1. Introduction
Natural products are widely used in the health field to prevent, relieve symptoms, and cure diseases. These products are obtained from medicinal plants rich in bioactive molecules that present biological activities of interest, such as antitumor, antimicrobial, antioxidant, analgesic, and wound healing potential. However, the use of bioactive compounds has some limitations, such as low stability, limited absorption, hydrophobicity, low bioavailability, and others [1].
Nanotechnology presents several tools that can be used in the pharmaceutical field as an ally for the development of new therapeutic systems [1]. Nanotechnology uses a variety of nanomaterials with different characteristics, such as size, shape, and composition, which at the nanometric scale (10−9 m) enables several applications such as cosmetics, food, and pharmaceutical use [1]. Nanoencapsulation of bioactive compounds can solve solubility and stability issues, as well as shield the bioavailability and unique properties of bioactive compounds present in plants [2].
Bixa orellana is a native tree from Brazil popularly known as annatto. The fruit is red, globular, and has ovoid capsules from which annatto oil and annatto extract can be obtained. It is commonly used as a natural dye, and it has been used as an insect repellent and sunscreen by traditional communities [3]. Several pharmacological studies have highlighted Bixa orellana’s therapeutic effects, encompassing photoprotective, antioxidant, antidiabetic, anti-inflammatory, antimicrobial, anticancer, and anthelmintic properties [4,5,6,7].
The use of annatto extracts and oil associated with nanostructures is observed both with the complete extract and the isolated bixin [2]. Due to its hydrophobic characteristic, the main nanostructures reported for association with annatto are solid lipid nanoparticles and nanoemulsions that allow its encapsulation inside the nanoparticle, promoting better dispersion and stability [8,9]. In addition to the encapsulation of oil/extract, the association of annatto can be incorporated in the green synthesis of metallic nanoparticles, for antimicrobial and antioxidant applications [10,11].
The present systematic review performed a study to evaluate the characteristics of the nanostructures in which the annatto oil or extract can be encapsulated, as well as its main biological applications and toxicity.
2. Methodology
2.1. Protocol and Registration
The present study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [12]. The protocol of this systematic review was registered in the International Prospective Register of Systematic Reviews [13] with registration number: CRD42023448167.
2.2. Eligibility Criteria
2.2.1. Inclusion Criteria
This systematic review used as inclusion criteria studies that performed nanostructuring of Bixa orellana oil or extract and evaluated biological activities or toxicological profile.
2.2.2. Exclusion Criteria
Studies were excluded for the following reasons: (I) Studies of non-nanostructured Bixa orellana. (II) Studies that performed nanostructuring of compounds isolated from Bixa orellana. (III) Studies that did not evaluate the parameters of morphology, hydrodynamic diameter, zeta potential, or polydispersion index of nanostructures. (IV) Studies that did not evaluate biological activity or toxicological profile of Bixa orellana nanostructures. (V) Review articles, book chapters, theses, letters, conference abstracts, and patents.
2.3. Information Sources and Search Strategy
Individual search strategies were designed for each of the following bibliographic databases: CINAHL, LILACS, Embase, FSTA, MEDLINE, ProQuest, PubMed, ScienceDirect, Scopus, and Web of Science (Supplementary Table S1). The search in the databases was conducted on 5 and 6 June 2023. No year of publication or language filter restrictions were applied. Duplicate references were eliminated using the reference management web application Rayyan® [14].
2.4. Study Selection
The articles were selected in two phases: screening of titles and abstracts (phase 1) and reading of full text (phase 2). For both phases, three pairs of authors (VS and NO; ED and PA; CR and GS) were formed to independently analyze the studies. In phase 1, the pairs reviewed the titles and abstracts of all references identified in the electronic databases and selected the articles that appeared to meet the inclusion criteria, using the systematic review web application (Rayyan®) [14]. In phase 2, the pairs analyzed the full text of the articles selected in phase 1 and excluded studies that did not meet the inclusion criteria (Supplementary Table S2). A third author was consulted if disagreements between the two initial reviewers were not resolved by consensus. With the selected articles, the pairs independently extracted the relevant data on materials and methods (plant part and extraction method used, extract characterization, nanoparticle type and production, storage conditions and stability analysis, model and evaluation of biological activity and/or toxicity, treatment regimen) and results (result of extract characterization, nanoparticle characterization, stability analysis, evaluation of biological activity and/or toxicity).
2.5. Risks of Bias and Quality in Individual Studies
The quality of the included articles was assessed by applying a 19-question form based on and adapted from the ARRIVE Guidelines (Supplementary Table S3) related to methodology and outcome measurement [15]. The questionnaire comprised 19 question options: YES for high study quality, NO for low study quality, UNCLEAR indicated that the information is present in the study but not entirely clear, NOT AVAILABLE when the information was absent, and NOT APPLICABLE when the question did not apply to the analyzed study. These questions were identified by the reviewers and used to classify the studies based on the proportion of YES responses according to the established criteria. Based on this assessment, the studies were categorized as high quality when they exhibited a rate above 70%, moderate quality in the 50% to 69% range, and low quality when they recorded a rate below 49%. A second questionnaire was administered for studies that underwent in vivo analysis using the 10-question SYRCLE RoB Toll to assess the risk of selection, performance, detection, attrition, and other biases (Supplementary Table S4) [16]. YES responses indicated a low risk of bias, NO indicated a high risk of bias, and UNCLEAR indicated that bias could not be attributed. The items were answered for each study by two reviewers individually, and disagreements were resolved by a third reviewer.
3. Results
3.1. Study Selection
A search conducted in the Scopus database on 6 June 2023, using the search string “(bixa OR bixaceae OR ‘bixa orellana’)” identified a total of 4271 documents. This substantial number of publications highlights the interest and relevance of topics related to Bixa orellana within the scientific community. Among these documents, the following regions/countries with the highest academic production stand out: Brazil > India > United States > China > United Kingdom > Mexico > Malaysia > Egypt > Spain > France. Notably, Brazil leads the production with 1018 publications, representing 23.83% of the total, followed by India with 17.91% of the contributions. This can be observed in Figure 1.
By applying a filter to the results using the search string “(bixa OR bixaceae OR “bixa orellana”) AND (“nano-material” OR “nano-scale material” OR “nano-scale structure” OR “nano-sized material” OR “nano-sized structure” OR “nano-structure” OR “nano-structured material” OR “nanoscale material” OR “nanoscale structure” OR “nanosized material” OR “nanosized structure” OR nanostructure OR “nanostructured material” OR nanostructures OR nanomaterial)”, to identify specific studies that addressed the relationship between annatto and NPs (nanoparticles), a total of 186 documents were retrieved. According to data from the Scopus database, the countries/regions that stood out in publications on the combination “bixaceae AND nanomaterial” were India (69 publications), Brazil (27 publications), and China (18 publications), among others.
By performing a bibliometric analysis of the results from the most recent search in the Scopus database, using VOSviewer 1.6.18 software, it was possible to identify 93 relevant terms. This survey was carried out considering the co-occurrence of at least five terms using “full count” settings. Figure 2 illustrates the interconnection of three distinct clusters among the most frequently used terms. Among these terms, the prominent interest of the scientific community in the topic evaluated by concepts such as plant extract, particle size, and nanoparticles stands out.
The data in Figure 1 and Figure 2 were acquired exclusively from the Scopus database to provide a comprehensive overview of the topics covered in this context. However, within this systematic review, a total of 708 studies were identified from different databases (24 from PubMed, 35 from Medline, 2 from LILACS, 8 from FSTA, 10 from CINAHL, 44 from Scopus, 57 from Web of Science, 143 from Science Direct, 20 from Embase and 365 from ProQuest) (Supplementary Table S1). After removing duplicates, 576 studies remained, and an assessment of ‘titles and abstracts’ resulted in the exclusion of 556 studies. The remaining 20 articles were subjected to a full-text analysis. This procedure resulted in the exclusion of 11 articles according to the exclusion criteria (Supplementary Table S2). In the end, 9 articles were retained and incorporated into this systematic review. A detailed flowchart of this process is displayed in Figure 3.
3.2. Characteristics of the Included Studies
All the included studies were research articles that explored the promising advantages with the association of nanostructures and annatto extract/oil. These studies were conducted in various countries: Brazil (n = 5), India (n = 1), Greece (n = 1), Cuba (n = 1), and Bangladesh (n = 1), with publication dates ranging from 2017 to 2023 and all of them being published in English. The main characteristics of these studies are summarized in Table 1.
The types of nanoparticles (NPs) utilized encompassed lipid nanoparticles (n = 3), nanofibers (n = 2), polymeric nanoparticles (n = 2), and metallic nanoparticles (n = 2). These nanoparticles were primarily characterized by their particle size (n = 5), zeta potential (n = 5), and polydispersity index (PdI) (n = 4) using dynamic light scattering and electrophoretic mobility. Additionally, several studies examined NP absorbance or undertook physicochemical characterization through UV-vis spectrophotometry. Furthermore, some studies also assessed encapsulation efficiency, pH, and morphology.
Six (n = 6) studies used Bixa orellana seed extract, with three (n = 3) using the maceration method with acetone, two (n = 2) using maceration with ethanol, and another two studies (n = 2) using water extraction. Two other studies used Bixa orellana oil and seed essential oil but did not specify the extraction methods.
Among all the included studies, all of them assessed biological activity in in vivo models, while only three (n = 3) evaluated both in vitro and in vivo activity, and one (n = 1) study assessed activity in an ex vivo model and human volunteers. In vitro studies evaluated cytotoxicity/proliferation (n = 6), photoprotective efficacy (n = 2), cell morphology and differentiation (n = 1), antileishmanial assay (n = 1), anti-amastigote (n = 1), and antimicrobial activity (n = 1). Animal models were considered adequate, and ethical committee approval was reported in all studies that utilized them.
3.3. Quality of Individual Studies
When evaluated according to the adapted ARRIVE Guidelines, as shown in Table 2, all included articles (n = 9) were classified as high quality. The majority of the articles clearly reported the source of annatto extract (n = 8), however, four did not present the extraction methodology applied (n = 4). Characterization of the annatto extract was conducted in five studies (n = 5). Among the selected articles, eight (n = 8) provided clear descriptions of the procedural steps in the experiments, seven studies (n = 7) detailed all characteristics of the animals and cells used, and some articles explicitly mentioned the presence of control groups (n = 7), relevant biological variables for the outcomes (n = 8), and indicated the absence of conflicts of interest (n = 9).
The assessment of bias risk based on the SYRCLE RoB Toll guidelines, applied to studies that presented in vivo activity, is summarized in Table 3. The evaluated studies did not clearly describe information regarding allocation, randomization, and blinding. The studies did not make it clear whether the animals were randomly housed and if the animals were randomly selected for outcome assessment. Two studies clearly indicated that the experimental groups were similar at the study’s outset. Only one study made it clear that allocations were adequately concealed, while two studies did not adequately address incomplete outcome data. Two of the studies were considered free from other issues that could result in a high risk of bias, and all the assessed studies were free from selective outcome reporting.
3.4. Synthesis of Results
The studies employed distinct types of extracts derived from Bixa orellana, with the majority utilizing the species’ oil (n = 4) and aqueous extract (n = 4), while solely one instance involved the employment of the powdered form of the species (n = 1). From this set of studies, three investigations presented a minimum of one extract characterization analysis, while two studies introduced a plurality of assays (n = 3). Four studies did not provide data regarding the characterization of the extract used to develop the nanoparticles (n = 4).
The research strategies for Bixa orellana nanostructures encompassed its application within various nanostructure types, including nanofibers (n = 2), solid-lipid nanoparticles (n = 1), nanostructured lipid carriers (n = 1), polymeric nanodispersions (n = 1), metallic nanoparticles (n = 2), chitosan nanoparticles (n = 1), and nanocochleates (n = 1). All nanostructures were minimally characterized in terms of size, measured in nanometers. Within the scope of the studies, the prevailing number of nanostructures exhibited dimensions below 200 nm (n = 5), whereas in the other cases, the sizes extended up to 500 nm.
The nanostructures were subjected to various biomedical applications analysis, including photoprotective effects (n = 2), effects against leishmaniasis (n = 2), and anti-inflammatory properties (n = 1). Two studies assessed both antimicrobial and anticancer effects within the same investigation. The assays regarding therapeutic effects encompassed diverse strategies, ranging from in vitro studies involving cells and/or animal investigations, with one conducted in rats and another in mice. Only one study evaluated the biological effect on human skin tissue. Solely one study evaluated the properties of the nanostructures to produce scaffolds for cultivated meat.
4. Discussion
To the best of our knowledge, this work is the first review addressing nanostructures containing raw annatto products (extracts and oils). The rich chemical matrix of natural products found in annatto can potentially enhance their biomedical effects due to the synergy among the various compounds [22,23]. Additionally, the use of raw materials derived from annatto can reduce the costs associated with the compound isolation process, which poses a challenge that may limit the large-scale production of biomedical products containing isolated compounds [24]. Therefore, this systematic review summarizes the literature on the physicochemical characteristics, biomedical efficacy, and toxicity of nanostructures containing extracts and oils obtained from annatto, with the aim of guiding further scientific investigations using these products.
The studies included in this review highlight the development of solid lipid nanoparticles, nanostructured lipid carriers, nanocochleates, polymeric nanodispersions, chitosan nanoparticles, nanofibers, and metallic nanoparticles (zinc and silver), using fixed and essential oils and aqueous and dry extracts from different annatto parts, such as bark, seeds, and leaves. Due to the heterogeneity of the nature of the nanostructures and annatto products used, this work is an attempt to provide a comprehensive view of the impacts of annatto products on the physicochemical characteristics of the nanostructures produced as well as the biological effectiveness of these nanomaterials.
4.1. Influence of Annatto Products on the Physicochemical Characteristics of Nanostructures
As described in Table 1, lipid nanostructures were the most used platform to nanostructure annatto products (33.3%; 3 of 9 studies included), followed by nanofibers (22.2%; 2 of 9 studies included), metallic (22.2%; 2 of 9 studies included), and polymeric (22.2%; 2 of 9 studies included). These nanostructures present very different physicochemical characteristics when compared.
Regarding size, lipid nanoparticles produced using fixed and essential annatto oils had sizes ranging from 52 to 200 nm [18,19]. The literature describes the size of these nanostructures as varying between 50 and 1000 nm [25]. Interestingly, in the study by Andréo-Filho (2017) [3], solid nanoparticles containing annatto oil ranged in size from 0.20 to 1.42 µm. This disparity in sizes is associated with the synthesis methodology used. The solid lipid nanoparticles containing annatto oil and produced using a high-energy homogenization process showed significantly smaller particle sizes (~0.20 µm) compared to the same formulation subjected to a low-energy process through heating (~1.42 µm) [3]. High-energy methodologies, such as ultrasonication and high-pressure homogenization, are widely used because they significantly reduce the size of nanoparticles. These methodologies focus on shear forces, cavitation, and collision of particles necessary to break larger particles into smaller ones [3,18].
Cellulose acetate nanofibers containing annatto seed extract ranged in size from 269 to 420 nm [9,21]. In these nanostructures, the presence of the extract had a relevant effect on size determination. The biomolecules bixin and norbixin are capable of interacting with the functional groups of cellulose, acting as plasticizers. This effect significantly reduced the size of the nanofibers from 468 to 269 nm and also reduced the stiffness of the nanofiber mesh compared to the formulation without the extract [9].
Annatto polymeric nanoparticles ranged in size from 53 to 340 nm. The interaction of annatto products with the nanoparticle components can impact the size of the nanostructure formed, as observed in the study by Ntohogian (2018) [20], in which it was possible to observe an increase from 250 to 287–340 nm in the size of chitosan nanoparticles in the presence of annatto dry extract.
Metallic nanoparticles are described as having particle sizes in the range of 10 to 100 nm. Among the studies included in the review, silver and zinc nanoparticles synthesized by green synthesis using annatto extract showed sizes ranging from 28.6 to 92.9 nm. In the study by Gharpure (2022) [11], the synthesis of zinc nanoparticles was carried out in a comparative way using extracts from the annatto seed husks, seeds, and leaves. These different extracts differ in their chemical composition, making it possible to observe that aromatic and vinylic compounds are present in aqueous extracts of the annatto leaf; the seeds contain phenolic and aromatic compounds, flavonoids, and fatty acids; phenolic compounds, steroids, flavonoids, carotenoids, fatty acids, and hydrocarbons are present in the seed husks [11].
These differences in chemical characterization were reflected in differences in the physicochemical characterization of the nanoparticles formed. Zinc nanoparticles synthesized with annatto seed extract presented an almond-like shape in the range of 220–440 nm, while nanoparticles synthesized from annatto leaves and seed husks presented a spherical shape in the range of 169–259 and 278–654 nm, respectively. Additionally, these nanoparticles also presented different surface areas, with the largest surface area observed in the nanoparticles synthesized using annatto leaf extract, followed by those synthesized with seed extract and the seed husks [11].
The zeta potential refers to the electrostatic charge of the nanoparticles’ surface. Systems that have a zeta potential of ± 30 mV are considered highly stable due to the repulsion effect between the charges [26]. Chitosan nanoparticles containing annatto extract showed a higher zeta potential value (47 mV) compared to the formulation without the extract (36 mV) [20]. Also, the presence of annatto oil in the formulation of nanostructured lipid carriers contributed to the stability of the system by increasing the modulus of the zeta potential [18]. Consequently, it was observed that nanocarriers containing annatto oil showed fewer variations in hydrodynamic size after 90 days of storage compared to nanocarriers without annatto oil [18]. In both formulations, not only the presence but also the concentration of annatto extract and oil determined changes in the zeta potential value, making it possible to observe that the increase in zeta potential was proportional to the increase in the concentration of annatto products [18,20].
The stability of a nanostructured system is also directly associated with the organization of its crystalline structure. In nanostructured lipid carriers, the interior of the nanoparticles presents a less organized crystalline structure compared to solid lipid nanoparticles. This low organization can increase the level of entrapment of the encapsulated bioactive compounds; on the other hand, it impairs the stability of the system [18]. The nanostructured lipid carriers containing annatto oil produced in the study by Ferreira et al. (2021) [18], showed greater fluidity and amorphous organization of the crystalline structure of their interior compared to carriers without the oil.
The development of nanostructures using annatto products is a tool capable of optimizing the interaction of annatto bioactive compounds with biological systems and enhancing their therapeutic activities [27]. Different biological applications were evaluated to determine the therapeutic efficacy and toxicity profile of the nanostructures containing annatto products. The results of these evaluations will be described below.
4.2. Therapeutic Efficacy Profile of the Nanostructures Containing Annatto Products
4.2.1. Photoprotective and Healing Activity
Solar irradiation by ultraviolet rays is the cause of more than 50% of skin tumors in humans [28]. Sun protection products consist of chemical agents, such as titanium and zinc dioxide, which protect against UV radiation by absorbing or reflecting the rays [3]. The association of sunscreen formulations with natural products that have photoprotective and antioxidant activities is relevant for increasing photoprotection. The presence of pigments, such as bixin and norbixin, guarantees photoprotective and antioxidant activities to annatto products. Bixin has already been described as capable of activating nuclear factor-E2-related factor 2 (NRF2) and triggering a series of protective responses against solar radiation-induced damage and carcinogenesis through DNA detoxification and repair mechanisms [29].
Nanoparticles can be used to encapsulate natural products and promote increased sun protection. This effect is a result of the higher surface area ratio promoted by the reduced size of the nanoparticles, where greater surface coverage is achieved [3]. The photoprotection of formulations is determined by the sun protection factor (SPF) value. SPF values between 2 and 12 result in minimal photoprotective activity, whereas SPF values between 12 and 30 result in moderate protective activity, but high photoprotective activity is found in formulations that present SPF values greater than 30 [20]. Chitosan nanoparticles containing 20, 40, and 60% natural and ultrafiltered annatto extract showed minimal photoprotective effect ranging in SPF values from 2.34 to 2.76 [20]. When associated with chemical compounds used in the formulation of sunscreens, the photoprotective activity is enhanced, as observed with solid lipid nanoparticles containing annatto oil and the compound octyl methoxycinnamate, presenting SPF values between 19.7 and 21.7 [3].
Nanofibers are a type of nanostructure quite relevant for therapeutic use in dermal wounds. The random alignment of the fibers results in the construction of a mesh similar to the structure of the extracellular matrix. This structure facilitates cell adhesion and diffusion of oxygen and nutrients, thus promoting cell proliferation and accelerating healing processes [9,21,30]. In the study by Santos et al. (2021), cellulose acetate nanofibers containing annatto seed extract facilitated the adhesion of fibroblasts to their surface in vitro and showed an immunomodulatory effect in vivo with inhibition of the recruitment of immune system cells and no scarring evidence at the implantation site 15 days after the intervention [9].
4.2.2. Leishmanicidal Activity
Leishmaniasis is an endemic disease of tropical regions of South and Central America, Asia, Africa, and Southern Europe. It is caused by infection with parasites of the genus Leishmania. Leishmaniasis is classified into visceral, cutaneous, mucosal, and post kala-azar dermal leishmaniasis. The infection begins after being bitten by mosquitoes of the Lutzomyia and Phlebotomus genus, in which the parasites in the promastigote form are transmitted to the human host, where they develop in the amastigote form, inside cells of the host’s phagocytic mononuclear system, mainly macrophages [31]. Treatments for leishmaniasis consist of meglumine antimoniate, sodium stibogluconate, amphotericin B, miltefosine, paromomycin, and pentamidine [31]. Despite being widely used, these drugs have high toxicity and high cost, and some are administered parenterally. These factors result in low adherence by patients [18].
Nanoparticles can direct antiparasitic molecules into organs rich in macrophages such as bone marrow, liver, lymph nodes, and kidneys, enhancing leishmanicidal activity. Furthermore, nanoparticles ranging in size from 50 to 500 nm are rapidly phagocytosed by macrophages, which may be interesting for the treatment of amastigotes of leishmania [32]. In the study by Ferreira et al. (2021) [18], nanostructured lipid carriers containing 2 and 4% annatto oil showed 70–90% leishmanicidal activity in reducing amastigote forms of L. major, being even significantly more effective than the standard drug meglumine antimoniate. Interestingly, free annatto oil did not have a leishmanicidal effect [18].
In the study by Machin et al. (2019) [19], nanocochleate formulations containing annatto essential oil showed lower in vitro leishmanicidal activity in amastigote forms of L. amazonensis compared to free annatto essential oil. Nevertheless, in an in vivo model, nanocochleates were able to reduce the size of lesions in animals infected with L. amazonensis to a greater extent compared to the free essential oil and in a similar way with animals treated with glucantime [19].
Nanocochleates are cylindrical lipid nanoparticles of the liposome family formed from the interaction between negative phospholipids and divalent cations [33]. The multilamellar characteristic of nanocochleates allows bioactive compounds to associate both externally and internally, being slowly released by desorption, dissolution, or diffusion [19]. The slow release of annatto essential oil may have impaired the in vitro leishmanicidal activity due to the short exposure time (48 h). In the in vivo test, the exposure time was longer, promoting the release of annatto essential oil and evidencing its leishmanicidal effectiveness [19].
4.2.3. Antioxidant and Antimicrobial Activity
Microbial resistance to the effect of antimicrobial drugs is a worldwide problem and has made the treatment of infections an arduous process [34]. Metallic nanoparticles have been described in the literature as a potential antimicrobial agent [34]. These nanoparticles can reduce the viability of bacteria through the production of reactive oxygen species and promoting changes in the structure of the microbial cell membrane, culminating in the leakage of intracellular content. Furthermore, Zinc ions (Zn2+) inhibit cellular active transport, inactivate enzymes, and disrupt amino acid metabolism. In fungi, metallic nanoparticles are responsible for the uncontrolled accumulation of cellular components and interference with cellular functioning [11].
The different bioactive compounds of annatto extract can be used in the green synthesis of metallic nanoparticles. Compounds such as flavonoids, steroids, and phenolic compounds act as chelating agents and form complexes with metal ions, stabilizing them and forming nanoparticles [11]. In addition to their role in the formation of nanoparticles, the bioactive compounds in the extract may present synergism in biological activities.
Zinc nanoparticles produced using annatto leaf, seed, and bark extract were tested for antibacterial activity on strains of Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Although the crude extracts of these products did not show antibacterial activity, when associated with zinc nanoparticles, the formulation was able to reduce the viability of strains of S. aureus, B. subtilis, and E. coli. However, it was not successful in reducing the viability of Penicillium sp., Aspergillus flavus, Fusarium oxysporum, and Rhizoctonia solani fungal strains [11]. Silver nanoparticles produced with aqueous extract of annatto seeds were tested for antibacterial activity against strains of S. aureus, E. coli, Shigella dysenteriae, and Shigella boydii but showed antibacterial activity restricted to only strains of S. dysenteriae [10].
It was also possible to observed that the physical-chemical parameters of nanostructures modulate interactions with cells. The process of cellular absorption and targeting between intracellular compartments is influenced by the size of the nanoparticle and its charge [18,35]. Zinc nanoparticles produced with extracts from annatto leaves showed smaller particle sizes and greater antibacterial activity against strains of S. aureus and B. subtilis, demonstrating that perhaps smaller nanoparticles are being more internalized in bacterial cells [11].
Oxidative stress is characterized by a high concentration of free radicals that promote changes in the structure and function of nucleic acids, lipids, and proteins. These changes are associated with the pathogenesis of neurodegenerative and cardiovascular diseases, and cancer [36]. The establishment of the oxidative stress state occurs due to the inefficiency of endogenous antioxidant mechanisms in neutralizing free radicals. In this sense, silver nanoparticles play a relevant antioxidant role because they have unpaired electrons capable of binding to free radicals and stabilizing them. This antioxidant activity was observed in the study by Maitra et al. (2023) [10], in which silver nanoparticles synthesized using annatto extract were 78.86% effective in reducing the DPPH radical [10].
Additionally, the association of bioactive compounds from the extract used in green synthesis on the structure of metal nanoparticles is a phenomenon already described in the literature, as demonstrated on the FTIR results found by Sharma et al. (2024) [37]. In this sense, the result found in the study by Maitra et al. (2023) can also be associated with the annatto extract itself, which in the study by Quiroz et al. (2019) showed antioxidant activity in the ABTS (2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)), FRAP (Ferric-Reducing Antioxidant Power) and DPPH tests [38].
4.2.4. Antitumoral Activity
Cancer is characterized by the occurrence of mutations associated with the activation of proto-oncogenes and the inactivation of tumor suppressor genes. These alterations lead to disordered proliferative rates in cells and other changes favoring tumor progression, such as immune system evasion, energy metabolism reprogramming, heightened angiogenesis, and the occurrence of metastases [39]. According to the Global Cancer Observatory, approximately 21.9 million new cases of cancer are expected to be reported worldwide by 2025 [40]. The shared characteristics between healthy and tumor cells, coupled with the high heterogeneity expressed in tumor cells, pose a significant challenge in cancer treatment.
Several studies have elucidated the potential of metallic nanoparticles in reducing the viability of tumor cells [41]. The dissolution of metals from nanoparticles can induce changes in mitochondrial functioning, DNA damage, increased intracellular concentrations of reactive oxygen species, and rupture of the cell membrane [42]. In a study conducted by Maitra (2023) [10], silver nanoparticles synthesized using the aqueous extract of annatto seed demonstrated the ability to inhibit the proliferation of MCF-7 breast cancer cells in a dose-dependent manner, exhibiting a maximum inhibition of 68.3% at a concentration of 31.25 µg/mL.
While zinc nanoparticles are described in the literature as potential antitumor agents, with reported efficacy in reducing the viability of HCT-116 colon cancer cells [43], a study by Gharpure (2022) [11] observed that zinc nanoparticles synthesized using extracts from the bark, seeds, and leaves of annatto did not exhibit antitumor activity in HCT-116 colon cancer cells.
4.3. Toxicity of Annatto Nanostructures
The widespread use of products obtained from annatto in the food industry and in traditional medicine reveals signs of their safety. Analyzing the composition of annatto extracts, it is possible to observe that bioactive compounds with high potential for toxicity, such as alkaloids, saponins, and glycosides, are present in low concentrations, while compounds with low potential for toxicity, such as terpenoids, flavonoids, and phenolics are present in high concentrations [44]. The clinical study by Zegarra et al. (2007) administered 250 mg of powdered extracts of annatto leaves to participants three times a day for 6 months and no harmful adverse effects were observed, evidencing the biocompatibility of these extracts [45].
One of the bases of nanotechnology is the principle of improvements of nanomaterials to present new physicochemical properties to the same materials structured on larger scales. These new properties may favor the biological activities of the compounds, but may also change their toxicological profile. Mechanisms of nanoparticle toxicity are associated with the production of reactive oxygen species, DNA damage, changes in the structure of proteins and cellular macromolecules, and cell membrane damage [46].
The studies included in this review carried out toxicity tests in vitro (n = 6), in vivo (n = 3), ex vivo (n = 1), and clinical (n = 1) models of annatto-containing nanostructures. In vitro tests were conducted with cell cultures of fibroblasts, keratinocytes (HaCaT), macrophages (from BALB/c mice), myoblasts (C2C12), and endothelial cells (HUVE). Significant cytotoxic effects were observed only in macrophages treated with nanocochleates containing annatto essential oil, presenting a CC50 value of 94.6 µg/mL, and in fibroblasts and keratinocytes treated with nanostructured lipid carriers containing 2 and 4% of annatto oil, which presented IC50 values of 153.64–181.93 µg/mL and 123.37–257.11 µg/mL in fibroblasts and keratinocytes, respectively [18,19].
In in vivo models, Wistar rats treated with cellulose acetate nanofibers and BALB/c mice treated with 30 mg/kg of nanocochleates containing annatto essential oil did not show clinical, biochemical, and histopathological signs of toxicity [9,19]. In the study by Carvalho et al. (2023), 1 to 10 mg/kg of nanoprecipitates containing annatto oil were injected intramuscularly in Wistar rats; only the 10 mg/kg dose showed toxic effects with associated histopathological changes in the animal’s muscles, with the appearance of areas of necrosis, infiltration of leukocytes and changes in the morphology of muscle fibers [17].
In the study by Andreo-Filho et al. (2017), solid lipid nanoparticles were topically applied to human skin at a concentration of 2 mg/cm2 and no changes in cell metabolism and skin cell morphology were observed. However, these biocompatibility results are limited to the small number of three participants in the study [3].
5. Considerations for the Nanostructuring of Annatto Products
Several factors can be considered to determine the choice of the ideal nanostructure for encapsulating annatto products. One of the main factors is the physical and chemical characteristics of the product. In the case of nonpolar products such as fixed and essential oils of annatto, lipid nanoparticles can provide a structural organization that favors greater stability, better encapsulation efficiency and better dispersion of the oil in aqueous media [47]. In the case of hydrophilic extracts, polar nanostructures, such as polymeric nanoparticles, can better encapsulate the bioactive compounds of the extract [48,49]. Among them, nanofibers have a high surface area that enhances the encapsulation efficiency of hydrophilic extracts and allows greater interaction with the biological components associated with the therapeutic effect [20]. Additionally, the choice of the ideal nanoparticle also depends on the context of the biological application, route of administration and biological targets to be achieved, which determine the physicochemical characteristics of the nanostructures that will best carry the annatto products.
The incorporation of annatto products into nanoparticles promotes the aggregation of value to these products by enhancing their biological activities and optimizing their physicochemical characteristics. These gains favor the development of effective and stable biomedical products, characteristics that are absent or incipient in the crude extract or oil [1]. Although the nanostructuring process involves the use of advanced technologies for production and characterization and consequently costs, the gains in efficacy, bioavailability and increased quality of the final product can outweigh these expenses [50]. In this sense, the experimental design for the development of pharmaceutical products must be aligned with the principles of translational research in which industrial reality scenarios are evaluated to make production scaling viable.
One of the most challenging aspects for the reproducibility and scaling of biomedical products using plant-based raw materials is the variations in chemical composition due to environmental conditions. This can make the levels of compounds responsible for the biological activities of the material inconsistent and, consequently, variations in biological response can occur [51]. The characterization and detection of the compounds responsible for the biological activities of annatto products is of great importance to promote their use in the development of pharmaceutical products. This knowledge can favor the establishment of rigorous quality control methodologies through the standardization of cultivation, extraction, and storage conditions of annatto products in order to contribute to the conservation of the compounds responsible for biological activities and the reproducibility of therapeutic activities [52].
6. Limitations
Limitations were observed in the development of this systematic review. The development of nanostructures with annatto extracts and oils is an approach that is still little explored in the scientific literature, making it difficult to find articles that meet the inclusion criteria. Additionally, the studies included are heterogeneous concerning the part of the plant used, extraction methodologies, and types of nanostructures developed. This scenario allows only partial comparisons between the efficacy and safety results found in different studies.
7. Conclusions
The main findings of the studies included in this review demonstrate that annatto extracts and oils can be used in the development of lipid, polymeric, metallic, and nanofiber nanostructures. The incorporation of annatto extracts and oils into the nanostructure optimized some physicochemical characteristics of the formulation, such as size reduction, increase in zeta potential modulus, and crystalline organization of the nanostructure. These improvements are capable of enhancing the therapeutic effects of annatto compounds, as demonstrated in the results of biological analyses in which the nanostructures showed leishmanicidal, photoprotective, antioxidant, antimicrobial, immunomodulatory efficacy, and tissue regeneration potential with no or low toxic effects in in vitro, in vivo, and clinical models. Therefore, the present work supports that the production of annatto extracts and oils nanostructures is a relevant approach to the development of new technologies for biomedical applications.
N.O.M., C.R.d.S., E.B.d.O.D., P.L.A. and G.d.O.S.: Methodology, Formal analysis, Investigation, Writing—Original Draft, Writing—Review & Editing. V.R.P.d.S.: Conceptualization, Methodology, Investigation, Formal analysis, Writing—Original Draft, Writing—Review & Editing, Supervision. M.L.B.C. and G.A.J.: Conceptualization, Methodology, Investigation, Formal analysis, Writing—Original Draft, Writing—Review & Editing, Supervision, Project administration, Funding acquisition. All authors have read and agreed to the published version of the manuscript.
The authors declare no conflicts of interest.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Enlarge this image.Figure 1. Number of publications listed in Scopus database by regions or countries. Data were obtained on 6 June 2023.
Enlarge this image.Figure 2. Bibliometric study of publications listed in the Scopus database, with MeSH terms for bixaceae and nanomaterials, using the VOSviewer program (version 1.6.18), with at least five co-occurrences and full count configurations. Data were obtained on 8 August 2023.
Summary of descriptive characteristics of the included studies.
| Study | Intervention | Population | Outcomes | |||
|---|---|---|---|---|---|---|
| Author, Year/Country | Fruit Species/Extraction Method | Fruit Characterization Analysis | Nanoparticle Type/Production Methodology | Nanoparticle Characterization | Biological Activity Assessed/Model/Treatment Regimen | Results |
| Andréo-Filho et al., 2017/Brazil | Bixa orellana oil | Not evaluated | - Solid-Lipid Nanoparticles (SLN) | OMC (P1): | - Photoprotective efficacy (SPF) in vitro (L) with 250–450 nm wavelength range; | |
| Carvalho et al., 2023/Brazil | Bixa orellana oil (commercial) | 72.6 ± 0.9% of δ-tocotrienol | - Polymeric Bixa orellana Nanodispersions (PBN); | PBN: | - Toxicity in 3-week-old Wistar rats (n = 4); | No clinical signs of PBN toxicity 4 days after injection; |
| Ferreira et al., 2021/Brazil | Bixa Orellana oil (commercial) | Not evaluated | - Nanostrutured lipid carrier (NLC) loaded with 2 and 4% (w/w) of annatto oil and 10% of CP (NLCcp2 and NLCcp4) or 10% of MM (NLCmm2 and NLCmm4) | NLCmm (2 and 4): | Cytotoxicity on BALB/c 3T3 (fibroblasts) and HaCaT (keratinocytes) cells (MTT 24 h); | |
| Gharpure et al., 2022/India | Bixa Orellana/Leaves (BL), Seeds (BS) and Seed Coats (BSc) extracts/Boiling Water extraction | - Presence of flavonoids, phenolics, and glycosides on BL, BS and BSc (UV-Vis); | - Zinc Nanoparticles (ZnO) | 341–353 nm (L-ZnO)/378–373 nm (S-ZnO)/327–337 nm (Sc-ZnO) before and after calcination, respectively (UV-vis absorption); | Anti-bacterial activity in vitro on S. aureus, B. subtilis, E. coli, and P. aeruginosa) (Well-based diffusion); | No anti-bacterial activity of free BL, BS, BSc, and calcinated ZnO nanoparticles; |
| Machin et al., 2019/Cuba | Bixa orellana/Seed essencial oil (AEO) | Not evaluated | - Nanocochleate loaded with AEO (NCA) prepared with purified phospholipids from soy lecithin | NCA: | - Anti-amastigote activity in vitro (L. amazonensis internalized in peritoneal macrophages from BALB/c mice) (Staining with Giemsa); | |
| Maitra et al., 2023/Bangladesh | Bixa orellana/Aqueous Seed extract | Peaks at 2930, 1615 and 1383 cm −1 (FTIR). | - Silver Nanoparticles (AgNPs) | AgNPs: | - Antioxidant activity (DPPH scavenging); | 50.76, 62.78 and 78.86% DPPH radical scavenging of AgNPs 50, 100, and 200 µg/mL, respectively; |
| Ntohogian et al., 2018/Greece | Bixa orellana/powder and ultrafiltrated (UF) (commercial) | Presence of bixin and norbixin on annatto and UF annatto (FTIR peaks of 3400, 2920, 2855, 1690, 1603 and 1149 cm−1) | - Chitosan Nanoparticles (CS) loaded with 20, 40, and 60% (w/w) of annatto (CNA) and UF annatto (CNAF) | Blank: | Cytotoxicity on HUVE cell line (MTT 24 h); | No alterations on nanoparticles morphology with different annatto %; |
| Santos et al., 2021/Brazil | Bixa orellana/seed extract/Solvent extraction (ethanol) | Presence of bixin and norbixin (UV-vis peaks of 353, 430, 455, and 482 nm and FTIR peaks of 1038, 989, and 845 cm−1) | - Cellulose Acetate/Annatto Nanofibers (CAAN) | CAAN: | Cytotoxicity by HET-CAM test (5 min) | 2.12 ± 0.24% of annatto global extraction yield; |
| Santos et al., 2023/Brazil | Bixa orellana seed extract/Solvent extraction (ethanol) | Bixin and norbixin absorption band at 410 nm (UV-vis spectroscopy) | - Cellulose Acetate/Annatto Nanofibers (CAAN) | CAAN: | Cytotoxicity (MTT 2 and 7 days), cell morphology (SEM) and differentiation analysis (RT-qPCR) on myoblast cells (C2C12) | 50 ± 3° contact angle of CAAN with water = hydrophilic property; CAAN presented smooth and homogenous porous interconnections mats; |
Legend: BJH = Teller, Brunauer, Emmett, Barrett, Joyner, Halenda; CC50 = 50% cytotoxic concentration; CP = cetyl palmitate; CPK = creatine kinase; DLS = Dynamic Light Scattering; DPPH = 2,2-Diphenyl-1-picrylhydrazyl; EDS = field emission scanning electron microscopy; EDX = Energy-dispersive X-ray spectroscopy; EE = Entrapment Efficiency; FESEM = Field Emission Scanning Electron Microscopy; FTIR = Fourier Transformation Infrared Spectroscopy; GC-MS = Gas Chromatography–Mass Spectrometry; HR-MS = High Resolution Mass Spectrometry; IC50 = half maximal inhibitory concentrations; LDH = Lactate dehydrogenase; MM = myristyl myristate; MPT-FLIM = Multiphoton Tomography with Fluorescence Lifetime Imaging Microscopy; MTS = 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium; MTT = 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide; NMR = Nuclear Magnetic Resonance spectroscopy; PdI = Polydispersivity index; PL = Photoluminescence; PLA = poly(L-lactide); PS = particle size; OMC = octyl methoxycinnamate; TEM = Transmission Electron Microscopy; TPP = Tripolyphosphate; UV-vis = Ultraviolet–visible spectroscopy; XRD = X-ray diffractometry; ZP = zeta potential;
Results of the quality analysis of the included studies.
| Quality Analysis | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Author | Year | Experimental Design/Scientific Report | Results | Ethical Statement | ||||||||||||||||
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | ||
| Andréo-Filho et al. [ | 2017 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Carvalho et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Ferreira et al [ | 2021 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Gharpure et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Machin et al. [ | 2019 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Maitra et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Ntohogian et al. [ | 2018 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Santos et al. [ | 2021 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Santos et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | - | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
[Image omitted. Please see PDF.] High quality, [Image omitted. Please see PDF.] Low quality, [Image omitted. Please see PDF.] Some concerns, [Image omitted. Please see PDF.] No information, - Not applicable.
Results of the risk of bias using Syrcle’s risk of bias of the in vivo included studies.
| Syrcle’s Risk of Bias | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Author | Year | Questions | |||||||||
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | ||
| Carvalho et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Maitra et al. [ | 2023 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
| Santos et al. [ | 2021 | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] | [Image omitted. Please see PDF.] |
[Image omitted. Please see PDF.] Low risk, [Image omitted. Please see PDF.] High risk, [Image omitted. Please see PDF.] Unclear.
Supplementary Materials
The following supporting information can be downloaded at:
References
1. Majumdar, M.; Shivalkar, S.; Pal, A.; Verma, M.L.; Sahoo, A.K.; Roy, D.N. Nanotechnology for Enhanced Bioactivity of Bioactive Compounds. Biotechnological Production of Bioactive Compounds; Elsevier: Amsterdam, The Netherlands, 2020; pp. 433-466.
2. Enayati, A.; Rezaei, A.; Falsafi, S.R.; Rostamabadi, H.; Malekjani, N.; Akhavan-Mahdavi, S.; Kharazmi, M.S.; Jafari, S.M. Bixin-Loaded Colloidal Nanodelivery Systems, Techniques and Applications. Food Chem.; 2023; 412, 135479. [DOI: https://dx.doi.org/10.1016/j.foodchem.2023.135479] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/36709686]
3. Andréo-Filho, N.; Bim, A.V.K.; Kaneko, T.M.; Kitice, N.A.; Haridass, I.N.; Abd, E.; Santos Lopes, P.; Thakur, S.S.; Parekh, H.S.; Roberts, M.S. et al. Development and Evaluation of Lipid Nanoparticles Containing Natural Botanical Oil for Sun Protection: Characterization and In Vitro and In Vivo Human Skin Permeation and Toxicity. Ski. Pharmacol. Physiol.; 2018; 31, pp. 1-9. [DOI: https://dx.doi.org/10.1159/000481691]
4. Muddapur, U.M.; Turakani, B.; Jalal, N.A.; Ashgar, S.S.; Momenah, A.M.; Alshehri, O.M.; Mahnashi, M.H.; Shaikh, I.A.; Khan, A.A.; Dafalla, S.E. Phytochemical Screening of Bixa orellana and Preliminary Antidiabetic, Antibacterial, Antifibrinolytic, Anthelmintic, Antioxidant, and Cytotoxic Activity against Lung Cancer (A549) Cell Lines. J. King Saud Univ.-Sci.; 2023; 35, 102683. [DOI: https://dx.doi.org/10.1016/j.jksus.2023.102683]
5. Kusmita, L.; Franyoto, Y.D.; Mutmainah, M.; Puspitaningrum, I.; Nurcahyanti, A.D.R. Bixa orellana L. Carotenoids: Antiproliferative Activity on Human Lung Cancer, Breast Cancer, and Cervical Cancer Cells In Vitro. Nat. Prod. Res.; 2022; 36, pp. 6421-6427. [DOI: https://dx.doi.org/10.1080/14786419.2022.2036144] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35133226]
6. Medina-Flores, D.; Ulloa-Urizar, G.; Camere-Colarossi, R.; Caballero-García, S.; Mayta-Tovalino, F.; del Valle-Mendoza, J. Antibacterial Activity of Bixa orellana L.(Achiote) against Streptococcus mutans and Streptococcus Sang. Asian Pac. J. Trop. Biomed.; 2016; 6, pp. 400-403. [DOI: https://dx.doi.org/10.1016/j.apjtb.2016.03.005]
7. Ashraf, A.; Ijaz, M.U.; Muzammil, S.; Nazir, M.M.; Zafar, S.; Zihad, S.M.N.K.; Uddin, S.J.; Hasnain, M.S.; Nayak, A.K. The Role of Bixin as Antioxidant, Anti-Inflammatory, Anticancer, and Skin Protecting Natural Product Extracted from Bixa orellana L. Fitoterapia; 2023; 169, 105612. [DOI: https://dx.doi.org/10.1016/j.fitote.2023.105612] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/37454777]
8. Selvakumar, V.; Chelliah, R.; Barathikannan, K.; Elahi, F.; Rubab, M.; Sanyal, S.; Yeon, S.J.; Oh, D.H. Seed-Based Oil in Nanomaterials Synthesis and Their Role in Drug Delivery and Other Applications. Secondary Metabolites Based Green Synthesis of Nanomaterials and Their Applications; Springer Nature: Singapore, 2022; [DOI: https://dx.doi.org/10.1007/978-981-99-0927-8_13]
9. Dos Santos, A.E.A.; Dos Santos, F.V.; Freitas, K.M.; Pimenta, L.P.S.; de Oliveira Andrade, L.; Marinho, T.A.; de Avelar, G.F.; da Silva, A.B.; Ferreira, R.V. Cellulose Acetate Nanofibers Loaded with Crude Annatto Extract: Preparation, Characterization, and In Vivo Evaluation for Potential Wound Healing Applications. Mater. Sci. Eng. C; 2021; 118, 111322. [DOI: https://dx.doi.org/10.1016/j.msec.2020.111322]
10. Maitra, B.; Khatun, M.H.; Ahmed, F.; Ahmed, N.; Kadri, H.J.; Rasel, M.Z.U.; Saha, B.K.; Hakim, M.; Kabir, S.R.; Habib, M.R. Biosynthesis of Bixa orellana Seed Extract Mediated Silver Nanoparticles with Moderate Antioxidant, Antibacterial and Antiproliferative Activity. Arab. J. Chem.; 2023; 16, 104675. [DOI: https://dx.doi.org/10.1016/j.arabjc.2023.104675]
11. Gharpure, S.; Yadwade, R.; Ankamwar, B. Non-Antimicrobial and Non-Anticancer Properties of ZnO Nanoparticles Biosynthesized Using Different Plant Parts of Bixa Orellana. ACS Omega; 2022; 7, pp. 1914-1933. [DOI: https://dx.doi.org/10.1021/acsomega.1c05324]
12. Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D.G. The PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. Ann. Intern. Med.; 2009; 151, pp. 264-269. [DOI: https://dx.doi.org/10.7326/0003-4819-151-4-200908180-00135]
13. Page, M.J.; Shamseer, L.; Tricco, A.C. Registration of Systematic Reviews in PROSPERO: 30,000 Records and Counting. Syst. Rev.; 2018; 7, 32. [DOI: https://dx.doi.org/10.1186/s13643-018-0699-4] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29463298]
14. Ouzzani, M.; Hammady, H.; Fedorowicz, Z.; Elmagarmid, A. Rayyan—A Web and Mobile App for Systematic Reviews. Syst. Rev.; 2016; 5, 210. [DOI: https://dx.doi.org/10.1186/s13643-016-0384-4]
15. Du Sert, N.P.; Hurst, V.; Ahluwalia, A.; Alam, S.; Avey, M.T.; Baker, M.; Browne, W.J.; Clark, A.; Cuthill, I.C.; Dirnagl, U. The ARRIVE Guidelines 2019: Updated Guidelines for Reporting Animal Research. bioRxiv; 2019; [DOI: https://dx.doi.org/10.1101/703181]
16. Hooijmans, C.R.; Rovers, M.M.; De Vries, R.B.M.; Leenaars, M.; Ritskes-Hoitinga, M.; Langendam, M.W. SYRCLE’s Risk of Bias Tool for Animal Studies. BMC Med. Res. Methodol.; 2014; 14, 43. [DOI: https://dx.doi.org/10.1186/1471-2288-14-43] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24667063]
17. de Oliveira Carvalho, H.; Sauma, A.L.R.; do Nascimento, A.L.; de Lima Teixeira, A.V.T.; Gonçalves, D.E.S.; Gomes, L.; da Costa Furtado, G.; da Silva, H.R.; de Souza, G.C.; Pereira, A.C.M. Intramuscular Compatibility of an Injectable Anti-Inflammatory Nanodispersion from a Standardized Bixa orellana Oil (Chronic®): A Toxicological Study in Wistar Rats. Inflammopharmacology; 2023; 31, pp. 877-886. [DOI: https://dx.doi.org/10.1007/s10787-023-01162-8] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/36853419]
18. Ferreira, M.A.; de Almeida Júnior, R.F.; Onofre, T.S.; Casadei, B.R.; Farias, K.J.S.; Severino, P.; de Oliveira Franco, C.F.; Raffin, F.N.; de Lima e Moura, T.F.A.; de Melo Barbosa, R. Annatto Oil Loaded Nanostructured Lipid Carriers: A Potential New Treatment for Cutaneous Leishmaniasis. Pharmaceutics; 2021; 13, 1912. [DOI: https://dx.doi.org/10.3390/pharmaceutics13111912] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34834327]
19. Machín, L.; Tamargo, B.; Piñón, A.; Atíes, R.C.; Scull, R.; Setzer, W.N.; Monzote, L. Bixa orellana L.(Bixaceae) and Dysphania ambrosioides (L.) Mosyakin & Clemants (Amaranthaceae) Essential Oils Formulated in Nanocochleates against Leishmania amazonensis. Molecules; 2019; 24, 4222. [DOI: https://dx.doi.org/10.3390/molecules24234222]
20. Ntohogian, S.; Gavriliadou, V.; Christodoulou, E.; Nanaki, S.; Lykidou, S.; Naidis, P.; Mischopoulou, L.; Barmpalexis, P.; Nikolaidis, N.; Bikiaris, D.N. Chitosan Nanoparticles with Encapsulated Natural and UF-Purified Annatto and Saffron for the Preparation of UV Protective Cosmetic Emulsions. Molecules; 2018; 23, 2107. [DOI: https://dx.doi.org/10.3390/molecules23092107]
21. dos Santos, A.E.A.; Cotta, T.; Santos, J.P.F.; Camargos, J.S.F.; do Carmo, A.C.C.; Alcântara, E.G.A.; Fleck, C.; Copola, A.G.L.; Nogueira, J.M.; Silva, G.A.B. Bioactive Cellulose Acetate Nanofiber Loaded with Annatto Support Skeletal Muscle Cell Attachment and Proliferation. Front. Bioeng. Biotechnol.; 2023; 11, 1116917. [DOI: https://dx.doi.org/10.3389/fbioe.2023.1116917]
22. Caesar, L.K.; Cech, N.B. Synergy and Antagonism in Natural Product Extracts: When 1 + 1 Does Not Equal 2. Nat. Prod. Rep.; 2019; 36, pp. 869-888. [DOI: https://dx.doi.org/10.1039/C9NP00011A]
23. da Silva, A.K.A.; dos Santos, C.R.; Carneiro, M.L.B.; Joanitti, G.A.; Luz, G.V.S.; Rosa, S.S.R.F.; Pinheiro, W.M.; Rosa, M.F.F.; Abreu, P.R.A.; Fukuoka, F.M.G. et al. Chapter 1—Bixa orellana L. and Its Implications in Human Health: Perspectives and New Trends. Studies in Natural Products Chemistry; Atta-ur-Rahman,. Elsevier: Amsterdam, The Netherlands, 2023; Volume 77, pp. 1-36. ISBN 1572-5995
24. Zhang, Q.W.; Lin, L.G.; Ye, W.C. Techniques for Extraction and Isolation of Natural Products: A Comprehensive Review. Chin. Med.; 2018; 13, 20. [DOI: https://dx.doi.org/10.1186/s13020-018-0177-x] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29692864]
25. Akbari, J.; Saeedi, M.; Ahmadi, F.; Hashemi, S.M.H.; Babaei, A.; Yaddollahi, S.; Rostamkalaei, S.S.; Asare-Addo, K.; Nokhodchi, A. Solid Lipid Nanoparticles and Nanostructured Lipid Carriers: A Review of the Methods of Manufacture and Routes of Administration. Pharm. Dev. Technol.; 2022; 27, pp. 525-544. [DOI: https://dx.doi.org/10.1080/10837450.2022.2084554] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35635506]
26. Clogston, J.D.; Patri, A.K. Zeta Potential Measurement. Characterization of Nanoparticles Intended for Drug Delivery; Humana Press: Totowa, NJ, USA, 2011; pp. 63-70.
27. Teja, P.K.; Mithiya, J.; Kate, A.S.; Bairwa, K.; Chauthe, S.K. Herbal Nanomedicines: Recent Advancements, Challenges, Opportunities and Regulatory Overview. Phytomedicine; 2022; 96, 153890. [DOI: https://dx.doi.org/10.1016/j.phymed.2021.153890] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35026510]
28. Passeron, T.; Krutmann, J.; Andersen, M.L.; Katta, R.; Zouboulis, C.C. Clinical and Biological Impact of the Exposome on the Skin. J. Eur. Acad. Dermatol. Venereol.; 2020; 34, pp. 4-25. [DOI: https://dx.doi.org/10.1111/jdv.16614] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32677068]
29. Rojo De La Vega, M.; Krajisnik, A.; Zhang, D.D.; Wondrak, G.T. Targeting NRF2 for Improved Skin Barrier Function and Photoprotection: Focus on the Achiote-Derived Apocarotenoid Bixin. Nutrients; 2017; 9, 1371. [DOI: https://dx.doi.org/10.3390/nu9121371]
30. Zhang, X.; Meng, Y.; Gong, B.; Wang, T.; Lu, Y.; Zhang, L.; Xue, J. Electrospun Nanofibers for Manipulating Soft Tissue Regeneration. J. Mater. Chem. B; 2022; 10, pp. 7281-7308. [DOI: https://dx.doi.org/10.1039/D2TB00609J]
31. Kumari, D.; Perveen, S.; Sharma, R.; Singh, K. Advancement in Leishmaniasis Diagnosis and Therapeutics: An Update. Eur. J. Pharmacol.; 2021; 910, 174436. [DOI: https://dx.doi.org/10.1016/j.ejphar.2021.174436]
32. de Souza, A.; Marins, D.S.S.; Mathias, S.L.; Monteiro, L.M.; Yukuyama, M.N.; Scarim, C.B.; Löbenberg, R.; Bou-Chacra, N.A. Promising Nanotherapy in Treating Leishmaniasis. Int. J. Pharm.; 2018; 547, pp. 421-431. [DOI: https://dx.doi.org/10.1016/j.ijpharm.2018.06.018]
33. Govardhane, S.; Shende, P. Phthalocyanine-Based Glucose-Responsive Nanocochleates for Dynamic Prevention of β-Cell Damage in Diabetes. J. Liposome Res.; 2024; 34, pp. 44-59. [DOI: https://dx.doi.org/10.1080/08982104.2023.2209642]
34. Gattu, R.; Ramesh, S.S.; Ramesh, S. Role of Small Molecules and Nanoparticles in Effective Inhibition of Microbial Biofilms: A Ray of Hope in Combating Microbial Resistance. Microb. Pathog.; 2024; 188, 106543. [DOI: https://dx.doi.org/10.1016/j.micpath.2024.106543]
35. De Macedo, E.F.; Santos, N.S.; Nascimento, L.S.; Mathey, R.; Brenet, S.; de Moura, M.S.; Hou, Y.; Tada, D.B. Interaction between Nanoparticles, Membranes and Proteins: A Surface Plasmon Resonance Study. Int. J. Mol. Sci.; 2022; 24, 591. [DOI: https://dx.doi.org/10.3390/ijms24010591]
36. Pisoschi, A.M.; Pop, A.; Iordache, F.; Stanca, L.; Predoi, G.; Serban, A.I. Oxidative Stress Mitigation by Antioxidants-an Overview on Their Chemistry and Influences on Health Status. Eur. J. Med. Chem.; 2021; 209, 112891. [DOI: https://dx.doi.org/10.1016/j.ejmech.2020.112891] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33032084]
37. Sharma Yashwant Singh Parmar, V.; Thakur Yashwant Singh Parmar, S.; Singh Parmar, Y. Evaluation of Antimicrobial and Antioxidant Effect of Biosynthesized Silver Nanoparticles from Sapindus Mukorossi Pericarp Extract; Research Square: Durham, NC, USA, 2024; [DOI: https://dx.doi.org/10.21203/rs.3.rs-3836555/v1]
38. Quintero Quiroz, J.; Naranjo Duran, A.M.; Silva Garcia, M.; Ciro Gomez, G.L.; Rojas Camargo, J.J. Ultrasound-Assisted Extraction of Bioactive Compounds from Annatto Seeds, Evaluation of Their Antimicrobial and Antioxidant Activity, and Identification of Main Compounds by LC/ESI-MS Analysis. Int. J. Food Sci.; 2019; 2019, 3721828. [DOI: https://dx.doi.org/10.1155/2019/3721828] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31392206]
39. Khursheed, R.; Dua, K.; Vishwas, S.; Gulati, M.; Jha, N.K.; Aldhafeeri, G.M.; Alanazi, F.G.; Goh, B.H.; Gupta, G.; Paudel, K.R. Biomedical Applications of Metallic Nanoparticles in Cancer: Current Status and Future Perspectives. Biomed. Pharmacother.; 2022; 150, 112951. [DOI: https://dx.doi.org/10.1016/j.biopha.2022.112951] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35447546]
40. Soerjomataram, I.; Bray, F. Planning for Tomorrow: Global Cancer Incidence and the Role of Prevention 2020–2070. Nat. Rev. Clin. Oncol.; 2021; 18, pp. 663-672. [DOI: https://dx.doi.org/10.1038/s41571-021-00514-z] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34079102]
41. da Silva, P.B.; Machado, R.T.A.; Pironi, A.M.; Alves, R.C.; De Araújo, P.R.; Dragalzew, A.C.; Dalberto, I.; Chorilli, M. Recent Advances in the Use of Metallic Nanoparticles with Antitumoral Action-Review. Curr. Med. Chem.; 2019; 26, pp. 2108-2146. [DOI: https://dx.doi.org/10.2174/0929867325666180214102918]
42. Alphandéry, E. Natural Metallic Nanoparticles for Application in Nano-Oncology. Int. J. Mol. Sci.; 2020; 21, 4412. [DOI: https://dx.doi.org/10.3390/ijms21124412]
43. Berehu, H.M.; Anupriya, S.; Khan, M.I.; Chakraborty, R.; Lavudi, K.; Penchalaneni, J.; Mohapatra, B.; Mishra, A.; Patnaik, S. Cytotoxic Potential of Biogenic Zinc Oxide Nanoparticles Synthesized From Swertia Chirayita Leaf Extract on Colorectal Cancer Cells. Front. Bioeng. Biotechnol.; 2021; 9, 788527. [DOI: https://dx.doi.org/10.3389/fbioe.2021.788527]
44. Stohs, S.J. Safety and Efficacy of Bixa orellana (Achiote, Annatto) Leaf Extracts. Phytother. Res.; 2014; 28, pp. 956-960. [DOI: https://dx.doi.org/10.1002/ptr.5088]
45. Zegarra, L.; Vaisberg, A.; Loza, C.; Aguirre, R.L.; Campos, M.; Fernandez, I.; Talla, O.; Villegas, L. Double-Blind Randomized Placebo-Controlled Study of Bixa orellana in Patients with Lower Urinary Tract Symptoms Associated to Benign Prostatic Hyperplasia. Int. Braz. J. Urol.; 2007; 33, pp. 493-501. [DOI: https://dx.doi.org/10.1590/S1677-55382007000400006]
46. Najahi-Missaoui, W.; Arnold, R.D.; Cummings, B.S. Safe Nanoparticles: Are We There Yet?. Int. J. Mol. Sci.; 2020; 22, 385. [DOI: https://dx.doi.org/10.3390/ijms22010385] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33396561]
47. Jurić, S.; Jurić, M.; Siddique, M.A.B.; Fathi, M. Vegetable Oils Rich in Polyunsaturated Fatty Acids: Nanoencapsulation Methods and Stability Enhancement. Food Rev. Int.; 2020; 38, pp. 32-69. [DOI: https://dx.doi.org/10.1080/87559129.2020.1717524]
48. Mosaddik, A.; Ravinayagam, V.; Elaanthikkal, S.; Fessi, H.; Badri, W.; Elaissari, A. Development and Use of Polymeric Nanoparticles for the Encapsulation and Administration of Plant Extracts. Natural Products as Source of Molecules with Therapeutic Potential: Research & Development, Challenges and Perspectives; Cechinel Filho, V. Springer International Publishing: Cham, Switzerland, 2018; pp. 391-463. ISBN 978-3-030-00545-0
49. Gali, L.; Pirozzi, A.; Donsì, F. Biopolymer- and Lipid-Based Carriers for the Delivery of Plant-Based Ingredients. Pharmaceutics; 2023; 15, 927. [DOI: https://dx.doi.org/10.3390/pharmaceutics15030927]
50. Taouzinet, L.; Djaoudene, O.; Fatmi, S.; Bouiche, C.; Amrane-Abider, M.; Bougherra, H.; Rezgui, F.; Madani, K. Trends of Nanoencapsulation Strategy for Natural Compounds in the Food Industry. Processes; 2023; 11, 1459. [DOI: https://dx.doi.org/10.3390/pr11051459]
51. Jadhav, R.R.; Khare, D. Green Biotherapeutics: Overcoming Challenges in Plant-Based Expression Platforms. Plant Biotechnol. Rep.; 2024; 18, pp. 465-486. [DOI: https://dx.doi.org/10.1007/s11816-024-00910-8]
52. Bodiwala, K.B.; Banker, N.; Lalwani, R.; Shah, M.B.; Gajjar, A.K. Quality Control Methods for Fruit Extracts of Kigelia Africana Using High Performance Thin Layer Chromatography. Nat. Prod. Res.; 2024; pp. 1-9. [DOI: https://dx.doi.org/10.1080/14786419.2024.2340762] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/38597203]
53. Barbosa, R.D.M.; Leite, A.M.; García-Villén, F.; Sánchez-Espejo, R.; Cerezo, P.; Viseras, C.; Faccendini, A.; Sandri, G.; Raffin, F.N.; Moura, T.F.A.D.L.E. Hybrid Lipid/Clay Carrier Systems Containing Annatto Oil for Topical Formulations. Pharmaceutics; 2022; 14, 1067. [DOI: https://dx.doi.org/10.3390/pharmaceutics14051067]
54. Bitencourt, A.P.; Duarte, J.L.; Oliveira, A.E.; Cruz, R.A.; Carvalho, J.C.; Gomes, A.T.; Ferreira, I.M.; Ribeiro-Costa, R.M.; Silva-Júnior, J.O.; Fernandes, C.P. Preparation of aqueous nanodispersions with annatto (Bixa orellana L.) extract using an organic solvent-free and low energy method. Food Chem.; 2018; 257, pp. 196-205. [DOI: https://dx.doi.org/10.1016/j.foodchem.2018.02.067]
55. Naranjo-Durán, A.M.; Quintero-Quiroz, J.; Rojas-Camargo, J.; Ciro-Gómez, G.L. Modified-release of encapsulated bioactive compounds from annatto seeds produced by optimized ionic gelation techniques. Sci Rep.; 2021; 11, 1317. [DOI: https://dx.doi.org/10.1038/s41598-020-80119-1]
56. Huamán, A.A.; Celestino, M.R.; Quintana, M.E. Theoretical and experimental study of solar cells based on nanostructured films of TiO2 sensitized with natural dyes extracted from Zea mays and Bixa orellana. RSC Adv.; 2021; 11, pp. 9086-9097. [DOI: https://dx.doi.org/10.1039/D1RA01043C]
57. Huamán Aguirre, A.A.; Salazar Salinas, K.; Quintana Cáceda, M. Molecular interaction of natural dye based on Zea mays and Bixa orellana with nanocrystalline TiO2 in dye sensitized solar cells. J. Electrochem. Sci. Eng.; 2021; 11, pp. 179-195. [DOI: https://dx.doi.org/10.5599/jese.1014]
58. Kumar, A.; Bera, S.; Singh, M.; Mondal, D. Molecular Interactions of Silica Nanoparticles and Biomolecule-Functionalized Silica Nanoparticles with Bixa orellana L. Plant DNA. Silicon; 2022; 14, pp. 1407-1419. [DOI: https://dx.doi.org/10.1007/s12633-020-00913-4]
59. Maurya, I.C.; Singh, S.; Senapati, S.; Srivastava, P.; Bahadur, L. Green synthesis of TiO2 nanoparticles using Bixa orellana seed extract and its application for solar cells. Sol. Energy; 2019; 194, pp. 952-958. [DOI: https://dx.doi.org/10.1016/j.solener.2019.10.090]
60. Pal, S.; Malhotra, S.; Naik, S. Development of cosmeceutical products from nano-sized active colour constituents of Ratanjot, Seabuckthorn and Annatto. Int. J. Pharm. Pharm. Sci.; 2016; 8, pp. 232-237.
61. Prada, A.L.; Bitencourt, A.P.; Amado, J.R.; Cruz, R.A.; Carvalho, J.C.; Fernandes, C.P. Development and Characterization of Cassia grandis and Bixa orellana Nanoformulations. Curr. Top. Med. Chem.; 2016; 16, pp. 2057-2065. [DOI: https://dx.doi.org/10.2174/1568026616666160215161103]
62. Oliveira, S.D.S.D.C.; Sarmento, E.D.S.; Marinho, V.H.; Pereira, R.R.; Fonseca, L.P.; Ferreira, I.M. Green Extraction of Annatto Seed Oily Extract and Its Use as a Pharmaceutical Material for the Production of Lipid Nanoparticles. Molecules; 2022; 27, 5187. [DOI: https://dx.doi.org/10.3390/molecules27165187] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/36014427]
63. Silva, E.K.; Meireles, M.A. Influence of the degree of inulin polymerization on the ultrasound-assisted encapsulation of annatto seed oil. Carbohydr. Polym.; 2015; 133, pp. 578-586. [DOI: https://dx.doi.org/10.1016/j.carbpol.2015.07.025] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/26344316]
64. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E. et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ; 2021; 372, n71. [DOI: https://dx.doi.org/10.1136/bmj.n71]
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
; Carolina Ramos dos Santos 3
; Elysa Beatriz de Oliveira Damas 4 ; Araujo, Paula Lauane 3 ; de Oliveira Silva, Gabriella 4
; Graziella Anselmo Joanitti 5
; Marcella Lemos Brettas Carneiro 6
1 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;
2 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;
3 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;
4 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;
5 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;
6 Laboratory of Bioactive Compounds and Nanobiotechnology (LCBNano), Campus Darcy Ribeiro, University of Brasilia, Brasilia 70910-900, Brazil;