Abstract

One of the potential candidates as a drug delivery agent that has been widely developed is mesoporous silica nanoparticle (MSN), which has several unique features. The high surface area and pore volume, tunable size particle, biocompatibility, and non-toxic are great features promising drug delivery carriers. The optimum condition to load the drug onto MSN is needed to maximize the loading of drugs. The drug loading is influenced by factors, such as silica to drug ratio, time, and pH condition. In this study, we had conducted the optimization of drug loading into MSN by implemented the Box-Behnken design of experiments. Also, the influence of each factor can be obtained through statistical calculation. The results showed that silica to drug ratio and pH condition significantly affect the loading capacity of MSN. The optimum condition obtained at silica to drug ratio, time, and pH conditions is 1, 48, and 3, respectively.

Details

Title
Loading Optimization of Mesoporous Silica Nanoparticle as Drug Delivery Agent
Author
Lestari, W A 1 ; Wibowo, F R 1 ; Wahyuningsih, S 1 ; Saputra, O A 1 ; Lestari, W W 1 ; Gomez-Ruiz, S 2 ; Mukti, R R 3 ; Martien, R 4 

 Chemistry Department, Faculty of Mathematic and Natural Sciences, Sebelas Maret University Surakarta, Indonesia 
 Departamento de Biología y Geología, Física y Química Inorgánica, Universidad Rey Juan Carlos, Móstoles, Madrid E-28933, Spain 
 Division of Inorganic and Physical Chemistry, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Indonesia 
 Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia 
Publication year
2021
Publication date
May 2021
Publisher
IOP Publishing
ISSN
17426588
e-ISSN
17426596
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2538370717
Copyright
© 2021. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.