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Abstract
Eulophia macrobulbon (E.C.Parish & Rchb.f.) Hook.f. contains a natural PDE5A1 inhibitor, phenanthrene, 1-(4'-hydroxybenzyl)-4,8- dimethoxyphenanthrene-2,7-diol (HDP), a potential agent for the treatment of erectile dysfunction. The aim of this study was to improve the extraction efficiency of HDP from E. macrobulbon by using a more environmentally friendly extraction method, subcritical liquid dimethyl ether extraction (sDME), instead of classical solvent extraction (CSE) and ultrasound-assisted extraction (UAE). The efficiency and quality of the extracts obtained were evaluated using the following criteria: %process yield; solvent amount; extraction time; temperature; %HDP content by LC–MS, bioactivity as inhibition of phosphodiesterase-5A1 (PDE5A1) by radio-enzymatic assay; and chemical profiles by LC-QTOF-MS. sDME provided the highest content of HDP in the extract at 4.47%, much higher than the use of ethanol (0.4–0.5%), ethyl acetate (1.2–1.7%), or dichloromethane (0.7–1.4%). The process yield for sDME (1.5–2.7%) was similar to or lower than the other solvents (0.9–17%), but as long as the process yield is not prohibitively low, the concentration is a more important measure for clinical use. The optimal conditions for sDME extraction were: Extraction time, 40 min; 200% water as co-solvent; sample-to-solvent ratio of 1:8; temperature, 35 °C. Phenanthrene aglycone and glycoside derivatives were the major constituents of the sDME extracts and lesser amounts of phenolic compounds and sugars. The inhibition of PDE5A1 by sDME (IC50 0.67 ± 0.22 µg/ml) was tenfold more potent than ethanolic extract and other extraction methods, suggesting a high probability of clinical efficacy. Thus, sDME was a more efficient, faster, solvent-saving and environmentally friendly extraction method and more selective for phenanthrene when extracted from E. macrobulbon.
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1 University of Phayao, Research and Innovation Center in Cosmetic Sciences and Natural Products, Department of Cosmetic Sciences, School of Pharmaceutical Sciences, Phayao, Thailand (GRID:grid.412996.1) (ISNI:0000 0004 0625 2209)
2 Naresuan University, Chemical Engineering Program, Department of Industrial Engineering, Faculty of Engineering, Phitsanulok, Thailand (GRID:grid.412029.c) (ISNI:0000 0000 9211 2704)
3 Naresuan University, Department of Pharmaceutical Chemistry and Pharmacognosy, Center of Excellence in Cannabis Research, Faculty of Pharmaceutical Sciences, Center of Excellence for Innovation in Chemistry, Phitsanulok, Thailand (GRID:grid.412029.c) (ISNI:0000 0000 9211 2704)
4 Naresuan University, Division of Applied Thai Traditional Medicine, Faculty of Public Health, Phitsanulok, Thailand (GRID:grid.412029.c) (ISNI:0000 0000 9211 2704)
5 Walailak University, Akkhraratchakumari Veterinary College, Nakhon Si Thammarat, Thailand (GRID:grid.412867.e) (ISNI:0000 0001 0043 6347)
6 Naresuan University, Science Laboratory Centre, Faculty of Science, Phitsanulok, Thailand (GRID:grid.412029.c) (ISNI:0000 0000 9211 2704)
7 University of Phayao, Research and Innovation Center in Cosmetic Sciences and Natural Products, Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences, Phayao, Thailand (GRID:grid.412996.1) (ISNI:0000 0004 0625 2209)