Triterpenoids are known for their promising biological activities, and there is a growing focus on green extraction methods for these compounds. In this study, ultrasound-assisted deep eutectic solvents were employed to extract triterpenoids from persimmon leaves, with choline chloride-lactic acid identified as an effective green solvent. The extraction conditions were carefully optimized using response surface methodology, resulting in an extraction efficiency of 12.41%, which is 1.54 times higher than that achieved with conventional organic solvents such as methanol. The triterpenoids were then successfully recovered using a solid-liquid extraction method based on AB-8 macroporous resins, achieving a 94.01% recovery rate with a final product triterpenoid content of 81.87%. These findings provide a strong foundation for the sustainable extraction of triterpenoids and other valuable compounds from biomass.
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http://dx.doi.org/10.1039/d4ay01885k | DOI Listing |
Anal Methods
January 2025
Faculty of Pharmacy, Hue University of Medicine and Pharmacy, Hue University, Hue City, Vietnam.
Triterpenoids are known for their promising biological activities, and there is a growing focus on green extraction methods for these compounds. In this study, ultrasound-assisted deep eutectic solvents were employed to extract triterpenoids from persimmon leaves, with choline chloride-lactic acid identified as an effective green solvent. The extraction conditions were carefully optimized using response surface methodology, resulting in an extraction efficiency of 12.
View Article and Find Full Text PDFFood Chem
January 2025
Toyo Institute of Food Technology, 23-2, Minami-Hanayashiki 4-Chome, Kawanishi City, Hyogo Prefecture 666-0026, Japan. Electronic address:
The simultaneous determination of pentacyclic triterpenoids, which are secondary metabolites in plants, is difficult because of the similarity in structure and minimal differences in polarity. In this study, we established a simple and sensitive method for the simultaneous determination of pentacyclic triterpenoids based on liquid chromatography-single-quadrupole mass spectrometry (LC-MS) using a C30 column. The established method completely separated 13 pentacyclic triterpenoids based on their different retention times.
View Article and Find Full Text PDFChem Biodivers
January 2025
Liverpool John Moores University, Centre for Natural Products Discovery, School of Pharmacy and Biomolecular Sciences, Byrom Street, Liverpool, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
Diospyros discolor Willd., commonly known as Velvet apple or Mabolo, is an underutilized fruit. Traditionally, various parts of D.
View Article and Find Full Text PDFHeliyon
May 2024
Natural and Medical Sciences Research Center, University of Nizwa, P.O. Box 33, Birkat Al Mauz, Nizwa 616, Sultanate of Oman.
The present article describes the muscle relaxant and antipyretic effects of pentacyclic triterpenes, oleanolic acid (), ursolic acid () and betulinic acid () isolated from roots of in animal models. The muscle relaxant effects of isolated pentacyclic triterpenes were determined by chimney and inclined plane tests. In the chimney test, pretreatment of pentacyclic triterpenes evoked significant dose dependent influence on muscle coordination.
View Article and Find Full Text PDFMolecules
April 2024
Guangdong Provincial Engineering Research Center for Modernization of TCM, Jinan University, Guangzhou 510632, China.
Six new 2-hydroxy ursane triterpenoids, 3---coumaroyloxy-2,19-dihydroxy-12-ursen-28-oic acid (), 3--coumaroyloxy-2,19-dihydroxy-12-ursen-28-oic acid (), 3---coumaroyloxy-2-hydroxy-12-ursen-28-oic acid (), 3--coumaroyloxy-2-hydroxy-12,20(30)-ursadien-28-oic acid (), 3-feruloyloxy-2-hydroxy-12,20(30)-ursadien-28-oic acid (), and 3-feruloyloxy-2-hydroxy-12,20(30)-ursadien-28-oic acid (), along with eleven known triterpenoids (-), were isolated from the leaves of . Their chemical structures were elucidated by comprehensive analysis of UV, IR, HRESIMS, and NMR spectra. All the isolated compounds were evaluated for their PTP1B inhibitory activity.
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