Affiliation:
1. Research Center for Pharmaceutical Ingredients and Traditional Medicine National Research, and Innovation Agency (BRIN) Kawasan Sains dan Teknologi (KST) B.J Habibie (PUSPIPTEK) Serpong 15314> South Tangerang Banten Indonesia
2. Research Center for Chemistry National Research and Innovation Agency (BRIN) Gd. 452 Kawasan Sains dan Teknologi (KST) B.J Habibie (PUSPIPTEK) Serpong South Tangerang Banten Indonesia 15314
Abstract
AbstractThis study was undertaken to analyse the potential bioactivities including antibacterial, antioxidant and antidiabetic derived from the methanolic extract and the column chromatography ethyl acetate fraction (AcOEt Fr) of Horsfieldia spicata leaves. Methanolic extract and 4 other fractions was calculated for total phenol and flavonoid contents along with tested for antibacterial, antioxidant and antidiabetic properties. Interestingly, the AcOEt Fr had the highest value for total flavonoid content and the best antioxidant, and antidiabetic activities. Therefore, the AcOEt Fr was further separated using column chromatography technique for obtaining 9 selected fractions namely fraction 1 (F1) ‐ fraction 9 (F9) which were further tested. The results showed that the AcOEt column chromatography fractions namely F2, F3, F4 and F6 had the best clear inhibition antibacterial value against all bacterial tested. In addition, these fractions also exhibited better Minimum Inhibitory Concentrations (MIC) and Minimum Bactericidal Concentrations (MBC) values than others. Antioxidant, 2,2‐diphenylpicrylhydrazyl (DPPH) assayed indicated that AcOEt Fr had the strongest IC50 value of 47.30 μg/mL. Further, F4 column chromatography fraction showed the best inhibition against α‐Glucosidase enzyme related to antidiabetic activity with an IC50 value of 6.11 μg/mL. Liquid chromatography tandem‐mass spectrometry (LC/MS/MS) analysis identified that F4 derived from AcOEt fraction had several compounds belonging to the flavonoid and phenolics such as 3′,5‐dihydroxy‐7,4′‐dimethoxyflavone, 5,7‐dihydroxy‐3‐(4′‐hydroxybenzyl)chromone, and Kadsurenin I.
Subject
Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering