4.6 Article

Ultrasound-Assisted Extraction of Antioxidants from Melastoma malabathricum Linn.: Modeling and Optimization Using Box-Behnken Design

Journal

MOLECULES
Volume 28, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28020487

Keywords

Melastoma malabathricum; ultrasound-assisted extraction (UAE); one-factor-at-a-time (OFAT); response surface methodology (RSM); Box-Behnken design (BBD); antioxidant assay; physicochemical characterization; phytochemical screening

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This study presents modeling and optimization of ultrasound-assisted extraction (UAE) of Melastoma malabathricum to evaluate its phytochemical properties. Through an OFAT procedure and response surface methodology, optimum conditions were established for maximum antioxidant extraction. The results showed that UAE at 37 kHz, X-ET 32 degrees C for X-UT 16 min, X-SC 70% ethanol concentration, and X-SLR 1:10 ratio yielded high scavenging effects on DPPH, as well as significant levels of total phenolic and flavonoid contents. GC-MS analysis confirmed the presence of important phytochemical compounds. This study provides valuable insights for further validation of the medicinal and cosmeceutical uses of Melastoma malabathricum.
This study presents modeling and optimization of ultrasound-assisted extraction (UAE) of Melastoma malabathricum with the objective of evaluating its phytochemical properties. This one-factor-at-a-time (OFAT) procedure was conducted to screen for optimization variables whose domains included extraction temperature (X-ET), ultrasonic time (X-UT), solvent concentration (X-SC), and sample-to-liquid ratio (X-SLR). Response surface methodology (RSM) coupled with Box-Behnken design (BBD) was applied to establish optimum conditions for maximum antioxidant extraction. Modeling and optimization conditions of UAE at 37 kHz, X-ET 32 degrees C for X-UT 16 min and dissolved in an X-SC 70% ethanol concentration at a X-SLR 1:10 ratio yielded scavenging effects on 2,2-diphenyl-1-picryl-hydrazyl (DPPH) at 96% +/- 1.48 and recorded values of total phenolic content (TPC) and total flavonoid content (TFC) at 803.456 +/- 32.48 mg GAE (gallic acid equivalents)/g, and 102.972 +/- 2.51 mg QE (quercetin equivalents)/g, respectively. The presence of high flavonoid compounds was verified using TWIMS-QTOFMS. Chromatic evaluation of phytochemicals using gas chromatography-mass spectrometry (GC-MS) revealed the presence of 14 phytocompounds widely documented to play significant roles in human health. This study provides a comparative evaluation with other studies and may be used for validation of the species' potential for its much-acclaimed medicinal and cosmeceutical uses.

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