Box-Behnken Design (BBD)-Based Optimization of Microwave-Assisted Extraction of Parthenolide from the Stems of Tarconanthus camphoratus and Cytotoxic Analysis
Parthenolide, a strong cytotoxic compound found in different parts of which motivated the authors to develop an optimized microwave-assisted extraction (MEA) method using Box-Behnken design (BBD) for efficient extraction of parthenolide from the stem of and its validation by high-performance thin-la...
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Published in: | Molecules (Basel, Switzerland) Vol. 26; no. 7; p. 1876 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
MDPI AG
26-03-2021
MDPI |
Subjects: | |
Online Access: | Get full text |
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Summary: | Parthenolide, a strong cytotoxic compound found in different parts of
which motivated the authors to develop an optimized microwave-assisted extraction (MEA) method using Box-Behnken design (BBD) for efficient extraction of parthenolide from the stem of
and its validation by high-performance thin-layer chromatography (HPTLC) and cytotoxic analysis. The optimized parameters for microwave extraction were determined as: 51.5 °C extraction temperature, 50.8 min extraction time, and 211 W microwave power. A quadratic polynomial model was found the most suitable model with
of 0.9989 and coefficient of variation (CV) of 0.2898%. The high values of adjusted
(0.9974), predicted
(0.9945), and signal-to-noise ratio (74.23) indicated a good correlation and adequate signal, respectively. HPTLC analyzed the parthenolide (R
= 0.16) content in
methanol extract (TCME) at λ
= 575 nm and found it as 0.9273% ± 0.0487%
/
, which was a higher than expected yield (0.9157%
/
). The TCME exhibited good cytotoxicity against HepG2 and MCF-7 cell lines (IC
= 30.87 and 35.41 µg/mL, respectively), which further supported our findings of high parthenolide content in TCME. This optimized MAE method can be further applied to efficiently extract parthenolide from marketed herbal supplements containing different
species. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules26071876 |