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Development and validation of an RP-HPLC method for the simultaneous determination of total withanolide glycosides and Withaferin A in Withania somnifera (Ashwagandha)
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Background:
Withanolide glycosides in Ashwagandha (Withania somnifera), are important
metabolites attributed with widely acclaimed therapeutic potential for which validated methods
for quantitative determination are limited.
Objective:
The primary objective was to develop and validate a Reversed-Phase High Performance
Liquid Chromatography (RP-HPLC) method for simultaneous quantification of total withanolide
glycosides (WG), withanoside IV and withaferin A present in ashwagandha extract.The study also
aimed to identify various other constituents present in the extract.
Materials and Methods:
Aqueous methanol extract (AME) of Ashwagandha was prepared and fractionated
into two viz. flavonoid rich fraction (FF) and withanolide rich fraction (WF). RP-HPLC
method was developed and validated for the estimation of total WG in ashwagandha extract according
to ICH guidelines. Preparative HPLC based purification of major compounds from WF fraction
was carried out and constituents were identified using spectroscopic techniques. HPLC chemical
profiling of WF before and after acid hydrolysis under controlled conditions was carried out to further
confirm the glycosidic compounds.
Results and Discussion:
The RP-HPLC method gave a precise differentiation of flavonoids, withanolides
and WG present in ashwagandha extract. The method demonstrated good reliability and
sensitivity, and can be conveniently used for the quantification of total WG, withanoside IV and
withaferin A present in ashwagandha extracts. According to this method, a purified fraction (WF)
prepared from roots and leaves of Ashwagandha comprise 35% of total WG, 3.27% of withanoside
IV and 2.40% of Withaferin A. The method was also applied to different products prepared from
Ashwagandha with total withanolide glycosides ranged from 1.5% to 60%, and the results were
found to be reproducible. Identification of the individual chemical constituents as well as the acid
hydrolytic pattern of the extract further supported the reliability of the developed method for the
quantitative determination of total WG. This study also reported a new withanolide glycoside
named, cilistol V-6’-O-glucoside (Aswanoside) along with some other known withanolide glycosides.
Conclusion:
A Reversed-Phase High Performance Liquid Chromatography (RP-HPLC) method
was developed and validated for the quantitative determination of total WG, withanoside IV and
withaferin A present in ashwagandha extract according to ICH guidelines. This study also reported
a new withanolide glycoside named, cilistol V-6’-O-glucoside (Aswanoside) along with some
other known WG.
Bentham Science Publishers Ltd.
Title: Development and validation of an RP-HPLC method for the simultaneous determination of total withanolide glycosides and Withaferin A in Withania somnifera (Ashwagandha)
Description:
Background:
Withanolide glycosides in Ashwagandha (Withania somnifera), are important
metabolites attributed with widely acclaimed therapeutic potential for which validated methods
for quantitative determination are limited.
Objective:
The primary objective was to develop and validate a Reversed-Phase High Performance
Liquid Chromatography (RP-HPLC) method for simultaneous quantification of total withanolide
glycosides (WG), withanoside IV and withaferin A present in ashwagandha extract.
The study also
aimed to identify various other constituents present in the extract.
Materials and Methods:
Aqueous methanol extract (AME) of Ashwagandha was prepared and fractionated
into two viz.
flavonoid rich fraction (FF) and withanolide rich fraction (WF).
RP-HPLC
method was developed and validated for the estimation of total WG in ashwagandha extract according
to ICH guidelines.
Preparative HPLC based purification of major compounds from WF fraction
was carried out and constituents were identified using spectroscopic techniques.
HPLC chemical
profiling of WF before and after acid hydrolysis under controlled conditions was carried out to further
confirm the glycosidic compounds.
Results and Discussion:
The RP-HPLC method gave a precise differentiation of flavonoids, withanolides
and WG present in ashwagandha extract.
The method demonstrated good reliability and
sensitivity, and can be conveniently used for the quantification of total WG, withanoside IV and
withaferin A present in ashwagandha extracts.
According to this method, a purified fraction (WF)
prepared from roots and leaves of Ashwagandha comprise 35% of total WG, 3.
27% of withanoside
IV and 2.
40% of Withaferin A.
The method was also applied to different products prepared from
Ashwagandha with total withanolide glycosides ranged from 1.
5% to 60%, and the results were
found to be reproducible.
Identification of the individual chemical constituents as well as the acid
hydrolytic pattern of the extract further supported the reliability of the developed method for the
quantitative determination of total WG.
This study also reported a new withanolide glycoside
named, cilistol V-6’-O-glucoside (Aswanoside) along with some other known withanolide glycosides.
Conclusion:
A Reversed-Phase High Performance Liquid Chromatography (RP-HPLC) method
was developed and validated for the quantitative determination of total WG, withanoside IV and
withaferin A present in ashwagandha extract according to ICH guidelines.
This study also reported
a new withanolide glycoside named, cilistol V-6’-O-glucoside (Aswanoside) along with some
other known WG.
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