Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices

Abstract The existing HPLC methods for the assaying of multiple markers in standardized herbal extracts use a single wavelength for quantification, which usually leads to lower assay than actual claims. It was because screening multiple phytochemical standards irrespective to their absorption maxima...

Full description

Bibliographic Details
Main Authors: Gnanabhaskar Danaboina, Rudramani Tiwari, Kurra Subrahmanyam, V. Shreekala, Ajay Kumar Meena
Format: Article
Language:English
Published: SpringerOpen 2023-11-01
Series:Future Journal of Pharmaceutical Sciences
Subjects:
Online Access:https://doi.org/10.1186/s43094-023-00555-4
_version_ 1797577579542085632
author Gnanabhaskar Danaboina
Rudramani Tiwari
Kurra Subrahmanyam
V. Shreekala
Ajay Kumar Meena
author_facet Gnanabhaskar Danaboina
Rudramani Tiwari
Kurra Subrahmanyam
V. Shreekala
Ajay Kumar Meena
author_sort Gnanabhaskar Danaboina
collection DOAJ
description Abstract The existing HPLC methods for the assaying of multiple markers in standardized herbal extracts use a single wavelength for quantification, which usually leads to lower assay than actual claims. It was because screening multiple phytochemical standards irrespective to their absorption maxima which drive decrease in peak are response which ultimately impact the assay. To overcome this issue, we have applied a methodology, called Mixed Standard Multi-Signal (MSMS) simultaneous detection, where multiple reference standards get extracted each with their respective λ max and quantification will be done at the same λ max in a single sequence data setup. This method was standardized using Single Signal Multi-Standards, Single Signal Single Standard, Multi-Signal Single Standard, for all individual reference standards, mixed reference standards, plant extracts, and Ayurvedic formulations. The results of our study demonstrate that higher assay reported total actives 5.04% by conventional detection and for current proposed method 13.81% with shorter span of analysis time and lesser solvent consumption. It helps to decide the actual standardization label claim on product which drives better commercial costings, and dosage regimen claims. Graphical Abstract
first_indexed 2024-03-10T22:11:14Z
format Article
id doaj.art-4194342131e846049a928a76744dd293
institution Directory Open Access Journal
issn 2314-7253
language English
last_indexed 2024-03-10T22:11:14Z
publishDate 2023-11-01
publisher SpringerOpen
record_format Article
series Future Journal of Pharmaceutical Sciences
spelling doaj.art-4194342131e846049a928a76744dd2932023-11-19T12:36:41ZengSpringerOpenFuture Journal of Pharmaceutical Sciences2314-72532023-11-019111210.1186/s43094-023-00555-4Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matricesGnanabhaskar Danaboina0Rudramani Tiwari1Kurra Subrahmanyam2V. Shreekala3Ajay Kumar Meena4Department of Chemistry, Regional Ayurveda Research Institute, Ministry of Ayush, Govt. of IndiaDepartment of Chemistry, Regional Ayurveda Research Institute, Ministry of Ayush, Govt. of IndiaDepartment of Pharmacology, Regional Ayurveda Research InstituteDepartment of Ayurveda, Regional Ayurveda Research InstituteDepartment of Chemistry, Regional Ayurveda Research Institute, Ministry of Ayush, Govt. of IndiaAbstract The existing HPLC methods for the assaying of multiple markers in standardized herbal extracts use a single wavelength for quantification, which usually leads to lower assay than actual claims. It was because screening multiple phytochemical standards irrespective to their absorption maxima which drive decrease in peak are response which ultimately impact the assay. To overcome this issue, we have applied a methodology, called Mixed Standard Multi-Signal (MSMS) simultaneous detection, where multiple reference standards get extracted each with their respective λ max and quantification will be done at the same λ max in a single sequence data setup. This method was standardized using Single Signal Multi-Standards, Single Signal Single Standard, Multi-Signal Single Standard, for all individual reference standards, mixed reference standards, plant extracts, and Ayurvedic formulations. The results of our study demonstrate that higher assay reported total actives 5.04% by conventional detection and for current proposed method 13.81% with shorter span of analysis time and lesser solvent consumption. It helps to decide the actual standardization label claim on product which drives better commercial costings, and dosage regimen claims. Graphical Abstracthttps://doi.org/10.1186/s43094-023-00555-4HPLCDADMSMSSimultaneous detectionBioactivesFood
spellingShingle Gnanabhaskar Danaboina
Rudramani Tiwari
Kurra Subrahmanyam
V. Shreekala
Ajay Kumar Meena
Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
Future Journal of Pharmaceutical Sciences
HPLC
DAD
MSMS
Simultaneous detection
Bioactives
Food
title Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
title_full Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
title_fullStr Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
title_full_unstemmed Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
title_short Multi-wavelength fusion spectral extraction-assisted HPLC for simultaneous quantification of multiple secondary metabolites in herbal matrices
title_sort multi wavelength fusion spectral extraction assisted hplc for simultaneous quantification of multiple secondary metabolites in herbal matrices
topic HPLC
DAD
MSMS
Simultaneous detection
Bioactives
Food
url https://doi.org/10.1186/s43094-023-00555-4
work_keys_str_mv AT gnanabhaskardanaboina multiwavelengthfusionspectralextractionassistedhplcforsimultaneousquantificationofmultiplesecondarymetabolitesinherbalmatrices
AT rudramanitiwari multiwavelengthfusionspectralextractionassistedhplcforsimultaneousquantificationofmultiplesecondarymetabolitesinherbalmatrices
AT kurrasubrahmanyam multiwavelengthfusionspectralextractionassistedhplcforsimultaneousquantificationofmultiplesecondarymetabolitesinherbalmatrices
AT vshreekala multiwavelengthfusionspectralextractionassistedhplcforsimultaneousquantificationofmultiplesecondarymetabolitesinherbalmatrices
AT ajaykumarmeena multiwavelengthfusionspectralextractionassistedhplcforsimultaneousquantificationofmultiplesecondarymetabolitesinherbalmatrices