HPTLC and UPLC-MS/MS Methods for Quality Control Analysis of Itrifal Formulations of Unani System of Medicine.


Journal

Journal of AOAC International
ISSN: 1944-7922
Titre abrégé: J AOAC Int
Pays: England
ID NLM: 9215446

Informations de publication

Date de publication:
01 Jun 2020
Historique:
pubmed: 28 10 2019
medline: 29 6 2021
entrez: 27 10 2019
Statut: ppublish

Résumé

Ultra-performance LC (UPLC)-tandem MS (MS/MS) and high-performance TLC (HPTLC) assay methods were developed for chemical fingerprinting and quantitative analysis of bioactive constituents of a certain "Itrifal formulation," a traditional kind of Unani medicine. In the present investigation, HPTLC and UPLC-MS/MS methods were developed and validated for the detection and quantification of major metabolites present in itrifal formulation. The metabolites present in the formulation were separated using modern chromatographic techniques, and a quantitative analysis was performed. Analytical performance of the proposed HPTLC and UPLC-MS/MS methods was validated as per the defined guidelines with respect to linearity, accuracy, precision, robustness, and specificity. The developed UPLC-MS/MS and HPTLC methods were used for quantification of gallic acid, tannic acid, catechin, and quercetin. All four constituents were quantified by UPLC-MS/MS, while two constituents were quantified by HPTLC in the commercial itrifal formulation. The calibration plot was found to be linear, accurate, precise, robust, and specific for both HPTLC and UPLC-MS/MS. The present methods were successfully applied for analysis of the given markers in itrifal formulations. The same can be used for QC and stability testing of itrifal formulations.

Sections du résumé

BACKGROUND BACKGROUND
Ultra-performance LC (UPLC)-tandem MS (MS/MS) and high-performance TLC (HPTLC) assay methods were developed for chemical fingerprinting and quantitative analysis of bioactive constituents of a certain "Itrifal formulation," a traditional kind of Unani medicine.
OBJECTIVE OBJECTIVE
In the present investigation, HPTLC and UPLC-MS/MS methods were developed and validated for the detection and quantification of major metabolites present in itrifal formulation.
METHODS METHODS
The metabolites present in the formulation were separated using modern chromatographic techniques, and a quantitative analysis was performed. Analytical performance of the proposed HPTLC and UPLC-MS/MS methods was validated as per the defined guidelines with respect to linearity, accuracy, precision, robustness, and specificity.
RESULTS RESULTS
The developed UPLC-MS/MS and HPTLC methods were used for quantification of gallic acid, tannic acid, catechin, and quercetin. All four constituents were quantified by UPLC-MS/MS, while two constituents were quantified by HPTLC in the commercial itrifal formulation. The calibration plot was found to be linear, accurate, precise, robust, and specific for both HPTLC and UPLC-MS/MS.
CONCLUSIONS CONCLUSIONS
The present methods were successfully applied for analysis of the given markers in itrifal formulations. The same can be used for QC and stability testing of itrifal formulations.

Identifiants

pubmed: 31653282
pii: 5718350
doi: 10.5740/jaoacint.19-0231
doi:

Substances chimiques

Gallic Acid 632XD903SP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

649-658

Informations de copyright

Copyright ©2020 by AOAC International, Inc. All rights reserved.

Auteurs

Rehan Abdur Rab (RA)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmaceutics, Nano Medicine Laboratory, New Delhi 110062, India.

Sultan Zahiruddin (S)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmacognosy and Photochemistry, Bioactive Natural Product Laboratory, New Delhi 110062, India.

Mohammad Ibrahim (M)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmacognosy and Photochemistry, Bioactive Natural Product Laboratory, New Delhi 110062, India.

Faisal Husain (F)

Rehbar Ayurvedic and Unani Medical College, Bhawanigarh, Punjab 148026, India.

Rabea Parveen (R)

Jamia Millia Islamia, Department of Biosciences, New Delhi 110025, India.

Washim Khan (W)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmacognosy and Photochemistry, Bioactive Natural Product Laboratory, New Delhi 110062, India.

Farhan J Ahmad (FJ)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmaceutics, Nano Medicine Laboratory, New Delhi 110062, India.

Asim A Khan (AA)

Ministry of AYUSH, Central Council for Research in Unani Medicine, New Delhi 110058, India.

Sayeed Ahmad (S)

Jamia Hamdard, School of Pharmaceutical Education and Research, Department of Pharmacognosy and Photochemistry, Bioactive Natural Product Laboratory, New Delhi 110062, India.

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