Determination of progesterone (steroid drug) in the semi‐solid dosage form (vaginal gel) using a stability‐indicating method by RP‐HPLC/PDA detector-Reference-Cited by-同舟云学术

Determination of progesterone (steroid drug) in the semi‐solid dosage form (vaginal gel) using a stability‐indicating method by RP‐HPLC/PDA detector

Published:2021-10-08 Issue:1 Volume:36 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Konduru Naresh¹^ORCID,Kethe Vijay Babu²,Gundla Rambabu³,Katari Naresh Kumar³,Mallavarapu Ravindra³

Affiliation:

1. Analytical Research and Development YunNan Longjin Careyou Pharmaceutical Co., Ltd., Yunnan Province Kunming City China

2. Analytical Research and Development WUXI STA Pharmaceutical Co., Ltd. Shanghai China

3. Department of Chemistry, School of Science GITAM (Deemed to be University) Hyderabad India

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bmc.5246

Reference19 articles.

1. Validated stability‐indicating RP‐HPLC method for the assay of Dienogest in bulk and tablet dosage form;Avilas B.;International Journal of Pharmaceutical Quality Assurance.,2013

2. Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines

3. Stability‐indicating HPLC method for simultaneous quantification of 14 impurities in excedrin tablet formulations and identification of new impurity by LC–MS in accelerated stability studies

4. Column selection approach for related substances determination of progesterone by high-performance liquid chromatography

5. ICH Q2A. (1994).validation of analytical procedure: Methodology International Conference on Harmonization Geneva October 1994.

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