Development and validation of a RP-UPLC method for the determination of betamethasone dipropionate impurities in topical formulations using a multivariate central composite design-Reference-Cited by-同舟云学术

Development and validation of a RP-UPLC method for the determination of betamethasone dipropionate impurities in topical formulations using a multivariate central composite design

Published:2021 Issue:33 Volume:13 Page:3705-3723
ISSN:1759-9660
Container-title:Analytical Methods
language:en
Short-container-title:Anal. Methods

Author:

Muchakayala Siva Krishna¹²^ORCID,Pavithra Kommera²,Katari Naresh Kumar²^ORCID,Marisetti Vishnu M.³^ORCID,Dongala Thirupathi⁴^ORCID,Vegesna Raju V. K.¹

Affiliation:

1. Analytical Research and Development, Douglas Pharma US Inc, 1035 Louis Drive, Warminster, Pennsylvania, USA, 18974

2. Department of Chemistry, School of Science, GITAM Deemed to be University, Hyderabad, Telangana, India, 502329

3. Analytical Research and Development, ScieGen Pharmaceuticals Inc, 89 Arkay Drive, Hauppauge, New York, 11788, USA

4. Quality Control, Aurex Laboratories LLC, 10 Lake Drive, East Windsor, New Jersey, USA, 08520

Abstract

A QbD based UPLC method for the determination of impurities present in cream and ointment formulations of betamethasone dipropionate (BMD).

Publisher

Royal Society of Chemistry (RSC)

Subject

General Engineering,General Chemical Engineering,Analytical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/AY/D1AY01096D

Reference20 articles.

1. THE EFFECT OF BETAMETHASONE DIPROPIONATE CREAM 0.05% (DIPROSONE) ON ADRENOCORTICAL FUNCTION

2. USP43-NF38 2S, United States Pharmacopeial Convention , Rockville, Maryland, USA

3. Development and Validation of a Stability-Indicating RP-HPLC Method for Simultaneous Assay of Betamethasone Dipropionate, Chlorocresol, and for the Estimation of Betamethasone Dipropionate Related Compounds in a Pharmaceutical Cream and Ointment

4. Development and validation of stability-indicating HPLC method for betamethoasone dipropionate and related substances in topical formulation

5. Development and validation of a stability-indicating HPLC method for simultaneous determination of salicylic acid, betamethasone dipropionate and their related compounds in Diprosalic Lotion®

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Liquid Chromatography–Mass Spectrometry Method for Determination of N‐Methyl‐N‐Nitrosopyridin‐4‐Amine in a Vonoprazan Fumarate Drug;SEPARATION SCIENCE PLUS;2024-07-25

2. A rapid and novel quantitative determination of Lecanemab monoclonal antibody for Alzheimer’s disease using reverse phase ultra performance liquid chromatography;Analytical Chemistry Letters;2024-07-03

3. QbD green analytical procedure for the quantification of tolvaptan by utilizing stability indicating UHPLC method;BMC Chemistry;2024-06-28

4. A sensitive UPLC-MS/MS method for the simultaneous assay and trace level genotoxic impurities quantification of SARS-CoV-2 inhibitor-Molnupiravir in its pure and formulation dosage forms using fractional factorial design;Results in Chemistry;2023-12

5. Fast on-site simultaneous electroanalysis of fusidic acid and betamethasone in pharmaceuticals and water samples using novel stochastic platform;Electrochemistry Communications;2023-12