Novel reversed‐phase HPLC method for simultaneous determination of ethynodiol diacetate (EDA)/ethinyl estradiol (EE) in pharmaceutical dosage form-Reference-Cited by-同舟云学术

Novel reversed‐phase HPLC method for simultaneous determination of ethynodiol diacetate (EDA)/ethinyl estradiol (EE) in pharmaceutical dosage form

Published:2021-01-07 Issue:5 Volume:35 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Chinta Srinivasa Reddy¹,Ponnam Vijetha²,Katari Naresh Kumar³^ORCID,Ediga Sasikiran Goud¹,Marisetti Vishnu Murthy⁴

Affiliation:

1. Department of Quality Operations Novast Laboratories Ltd Nantong Jiangsu Province China

2. Department of Chemical Engineering, Vignan’s Foundation for Science Technology and Research University Guntur Andhra Pradesh India

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

4. Analytical Research and Development ScieGen Pharmaceuticals, Inc. New York USA

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.5055

Reference22 articles.

1. Direct quantitative thin-layer chromatographic determination of levonorgestrel and ethinyloestradiol in oral contraceptives by diffuse reflection and fluorescence methods

2. Estimation of impurity profiles of drugs and related materials

3. Quantitative Analysis of Ethynodiol Diacetate and Ethinyl Estradiol/Mestranol in Oral Contraceptive Tablets by High-Performance Liquid Chromatography

4. Food and Drug Administration (FDA)(2010).Highlights of PrescribingInformation.http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021998lbl.pdfaccessed.

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1. Quantification of Drospirenone- and Ethinyl Estradiol-Related Impurities in a Combined Pharmaceutical Dosage Form by a Chromatography Method With a QbD Robustness Study;Journal of AOAC International;2023-09-27