Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines-Reference-Cited by-同舟云学术

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

Published:2019-08-08 Issue: Volume: Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Dongala Thirupathi¹²^ORCID,Katari Naresh Kumar²³^ORCID,Palakurthi Ashok Kumar¹,Jonnalagadda Sreekantha B.³^ORCID

Affiliation:

1. Aurex Laboratories LLC NJ USA

2. Department of ChemistryGITAM deemed to be University Hyderabad Telangana India

3. School of Chemistry & Physics, College of Agriculture, Engineering and Science, Westville CampusUniversity of KwaZulu‐Natal Durban South Africa

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.4641

Reference29 articles.

1. Simultaneous determination of ambroxol hydrochloride and guaifenesin by HPLC, TLC spectrodensitometric and multivariate calibration methods in pure form and in cough–cold formulations;Abdelkawy M.;Journal of Chromatography and Separation Techniques,2011

2. A new hydrophilic interaction liquid chromatographic (HILIC) procedure for the simultaneous determination of pseudoephedrine hydrochloride (PSH), diphenhydramine hydrochloride (DPH) and dextromethorphan hydrobromide (DXH) in cough–cold formulations;Ali M. S.;Journal of Pharmaceutical and Biomedical Analysis,2007

3. Spectrophotometric estimation of guaifenesin and salbutamol in pure and tablet dosage form by using different methods;Bankar A. A.;Der Pharma Chemica.,2013

4. A rapid HPLC assay for the determination of dextro‐propoxyphene related substance in combination with aspirin, acetaminophen, and caffeine in tablet and capsule formulations;Burge L. J.;Journal of Liquid Chromatography,2003

5. HPLC method development and validation:simultaneous determination of active ingredients in cough and cold pharmaceuticals;Çaglar H.;International Journal of Pharmacy and Pharmaceutical Sciences,2014

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