Development of a rapid and validated stability-indicating UPLC-PDA method for concurrent quantification of impurity profiling and an assay of ipratropium bromide and salbutamol sulfate in inhalation dosage form-Reference-Cited by-同舟云学术

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Development of a rapid and validated stability-indicating UPLC-PDA method for concurrent quantification of impurity profiling and an assay of ipratropium bromide and salbutamol sulfate in inhalation dosage form

Published:2023-03 Issue:2 Volume:81 Page:300-314
ISSN:0003-4509
Container-title:Annales Pharmaceutiques Françaises
language:en
Short-container-title:Annales Pharmaceutiques Françaises

Author:

Kondra S.^ORCID,Pawar A.K.M^ORCID,Bapuji A.T^ORCID,Shankar P.D.S^ORCID

Publisher

Elsevier BV

Subject

Pharmaceutical Science,Pharmacology

Reference28 articles.

1. The Merck Index – an encyclopedia of chemicals, drugs and biologicals;O’Neil,2006

2. Clinical pharmacology made incredibly easy;Springhouse,2008

3. Ipratropium bromide: physical properties;Abdine;Profiles Drug Subst Excipients Relat Methodol,2003

4. Bronchodilator efficacy of the fixed combination of ipratropium and albuterol compared to albuterol alone in moderate-to-severe persistent asthma;Gelb;Pulm Pharmacol Ther,2008

5. Development and validation of a HPLC method for the simultaneous estimation of the salbutamol sulphate and ipratropium in inhalation dosage forms;Jyothi;Int J Pharm Sci,2012

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