Literature DB >> 3584319

General method for the analysis of pharmaceutical dosage forms by high-performance liquid chromatography.

A S Sidhu, J M Kennedy, S Deeble.   

Abstract

A reliable and simple method for the routine analysis of pharmaceutical dosage forms by high-performance liquid chromatography using a C18 Bondapak reversed-phase column with a binary solvent system consisting of acetonitrile and 0.05 M potassium dihydrogen phosphate has been developed. Standardised extraction procedures for drugs in various dosage forms have been developed and successfully applied to a wide range of current pharmaceutical formulations.

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Year:  1987        PMID: 3584319     DOI: 10.1016/s0021-9673(01)94319-5

Source DB:  PubMed          Journal:  J Chromatogr


  3 in total

1.  Validated gradient stability indicating HPLC method for determining Diltiazem Hydrochloride and related substances in bulk drug and novel tablet formulation.

Authors:  Vivekanand A Chatpalliwar; Pawan K Porwal; Neeraj Upmanyu
Journal:  J Pharm Anal       Date:  2012-02-04

2.  Determination of naphazoline HCl, pheniramine maleate and their official impurities in eye drops and biological fluid rabbit aqueous humor by a validated LC-DAD method.

Authors:  Khadiga M Kelani; Maha A Hegazy; Amal M Hassan; Mahmoud A Tantawy
Journal:  RSC Adv       Date:  2021-02-10       Impact factor: 3.361

3.  A green TLC densitometric method for the simultaneous detection and quantification of naphazoline HCl, pheniramine maleate along with three official impurities.

Authors:  Khadiga M Kelani; Maha A Hegazy; Amal M Hassan; Mahmoud A Tantawy
Journal:  BMC Chem       Date:  2022-04-04
  3 in total

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