Literature DB >> 18966892

Drug impurity profiling strategies.

S Görög1, M Babják, G Balogh, J Brlik, A Csehi, F Dravecz, M Gasdag, P Horváth, A Laukó, K Varga.   

Abstract

A general scheme is set up for the estimation of the impurity profile of bulk drug substances by the complex use of chromatographic, spectroscopic and hyphenated techniques. Several examples are presented as illustrations to the scheme from the authors' laboratory involving the use of chromatographic methods such as thin-layer-(TLC), gas-(GC), analytical and preparative high-performance liquid chromatography (HPLC), spectroscopic methods such as mass spectrometry (MS) and NMR spectroscopy as well as hyphenated techniques (HPLC/diode-array UV, GC/MS and HPLC/MS). In addition to summarizing earlier work, new examples are also presented: identification of an impurity (propyl 4-[diethylcarbamoyl(methoxy)]-3-methoxy phenylglyoxylate, II) in propanidid (I) and two unsaturated impurities in allylstrenol (VII) by GC/MS and HPLC/diode-array UV as well as estimation of the impurity profile of mazipredone (III) by HPLC/MS and HPLC/diode-array UV.

Entities:  

Year:  1997        PMID: 18966892

Source DB:  PubMed          Journal:  Talanta        ISSN: 0039-9140            Impact factor:   6.057


  5 in total

1.  A RP-HPLC Method for the Analysis of Neostigmine Methylsulfate and Process-Related Impurities, Forced Degradation Studies, in the Injection Formulation.

Authors:  Manali Parab; Vaishali A Shirsat; Yogita M Kodgule; Mandar Kodgule
Journal:  Int J Anal Chem       Date:  2021-05-11       Impact factor: 1.885

2.  Development and Validation of a Stability-Indicating RP-HPLC Method for the Estimation of Drotaverine Impurities in API and Pharmaceutical Formulation.

Authors:  Veera Raghava Raju Thummala; Satya Sankarsana Jagan Mohan Tharlapu; Vijay Kumar Rekulapalli; Mrutyunjaya Rao Ivaturi; Someswara Rao Nittala
Journal:  Sci Pharm       Date:  2013-10-21

3.  A Validated RP-HPLC Stability Method for the Estimation of Chlorthalidone and Its Process-Related Impurities in an API and Tablet Formulation.

Authors:  Chaitali Kharat; Vaishali A Shirsat; Yogita M Kodgule; Mandar Kodgule
Journal:  Int J Anal Chem       Date:  2020-04-10       Impact factor: 1.885

4.  Development and Validation of a Precise, Single HPLC Method for the Determination of Tolperisone Impurities in API and Pharmaceutical Dosage Forms.

Authors:  Thummala Veera Raghava Raju; Raja Kumar Seshadri; Srinivas Arutla; Tharlapu Satya Sankarsana Jagan Mohan; Ivaturi Mrutyunjaya Rao; Someswara Rao Nittala
Journal:  Sci Pharm       Date:  2012-11-05

5.  Development and Validation of a Stability-Indicating RP-UPLC Method for the Estimation of Impurities in Cinacalcet Hydrochloride API and its Formulation.

Authors:  Pingili Sunil Reddy; Thummala Veera Raghava Raju; Penmetsa Satyanarayana Raju; Nadimpalli Sunil Varma; Kondra Sudhakar Babu
Journal:  Sci Pharm       Date:  2015-04-16
  5 in total

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