Journal: Drug Invention Today

Article Id: JPRS-CPS-0000861
Title: Impurity profile- A review
Category: Chemistry and Parallel Synthesis
Section: Review Article
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    Impurity profiling is the common name of a group of analytical activities, the aim of which is the detection, identification/structure elucidation and quantitative determination of organic and inorganic impurities, as well as residual solvents in bulk drugs and pharmaceutical formulations. Since this is the best way to characterize the quality and stability of bulk drugs and pharmaceutical formulations, this is the core activity in modern drug analysis. Due to the very rapid development of the analytical methodologies available for this purpose and the similarly rapid increase of the demands as regards the purity of drugs it is an important task to review a summary of the problems and the various possibilities offered by modern analytical chemistry for their solution. Various regulatory authorities like ICH, USFDA, Canadian Drug and Health Agency are emphasizing on the purity requirements and the identification of impurities in Active Pharmaceutical Ingredient’s (API’s). Qualification of the impurities is the process of acquiring and evaluating data that establishes biological safety of an individual impurity; thus, revealing the need and scope of impurity profiling of drugs in pharmaceutical research. Identification of impurities is done by variety of Chromatographic and Spectroscopic techniques, either alone or in combination with other techniques. There are different methods for detecting and characterizing impurities with TLC, HPLC, HPTLC, AAS etc. Conventional Liquid Chromatography, particularly, HPLC has been exploited widely in field of impurity profiling; the wide range of detectors, and stationary phases along with its sensitivity and cost effective separation have attributed to its varied applications. Among the various Planar Chromatographic Methods; TLC is the most commonly used separation technique, for isolation of impurities; due to its ease of operation and low cost compared to HPLC. An advancement of thin layer chromatography HPTLC is a well-known technique for the impurity isolation.Headspace GC is one of the most preferred techniques for identification of residual solvents. The advent of hyphenated techniques has revolutionized impurity profiling, by not only separation but structural identification of impurities as well. Among all hyphenated techniques, the most exploited techniques, for impurity profiling of drugs are LC-MS-MS, LC-NMR, LCNMR- MS, GC-MS, and LC-MS.

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  • About the authors and Affiliations

    Author(s) Name:

    Vasanti S* , Sulabha S.

    Affiliation(s) Name:

    *S.V.K.M’S, Dr. Bhanuben Nanavati College of Pharmacy, Mithibhai College Campus, V.M. Road. Vile Parle- (W), Mumbai - 400 056. (India)

    *Corresponding author.
    Vasanti S
    Department of Pharma Chemistry
    S.V.K.M’S, Dr. Bhanuben Nanavati College of Pharmacy, Mithibhai College
    V.M. Road. Vile Parle- (W),
    Mumbai - 400 056. India

    Received on: 20-07-2009; Revised on: 21-08- 2009; Accepted on:14-10-2009

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    Vasanti S* , Sulabha S.

    Title:Impurity profile- A review
    Journal:Drug Invention Today
    Vol(issue):1 (December)
    Page No: (81-88)
  • Experimental Methods Keywords

    Methodology:Analytical method development, Spectrophotometry, Chromatography
    Research Materials: Drug Impurities


Impurity Analytical method development Spectrophotometry Chromatography

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