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      Development of forced degradation and stability indicating studies of drugs—A review

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          Abstract

          Forced degradation is a degradation of new drug substance and drug product at conditions more severe than accelerated conditions. It is required to demonstrate specificity of stability indicating methods and also provides an insight into degradation pathways and degradation products of the drug substance and helps in elucidation of the structure of the degradation products. Forced degradation studies show the chemical behavior of the molecule which in turn helps in the development of formulation and package. In addition, the regulatory guidance is very general and does not explain about the performance of forced degradation studies. Thus, this review discusses the current trends in performance of forced degradation studies by providing a strategy for conducting studies on degradation mechanisms and also describes the analytical methods helpful for development of stability indicating method.

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          Development of validated stability-indicating assay methods--critical review.

          This write-up provides a review on the development of validated stability-indicating assay methods (SIAMs) for drug substances and products. The shortcomings of reported methods with respect to regulatory requirements are highlighted. A systematic approach for the development of stability-indicating methods is discussed. Critical issues related to development of SIAMs, such as separation of all degradation products, establishment of mass balance, stress testing of formulations, development of SIAMs for combination products, etc. are also addressed. The applicability of pharmacopoeial methods for the analysis of stability samples is discussed. The requirements of SIAMs for stability study of biotechnological substances and products are also touched upon.
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            The role of degradant profiling in active pharmaceutical ingredients and drug products.

            Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products. In order to fulfill development and regulatory needs, this publication provides a roadmap for when and how to perform studies, helpful tools in designing rugged scientific studies, and guidance on how to record and communicate results.
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              Identification of Pharmaceutical Impurities

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                Author and article information

                Contributors
                Journal
                J Pharm Anal
                J Pharm Anal
                Journal of Pharmaceutical Analysis
                Xi'an Jiaotong University
                2095-1779
                2214-0883
                17 September 2013
                June 2014
                17 September 2013
                : 4
                : 3
                : 159-165
                Affiliations
                [0005]Department of Pharmaceutical Analysis, Institute of Research and Development, Gujarat Forensic Sciences University, Sector-18A, Nr. Police Bhavan, Gandhinagar 382007, Gujarat, India
                Author notes
                [* ]Corresponding author. Tel.: +91 9723001703; fax: +91 079 23247465. blessy_51289@ 123456yahoo.co.in
                Article
                S2095-1779(13)00100-7
                10.1016/j.jpha.2013.09.003
                5761119
                29403878
                a7d1b474-1757-492f-8d50-ea2c7808e8d7
                © 2013 Xi’an Jiaotong University. Production and hosting by Elsevier B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).

                History
                : 24 January 2013
                : 10 September 2013
                Categories
                Review Article

                degradation conditions,degradation product,forced degradation,stability indicating method,stress testing

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