Transcription of HPLC METHOD DEVELOPMENT -A REVIEW
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HPLC METHOD DEVELOPMENT -A REVIEW
Pallaviet of PharmaceuticalResearch &Education, 2017, 1(2), 243-260243 ReviewArticleJournal of Pharmaceutical Research & EducationJournal homepage: METHOD DEVELOPMENT -AREVIEWMs Pallavi Nemgonda Patil*Suresh GyanViharUniversity,Jaipur, may be utilized as the basis for decisions relating to administering the drug to patients,play important roles in new discovery, DEVELOPMENT , manufacture of pharmaceutical drugs andvarious other studies related to humans and METHOD validation requiredduring drug DEVELOPMENT and manufacturing and these analytical methods are fit for theirintended purpose. To comply with the requirements of GMP pharmaceutical industries shouldhave an overall validation policy which documents howvalidation will be mainly focuses on the optimization of HPLC sequence of events requiredfor METHOD DEVELOPMENT and analytical validation are Words:HPLC,Analytical METHOD validation, Pharmaceuticalanalysis, Specificity,Precision, CHROMATOGRAPHYP artition chromatography can be subdivided into(i) liquid-liquid chromatography and(ii) bonded-phase chromatography.
1. Understand the physicochemical properties of drug molecule Physicochemical properties of a drug molecule play an important role in method development. For Method development one has to study the physical properties like solubility, polarity, pKa and pH of the drug molecule. Polarity is a physical property of a compound. It helps an analyst,
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