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Inventi Rapid: Pharm Analysis & Quality Assurance

Articles

  • Inventi:prpaqa/20163/21
    RP-HPLC Method Development and Validation for the Estimation of Lamivudine in Bulk Form
    01-Oct-2016 Research 2016 : October-December
    A Indira*, A Varada Reddy, K Satyanarayana, J Nageswara Rao, Geetha Priyadarshini

    A new RP-HPLC method for lamivudine has been developed and validated. The developed method was simple and accurate and validated for various parameters as per ICH guidelines. The drug has shown �»max at 226 nm in UV. The linearity concentration range for the drug was found to be 100-500 �¼g/ml and co-relation coefficient was found to 0.998 for RP-HPLC method respectively. The validation parameters as per the ICH guidelines were determined and found to be within the limits.

    How to Cite this Article
    A Indira, A Varada Reddy, K Satyanarayana et al. RP-HPLC Method Development and Validation for the Estimation of Lamivudine in Bulk Form. Inventi Rapid: Pharm Analysis & Quality Assurance, 2016(4):1-5, 2016.
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