Stress studies of tenofovir disoproxil fumarate by HPTLC in bulk drug and pharmaceutical formulation

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Abstract

A stability-indicating high-performance thin-layer chromatographic (HPTLC) method for determination of tenofovir disoproxil fumarate in bulk drug and in tablet has been developed and validated. The mobile phase selected was chloroform:methanol (9.0:1.0, v/v) with ultraviolet (UV) detection at 260nm. The retention factor was found to be 0.490.03 with correlation coefficients of 0.9994 in the range 300-1500ng/spot and with an accuracy of 99.25%. Method had the potential to determine tenofovir disoproxil fumarate from tablet without any interference, and it was a stability-indicating one. Copyright 2012 Shweta Havele and Sunil R. Dhaneshwar.

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Havele, S., & Dhaneshwar, S. R. (2012). Stress studies of tenofovir disoproxil fumarate by HPTLC in bulk drug and pharmaceutical formulation. The Scientific World Journal, 2012. https://doi.org/10.1100/2012/894136

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