DEVELOPMENT AND VALIDATION OF A HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD DETERMINATION OF ZIDOVUDINE ENCAPSULATED IN PCL NANOPARTICLES

DEVELOPMENT AND VALIDATION OF A HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD DETERMINATION OF ZIDOVUDINE ENCAPSULATED IN PCL NANOPARTICLES

A reversed-phase high-performance liquid chromatographic (HPLC) method was developed and validated for the determination of encapsulation efficiency of zidovudine in nanoparticules. The method was carried out in isocratic mode using 0.040M sodium acetate: methanol: acetonitrile: glacial acetic acid...

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Bibliographic Details
Published in:Drug Analytical Research Vol. 1; no. 2; pp. 1 - 8
Main Authors: Ribeiro Souza Magalhães, Milena Cristina, Portes Caldeira, Alisson Samuel, De Sousa Rocha Almeida, Hanna, Ligório Fialho, Sílvia, Da Silva Cunha Junior, Armando
Format: Journal Article
Language:English
Published: Universidade Federal do Rio Grande do Sul 28-12-2017
Online Access:Get full text
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Summary:A reversed-phase high-performance liquid chromatographic (HPLC) method was developed and validated for the determination of encapsulation efficiency of zidovudine in nanoparticules. The method was carried out in isocratic mode using 0.040M sodium acetate: methanol: acetonitrile: glacial acetic acid (880:100:20:2) as mobile phase, a C8 column at 25ºC and UV detection at 240 nm. The method was linear (r2 ˃ 0.99) over the range of 25.0-150.0 μg/mL, precise (RSD ˂ 5%), accurate (recovery = 100.5%), robust and selective. The validated HPLC-UV method can be successfully applied to determine the rate of zidovudine in nanoparticules.
ISSN:2527-2616
2527-2616
DOI:10.22456/2527-2616.79216