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Title: | Quantitative Analysis of Tenofovir by Titrimetric, Extractive Ion-pair Spectophotometric and Charge- Transfer Complexation Methods |
Authors: | Onah, Johnson O. Ukpe, Ajima |
Keywords: | Extractive spectrophotmetry Titrimetric analysis. Tenofovir disoproxil fumarate Extractive spectro photmetry |
Issue Date: | Feb-2011 |
Publisher: | Tropical Journal of Pharmaceutical Research |
Series/Report no.: | Vol. 10;No. 1; Pp 89-96 |
Abstract: | Purpose: Tenofovir disoproxil is an antiretroviral agent belonging to the class of nucleoside reversetranscriptase
inhibitors (NRTI’s) used in the management of HIV infection in adults. This study is aimed
at developing and validating four simple, sensitive and cost-effective analytical methods for ascertaining
the drug’s quality.
Methods: Tenofovir disoproxil forms a complex of 1:1 molar ratio with fumaric acid that was employed
in its aqueous titration with sodium hydroxide. Non-aqueous titration was also employed for its
determination. Extractive ion-pair spectrophotometric technique using methyl orange was similarly
employed to evaluate quantitatively the amount of tenofovir in the formulation. The drug was further
assayed by forming a charge-transfer complex with chloranilic acid and the coloured complex assayed
spectrophotometrically.
Results: Recovery experiments carried out by the proposed methods showed that aqueous titration
gave mean recovery of 97.7 % while non-aqueous titration gave 97.5 % recovery. The technique of
extractive ion-pair spectrophotometry similarly gave 98.7 % mean recovery while charge transfer
spectrophotometry gave 99.6 % for the same parameter.
Conclusion: These results show that the proposed methods are accurate, precise and sensitive. In
addition to being simple and cost-effective, they can conveniently be used for the assay of tenofovir
which has yet no official assay procedure. This investigation, therefore, contributes to the knowledge on
the development of assay techniques for a drug that is already extensively distributed in the market. |
URI: | http://hdl.handle.net/123456789/933 |
Appears in Collections: | Pharmaceutical Chemistry
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