UV Spectrophotometric method for the identification and solubility determination of nevirapine

Pharmazie

Volumn 64, Issue 10, 2009, Pages 690-691

  Stieger, Nicole ^a   Liebenberg, W ^a   Wessels, J C ^a  

^a NORTH WEST UNIVERSITY   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROCHLORIC ACID; METHANOL; NEVIRAPINE; WATER; SOLVENT;

ANALYTIC METHOD; ARTICLE; DRUG DETERMINATION; DRUG SOLUBILITY; QUANTITATIVE ANALYSIS; ULTRAVIOLET SPECTROPHOTOMETRY; CHEMISTRY; SOLUBILITY; STANDARD;

HYDROCHLORIC ACID; METHANOL; NEVIRAPINE; REFERENCE STANDARDS; SOLUBILITY; SOLVENTS; SPECTROPHOTOMETRY, ULTRAVIOLET; WATER;

EID: 74949098148     PISSN: 00317144     EISSN: None     Source Type: Journal    
DOI: 10.1691/ph.2009.9163     Document Type: Article

References (8)

1. Anbazhagan S, Indumathy N, Shanmugapandiyan P, Sridhar SK (2005) Simultaneous quantification of stavudine, lamivudine and nevirapine by UV spectroscopy, reverse phase HPLC and HPTLC in tablets. J Pharm Biomed Anal 39: 801-804.
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4. rd ed. London: Pharmaceutical Press. p. 1329-1330.
5. th ed. Whitehouse Station, NJ: Merck Research Laboratories. p. 1123.
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8. United States Pharmacopoeia (2009) Monographs: Nevirapine. [Web:] http://www.uspnf.com/uspnf/pub/data/v32270/usp32nf27s0 m56485.xml. [Date of access: 19 May 2009].