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Nandi, U., Das, A., Roy, B., Choudhury, H., Gorain, B. and Pal, T.K. (2012) Development and Validation of an HPLC-UV Method for Simultaneous Determination of Zidovudine, Lamivudine, and Nevirapine in Human Plasma and Its Application to Pharmacokinetic Study in Human Volunteers. Drug Testing and Analysis, 5, 485-491.
https://pubmed.ncbi.nlm.nih.gov/22374835
https://doi.org/10.1002/dta.419

has been cited by the following article:

• TITLE: Development, Validation and Application of a Spectrofluorimetric Method for the Quantification of Nevirapine in Pharmaceutical Formulations Tablets and Suspensions

  AUTHORS: Lucien Murhula Namegabe, Aladin Ombeni Mahano, Serigne Omar Sarr

  KEYWORDS: Spectrofluorimetric Method, Validation Nevirapine, Sodium Hypochlorite

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.13 No.6, June 30, 2022

  ABSTRACT: The development of the spectrofluorimetric method can be considered a promising alternative that is relatively less expensive and sufficiently reliable. In the current literature, no method for the analysis of nevirapine by spectro-fluorimetric has been reported. The proposed method is based on the transformation of naturally non-fluorescent nevirapine into a fluorescent derivative after chemical synthesis. Maximum excitation and emission wavelengths are 290 nm and 357 nm respectively. The analytical performance of the method demonstrates linearity in the concentration range 1.5 × 10-2 and 13.5 × 10-2 μg/mL with a correlation coefficient (r) greater than 0.999. The detection (LOD) and quantification (LOQ) limits found are 1.97 × 10-3 μg/mL and 5.48 × 10-3 μg/mL respectively. Recovery is achieved with 99.9% and 100.3% trueness, intra-day precision with a coefficient of variation of repeatability (CVr) of 0.99% and inter-day precision with a coefficient of variation of precision (CVR) of 1.7%. The method has been successfully applied in the analysis of 10 batches of nevirapine tablets and suspensions.