Novel approaches for determination of antiretroviral reverse transcriptase inhibitor agent in commercial dosage forms by using spectrofluorimetric, first derivative spectrophotometric, and HPLC methods

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TIRIS G., Ciloglu E., ERK N.

FUTURE JOURNAL OF PHARMACEUTICAL SCIENCES, cilt.6, sa.1, 2020 (ESCI) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 6 Sayı: 1
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1186/s43094-020-00070-w
  • Dergi Adı: FUTURE JOURNAL OF PHARMACEUTICAL SCIENCES
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI)
  • Anahtar Kelimeler: Tenofovir, Spectrofluorimetry, HPLC, First derivative spectrophotometry, Quantitative analysis, TENOFOVIR DISOPROXIL FUMARATE, PERFORMANCE LIQUID-CHROMATOGRAPHY, MASS-SPECTROMETRY METHOD, HUMAN PLASMA, SIMULTANEOUS QUANTIFICATION, VALIDATION, LAMIVUDINE, EFAVIRENZ, EMTRICITABINE, ELVITEGRAVIR
  • Ankara Üniversitesi Adresli: Evet

Özet

Background: Rapid, simple, and sensitive spectrofluorimetric, first derivative spectrophotometric, and high-performance liquid chromatographic (HPLC) methods have been developed and validated for determination of tenofovir in pharmaceutical preparations. Spectrofluorimetric method is based on measuring the native fluorescence intensity of tenofovir at 375.0 nm after excitation at 275.0 nm. Calibration graphics were plotted and were found linear over 4.72-15.75 mu g/mL concentration range (r(2)= 0.9994). The second method developed was the first derivative spectrophotometric method for the analysis of tenofovir performed by measuring the amplitude at 251.7 and 272.6 nm. Linearity was observed in the concentration range 10.0-28.0 mu g/mL (r(2)= 0.9998). On the other hand, HPLC with a diode array detector (DAD). Ritonavir was used as internal standard (IS). HPLC analysis was carried out on a C(18)column (Wakosil-II 5 C-18 AR, 4.6 x 250 mm) using a mobile phase consisting of acetonitrile: 0.5% formic acid (99.5:0.5; v/v) at a flow rate of 1.0 mL/min. Injection volume was 5.0 mu L. DAD signals at 260.0 nm were used. HPLC method was found to be linear over the concentration range of 10.0-100.0 mu g/mL (r(2)= 0.9990).