RAPID ANALYSIS OF RILPIVIRINE, EMTRICITABINE AND TENOFOVIR ACTIVE INGREDIENTS BY NOVEL HPLC METHOD RİLPİVİRİN, EMTRİSİTABİN VE TENOFOVİR AKTİF BİLEŞENLERİNİN YENİ HPLC YÖNTEMİYLE HIZLI ANALİZİ


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BAY M., Genc A. A., Bouali W., TIRIS G., ERK N.

Ankara Universitesi Eczacilik Fakultesi Dergisi, cilt.50, sa.1, ss.79-87, 2026 (Scopus, TRDizin) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 50 Sayı: 1
  • Basım Tarihi: 2026
  • Doi Numarası: 10.33483/jfpau.1632572
  • Dergi Adı: Ankara Universitesi Eczacilik Fakultesi Dergisi
  • Derginin Tarandığı İndeksler: Scopus, Central & Eastern European Academic Source (CEEAS), TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.79-87
  • Anahtar Kelimeler: Emtricitabine, rilpivirine, RP-HPLC, simultaneous determination, tenofovir
  • Bezmiâlem Vakıf Üniversitesi Adresli: Evet

Özet

Objective: A novel high-performance liquid chromatography (HPLC) method was developed for the simultaneous determination of Emtricitabine (EMT), Tenofovir (TNF), and Rilpivirine (RLP). Material and Method: The analysis was performed using a Waters XBridge C18 (3.5 µm, 4.6 × 150 mm) column. The mobile phase consisted of methanol and triethylamine buffer (pH 3.15) in a 60:40 (v/v) ratio, with a flow rate of 1.2 ml/min. The developed method was successfully applied to standard mixtures and pharmaceutical tablet formulations containing EMT, TNF, and RLP, without matrix interference. Result and Discussion: The proposed technique exhibited good linearity, with correlation coefficients (R²) of 0.999 for EMT, 0.999 for TNF, and 1.000 for RLP. The calibration ranges were 10.0–600.0 µg/ml for EMT, 2.0–75.0 µg/ml for TNF, and 2.0–75.0 µg/ml for RLP. The method was validated in accordance with ICH guidelines, demonstrating high sensitivity, precision, and accuracy. It was found to be a rapid, economical, and efficient approach for the simultaneous determination of these active pharmaceutical ingredients.