Hacettepe University, Faculty of Pharmacy, Department of Analytical Chemistry, 06230 Ankara, Turkey; Drogsan Pharmaceuticals R&D Department, 06830 Gölbaşı, Ankara, Turkey.
Hacettepe University, Faculty of Pharmacy, Department of Analytical Chemistry, 06230 Ankara, Turkey.
J Pharm Biomed Anal. 2021 Jun 5;200:114075. doi: 10.1016/j.jpba.2021.114075. Epub 2021 Apr 20.
Tazarotene, a member of the acetylenic class of retinoids, is a third-generation prescription topical retinoid sold as a cream, gel, or foam. In its gel or cream formulations, tazarotene is at a concentration of either 0.1 % or 0.05 %. Fabric phase sorptive extraction membranes are used to selectively isolate and preconcentrate target analytes from different sample matrices. In this study, the tazarotene gel formulation was directly applied to fabric phase sorptive extraction membranes and extracted through a mixture of acetonitrile and water (80:20, v/v) to obtain a clean product free of colloidal suspension of tazarotene gel formulation. The final solutions were injected into an HPLC system equipped with a Zorbax 5 μm Phenyl-Hexyl LC Column (250 × 4.6 mm). Injection volume was 50 μL and UV detection was performed at 326 nm. The flow rate was 1.0 mL min while using an isocratic elution with a mixture of ammonium acetate (50 mM) and methanol (15:85, v/v) as the mobile phase. The method was validated according to ICH guideline Q2 (R1) and successfully applied to gel formulations including 0.01 % tazarotene. This is the first reported application of fabric phase sorptive extraction in the analyses of gel formulations. The capability of fabric phase sorptive extraction membranes to clean up the sample matrix and prepare active pharmaceutical ingredients to be analyzed with acceptable recovery (>98.0 %) and reproducibility may encourage quality control laboratories to use fabric phase sorptive extraction in routine applications.
他扎罗汀是类视黄醇的炔属化合物,是第三代处方局部用维 A 酸,以乳膏、凝胶或泡沫剂的形式出售。其凝胶或乳膏制剂中他扎罗汀的浓度分别为 0.1%或 0.05%。纤维相固相萃取膜用于选择性地从不同的样品基质中分离和浓缩目标分析物。在这项研究中,他扎罗汀凝胶制剂直接应用于纤维相固相萃取膜,然后通过乙腈和水(80:20,v/v)的混合物提取,以获得无胶体悬浮的清洁产物。最后将溶液注入配备 Zorbax 5 μm 苯基己基 LC 柱(250×4.6mm)的 HPLC 系统。进样量为 50μL,在 326nm 处进行紫外检测。流速为 1.0mL/min,采用乙酸铵(50mM)和甲醇(15:85,v/v)的混合物作为流动相进行等度洗脱。该方法按照 ICH 指南 Q2(R1)进行验证,并成功应用于包括 0.01%他扎罗汀的凝胶制剂。这是纤维相固相萃取在凝胶制剂分析中的首次报道应用。纤维相固相萃取膜能够净化样品基质并准备待分析的活性药物成分,具有可接受的回收率(>98.0%)和重现性,这可能鼓励质量控制实验室在常规应用中使用纤维相固相萃取。