Hassib Sonia T, Mahrouse Marianne A, Elkady Ehab F, Sayed Rawda M
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo, Egypt.
J Chromatogr Sci. 2018 Sep 1;56(8):716-723. doi: 10.1093/chromsci/bmy047.
Topical pharmaceutical preparations containing betamethasone esters are widely prescribed for treatment of severe inflammatory skin conditions. Some betamethasone esters-containing preparations are formulated with either an antibacterial or an antifungal agent or a vitamin D3 derivative. A fast reversed-phase high-performance liquid chromatography method has been developed for the simultaneous determination of three betamethasone esters-containing binary mixtures along with the excipients of their dosage forms using clobetasone butyrate as internal standard. The first mixture was betamethasone valerate and fusidic acid (Mixture I) with chlorocresol as preservative. The second mixture was betamethasone dipropionate (BTD) and clotrimazole (Mixture II) with benzyl alcohol as preservative. The third mixture was BTD and calcipotriol monohydrate (Mixture III). Optimized chromatographic separation was achieved on a Discovery® C18 (4.6 × 250 mm, 5 μm) column, using water: acetonitrile (35:65, v/v) as mobile phase at flow rate of 1 mL/min with UV detection at 230 nm. The method was validated according to ICH guidelines. The regression coefficients were > 0.999 for all drugs. The method was successfully applied for the determination of the studied drugs in bulk, synthetic mixtures and dosage forms. The developed method is accurate, sensitive, selective and precise and can be used for routine analysis in quality control laboratories.
含有倍他米松酯的局部用药物制剂被广泛用于治疗严重的炎症性皮肤病。一些含有倍他米松酯的制剂还与抗菌剂、抗真菌剂或维生素D3衍生物一起配制。已开发出一种快速反相高效液相色谱法,以丁酸氯倍他索作为内标,同时测定三种含倍他米松酯的二元混合物及其剂型的辅料。第一种混合物是戊酸倍他米松和夫西地酸(混合物I),以氯甲酚作为防腐剂。第二种混合物是二丙酸倍他米松(BTD)和克霉唑(混合物II),以苯甲醇作为防腐剂。第三种混合物是BTD和一水钙化醇(混合物III)。在Discovery® C18(4.6×250 mm,5μm)色谱柱上实现了优化的色谱分离,使用水:乙腈(35:65,v/v)作为流动相,流速为1 mL/min,在230 nm处进行紫外检测。该方法根据ICH指南进行了验证。所有药物的回归系数均>0.999。该方法已成功应用于原料药、合成混合物和剂型中所研究药物的测定。所开发的方法准确、灵敏、选择性好且精密,可用于质量控制实验室的常规分析。