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更昔洛韦眼用在体凝胶剂的制备及其含量测定 被引量:3

Determination of Ganciclovir in In-situ Ophthalmic Gel by RP-HPLC
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摘要 试验制备了更昔洛韦眼用在体凝胶剂并测定更昔洛韦的含量。采用RP-HPLC法,色谱柱:Dikma C 18柱(150 mm×4.6 mm,5μm);流动相:V(甲醇)∶V(水)=10∶90;检测波长:254 nm;柱温:室温;流速:1.0 mL/min。更昔洛韦在10.0~60.0μg/mL范围内线性关系良好(r2=0.999 5);更昔洛韦的平均回收率为99.9%,RSD为0.23%。该方法简单、快捷,回收率和重复性良好,可作为更昔洛韦在体凝胶剂质量评价的方法。 The ganciclovir in-situ ophthalmic gel was prepared and ganciclovir content in in-situ ophthalmic gel was determined by chromatography.Chromatography was performed using a Dikma C18(150 mm×4.6 mm,5 μm)column with mobile phase consisting of a mixture of methanol-water(V(methanol)∶V(water)= 10∶90).The monitoring wavelength was set at 254 nm.The flow rate was 1.0 mL/min at room temperature.A good linearity was found in the range of 10.0~60.0 μg/mL(r2 = 0.999 5).The average recoveries was 99.9%(RSD=0.23%).The method is simple,rapid,satisfactory recoveries and good reproducibility.It can be used to control the quality of ganciclovir in-situ gel.
出处 《当代化工》 CAS 2010年第2期126-128,共3页 Contemporary Chemical Industry
关键词 更昔洛韦 高效液相色谱 在体凝胶剂 Ganciclovir RP-HPLC In-situ gel
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