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RP-HPLC法测定黄芩苷脂质体的体外释放度 被引量:8

Determination of in Vitro Drug Release of Baicalin Liposomes by HPLC
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摘要 目的:建立以反相高效液相色谱法测定黄芩苷脂质体的体外释放度的方法。方法:色谱柱为岛津C18(150mm×4.6mm,5μm),流动相为甲醇-水-磷酸(47∶53∶0.2),流速为1.0mL.min-1,检测波长为280nm,柱温为25℃,进样量为10μL。结果:黄芩苷检测浓度在1.01~80.80μg.mL-1范围内与峰面积积分值呈良好线性关系(r=0.9998);平均加样回收率为100.05%,RSD=0.93%。结论:本方法灵敏、简便、准确,可用于黄芩苷脂质体的体外释放研究。 OBJECTIVE: To establish a HPLC method for the determination of in vitro drug release of Baicalin liposomes. METHODS: The separation was performed on a C18 column (150mm × 4.6mm, 5μm) at 25℃ ; the mobile phase was composed of methanol - water - phosohoric acid (47 : 53 : 0.2) at a flow rate of 1.0mL · min^-1.The ultraviolet wavelength was set at 280nm and the sample size was 10μL. RESULTS: The calibration curve showed good linearity in the range of 1.01 80.80μg · mL^-l(r-= 0.999 8) and the average recovery rate was 100.05% (RSD = 0.93%) .CONCLUSION: The method is sensitive, simple and accurate, and applicable for the study of in vitro drug release of Baicalin liposomes.
出处 《中国药房》 CAS CSCD 北大核心 2007年第33期2594-2596,共3页 China Pharmacy
关键词 反相高效液相色谱法 黄芩苷 脂质体 体外释放度 RP-HPLC Baicalin Liposomes In vitro release
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