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To determine entrapment efficiency of sparfloxacin lactate liposome with cation exchange resin-HPLC

机译:用阳离子交换树脂-HPLC测定施霉素血红素脂质体的血小板血红素脂质体的夹紧效率

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OBJECTIVE: To determine the entrapment efficiency of sparfloxacin lactate liposome. METHOD: The cation exchange resin was adopted to separate free sparfloxcain lactate from liposome dispersions. The content of sparfloxacin was determined by HPLC with Hypersil ODS2 column (250mm×4.6mm, 5μm). The mobile phase was 0.2mol·L-1 ammonium acetate solution acetonitrile (70:30 v/v, adjusted to pH 3.5 with acetic acid). The flow rate and UV detection were set respectively at 1.0mL·min-1 and 298nm. RESULTS: The free sparfloxacin was well separated from liposome dispersions and was adsorbed up to 9643% by cation exchange resin, but liposome was less than 2.63%. Sparfloxacin had a good linear relation in the range of 4.2-50.4μg·mL-1 (R2=1), the precision (RSD) was less than 1.30%, the sample recoveries were 99.96%-102.11%. CONCLUSION: This method is technically simple, rapid and efficient to separate and determine entrapment efficiency of sparfloxacin liposome.
机译:目的:确定施霉素乳酸脂质体的血小板血管素。方法:采用阳离子交换树脂与脂质体分散体分离自由蜘蛛乳酸乳酸盐。通过HPLC与Hypersil ODS2柱(250mm×4.6mm,5μm)测定Sparfloxacin的含量。流动相是0.2mol·L-1乙酸铵溶液乙腈(70:30V / V,用乙酸调节至pH 3.5)。流速和UV检测分别设置在1.0ml·min-1和298nm。结果:自由素氟辛酸与脂质体分散体分离得很好,并通过阳离子交换树脂吸附高达9643%,但脂质体小于2.63%。 Sparfloxacin在4.2-50.4μg·mL-1(R2 = 1)的范围内具有良好的线性关系,精度(RSD)小于1.30%,样品回收率为99.96%-102.11%。结论:这种方法在技术上简单,快速有效地分离和确定素脂素脂质体的夹带效率。

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