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A pre-column derivatization-HPLC method for determination of oxalipIatin(L-OHP)content and entrapment efficiency in nanoparticles

机译:纳米粒子中氧化素(L-OHP)含量(L-OHP)含量和熵效率的柱衍生 - HPLC方法

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Purpose: To develop an improved -HPLC method for the determination of oxaliplatin(L-OHP) content and entrapment efficiency in nanoparticles. Methods: After derivatization with sodium diethyldithiocarbamate (DDTC), Pt(DDTC)2 and diazepam (the internal standard) was separated on C18 column (250 mm×4.6 mm, 5 urn) at 30°Cusing a mobile phase consisting of methol and water (75:25, v/v) at flow rate of 1 ml-min-1; The method was validated with respect to selectivity, linearity, precision and accuracy, limit of quantification and stability. The ultrafiltration was employed to separate the free L-OHP from nanoparticles to calculate the entrapment efficiency. Results: The calibration curve of L-OHP was linear in the concentration range of 5.26-31.53 ugml-1. (r= 0.9997) with the limit of quantification (LOQ) of 0.42 ug/mL. The variation coefficients were not more than 1.63%. The mean recoveries was from 98.29% to 100.45%. The content and the encapsulation efficiency of L-OHP nanoparticles were 1.69mg/ml and 63%, respectively. Conclusion:The present method can be used to determine L-OHP content in prepared nanoparticles.as well as entrapment efficiency.
机译:目的:开发一种改进的-HPLC方法,用于测定纳米颗粒中的奥沙利​​铂(L-OHP)含量和熵效率。方法:用二乙基二硫代氨基甲酸钠(DDTC)衍生化,Pt(DDTC)2和DiazePam(内标)在C18柱(250mm×4.6mm,5瓮)上,在30°勾勒出由甲基和水组成的流动相(75:25,v / v),流速为1 ml-min-1;该方法是关于选择性,线性,精度和精度,量化极限和稳定性的验证。采用超滤将自由L-OHP与纳米颗粒分离以计算截留效率。结果:L-OHP的校准曲线在浓度范围内为5.26-31.53 UGML-1。 (r = 0.9997),定量限为0.42 ug / ml。变异系数不大于1.63%。平均回收率为98.29%至100.45%。 L-OHP纳米颗粒的含量和封装效率分别为1.69mg / mL和63%。结论:本方法可用于确定制备的纳米颗粒中的L-OHP含量。作为截留效率。

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