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Capillary electrophoresis to determine entrapment efficiency of a nanostructured lipid carrier loaded with piroxicam

机译:毛细管电泳确定载有吡罗昔康的纳米结构脂质载体的包封率

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摘要

A simple and fast capillary electrophoresis method has been developed to determine the amount of piroxicam loaded in a drug delivery system based on nanostructured lipid carriers (NLC). The entrapment efficiency of the nanostructured lipid carrier was estimated by measuring the concentration of drug not entrapped in a suspension of NLC. The influence of different parameters on migration times, peak symmetry, efficiency and resolution was studied; these parameters included the pH of the electrophoretic buffer solution and the applied voltage. The piroxicam peak was obtained with a satisfactory resolution. The separation was carried out using a running buffer, which it is composed of 50 mmol L-1 ammonium acetate and 13.75 mmol L-1 ammonia at pH 9. The optimal voltage was 20kV and the cartridge temperature was 20°C. The corresponding calibration curve was linear over the range of 2.7 ? 5.4 µg mL-1 of NLC suspension. The reproducibility of migration time and peak area were investigated, and the obtained RSD% values (n = 5) were 0.99 and 2.13, respectively.
机译:已经开发出一种简单而快速的毛细管电泳方法来确定基于纳米结构脂质载体(NLC)的药物输送系统中吡罗昔康的含量。纳米结构脂质载体的包封效率通过测量未截留在NLC悬浮液中的药物浓度来估算。研究了不同参数对迁移时间,峰对称性,效率和分离度的影响;这些参数包括电泳缓冲溶液的pH值和施加的电压。以满意的分辨率获得吡罗昔康峰。使用运行缓冲液进行分离,该缓冲液由50 mmol L-1乙酸铵和13.75 mmol L-1氨在pH 9下组成。最佳电压为20kV,色谱柱温度为20°C。相应的校准曲线在2.7Ω范围内呈线性。 5.4 µg mL-1的NLC悬浮液。研究了迁移时间和峰面积的重现性,获得的RSD%值(n = 5)分别为0.99和2.13。

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