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Preparation and Pharmacokinetics of Candesartan Cilexetil with Polymer Materials in Self-Microemulsifying Drug Delivery Systems

机译:用自我乳化药物递送系统中的聚合物材料制备和药代动力学

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The candesartan cilexetil SMEDDS with PEG-PLA as long-circulating materials were successfully prepared and characterized by appearance, size and size distribution, morphology of emulsion and stability. The emulsion showed a narrow size distribution, well-proportioned in good agreement with polydispersity index of 0.005 and 3.6 nm diameter. The candesartan cilexetil SMEDDS were precipitated for 30 days at 25 °C or 37 °C. Meanwhile, Pharmacokinetics experiments illuminated that the candesartan cilexetil SMEDDS in rats had a larger drug curve concentration (AUC) compared to the tablets in the experiments.
机译:用PEG-PLA作为长循环材料的Candaartan Cilexetil Smedds通过外观,尺寸和尺寸分布,乳液和稳定性的形貌,表征。乳液显示出窄尺寸分布,与0.005和3.6nm的多分散指数良好的良好相一致。 Candesartan Cilexetil Smedds在25℃或37℃下沉淀30天。同时,与实验中的片剂相比,药代动力学实验照亮了大鼠中的坎德坦纤维曲线Smedds具有较大的药物曲线浓度(AUC)。

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