[Study on chitosan-modified tripterygium glycoside nanoparticles and its renal targeting property].

Q3 Pharmacology, Toxicology and Pharmaceutics
Xiuxia Chen, Yinghui Wei, Jin-Na Yao, Yan-min Zhao, Xiao-Guang Shang, Fan-zhu Li
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引用次数: 3

Abstract

OBJECTIVE To prepare chitosan-modified tripterygium glycoside nanoparticles (LMWC-TG-PLA-NPs), and assess its renal targeting property in rats. METHOD Chitosan-modified tripterygium glycoside nanoparticles (LMWC-TG-PLA-NPs) were prepared by modified spontaneous emulsification solvent evaporation method, and modified with 50% deacetylated low molecular weight chitosan (LMWC). The shape of nanoparticles was observed under a transmission electron microscope. The mean diameter of nanoparticles was measured by particle size analyzer. The drug encapsulation efficiency and drug loading were measured by centrifuge method. The in vitro release behavior was studied with dialysis bags. Renal microdialysis technique and renal artery administration technique were combined to study the renal targeting property of nanopartcles. LMWC-TG-PLA-NPs were administrated in rats by tail vein injection (TVI) and renal artery administration (RAA), respectively, with TG-PLA-NPs as the control group. Renal dialysis fluid was regularly collected to determine the drug concentration in the dialysis fluid, map drug concentration-time curves, and calculate AUC ratio in kidneys through the two injection approaches as the renal targeting parameter (RTP), in order to assess the renal targeting property of LMWC-TG-PLA-NPs. RESULTS The prepared LMWC-TG-PLA-NPs looked smooth and round. Their average diameter, polydispersity index, encapsulation efficiency and drug loading were (207.6 +/- 3.4) nm, (0.078 +/- 0.009)%, (61.83 +/- 2.43)%, and (10.70 +/- 0.37)%, respectively. The pH 7.4 PBS buffer solution containing 20% ethanol showed obvious sustained release behavior. LMWC-TG-PLA-NPs showed a RTP of 71.97%, which was 3.6 times of TG-PLA-NPs of the control group. CONCLUSION The prepared LMWC-TG-PLA-NPs showed high drug encapsulation efficiency and drug loading, with obvious sustained release characteristics and renal targeting property. LMWC-TG-PLA-NPs are expected to become a new type vector for reducing toxic and side effects of tripterygium glycoside. Meanwhile, a new method is established for assessing renal targeting property with AUC ratio in kidneys after administrated through caudal veins and renal arteries as the renal targeting parameter.
壳聚糖修饰雷公藤苷纳米颗粒及其肾靶向性研究。
目的制备壳聚糖修饰的雷公藤苷纳米颗粒(LMWC-TG-PLA-NPs),并评价其大鼠肾靶向性。方法采用改性自发乳化溶剂蒸发法制备壳聚糖修饰雷公藤苷纳米粒子(LMWC- tg - pla - nps),并以50%脱乙酰化低分子量壳聚糖(LMWC)修饰。在透射电镜下观察纳米颗粒的形状。采用粒径分析仪测定纳米颗粒的平均粒径。采用离心法测定药物包封率和载药量。用透析袋研究其体外释放行为。将肾微透析技术与肾动脉给药技术相结合,研究纳米颗粒的肾靶向性。大鼠分别通过尾静脉注射(TVI)和肾动脉给药(RAA)给药LMWC-TG-PLA-NPs,对照组TG-PLA-NPs。定期采集肾透析液,测定透析液中药物浓度,绘制药物浓度-时间曲线,并通过两种注射方式计算肾脏内AUC比值作为肾靶向参数(RTP),以评价LMWC-TG-PLA-NPs的肾靶向性。结果制备的LMWC-TG-PLA-NPs表面光滑圆润。其平均直径为(207.6 +/- 3.4)nm,多分散指数为(0.078 +/- 0.009)%,包封率为(61.83 +/- 2.43)%,载药量为(10.70 +/- 0.37)%。含20%乙醇的ph7.4 PBS缓冲液表现出明显的缓释行为。LMWC-TG-PLA-NPs的RTP为71.97%,是对照组TG-PLA-NPs的3.6倍。结论制备的LMWC-TG-PLA-NPs包封效率高,载药量大,具有明显的缓释特性和肾靶向性。LMWC-TG-PLA-NPs有望成为降低雷公藤苷毒副作用的新型载体。同时,建立了以尾静脉和肾动脉给药后肾脏AUC比值作为肾脏靶向参数评价肾脏靶向性的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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