首页> 外文期刊>Journal of biomedical nanotechnology >Comparative receptor based brain delivery of tramadol-loaded poly(lactic-co-glycolic acid) nanoparticles
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Comparative receptor based brain delivery of tramadol-loaded poly(lactic-co-glycolic acid) nanoparticles

机译:负载曲马多的聚乳酸-乙醇酸纳米粒子的基于受体的比较脑传递

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摘要

Receptor mediated endocytosis or transcytosis has been reported for drug delivery across Bloodbrain barrier (BBB) and hence, the aim of the present investigations was to prepare and compare brain targeting efficiency of tramadol-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles surface modified with transferrin (Tf) and lactoferrin (Lf). Nanoparticles of tramadol were prepared using nanoprecipitation technique and surface conjugated with Tf and Lf using epoxy linker. Prepared nanoparticles were characterized for their size, surface charge, drug entrapment, transmission electron microscopy and in vitro drug release. The surface density of Tf and Lf was estimated by protein estimation. The drug distribution in blood, brain and other tissues was studied in mice after intravenous administration. Tf and Lf anchored nanoparticles exhibit enhanced uptake with 2.38 and 3.85 folds higher targeting respectively in the brain when compared with unconjugated nanoparticles. The brain targeting observed for Lf anchored PLGA nanoparticles (Lf-TMD-PLGA-NP) was 1.62 folds that of Tf anchored PLGA nanoparticles (Tf-TMD-PLGA-NP). Hence, the study revealed Tf and specially Lf as promising ligand for enhanced brain deposition of tramadol.
机译:据报道,受体介导的内吞或胞吞作用可通过血脑屏障(BBB)进行药物输送,因此,本研究的目的是准备和比较负载曲马多的聚乳酸-乙醇酸(PLGA)的脑靶向效率用转铁蛋白(Tf)和乳铁蛋白(Lf)表面改性的纳米颗粒。使用纳米沉淀技术制备曲马多的纳米颗粒,并使用环氧连接剂将其与Tf和Lf表面共轭。制备的纳米颗粒的尺寸,表面电荷,药物截留,透射电子显微镜和体外药物释放均经过表征。 Tf和Lf的表面密度通过蛋白质估计来估计。静脉内给药后,在小鼠中研究了在血液,大脑和其他组织中的药物分布。与未结合的纳米粒子相比,Tf和Lf锚定的纳米粒子在大脑中的摄取增强,分别具有2.38和3.85倍的高靶向性。 Lf锚定PLGA纳米粒子(Lf-TMD-PLGA-NP)观察到的大脑靶向是Tf锚定PLGA纳米粒子(Tf-TMD-PLGA-NP)的1.62倍。因此,研究表明Tf,特别是Lf是有希望的配体,可增强曲马多的脑沉积。

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