Feng Si-Shen, Zeng Wutao, Teng Lim Yean, Zhao Lingyun, Yin Win Khin, Oakley Reida, Hin Teoh Swee, Hang Lee Ronald Chi, Pan Shirong
Department of Chemical & Biomolecular Engineering, National University of Singapore, Singapore.
Nanomedicine (Lond). 2007 Jun;2(3):333-44. doi: 10.2217/17435889.2.3.333.
Paclitaxel is one of the most effective antiproliferative agents and it has been applied in the development of drug-eluting stents. There are difficulties, however, in using paclitaxel in clinical applications owing to its poor solubility and side effects. We have synthesized nanoparticles of biodegradable polymers for the effective and sustainable delivery of paclitaxel and other antiproliferative agents for restenosis treatment.
METHODS & RESULTS: Paclitaxel-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles were prepared by a modified solvent extraction/evaporation method with D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS) or polyvinyl alcohol (PVA) as an emulsifier. Drug-loaded nanoparticles were characterized for size and size distribution, surface morphology, surface charge, drug-encapsulation efficiency and in vitro drug-release kinetics. Cellular uptake of fluorescent nanoparticles was investigated in vitro in coronary artery smooth muscle cells and in vivo in the carotid arteries of rabbits. The antiproliferative effects of the nanoparticle formulations were assessed in vitro in close comparison with Taxol((R)). Both the PVA- and TPGS-emulsified nanoparticles have similar size and size distribution, surface morphology and dispersion stability and showed great advantages over paclitaxel in in vitro cellular uptake and cytotoxicity than Taxol. The TPGS-emulsified nanoparticle formulation has higher drug-encapsulation efficiency, cellular uptake and cytotoxicity than the PVA-emulsified nanoparticle formulation. IC(50) in 24-h culture with coronary artery smooth muscle cells is 748 ng/ml for paclitaxel, 708 ng/ml for PVA-emulsified nanoparticles and 474 ng/ml for TPGS-emulsified nanoparticles, respectively.
TPGS-emulsified PLGA nanoparticles have great potential for the effective and sustainable delivery of antiproliferative agents and for the development of nanoparticle-coated stents, which may become the third generation of cardiovascular stents.
紫杉醇是最有效的抗增殖药物之一,已应用于药物洗脱支架的研发。然而,由于其溶解性差和副作用,紫杉醇在临床应用中存在困难。我们合成了可生物降解聚合物纳米颗粒,用于有效且持续地递送紫杉醇及其他抗增殖药物以治疗再狭窄。
采用改良的溶剂萃取/蒸发法,以聚乙二醇1000维生素E琥珀酸酯(TPGS)或聚乙烯醇(PVA)为乳化剂,制备了负载紫杉醇的聚乳酸-羟基乙酸共聚物(PLGA)纳米颗粒。对载药纳米颗粒的尺寸及尺寸分布、表面形态、表面电荷、药物包封率和体外药物释放动力学进行了表征。在体外冠状动脉平滑肌细胞和体内兔颈动脉中研究了荧光纳米颗粒的细胞摄取情况。与紫杉醇(Taxol®)密切比较,评估了纳米颗粒制剂的体外抗增殖作用。PVA和TPGS乳化的纳米颗粒具有相似的尺寸及尺寸分布、表面形态和分散稳定性,并且在体外细胞摄取和细胞毒性方面比紫杉醇表现出更大优势。TPGS乳化的纳米颗粒制剂比PVA乳化的纳米颗粒制剂具有更高的药物包封率、细胞摄取率和细胞毒性。在冠状动脉平滑肌细胞24小时培养中,紫杉醇的IC50为748 ng/ml,PVA乳化纳米颗粒为708 ng/ml,TPGS乳化纳米颗粒为474 ng/ml。
TPGS乳化的PLGA纳米颗粒在有效且持续地递送抗增殖药物以及开发纳米颗粒涂层支架方面具有巨大潜力,这可能成为第三代心血管支架。