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Paclitaxel-loaded star-shaped copolymer nanoparticles for enhanced malignant melanoma chemotherapy against multidrug resistance

机译:负载紫杉醇的星形共聚物纳米颗粒可增强恶性黑色素瘤化学疗法的多药耐药性

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Malignant melanoma (MM) is the most dangerous type of skin cancer with annually increasing incidence and death rates. However, chemotherapy for MM is restricted by low topical drug concentration and multidrug resistance. In order to surmount the limitation and to enhance the therapeutic effect on MM, a new nanoformulation of paclitaxel (PTX)-loaded cholic acid (CA)-functionalized star-shaped poly(lactide-co-glycolide) (PLGA)-d-α-tocopheryl polyethylene glycol 1000 succinate (TPGS) nanoparticles (NPs) (shortly PTX-loaded CA-PLGA-TPGS NPs) was fabricated by a modified method of nanoprecipitation. The particle size, zeta potential, morphology, drug release profile, drug encapsulation efficiency, and loading content of PTX-loaded NPs were detected. As shown by confocal laser scanning, NPs loaded with coumarin-6 were internalized by human melanoma cell line A875. The cellular uptake efficiency of CA-PLGA-TPGS NPs was higher than those of PLGA NPs and PLGA-TPGS NPs. The antitumor effects of PTX-loaded NPs were evaluated by the MTT assay in vitro and by a xenograft tumor model in vivo, demonstrating that star-shaped PTX-loaded CA-PLGA-TPGS NPs were significantly superior to commercial PTX formulation Taxol?. Such drug delivery nanocarriers are potentially applicable to the improvement of clinical MM therapy.
机译:恶性黑色素瘤(MM)是皮肤癌中最危险的类型,其发病率和死亡率逐年增加。但是,MM的化疗受到局部药物浓度低和多药耐药性的限制。为了克服这一局限性并增强对MM的治疗效果,负载紫杉醇(PTX)的胆酸(CA)功能化星形聚丙交酯-乙交酯(PLGA)-d-α的新纳米制剂-生育酚聚乙二醇1000琥珀酸酯(TPGS)纳米颗粒(NPs)(短时间负载PTX的CA-PLGA-TPGS NPs)是通过改良的纳米沉淀方法制备的。检测了PTX负载的NP的粒径,ζ电位,形态,药物释放曲线,药物包封效率和负载量。如共聚焦激光扫描所示,载有香豆素6的NP被人黑素瘤细胞系A875内化。 CA-PLGA-TPGS NPs的细胞吸收效率高于PLGA NPs和PLGA-TPGS NPs。通过体外MTT分析和体内异种移植肿瘤模型评估了PTX负载的NPs的抗肿瘤作用,表明星形PTX负载的CA-PLGA-TPGS NPs明显优于商业PTX制剂Taxol ?。这样的药物递送纳米载体潜在地可用于改善临床MM疗法。

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