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首页> 外文期刊>International Journal of Pharmaceutics >Size-based anti-tumoral effect of paclitaxel loaded albumin microparticle dry powders for inhalation to treat metastatic lung cancer in a mouse model
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Size-based anti-tumoral effect of paclitaxel loaded albumin microparticle dry powders for inhalation to treat metastatic lung cancer in a mouse model

机译:基于紫杉醇负载白蛋白微粒干粉的抗肿瘤作用,用于吸入以治疗小鼠模型中的转移性肺癌

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摘要

In this study, we prepared paclitaxel (PTX) loaded bovine serum albumin (BSA) microparticles (MPs) of different sizes (0.5, 1.0, and 3.0 mu m) and converted them into dry powders (DPs) of a uniform size (similar to 5.0 mu m) through spray-drying techniques. The aim of preparing different sized PTX-MPs is to investigate the size-based in vivo biodistribution and retention of PTX in the lungs after intratracheal administration. Following the in vitro characterizations, the anti-tumor efficacy of the DPs containing differently sized PTX-BSA-MPs administered through intratracheal insufflation was compared with intravenously administered PTX solution (Taxol). While the fastest drug release was found for the 0.5 mu m group, the 1.0 and 3.0 mu m groups showed the highest antitumor efficiency in vivo. Taken together, our results demonstrate that the initial particle size of the incorporated particles, i.e., MPs, is crucial for the anti-tumor efficacy of DPs administered by inhalation, and the initial particle size should be regarded as one of the key factors in the development and quality control of such preparations.
机译:在这项研究中,我们制备了不同尺寸(0.5,1.0和3.0μm)的紫杉醇(PTX)牛血清白蛋白(BSA)微粒(MPS),并将其转化为均匀尺寸的干粉(DPS)(类似于5.0 mu m)通过喷雾干燥技术。制备不同大小的PTX-MPS的目的是探讨基于体内生物分布的大小,并在肿瘤内给药后的PTX保留。在体外表征之后,将含有通过内腹腔内灌注施用的不同大小的PTX-BSA-MP的DPS的抗肿瘤疗效与静脉内施用的PTX溶液(紫杉醇)进行比较。虽然发现最快的药物释放对于0.5μm,但1.0和3.0μm的组在体内显示出最高的抗肿瘤效率。我们的结果表明,掺入颗粒的初始粒径,即MPS,对于通过吸入给药的DP的抗肿瘤效果至关重要,并且初始粒度应被视为其中一个关键因素之一这种准备的发展和质量控制。

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