首页> 外文期刊>Journal of drug targeting >Magnetic poly epsilon-caprolactone nanoparticles containing Fe3O4 and gemcitabine enhance anti-tumor effect in pancreatic cancer xenograft mouse model.
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Magnetic poly epsilon-caprolactone nanoparticles containing Fe3O4 and gemcitabine enhance anti-tumor effect in pancreatic cancer xenograft mouse model.

机译:含Fe3O4和吉西他滨的磁性聚ε-己内酯纳米颗粒在胰腺癌异种移植小鼠模型中增强抗肿瘤作用。

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摘要

We prepared magnetic (Fe(3)O(4)) poly epsilon-caprolactone (PCL) nanoparticles (mean diameter 164 +/- 3 nm) containing an anticancer drug (gemcitabine) using emulsion-diffusion method in order to develop more efficient drug delivery for cancer treatment. Nanoparticles were smooth, well individualized and homogeneous in size. The values of magnetizations for the magnetic PCL nanoparticles were observed around 10.2 emu/g at 2000 Oe magnetic field intensity and showed super-paramagnetic property. In case of the drug, the drug loading contents was 18.6% and entrapment efficiency was 52.2%. The anti-tumor effects caused by these particles were examined using nude mice bearing subcutaneous human pancreatic adenocarcinoma cells (HPAC) in vivo. We divided that these mice were randomly assigned to one of five treatment groups for experimental contrast. The antitumor effect was showed with 15-fold higher dose when compared to free gemcitabine. From the result, the magnetic PCL nanoparticles may provide a therapeutic benefit by delivering drugs efficiently to magnetically targeted tumor tissues, thus achieving safe and successful anti-tumor effects with low toxicity.
机译:我们使用乳液扩散法制备了包含抗癌药物(吉西他滨)的磁性(Fe(3)O(4))聚ε-己内酯(PCL)纳米粒子(平均直径164 +/- 3 nm),以便开发出更有效的药物用于癌症治疗。纳米颗粒是光滑的,个体化的并且尺寸均匀。在2000 Oe磁场强度下,磁性PCL纳米颗粒的磁化强度值约为10.2 emu / g,并显示出超顺磁性。在使用药物的情况下,药物载量为18.6%,包封率为52.2%。使用体内携带皮下人胰腺腺癌细胞(HPAC)的裸鼠检查了由这些颗粒引起的抗肿瘤作用。我们将这些小鼠随机分为五个治疗组之一进行实验对比。与游离吉西他滨相比,抗肿瘤作用的剂量高出15倍。结果,磁性PCL纳米颗粒可通过将药物有效地递送至磁性靶向的肿瘤组织而提供治疗益处,从而以低毒性实现安全且成功的抗肿瘤作用。

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