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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Synergistic anticancer efficacy of Bendamustine Hydrochloride loaded bioactive Hydroxyapatite nanoparticles: In-vitro, ex-vivo and in-vivo evaluation
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Synergistic anticancer efficacy of Bendamustine Hydrochloride loaded bioactive Hydroxyapatite nanoparticles: In-vitro, ex-vivo and in-vivo evaluation

机译:盐酸苯达莫司汀负载生物活性羟基磷灰石纳米颗粒的协同抗癌功效:体外,离体和体内评估

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摘要

The present work evaluates the synergistic anticancer efficacy of bioactive Hydroxyapatite (HA) nanoparticles (HA NPs) loaded with Bendamustine HCl. Hydroxyapatite is a material with an excellent biological compatibility, a well-known fact which was also supported by the results of the Hemolytic studies and a high IC50 value observed in the MTT assay. HA NPs were prepared by the chemical precipitation method and loaded with the drug via physical adsorption. In-vitro release study was performed, which confirmed the sustained release of the drug from the drug loaded HA NPs. MTT assay, Cell Uptake and FACS studies on JURKAT E6.1 cell line and in-vivo pharmacokinetic studies in Wistar rats revealed that the drug loaded HA NPs could be easily internalized by the cells and release drug in a sustained manner. The drug loaded HA NPs showed cytotoxicity similar to the drug solution at 1/10th of the drug content, which indicates a possible synergism between the activity of the anticancer drug and calcium ions derived from the carrier. An increase in intracellular Ca2+ ions is reported to induce apoptosis in cells. Tumor regression study in Balb/c mice Ehrlich's ascites model presented a similar synergistic efficacy. The drug solution was able to decrease the tumor volume by half, while the drug loaded HA NPs reduced the tumor size by 6 times. (C) 2016 Elsevier B.V. All rights reserved.
机译:本工作评估了负载盐酸苯达莫司汀的生物活性羟基磷灰石(HA)纳米颗粒(HA NPs)的协同抗癌功效。羟基磷灰石是一种具有极佳生物相容性的材料,这一众所周知的事实也得到了溶血研究结果和MTT分析中观察到的高IC50值的支持。 HA NPs是通过化学沉淀法制备的,并通过物理吸附法负载了药物。进行了体外释放研究,该研究证实了药物从载药HA NP中持续释放。在Wistar大鼠中对JURKAT E6.1细胞系进行的MTT分析,细胞摄取和FACS研究以及在Wistar大鼠中进行的体内药代动力学研究表明,载有药物的HA NP可以很容易地被细胞内在化并持续释放药物。载有药物的HA NP在药物含量的1/10时显示出与药物溶液相似的细胞毒性,这表明抗癌药物的活性与源自载体的钙离子之间可能存在协同作用。据报道细胞内Ca 2+离子的增加诱导细胞凋亡。 Balb / c小鼠的肿瘤消退研究Ehrlich腹水模型表现出相似的协同功效。药物溶液能够将肿瘤体积减少一半,而载有药物的HA NP将肿瘤尺寸减少6倍。 (C)2016 Elsevier B.V.保留所有权利。

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