叶酸偶联丝素蛋白纳米载体靶向给药。

IF 1.4
Bano Subia, Sourov Chandra, Sarmistha Talukdar, Subhas C Kundu
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引用次数: 73

摘要

疾病治疗过程主要集中在开发无毒、可生物降解、非免疫原性、生物相容性、能够控制和长期释放生物分子的材料。本研究利用热带非桑蚕(Antheraea mylitta)的丝蛋白丝素制备纳米颗粒作为药物递送系统。叶酸是一种维生素,通过叶酸受体进入健康细胞和癌细胞。通过对细胞活力、增殖和内吞作用的分析,评价了载抗肿瘤药物阿霉素的叶酸丝素纳米颗粒的效率。因此,通过叶酸偶联丝素纳米颗粒刺激巨噬细胞,检测TNF-α、IL-1β和一氧化氮等细胞因子对促炎反应的影响。纤维蛋白-叶酸纳米载体无毒,易于被细胞吸收,并且能够持续释放药物。携带抗癌药物阿霉素的纳米颗粒靶向癌细胞。结果表明,丝素-叶酸纳米颗粒在生物医学和纳米技术在癌症研究中的应用前景广阔。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Folate conjugated silk fibroin nanocarriers for targeted drug delivery.

Disease treatment processes mainly focus on the development of nontoxic, biodegradable, non-immunogenic, biocompatible materials capable of controlled and long-term release of biomolecules. In this work silk protein fibroin from non-mulberry tropical tasar silkworm, Antheraea mylitta, is used to prepare nanoparticles as a drug delivery system. Folate is a vitamin, which is brought into healthy and cancerous cells by folate receptors. The efficiency of silk fibroin-folate nanoparticles loaded with anticancer drug doxorubicin was evaluated by analysing the cell viability, proliferation and endocytosis. Consequently the effects of pro-inflammatory responses by cytokines such as TNF-α, IL-1β and nitric oxide were checked by stimulating the macrophages with folate conjugated silk fibroin nanoparticles. The fibroin-folate nanocarriers are nontoxic, easily taken up by cells and capable of sustained drug release. Nanoparticles loaded with anticancer drug doxorubicin target cancer cells. The results show that silk fibroin-folate nanoparticles may serve as promising nanocarriers for different biomedical and nanotechnology applications in cancer research.

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