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用于递送甲氨蝶呤的聚赖氨酸树枝状纳米载体靶向表皮生长因子受体过表达的乳腺癌

Poly-Lysine Dendritic Nanocarrier to Target Epidermal Growth Factor Receptor Overexpressed Breast Cancer for Methotrexate Delivery.

作者信息

Narayanan Pratibha, Anitha Anju Krishnan, Ajayakumar Neethu, Kumar Kesavakurup Santhosh

机构信息

Pathogen Biology Division, Rajiv Gandhi Centre for Biotechnology, Bio-Innovation Centre, KINFRA Park, Chanthavila (PO), Thiruvananthapuram 695585, Kerala, India.

出版信息

Materials (Basel). 2022 Jan 21;15(3):800. doi: 10.3390/ma15030800.

Abstract

A fourth generation poly-lysine dendritic nanocarrier (PLDN)-based targeted chemotherapy for breast cancer is attempted by incorporating an epidermal growth factor receptor (EGFR)-specific short peptide E2 (ARSHVGYTGAR) and the drug methotrexate (MTX) into a nanocarrier system. The drug is incorporated into the nanocarrier using a cathepsin B cleavable spacer: glycine-phenylalanine-leucine-glycine (GFLG). The in vitro analysis of the time-dependent drug release, binding and internalization ability, and the cytotoxic nature showed that this drug delivery system (DDS) is highly effective. The efficacy analysis using non-obese diabetic/severe combined immunodeficiency (NOD-SCID) mice also showed that compared to the control group, the DDS can effectively reduce tumor volume. The mice that received the DDS appeared to gain weight more rapidly than the free drug, which suggests that the dendrimer is more easily tolerated by mice than the free drug.

摘要

通过将表皮生长因子受体(EGFR)特异性短肽E2(ARSHVGYTGAR)和药物甲氨蝶呤(MTX)整合到纳米载体系统中,尝试构建基于第四代聚赖氨酸树枝状纳米载体(PLDN)的乳腺癌靶向化疗方法。药物通过组织蛋白酶B可裂解的间隔子:甘氨酸-苯丙氨酸-亮氨酸-甘氨酸(GFLG)整合到纳米载体中。对时间依赖性药物释放、结合和内化能力以及细胞毒性的体外分析表明,这种药物递送系统(DDS)非常有效。使用非肥胖糖尿病/严重联合免疫缺陷(NOD-SCID)小鼠进行的疗效分析还表明,与对照组相比,DDS可有效减小肿瘤体积。接受DDS的小鼠似乎比接受游离药物的小鼠体重增加更快,这表明树枝状聚合物比游离药物更容易被小鼠耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ad6/8836561/ff6200208b3b/materials-15-00800-sch001.jpg

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