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叶酸基碳点功能化硬脂酸-g-聚乙烯亚胺两亲性纳米胶束:用于三阴性乳腺癌的靶向药物递送和成像。

Folic acid based carbon dot functionalized stearic acid-g-polyethyleneimine amphiphilic nanomicelle: Targeted drug delivery and imaging for triple negative breast cancer.

机构信息

Gene Therapy and Tissue Engineering Lab, Department of Polymer Science and Technology, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India.

Gene Therapy and Tissue Engineering Lab, Department of Polymer Science and Technology, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India.

出版信息

Colloids Surf B Biointerfaces. 2021 Jan;197:111382. doi: 10.1016/j.colsurfb.2020.111382. Epub 2020 Oct 27.

Abstract

Development of advanced therapeutic modalities for the treatment of cancer are become a thirst area in the field of biomedical science now a day. Current therapeutic approaches to treat this fatal disease always refer to partial curability with unavoidable obstacles. Here, we have developed stearic-g-polyethyleneimine acid amphiphilic nanomicelle functionalized with folic acid-based carbon dots (CDs) for targeted anticancer drug (doxorubicin, DOX) delivery and concurrent bio-imaging for triple negative breast cancer (TNBC). Developed nanomicelle was characterized by FTIR, XRD, H NMR, fluorescence spectroscopy, TEM etc. Highest DOX release from the nanomicelle was observed at slightly acidic pH. It was also found that the nanomicelle can be successfully internalized by the MDA-MB-231 cells and able to inhibit cell proliferation. The IC value by free DOX against TNBC was around 10 μg/mL, whereas, DOX loaded CD functionalized stearic-g-polyethyleneimine (25 kDa) (DOX-CDSP-25) showed similar cytotoxicity on TNBC at the concentration of only 1.0 μg/mL, indicating the efficiency of the delivery system compared to that of free DOX. Scanning electron microscopy (SEM) analysis revealed the effect of DOX-CDSP-25 on MDA-MB-231 cellular morphology in 24 h. Along with, the fluorescence property offered by folic acid derived CD allowed CDSP-25 to be acted as a promising bio-imaging tool for TNBC.

摘要

如今,开发用于治疗癌症的先进治疗方法已成为生物医学科学领域的热门领域。目前治疗这种致命疾病的方法总是指部分治愈,且不可避免地存在障碍。在这里,我们开发了一种基于叶酸的碳点(CDs)功能化的硬脂酸-g-聚乙烯亚胺酸两亲性纳米胶束,用于靶向抗癌药物(阿霉素,DOX)递送和三重阴性乳腺癌(TNBC)的同时生物成像。所开发的纳米胶束通过傅里叶变换红外光谱(FTIR)、X 射线衍射(XRD)、核磁共振(H NMR)、荧光光谱、透射电子显微镜(TEM)等进行了表征。在略酸性 pH 值下,从纳米胶束中观察到最高的 DOX 释放。还发现纳米胶束可以被 MDA-MB-231 细胞成功内化,并能够抑制细胞增殖。游离 DOX 对 TNBC 的 IC 值约为 10 μg/mL,而负载 DOX 的 CD 功能化硬脂酸-g-聚乙烯亚胺(25 kDa)(DOX-CDSP-25)在仅 1.0 μg/mL 的浓度下对 TNBC 表现出相似的细胞毒性,表明与游离 DOX 相比,该递送系统的效率更高。扫描电子显微镜(SEM)分析揭示了 DOX-CDSP-25 在 24 小时内对 MDA-MB-231 细胞形态的影响。此外,叶酸衍生的 CD 提供的荧光特性使 CDSP-25 能够成为 TNBC 的一种有前途的生物成像工具。

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