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基于多酚的紫杉醇前药自组装纳米平台用于肿瘤协同治疗。

Polyphenol-Based Paclitaxel Prodrug Self-Assembled Nanoplatform for Tumor Synergistic Therapy.

机构信息

Institute of Pharmaceutical Biotechnology, School of Biology and Food Engineering, Key Laboratory of Spin Electron and Nanomaterials of Anhui Higher Education Institutes, Suzhou University, Suzhou 234000, P. R. China.

Anhui Xinximeng Biological Technology Co., Ltd., Suzhou 234000, P. R. China.

出版信息

J Biomed Nanotechnol. 2021 Nov 1;17(11):2198-2209. doi: 10.1166/jbn.2021.3180.

Abstract

With the development of nanomedicine, studies focus on self-assembled nanoplatforms to reduce the toxicity of paclitaxel (PTX), promote the immune function at low-toxicity PTX, and achieve tumor synergistic therapy. Herein, a new nanoplatform was prepared with self-assembled 5-hydroxydopamine (DA)-PTX@tannic acid (TA)-Fe nanoparticles (TDPP NPs) by consolidation of targeted DA-PTX and TA with the assistance of coordination between polyphenols and Fe. The polyphenol-based TDPP NPs can reduce the toxicity of PTX and thereby realize the and synergistic effect against tumors. The low-toxicity TDPP NPs can enhance the expression of CD40 immune protein. Moreover, the TDPP NPs possessed a small size (52.2±4 nm), high drug loading efficiency (95%), and stable pharmacokinetics, ensuring high tumor accumulation of TDPP NPs by enhanced permeability and retention effect. Our work sheds new light on the nanoformulation of PTX with low toxicity and synergistic therapy effect, which may find clinical applications in the future.

摘要

随着纳米医学的发展,研究集中在自组装纳米平台上,以降低紫杉醇(PTX)的毒性,促进低毒性 PTX 的免疫功能,并实现肿瘤协同治疗。本文通过整合靶向 5-羟多巴胺(DA)-PTX 和单宁酸(TA)与多酚和 Fe 之间的配位,制备了一种新的纳米平台,即自组装的 5-羟多巴胺(DA)-PTX@单宁酸(TA)-Fe 纳米粒子(TDPP NPs)。基于多酚的 TDPP NPs 可以降低 PTX 的毒性,从而实现抗肿瘤的协同作用。低毒性的 TDPP NPs 可以增强 CD40 免疫蛋白的表达。此外,TDPP NPs 具有较小的尺寸(52.2±4nm)、高载药效率(95%)和稳定的药代动力学,通过增强的通透性和保留效应,确保 TDPP NPs 高度积聚在肿瘤中。我们的工作为具有低毒性和协同治疗效果的 PTX 的纳米制剂提供了新的思路,这可能在未来的临床应用中找到。

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