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载紫杉醇的藻蓝蛋白纳米颗粒的简明纳米平台用于协同化疗-声动力学抗肿瘤治疗。

Concise Nanoplatform of Phycocyanin Nanoparticle Loaded with Docetaxel for Synergetic Chemo-sonodynamic Antitumor Therapy.

机构信息

School of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013 Jiangsu, P. R. China.

Zhenjiang First People's Hospital, 8 Dianli Road, Zhenjiang, 212002 Jiangsu, P. R. China.

出版信息

ACS Appl Bio Mater. 2021 Sep 20;4(9):7176-7185. doi: 10.1021/acsabm.1c00745. Epub 2021 Aug 20.

DOI:10.1021/acsabm.1c00745
PMID:35006949
Abstract

Combined chemotherapy and sonodynamic therapy (chemo-SDT) based on the nanoplatform/nanocarrier is a potential antitumor strategy that has shown higher therapeutic efficacy than any monotherapy. Therefore, a safe and effective multifunctional system with a concise design and simple preparation process is urgently needed. In this work, by using a one-step cross-linking method, a multifunctional nanosystem, which employs phycocyanin nanoparticles (PCNPs) as a nanocarrier to deliver the chemotherapy drug docetaxel (DTX) and a nanosonosensitizer to generate reactive oxygen species (ROS), was prepared and evaluated (PCNP-DTX). Under low-intensity ultrasound irradiation, PCNP-DTX retained the ROS generation ability of phycocyanin and caused the destruction of mitochondrial potential. PCNP was also revealed to be an acidic and ultrasound-sensitive carrier with good biocompatibility. In addition to its cumulation behavior in tumors, PCNP can achieve tumor-targeted delivery and release of DTX. PCNP-DTX has also been proven to have a significant chemo-SDT synergy effect when low-intensity ultrasound was applied, showing enhanced antitumor activity both in vitro and in vivo. This study provides a concise yet promising nanoplatform based on the natural protein phycocyanin for achieving an effective, targeted, and synergetic chemo-SDT for antitumor therapy.

摘要

基于纳米平台/载体的联合化疗和声动力学疗法(chemo-SDT)比任何单一疗法都显示出更高的疗效,因此,迫切需要一种安全有效的多功能系统,具有简洁的设计和简单的制备工艺。在这项工作中,通过使用一步交联法,制备并评价了一种多功能纳米系统(PCNP-DTX),该系统以藻蓝蛋白纳米颗粒(PCNPs)作为纳米载体来递送化疗药物多西紫杉醇(DTX)和纳米声敏剂以产生活性氧(ROS)。在低强度超声辐射下,PCNP-DTX 保留了藻蓝蛋白产生 ROS 的能力,并导致线粒体电位破坏。PCNP 还被证明是一种具有良好生物相容性的酸性和超声敏感载体。除了在肿瘤中的积累行为外,PCNP 还可以实现 DTX 的肿瘤靶向递送和释放。当应用低强度超声时,PCNP-DTX 还被证明具有显著的 chemo-SDT 协同效应,在体外和体内均显示出增强的抗肿瘤活性。本研究提供了一种基于天然蛋白藻蓝蛋白的简洁但有前途的纳米平台,用于实现有效的、靶向的、协同的抗肿瘤化疗和声动力学疗法。

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