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通过532nm光聚合制备的共负载紫杉醇和姜黄素的纳米凝胶用于协同抑制乳腺肿瘤。

Nanogels co-loading paclitaxel and curcumin prepared through photopolymerization at 532 nm for synergistically suppressing breast tumors.

作者信息

Song Xiaoyan, Feng Zujian, Peng Yuanyuan, Yu Siyuan, Du Xinjing, Huang Pingsheng, Wang Weiwei, Xing Jinfeng

机构信息

Tiangong University, School of Material Science and Engineering, Tianjin 300387, P. R. China.

Tianjin Key Laboratory of Biomaterial Research, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin 300192, P. R. China.

出版信息

J Mater Chem B. 2023 Feb 22;11(8):1798-1807. doi: 10.1039/d2tb02254k.

Abstract

Combined chemotherapy plays an increasingly important and practical role in the clinical treatment of malignant tumor. In this study, paclitaxel (PTX) and curcumin (Cur) are simultaneously encapsulated into nanogels (termed as NG-PC) by microemulsion photopolymerization at 532 nm for synergistically suppressing breast tumors. NG-PC with a size of 180 nm and a low polydispersity index (PDI < 0.2) presents a controlled and cumulative release of PTX and Cur within 90 h. Moreover, NG-PC displays a remarkable killing effect against 4T1 and MCF-7 cells. antitumor evaluation on 4T1 tumor-bearing mice demonstrates that NG-PC has significantly higher ability to inhibit tumor growth, inducing necrosis, apoptosis and suppression of proliferation than that of a single drug. Our research provides a facile method to prepare a nano-drug delivery platform with excellent drug co-loading ability and synergistic antitumor effect.

摘要

联合化疗在恶性肿瘤的临床治疗中发挥着越来越重要且切实可行的作用。在本研究中,通过在532nm处的微乳液光聚合将紫杉醇(PTX)和姜黄素(Cur)同时封装到纳米凝胶中(称为NG-PC),以协同抑制乳腺肿瘤。尺寸为180nm且多分散指数低(PDI<0.2)的NG-PC在90小时内呈现出PTX和Cur的可控且累积释放。此外,NG-PC对4T1和MCF-7细胞显示出显著的杀伤作用。对4T1荷瘤小鼠的抗肿瘤评估表明,NG-PC比单一药物具有显著更高的抑制肿瘤生长、诱导坏死、凋亡和抑制增殖的能力。我们的研究提供了一种简便的方法来制备具有优异药物共负载能力和协同抗肿瘤作用的纳米药物递送平台。

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