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用于成像和化疗的吲哚菁绿增强型紫杉醇纳米前药

Indocyanine green potentiated paclitaxel nanoprodrugs for imaging and chemotherapy.

作者信息

Xiang Xiujuan, Feng Xuan, Lu Shaojin, Jiang Bowen, Hao Dengyuan, Pei Qing, Xie Zhigang, Jing Xiabin

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin China.

University of Science and Technology of China Hefei China.

出版信息

Exploration (Beijing). 2022 Jun 4;2(4):20220008. doi: 10.1002/EXP.20220008. eCollection 2022 Aug.

Abstract

Self-assembled prodrug nanoparticles with tumor-responsive capacity have great potential in tumor visualization and treatment. However, the nanoparticle formulas usually contain multiple components, especially polymeric materials, which result in various potential issues. Herein, we report an indocyanine green (ICG)-driven assembly of paclitaxel prodrugs integrating near-infrared fluorescence imaging and tumor-specific chemotherapy. By feat of the hydrophilic merit of ICG, paclitaxel dimer could form more uniformly monodispersed nanoparticles. This two-in-one strategy reinforces the complementary advantages, resulting in superior assembly behavior, robust colloidal stability, enhanced tumor accumulation as well as desirable near-infrared imaging and in vivo feedback of chemotherapy. The in vivo experiments validated the prodrug activation at tumor sites as evidenced by enhanced fluorescence intensity, potent tumor growth suppression, and reduced systemic toxicity compared with commercial Taxol. The universality of ICG potentiated strategy toward photosensitizers and fluorescence dyes was confirmed. This presentation provides deep insight into the feasibility of constructing clinical-close alternatives for improving antitumor efficacy.

摘要

具有肿瘤响应能力的自组装前药纳米颗粒在肿瘤可视化和治疗方面具有巨大潜力。然而,纳米颗粒配方通常包含多种成分,尤其是聚合物材料,这会导致各种潜在问题。在此,我们报告了一种由吲哚菁绿(ICG)驱动的紫杉醇前药组装,集成了近红外荧光成像和肿瘤特异性化疗。借助ICG的亲水性优点,紫杉醇二聚体可形成更均匀的单分散纳米颗粒。这种二合一策略强化了互补优势,产生了优异的组装行为、强大的胶体稳定性、增强的肿瘤积累以及理想的近红外成像和化疗的体内反馈。体内实验验证了前药在肿瘤部位的激活,与市售紫杉醇相比,荧光强度增强、有效抑制肿瘤生长以及全身毒性降低证明了这一点。证实了ICG增强策略对光敏剂和荧光染料的通用性。本报告深入洞察了构建临床近似替代物以提高抗肿瘤疗效的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f671/10190853/b9823d0f4467/EXP2-2-20220008-g002.jpg

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