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Investigating the Effect of Chemical Structure of Semiconducting Polymer Nanoparticle on Photothermal Therapy and Photoacoustic Imaging

机译:研究半导体高分子纳米粒子的化学结构对光热疗法和光声成像的影响

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摘要

The donor-acceptor semiconducting polymers (SPs) have robust absorbance in near-infrared (NIR) region, great photostability, high photothermal conversion efficiency, and good biocompatibility. Thus, the SPs exhibit great potentials for photothermal therapy (PTT) and photoacoustic imaging (PAI). However, poor understanding of the underlying mechanisms and the correlation between the SP polymer chemical structures and their performances of PTT and PAI have significantly hindered their biomedical application. Herein, a series of acceptor-π-acceptor type (A1-π-A2) type SPs were synthesized. The diketopyrrolopyrrole (DPP) and thiophene are used as A1 electron accepting block and π-bridge, and the chemical structure of A2 unit was variable. The SPs were formulated into PEGylated nanoparticles, which ensured these SP-based nanoparticles (SP@NPs) exhibited similar size, shape, and physiological stability. Thus, the chemical structure of A2 unit was the only variable. The effects of the SP chemical structures are carefully and comprehensively evaluated through both in vitro and in vivo experiments. Our results demonstrated the chemical structure of A2 unit simultaneously impact their absorption spectra and photothermal (PT) conversion efficiency, which finally determined their PTT and PAI performances. Among these A2 acceptors, thieno[3,2-b]thiophene (TT) unit exhibited the best in vitro and in vivo anticancer efficacies and PAI performances. This study not only provides molecular insights into the design of efficient SPs for PTT and PAI but also highlights the flexibility and potential of SP@NPs for biomedical application. Thus, SP@NPs can act as a versatile nanoplatform for the development of novel light intensive imaging and therapeutic approaches.
机译:供体-受体半导体聚合物(SP)在近红外(NIR)区域具有强大的吸光度,具有出色的光稳定性,高的光热转化效率和良好的生物相容性。因此,SPs具有光热疗法(PTT)和光声成像(PAI)的巨大潜力。但是,对潜在机理以及SP聚合物化学结构与PTT和PAI的性能之间的相关性的了解不足,严重阻碍了其生物医学应用。在此,合成了一系列受体-π-受体型(A1-π-A2)型SP。二酮吡咯并吡咯(DPP)和噻吩被用作A1电子接受嵌段和π桥,A2单元的化学结构是可变的。将SP配制成PEG化的纳米颗粒,以确保这些基于SP的纳米颗粒(SP @ NP)表现出相似的尺寸,形状和生理稳定性。因此,A2单元的化学结构是唯一的变量。通过体外和体内实验,仔细,全面地评估了SP化学结构的影响。我们的结果表明,A2单元的化学结构同时影响其吸收光谱和光热(PT)转换效率,最终决定了它们的PTT和PAI性能。在这些A2受体中,噻吩并[3,2-b]噻吩(TT)单元表现出最好的体外和体内抗癌功效和PAI性能。这项研究不仅为PTT和PAI的高效SP的设计提供了分子见解,而且还突出了SP @ NP在生物医学应用中的灵活性和潜力。因此,SP @ NPs可以作为通用纳米平台,用于开发新型光密集型成像和治疗方法。

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