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Functionalised thermally induced phase separation (TIPS) microparticles enabled for 'click' chemistry

机译:功能化的热诱导相分离(TIPS)微粒可实现“点击”化学反应

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Due to their homogeneity, tuneable properties, low cost and ease of manufacture, thermally induced phase separation (TIPS) polymeric microparticles are emerging as an exciting class of injectable device for the treatment of damaged tissue or complex diseases, such as cancer. However, relatively little work has explored enhancing surface functionalisation of this system. Herein, we present the functionalisation of TIPS microparticles with both small molecules and an antibody fragment of Herceptin™, via a heterobifunc-tional pyridazinedione linker capable of participating in SPAAC "click" chemistry, and compare it to the traditional method of preparing active-targeted microparticle systems, that is, physisorption of antibodies to the microparticle surface. Antigen-binding assays demonstrated that functionalisation of microparticles with Herceptin Fab, via a pyridazinedione linker, provided an enhanced avidity to HER2+ when compared to traditional physisorption methods.
机译:由于它们的均质性,可调节的特性,低成本和易于制造,热诱导相分离(TIPS)聚合物微粒正成为令人兴奋的一类用于治疗受损组织或复杂疾病(例如癌症)的注射装置。然而,相对较少的工作已经探索了增强该系统的表面功能化。本文中,我们通过能够参与SPAAC“点击”化学反应的杂合吡啶并二酮连接体,展示了具有小分子和Herceptin™抗体片段的TIPS微粒的功能化,并将其与制备活性靶标的传统方法进行了比较微粒系统,即抗体对微粒表面的物理吸附。抗原结合测定表明,与传统的物理吸附方法相比,通过哒嗪二酮连接体将具有Herceptin Fab的微粒功能化后,对HER2 +的亲和力增强。

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