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In Situ Construction and Characterization of Chlorin-Based Supramolecular Aggregates in Tumor Cells

机译:肿瘤细胞中基于氯的超分子聚集体的原位构建和表征

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We demonstrate in situ construction and characterization of supramolecular aggregates from chlorin p6 (Cp6) molecules in tumor cells. Fully deprotonated Cp6 molecules in neutral condition were partially protonated inside the acidic lysosomes of cells and significantly increased the hydrophobicity of them that resulted in simultaneous formation of J-type aggregates. Importantly, the formation of J-aggregates was fully characterized in artificial tissues by UV-vis, circular dichroism (CD) and transmission electron microscope (TEM) techniques. Compared to the monomers, the J-aggregates exhibited 55-fold enhanced thermal conversion efficiency (eta) at the optimal excitation wavelength (690 nm). The remarkably increased heat effect contributed to the stronger photoacoustic (PA) signals, leading to at least 2 orders of magnitude increase of the tumor-to-normal tissue ratio (TIN), which was defined as the PA signal ratio between tumor site and surrounding normal tissue. We envision that this proof-of-concept study will open a new way to develop tumor environment-induced-self-assembly for variable biomedical applications.
机译:我们从肿瘤细胞中的二氢卟酚p6(Cp6)分子证明了超分子聚集体的原位构建和表征。在中性条件下,完全去质子化的Cp6分子在细胞的酸性溶酶体内被部分质子化,并显着增加了它们的疏水性,从而导致J型聚集体的同时形成。重要的是,通过紫外线可见,圆二色性(CD)和透射电子显微镜(TEM)技术可以充分表征人造组织中J聚集体的形成。与单体相比,在最佳激发波长(690 nm)下,J聚集体的热转化效率(η)提高了55倍。显着增加的热效应有助于产生更强的光声(PA)信号,从而导致肿瘤与正常组织之比(TIN)至少增加2个数量级,这被定义为肿瘤部位与周围组织之间的PA信号之比正常组织。我们预想,这项概念验证研究将为开发用于可变生物医学应用的肿瘤环境诱导的自组装开辟新途径。

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