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通过白蛋白和全氟碳协同整合来重激活光敏剂以增强光动力疗法。

Relighting Photosensitizers by Synergistic Integration of Albumin and Perfluorocarbon for Enhanced Photodynamic Therapy.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology, Medical School of Nanjing University , Nanjing 210093, China.

State Key Laboratory of Natural Medicines, China Pharmaceutical University , Nanjing 210009, China.

出版信息

ACS Appl Mater Interfaces. 2017 Feb 1;9(4):3463-3473. doi: 10.1021/acsami.6b14885. Epub 2017 Jan 18.

Abstract

Photodynamic therapy (PDT) is hampered by poor water solubility and skin phototoxicity of photosensitizers (PSs). Incorporation of PSs into nanocarrier (Nano-PDT) has been designed to overcome these problems. However, self-quenching of PSs highly condensed in Nano-PDT significantly reduced singlet oxygen (O) generation, resulting in unsatisfactory PDT efficacy. Here, we developed a novel tripleffect Nano-PDT, which has a special core-shell nanostructure by synergistic integration of perfluorotributylamine (PFTBA) and human serum albumin (HSA) to improve PDT. It has three mechanisms to relight quenched PSs, thereby generating more O. First, PSs uniformly dispersed in the shell, preventing self-quenching caused by π-π stacking. Second, HSA as nanocarrier extends the triplet-state lifetimes of PSs, increasing the amount of O. Third, PFTBA as core dissolves and protects O to extend the duration time of action of O. Compared with PS-encapsulated Nano-PDT, the self-quenching of PSs in tripleffect Nano-PDT can be effectively overcome. The fluorescence and O generation of PS are increased by approximately 100-fold and 15-fold, respectively. After intravenous injection into tumor-bearing mice, the tumor growth is significantly inhibited, while the PS-encapsulated Nano-PDT has almost no effect. The novel tripleffect Nano-PDT may guide improvement of existing clinical PDT and future PDT design.

摘要

光动力疗法(PDT)受到光敏剂(PSs)较差的水溶性和皮肤光毒性的阻碍。将 PSs 纳入纳米载体(Nano-PDT)的设计旨在克服这些问题。然而,高度浓缩在 Nano-PDT 中的 PSs 的自猝灭极大地降低了单线态氧(O)的生成,导致 PDT 效果不理想。在这里,我们开发了一种新型的三重效应 Nano-PDT,它通过协同整合全氟三丁胺(PFTBA)和人血清白蛋白(HSA)具有特殊的核壳纳米结构,以改善 PDT。它有三种机制来重新点亮猝灭的 PSs,从而产生更多的 O。首先,PSs 均匀分散在壳中,防止由于π-π堆积引起的自猝灭。其次,HSA 作为纳米载体延长 PSs 的三重态寿命,增加 O 的数量。第三,作为核心的 PFTBA 溶解并保护 O,从而延长 O 的作用持续时间。与 PS 封装的 Nano-PDT 相比,可以有效克服三重效应 Nano-PDT 中 PSs 的自猝灭。PS 的荧光和 O 生成分别增加了约 100 倍和 15 倍。静脉注射到荷瘤小鼠后,肿瘤生长明显受到抑制,而 PS 封装的 Nano-PDT 几乎没有效果。新型三重效应 Nano-PDT 可能指导现有临床 PDT 的改进和未来 PDT 的设计。

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