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载叶绿素铜钠和量子点的聚(丙交酯-乙交酯)纳米粒作为光动力治疗试剂。

Poly(Lactide-Co-Glycolide) Nanoparticles Co-Loaded with Chlorophyllin and Quantum Dots as Photodynamic Therapy Agents.

机构信息

NEST, Scuola Normale Superiore, Piazza San Silvestro 12, 56127, Pisa, Italy.

Fondazione Pisana per la Scienza, Via Ferruccio Giovannini 13, 56017, San Giuliano Terme, Pisa, Italy.

出版信息

Chempluschem. 2019 Nov;84(11):1653-1658. doi: 10.1002/cplu.201900342. Epub 2019 Aug 21.

Abstract

Photodynamic therapy (PDT) is an approach to treating cancer and involves light-induced activation of a photosensitizer that triggers the formation of reactive oxygen species (ROS) in targeted cells and subsequent cell death. Examples of photosensitizers are porphyrins, including the natural compound chlorophyll. These molecules can be delivered alone or co-formulated with an agent, such as quantum dots (QDs), that is able to excite them through a fluorescence resonance energy transfer (FRET)-based mechanism. We encapsulated a chlorophyllin copper complex and CdSe/ZnS core-shell QDs into biodegradable nanoparticles (NPs) composed of poly(lactide-co-glycolide) (PLGA), that allow modification with specific targeting ligands. When excited at 365 nm, FRET occurs between co-encapsulated QDs and chlorophyllin to result in the formation of ROS. This chlorophyllin-QD coformulation allows generation of ROS both in an aqueous environment and in cells, thus confirming the potential of this formulation in PDT.

摘要

光动力疗法(PDT)是一种治疗癌症的方法,涉及光诱导光敏剂的激活,该光敏剂在靶细胞中引发活性氧(ROS)的形成,随后导致细胞死亡。光敏剂的例子包括卟啉,包括天然化合物叶绿素。这些分子可以单独递送,也可以与能够通过基于荧光共振能量转移(FRET)的机制激发它们的试剂(例如量子点(QD))共同配制。我们将叶绿素铜配合物和 CdSe/ZnS 核壳 QD 封装到由聚(乳酸-共-乙醇酸)(PLGA)组成的可生物降解的纳米颗粒(NP)中,这些 NP 允许用特定的靶向配体进行修饰。当用 365nm 激发时,共封装的 QD 和叶绿素之间发生 FRET,导致 ROS 的形成。这种叶绿素-QD 共制剂允许在水相环境中和细胞中生成 ROS,从而证实了该制剂在 PDT 中的潜力。

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