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磷脂微团中单个量子点的合成、封装、纯化及偶联,用于细胞和体内成像。

Synthesis, encapsulation, purification and coupling of single quantum dots in phospholipid micelles for their use in cellular and in vivo imaging.

作者信息

Carion Olivier, Mahler Benoît, Pons Thomas, Dubertret Benoit

机构信息

Laboratoire Photons et Matière, CNRS UPRA5, ESPCI, 10, rue Vauquelin, 75231 Paris Cedex 05, France.

出版信息

Nat Protoc. 2007;2(10):2383-90. doi: 10.1038/nprot.2007.351.

Abstract

A detailed protocol for the synthesis of core/shell semiconductor nanocrystal, their encapsulation into phospholipid micelles, their purification and their coupling to a controlled number of small molecules is given. The protocol for the core/shell quantum dot (QD) CdSe/CdZnS synthesis has been specifically designed with two constraints in mind: green and reproducible core/shell QD synthesis with thick shell structure and QDs that can easily be encapsulated in poly(ethylene glycol)-phospholipid micelles with one QD per micelle. We present two procedures for the QD purification that are suitable for the use of QD micelles for in vivo imaging: ultracentrifugation and size-exclusion chromatography. We also discuss the different coupling chemistry for covalently linking a controlled number of molecules to the QD micelles. The total time durations for the different protocols are as follows: QD synthesis: 6 h; encapsulation: 15 min; purification: 1-4 h; coupling: reaction dependent.

摘要

本文给出了一种合成核壳半导体纳米晶体的详细方案,包括将其封装到磷脂胶束中、进行纯化以及与一定数量的小分子进行偶联。核壳量子点(QD)CdSe/CdZnS的合成方案是经过专门设计的,设计时考虑了两个限制因素:以绿色且可重复的方式合成具有厚壳结构的核壳量子点,以及合成能够轻松封装在聚乙二醇 - 磷脂胶束中且每个胶束包含一个量子点的量子点。我们介绍了两种适用于将量子点胶束用于体内成像的量子点纯化方法:超速离心法和尺寸排阻色谱法。我们还讨论了将一定数量的分子共价连接到量子点胶束上的不同偶联化学方法。不同方案的总时长如下:量子点合成:6小时;封装:15分钟;纯化:1 - 4小时;偶联:取决于反应。

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