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微胶囊化减轻量子点细胞毒性。

Mitigation of quantum dot cytotoxicity by microencapsulation.

机构信息

Interdisciplinary Program of Toxicology, Texas A&M University, College Station, Texas, United States of America.

出版信息

PLoS One. 2011;6(7):e22079. doi: 10.1371/journal.pone.0022079. Epub 2011 Jul 21.

Abstract

When CdSe/ZnS-polyethyleneimine (PEI) quantum dots (QDs) are microencapsulated in polymeric microcapsules, human fibroblasts are protected from acute cytotoxic effects. Differences in cellular morphology, uptake, and viability were assessed after treatment with either microencapsulated or unencapsulated dots. Specifically, QDs contained in microcapsules terminated with polyethylene glycol (PEG) mitigate contact with and uptake by cells, thus providing a tool to retain particle luminescence for applications such as extracellular sensing and imaging. The microcapsule serves as the "first line of defense" for containing the QDs. This enables the individual QD coating to be designed primarily to enhance the function of the biosensor.

摘要

当 CdSe/ZnS-聚乙烯亚胺(PEI)量子点(QD)被微封装在聚合物微胶囊中时,人类成纤维细胞可以免受急性细胞毒性作用的影响。在用微封装或未封装的 QD 处理后,评估细胞形态、摄取和活力的差异。具体来说,用聚乙二醇(PEG)终止的微胶囊中的 QD 可以减轻与细胞的接触和摄取,从而为细胞外传感和成像等应用提供一种保留颗粒发光的工具。微胶囊作为包含 QD 的“第一道防线”。这使得可以主要设计单个 QD 涂层来增强生物传感器的功能。

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