Quantum dots - Nano-sized probes for the exploration of cellular and intracellular targeting

Hild, W. A. and Breunig, M. and Goepferich, A. (2008) Quantum dots - Nano-sized probes for the exploration of cellular and intracellular targeting. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 68 (2). pp. 153-168. ISSN 0939-6411

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Abstract

Nanoparticles emerged as promising tool in drug targeting, since, after appropriate modification, they are able to deliver their payload to specific sites, like tissues, cells, or even certain cellular organelles. In this context, the delivery of nanoparticles from the circulation into the target cells represents a crucial step. Here, model drug delivery systems such as quantum dots are ideal candidates to elucidate this process in more detail, since they provide outstanding features like a small and uniform size, unique optical properties for most sensitive detection and modifiable surfaces. Recent progress in the surface chemistry of quantum dots expanded their use in biological applications, reduced their cytotoxicity and rendered quantum dots a powerful tool for the investigation of distinct cellular processes, like uptake, receptor trafficking and intracellular delivery. In this review, we will not only describe the ideal attributes of QDs for biological applications and imaging but also their distinct specific and non-specific pathways into the cells as well as their intracellular fate. (c) 2007 Elsevier B.V. All rights reserved.

Item Type: Article
Uncontrolled Keywords: PROTEIN-COUPLED RECEPTOR; IN-VIVO; GENE DELIVERY; PENETRATING PEPTIDES; TUMOR VASCULATURE; MAMMALIAN-CELLS; LIVING CELLS; LIVE CELLS; POLYMERIC NANOPARTICLES; MEDIATED ENDOCYTOSIS; drug targeting; quantum dot; nanoparticle; cellular uptake; endocytosis; cytotoxicity
Subjects: 600 Technology > 615 Pharmacy
Divisions: Chemistry and Pharmacy > Institute of Pharmacy > Pharmaceutical Technology (Prof. Göpferich)
Depositing User: Petra Gürster
Date Deposited: 18 Dec 2020 10:15
Last Modified: 18 Dec 2020 10:15
URI: https://pred.uni-regensburg.de/id/eprint/31412

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