Supramolecular vesicles for stimulus-responsive drug delivery
Developing smart controlled‐release systems for cancer therapy is highly desired in biomedicine. In order to improve therapeutic efficacy and lower undesired side effects, the construction of stimulus‐responsive nanocarriers is a favorable solution. Emerging supramolecular self‐assemblies possessing...
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sg-ntu-dr.10356-1385342020-06-01T10:26:33Z Supramolecular vesicles for stimulus-responsive drug delivery Xing, Pengyao Zhao, Yanli School of Materials Science & Engineering School of Physical and Mathematical Sciences Science::Medicine Cancer Therapy Drug Release Developing smart controlled‐release systems for cancer therapy is highly desired in biomedicine. In order to improve therapeutic efficacy and lower undesired side effects, the construction of stimulus‐responsive nanocarriers is a favorable solution. Emerging supramolecular self‐assemblies possessing intrinsic dynamic and adaptive features present promising capabilities for the fabrication of stimulus‐responsive drug‐release systems. Dynamic supramolecular vesicles have attracted considerable attention as therapeutic carriers ascribed to their advantages of high‐cargo‐loading capacity/feasibility, excellent biocompatibility, and facile functionalization. Here, a summary and discussion of recent significant development of vesicles constructed by supramolecular self‐assembly for stimulus‐responsive drug delivery and therapeutics is given. Through presenting some representative studies, strategies regarding the design, synthesis, characterization, and biomedical applications of supramolecular vesicle carriers are highlighted according to various stimulus triggers. The aim is to provide a quick research update in this rapidly developing field. NRF (Natl Research Foundation, S’pore) 2020-05-08T01:05:43Z 2020-05-08T01:05:43Z 2018 Journal Article Xing, P., & Zhao, Y. (2018). Supramolecular vesicles for stimulus-responsive drug delivery. Small Methods, 2(4), 1700364-. doi:10.1002/smtd.201700364 2366-9608 https://hdl.handle.net/10356/138534 10.1002/smtd.201700364 4 2 en Small Methods © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. |
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Science::Medicine Cancer Therapy Drug Release Xing, Pengyao Zhao, Yanli Supramolecular vesicles for stimulus-responsive drug delivery |
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Developing smart controlled‐release systems for cancer therapy is highly desired in biomedicine. In order to improve therapeutic efficacy and lower undesired side effects, the construction of stimulus‐responsive nanocarriers is a favorable solution. Emerging supramolecular self‐assemblies possessing intrinsic dynamic and adaptive features present promising capabilities for the fabrication of stimulus‐responsive drug‐release systems. Dynamic supramolecular vesicles have attracted considerable attention as therapeutic carriers ascribed to their advantages of high‐cargo‐loading capacity/feasibility, excellent biocompatibility, and facile functionalization. Here, a summary and discussion of recent significant development of vesicles constructed by supramolecular self‐assembly for stimulus‐responsive drug delivery and therapeutics is given. Through presenting some representative studies, strategies regarding the design, synthesis, characterization, and biomedical applications of supramolecular vesicle carriers are highlighted according to various stimulus triggers. The aim is to provide a quick research update in this rapidly developing field. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Xing, Pengyao Zhao, Yanli |
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Article |
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Xing, Pengyao Zhao, Yanli |
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Xing, Pengyao |
title |
Supramolecular vesicles for stimulus-responsive drug delivery |
title_short |
Supramolecular vesicles for stimulus-responsive drug delivery |
title_full |
Supramolecular vesicles for stimulus-responsive drug delivery |
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Supramolecular vesicles for stimulus-responsive drug delivery |
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Supramolecular vesicles for stimulus-responsive drug delivery |
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supramolecular vesicles for stimulus-responsive drug delivery |
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2020 |
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https://hdl.handle.net/10356/138534 |
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1681057727016599552 |