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Si-Xue Cheng

Researcher at Wuhan University

Publications -  238
Citations -  12634

Si-Xue Cheng is an academic researcher from Wuhan University. The author has contributed to research in topics: Drug carrier & Micelle. The author has an hindex of 54, co-authored 236 publications receiving 10754 citations. Previous affiliations of Si-Xue Cheng include Sichuan University & University of South China.

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Vascular disrupting agent induced aggregation of gold nanoparticles for photothermally enhanced tumor vascular disruption

TL;DR: Results indicate that this strategy for VDA-induced aggregation of gold nanoparticles to further destroy tumor vascular by photothermal effect has great potential in tumor treatment and could effectively enhance tumor vascular damage and avoid the side effects caused by frequent administration.
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Self‐Assembled, Thermosensitive PCL‐g‐P(NIPAAm‐co‐HEMA) Micelles for Drug Delivery

TL;DR: It was found that micelles loaded with prednisone acetate showed improved drug release behavior due to the special micellar structure and cytotoxicity study showed that the PCL-g-P(NIPAAm-co-HEMA) copolymer exhibits good biocompatibility.
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Self‐assembled thermosensitive micelles based on poly(L‐lactide‐star block‐N‐isopropylacrylamide) for drug delivery

TL;DR: In vitro release behavior of MTX was investigated, which showed a drastic thermoresponsive fast/slow switching behavior according to the temperature-responsive structural changes of a micellar shell structure.
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Aptamer-functionalized albumin-based nanoparticles for targeted drug delivery.

TL;DR: Proteins have been extensively explored as versatile nanocarriers for drug delivery due to their complete biocompatibility, ease of surface modification, and lack of toxicity and immunogenicity, and aptamer-modified nanoparticles exhibit a significantly improved capability in up-regulating p16, p21 and E-cadherin, and down- Regulating EpCAM, vimentin, Snail, MMP-9, CD44 and CD133.
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Coassembly of oppositely charged short peptides into well-defined supramolecular hydrogels.

TL;DR: The strategy demonstrated in this study can be developed as a convenient approach for different types of short peptides to coassemble into a supramolecular hydrogel with multiple functions for the biomedical applications.