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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.3c01341
|2 doi
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|a pubmed24n1204.xml
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|a (DE-627)NLM361454368
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|a (NLM)37647573
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Liu, Yehong
|e verfasserin
|4 aut
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|a Construction of Core-Cross-Linked Polymer Micelles with High Biocompatibility and Stability for pH/Reduction Controllable Drug Delivery
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|c 2023
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 13.09.2023
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|a Date Revised 21.09.2023
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Polymer micelles have been studied extensively in drug delivery systems (DDS), and their stability is well known to directly affect drug delivery. In this article, a series of amphiphilic copolymers LA-PDPAn-PVPm were synthesized to prepare core-cross-linked nanoparticles (CNP) applied to controllable and targeted anticancer drug delivery. The copolymers could self-assemble in aqueous solution and form homogeneous spherical micelles with particle sizes of between 100 and 150 nm. A comparison between un-cross-linked UCNP and CNP showed that the cross-linking of LA could significantly improve the stability and responsive ability of the nanoparticles. From the in vitro-simulated drug release experiments, CNP was found to have great drug blocking ability under normal physiological conditions and could achieve rapid and efficient drug release under acidic/reducing conditions. In addition, cell experiments showed that CNP had superior biocompatibility and could target tumor cells for drug release. In conclusion, a drug carrier based on copolymer LA-PDPA-PVP realized effective controlled drug release due to the cross-linking of LA. The results will provide guidance for the design strategy of polymer micelles for drug carriers
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Micelles
|2 NLM
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|a Drug Carriers
|2 NLM
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|a Polymers
|2 NLM
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|a Chen, Miaoxin
|e verfasserin
|4 aut
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|a Li, Gaoyang
|e verfasserin
|4 aut
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|a Xu, Shouhong
|e verfasserin
|4 aut
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1 |
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|a Liu, Honglai
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 39(2023), 36 vom: 12. Sept., Seite 12671-12679
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:39
|g year:2023
|g number:36
|g day:12
|g month:09
|g pages:12671-12679
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|u http://dx.doi.org/10.1021/acs.langmuir.3c01341
|3 Volltext
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|d 39
|j 2023
|e 36
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|h 12671-12679
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