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231226s2022 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.2c02896
|2 doi
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|a pubmed24n1167.xml
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|a (DE-627)NLM35028217X
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|a (NLM)36516233
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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 Belkhir, Kedafi
|e verfasserin
|4 aut
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|a Synthesis and Self-Assembly of UV-Cross-Linkable Amphiphilic Polyoxazoline Block Copolymers
|b Importance of Multitechnique Characterization
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|c 2022
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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
|b cr
|2 rdacarrier
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|a Date Completed 28.12.2022
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|a Date Revised 06.01.2023
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a In the nanomedicine field, there is a need to widen the availability of nanovectors to compensate for the increasingly reported side effects of poly(ethene glycol). Nanovectors enabling cross-linking can further optimize drug delivery. Cross-linkable polyoxazolines are therefore relevant candidates to address these two points. Here we present the synthesis of coumarin-functionalized poly(2-alkyl-2-oxazoline) block copolymers, namely, poly(2-methyl-2-oxazoline)-block-poly(2-phenyl-2-oxazoline) and poly(2-methyl-2-oxazoline)-block-poly(2-butyl-2-oxazoline). The hydrophilic ratio and molecular weights were varied in order to obtain a range of possible behaviors. Their self-assembly after nanoprecipitation or film rehydration was examined. The resulting nano-objects were fully characterized by transmission electron microscopy (TEM), cryo-TEM, multiple-angle dynamic and static light scattering. In most cases, the formation of polymer micelles was observed, as well as, in some cases, aggregates, which made characterization more difficult. Cross-linking was performed under UV illumination in the presence of a coumarin-bearing cross-linker based on polymethacrylate derivatives. Addition of the photo-cross-linker and cross-linking resulted in better-defined objects with improved stability in most cases
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a poly(2-methyl-2-oxazoline)
|2 NLM
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|a Polymers
|2 NLM
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|a Polyamines
|2 NLM
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|a Micelles
|2 NLM
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|a Cerlati, Orélia
|e verfasserin
|4 aut
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|a Heaugwane, Diana
|e verfasserin
|4 aut
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|a Tosi, Alice
|e verfasserin
|4 aut
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|a Benkhaled, Belkacem Tarek
|e verfasserin
|4 aut
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|a Brient, Pierre-Louis
|e verfasserin
|4 aut
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|a Chatard, Camille
|e verfasserin
|4 aut
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|a Graillot, Alain
|e verfasserin
|4 aut
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|a Catrouillet, Sylvain
|e verfasserin
|4 aut
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|a Balor, Stéphanie
|e verfasserin
|4 aut
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|a Goudounèche, Dominique
|e verfasserin
|4 aut
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|a Payré, Bruno
|e verfasserin
|4 aut
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|a Laborie, Pascale
|e verfasserin
|4 aut
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|a Lim, Jia-Hui
|e verfasserin
|4 aut
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|a Putaux, Jean-Luc
|e verfasserin
|4 aut
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|a Vicendo, Patricia
|e verfasserin
|4 aut
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|a Gibot, Laure
|e verfasserin
|4 aut
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|a Lonetti, Barbara
|e verfasserin
|4 aut
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|a Mingotaud, Anne-Françoise
|e verfasserin
|4 aut
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|a Lapinte, Vincent
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 38(2022), 51 vom: 27. Dez., Seite 16144-16155
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:38
|g year:2022
|g number:51
|g day:27
|g month:12
|g pages:16144-16155
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|u http://dx.doi.org/10.1021/acs.langmuir.2c02896
|3 Volltext
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|a AR
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|d 38
|j 2022
|e 51
|b 27
|c 12
|h 16144-16155
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