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Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers

In contrast with traditional chemotherapy, controlled drug delivery systems provide many advantages. Herein, a thermosensitive star polymer pompon with a core–arm structure was synthesized using a grafting-on method as a thermo-responsive controlled release drug carrier. Single-chain cyclized/knotte...

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Autores principales: Xu, Na, Huang, Xiaobei, Yin, Guangfu, Bu, Meijiao, Pu, Ximing, Chen, Xianchun, Liao, Xiaoming, Huang, Zhongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080076/
https://www.ncbi.nlm.nih.gov/pubmed/35539452
http://dx.doi.org/10.1039/c8ra02117a
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author Xu, Na
Huang, Xiaobei
Yin, Guangfu
Bu, Meijiao
Pu, Ximing
Chen, Xianchun
Liao, Xiaoming
Huang, Zhongbing
author_facet Xu, Na
Huang, Xiaobei
Yin, Guangfu
Bu, Meijiao
Pu, Ximing
Chen, Xianchun
Liao, Xiaoming
Huang, Zhongbing
author_sort Xu, Na
collection PubMed
description In contrast with traditional chemotherapy, controlled drug delivery systems provide many advantages. Herein, a thermosensitive star polymer pompon with a core–arm structure was synthesized using a grafting-on method as a thermo-responsive controlled release drug carrier. Single-chain cyclized/knotted poly tetra(ethylene glycol) diacrylate (polyTEGDA) was used as the hydrophobic core, and thermosensitive linear poly(N-isopropylacrylamide-co-N-methylolacrylamide) (poly(NIPAM-co-NMA)) was selected as the hydrophilic arm. Below or above its lower critical solution temperature (LCST), the linear poly(NIPAM-co-NMA) grafted onto the polyTEGDA core adopted a stretched or curled status, respectively, then the drug could be loaded in or extruded out. The LCST of star polyTEGDA-b-poly(NIPAM-co-NMA) was adjusted to slightly above body temperature (37 °C). The antitumor drug doxorubicin (DOX) was successfully loaded into the pompons with a high loading capacity of 19.45%. The cumulative release of DOX from loaded pompons in vitro for 72 hours was 71% and 20.7% at 42 °C and 37 °C, respectively, indicating that the excellent temperature-controlled release characteristics result from the unique thermo-responsive extrusion effect. Moreover, DOX loaded polyTEGDA-b-poly(NIPAM-co-NMA) pompons achieved better antitumor ability against ovarian carcinoma SKOV3 cells at 42 °C compared with that at 37 °C. These results suggest that star polyTEGDA-b-poly(NIPAM-co-NMA) pompons have considerable promise as thermo-responsive controlled drug delivery carriers.
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spelling pubmed-90800762022-05-09 Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers Xu, Na Huang, Xiaobei Yin, Guangfu Bu, Meijiao Pu, Ximing Chen, Xianchun Liao, Xiaoming Huang, Zhongbing RSC Adv Chemistry In contrast with traditional chemotherapy, controlled drug delivery systems provide many advantages. Herein, a thermosensitive star polymer pompon with a core–arm structure was synthesized using a grafting-on method as a thermo-responsive controlled release drug carrier. Single-chain cyclized/knotted poly tetra(ethylene glycol) diacrylate (polyTEGDA) was used as the hydrophobic core, and thermosensitive linear poly(N-isopropylacrylamide-co-N-methylolacrylamide) (poly(NIPAM-co-NMA)) was selected as the hydrophilic arm. Below or above its lower critical solution temperature (LCST), the linear poly(NIPAM-co-NMA) grafted onto the polyTEGDA core adopted a stretched or curled status, respectively, then the drug could be loaded in or extruded out. The LCST of star polyTEGDA-b-poly(NIPAM-co-NMA) was adjusted to slightly above body temperature (37 °C). The antitumor drug doxorubicin (DOX) was successfully loaded into the pompons with a high loading capacity of 19.45%. The cumulative release of DOX from loaded pompons in vitro for 72 hours was 71% and 20.7% at 42 °C and 37 °C, respectively, indicating that the excellent temperature-controlled release characteristics result from the unique thermo-responsive extrusion effect. Moreover, DOX loaded polyTEGDA-b-poly(NIPAM-co-NMA) pompons achieved better antitumor ability against ovarian carcinoma SKOV3 cells at 42 °C compared with that at 37 °C. These results suggest that star polyTEGDA-b-poly(NIPAM-co-NMA) pompons have considerable promise as thermo-responsive controlled drug delivery carriers. The Royal Society of Chemistry 2018-04-25 /pmc/articles/PMC9080076/ /pubmed/35539452 http://dx.doi.org/10.1039/c8ra02117a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Xu, Na
Huang, Xiaobei
Yin, Guangfu
Bu, Meijiao
Pu, Ximing
Chen, Xianchun
Liao, Xiaoming
Huang, Zhongbing
Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title_full Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title_fullStr Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title_full_unstemmed Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title_short Thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
title_sort thermosensitive star polymer pompons with a core–arm structure as thermo-responsive controlled release drug carriers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080076/
https://www.ncbi.nlm.nih.gov/pubmed/35539452
http://dx.doi.org/10.1039/c8ra02117a
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