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Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery

To study the effects of X-shaped amphiphilic block copolymers on delivery of docetaxel (DTX) and the reduction-sensitive property on drug release, a novel reduction-sensitive amphiphilic copolymer, (PLGA)(2)-SS-4-arm-PEG(2000) with a Gemini-like X-shape, was successfully synthesized. The formation o...

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Autores principales: Xiao, Haijun, Wang, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554410/
https://www.ncbi.nlm.nih.gov/pubmed/26346880
http://dx.doi.org/10.2147/IJN.S85230
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author Xiao, Haijun
Wang, Lu
author_facet Xiao, Haijun
Wang, Lu
author_sort Xiao, Haijun
collection PubMed
description To study the effects of X-shaped amphiphilic block copolymers on delivery of docetaxel (DTX) and the reduction-sensitive property on drug release, a novel reduction-sensitive amphiphilic copolymer, (PLGA)(2)-SS-4-arm-PEG(2000) with a Gemini-like X-shape, was successfully synthesized. The formation of nanomicelles was proved with respect to the blue shift of the emission fluorescence as well as the fluorescent intensity increase of coumarin 6-loaded particles. The X-shaped polymers exhibited a smaller critical micelle concentration value and possessed higher micellar stability in comparison with those of linear ones. The size of X-shaped (PLGA)(2)-SS-4-arm-PEG(2000) polymer nanomicelles (XNMs) was much smaller than that of nanomicelles prepared with linear polymers. The reduction sensitivity of polymers was confirmed by the increase of micellar sizes as well as the in vitro drug release profile of DTX-loaded XNMs (DTX/XNMs). Cytotoxicity assays in vitro revealed that the blank XNMs were nontoxic against A2780 cells up to a concentration of 50 µg/mL, displaying good biocompatibility. DTX/XNMs were more toxic against A2780 cells than other formulations in both dose- and time-dependent manners. Cellular uptake assay displayed a higher intracellular drug delivery efficiency of XNMs than that of nanomicelles prepared with linear polymers. Besides, the promotion of tubulin polymerization induced by DTX was visualized by immunofluorescence analysis, and the acceleration of apoptotic process against A2780 cells was also imaged using a fluorescent staining method. Therefore, this X-shaped reduction-sensitive (PLGA)(2)-SS-4-arm-PEG(2000) copolymer could effectively improve the micellar stability and significantly enhance the therapeutic efficacy of DTX by increasing the cellular uptake and selectively accelerating the drug release inside cancer cells.
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spelling pubmed-45544102015-09-04 Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery Xiao, Haijun Wang, Lu Int J Nanomedicine Original Research To study the effects of X-shaped amphiphilic block copolymers on delivery of docetaxel (DTX) and the reduction-sensitive property on drug release, a novel reduction-sensitive amphiphilic copolymer, (PLGA)(2)-SS-4-arm-PEG(2000) with a Gemini-like X-shape, was successfully synthesized. The formation of nanomicelles was proved with respect to the blue shift of the emission fluorescence as well as the fluorescent intensity increase of coumarin 6-loaded particles. The X-shaped polymers exhibited a smaller critical micelle concentration value and possessed higher micellar stability in comparison with those of linear ones. The size of X-shaped (PLGA)(2)-SS-4-arm-PEG(2000) polymer nanomicelles (XNMs) was much smaller than that of nanomicelles prepared with linear polymers. The reduction sensitivity of polymers was confirmed by the increase of micellar sizes as well as the in vitro drug release profile of DTX-loaded XNMs (DTX/XNMs). Cytotoxicity assays in vitro revealed that the blank XNMs were nontoxic against A2780 cells up to a concentration of 50 µg/mL, displaying good biocompatibility. DTX/XNMs were more toxic against A2780 cells than other formulations in both dose- and time-dependent manners. Cellular uptake assay displayed a higher intracellular drug delivery efficiency of XNMs than that of nanomicelles prepared with linear polymers. Besides, the promotion of tubulin polymerization induced by DTX was visualized by immunofluorescence analysis, and the acceleration of apoptotic process against A2780 cells was also imaged using a fluorescent staining method. Therefore, this X-shaped reduction-sensitive (PLGA)(2)-SS-4-arm-PEG(2000) copolymer could effectively improve the micellar stability and significantly enhance the therapeutic efficacy of DTX by increasing the cellular uptake and selectively accelerating the drug release inside cancer cells. Dove Medical Press 2015-08-24 /pmc/articles/PMC4554410/ /pubmed/26346880 http://dx.doi.org/10.2147/IJN.S85230 Text en © 2015 Xiao and Wang. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Xiao, Haijun
Wang, Lu
Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title_full Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title_fullStr Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title_full_unstemmed Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title_short Effects of X-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
title_sort effects of x-shaped reduction-sensitive amphiphilic block copolymer on drug delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554410/
https://www.ncbi.nlm.nih.gov/pubmed/26346880
http://dx.doi.org/10.2147/IJN.S85230
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