Glucose- and pH-Responsive Nanogated Ensemble Based on Polymeric Network Capped Mesoporous Silica
In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acryla...
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Published in | ACS applied materials & interfaces Vol. 7; no. 11; pp. 6310 - 6316 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
25.03.2015
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Abstract | In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acrylate and the subsequent hydrolysis of the ester bond. Then the PAA was glycosylated with glucosamine to obtain P(AA-AGA). To block the pore of silica, the P(AA-AGA) chains were cross-linked through the formation of boronate esters between 4,4-(ethylenedicarbamoyl)phenylboronic acid (EPBA) and the hydroxyl groups of P(AA-AGA). The boronate esters disassociated in the presence of glucose or in acidic conditions, which lead to opening of the mesoporous channels and the release of loaded guest molecules. The rate of release could be tuned by varying the pH or the concentration of glucose in the environment. The combination of two stimuli exhibited an obvious enhanced release capacity in mild acidic conditions (pH 6.0). |
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AbstractList | In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acrylate and the subsequent hydrolysis of the ester bond. Then the PAA was glycosylated with glucosamine to obtain P(AA-AGA). To block the pore of silica, the P(AA-AGA) chains were cross-linked through the formation of boronate esters between 4,4-(ethylenedicarbamoyl)phenylboronic acid (EPBA) and the hydroxyl groups of P(AA-AGA). The boronate esters disassociated in the presence of glucose or in acidic conditions, which lead to opening of the mesoporous channels and the release of loaded guest molecules. The rate of release could be tuned by varying the pH or the concentration of glucose in the environment. The combination of two stimuli exhibited an obvious enhanced release capacity in mild acidic conditions (pH 6.0). In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acrylate and the subsequent hydrolysis of the ester bond. Then the PAA was glycosylated with glucosamine to obtain P(AA-AGA). To block the pore of silica, the P(AA-AGA) chains were cross-linked through the formation of boronate esters between 4,4-(ethylenedicarbamoyl)phenylboronic acid (EPBA) and the hydroxyl groups of P(AA-AGA). The boronate esters disassociated in the presence of glucose or in acidic conditions, which lead to opening of the mesoporous channels and the release of loaded guest molecules. The rate of release could be tuned by varying the pH or the concentration of glucose in the environment. The combination of two stimuli exhibited an obvious enhanced release capacity in mild acidic conditions (pH 6.0).In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acrylate and the subsequent hydrolysis of the ester bond. Then the PAA was glycosylated with glucosamine to obtain P(AA-AGA). To block the pore of silica, the P(AA-AGA) chains were cross-linked through the formation of boronate esters between 4,4-(ethylenedicarbamoyl)phenylboronic acid (EPBA) and the hydroxyl groups of P(AA-AGA). The boronate esters disassociated in the presence of glucose or in acidic conditions, which lead to opening of the mesoporous channels and the release of loaded guest molecules. The rate of release could be tuned by varying the pH or the concentration of glucose in the environment. The combination of two stimuli exhibited an obvious enhanced release capacity in mild acidic conditions (pH 6.0). In this paper, a glucose and pH-responsive release system based on polymeric network capped mesoporous silica nanoparticles (MSN) has been presented. The poly(acrylic acid) (PAA) brush on MSN was obtained through the surface-initiated atom transfer radical polymerization (SI-ATRP) of t-butyl acrylate and the subsequent hydrolysis of the ester bond. Then the PAA was glycosylated with glucosamine to obtain P(AA-AGA). To block the pore of silica, the P(AA-AGA) chains were cross-linked through the formation of boronate esters between 4,4-(ethylenedicarbamoyl)phenylboronic acid (EPBA) and the hydroxyl groups of P(AA-AGA). The boronate esters disassociated in the presence of glucose or in acidic conditions, which lead to opening of the mesoporous channels and the release of loaded guest molecules. The rate of release could be tuned by varying the pH or the concentration of glucose in the environment. The combination of two stimuli exhibited an obvious enhanced release capacity in mild acidic conditions (pH 6.0). |
Author | Tang, Zhao-Wen Xiao, Jian-Yun Wu, Hai-Xia Yang, Mei-Yan Tan, Lei Zhuo, Ren-Xi Liu, Chuan-Jun |
AuthorAffiliation | Wuhan University College of Chemistry and Chemical Engineering Luoyang Normal University College of Chemistry and Molecular Science |
AuthorAffiliation_xml | – name: College of Chemistry and Chemical Engineering – name: Luoyang Normal University – name: College of Chemistry and Molecular Science – name: Wuhan University |
Author_xml | – sequence: 1 givenname: Lei surname: Tan fullname: Tan, Lei organization: Wuhan University – sequence: 2 givenname: Mei-Yan surname: Yang fullname: Yang, Mei-Yan organization: Wuhan University – sequence: 3 givenname: Hai-Xia surname: Wu fullname: Wu, Hai-Xia organization: Luoyang Normal University – sequence: 4 givenname: Zhao-Wen surname: Tang fullname: Tang, Zhao-Wen organization: Wuhan University – sequence: 5 givenname: Jian-Yun surname: Xiao fullname: Xiao, Jian-Yun organization: Wuhan University – sequence: 6 givenname: Chuan-Jun surname: Liu fullname: Liu, Chuan-Jun email: cjliu@whu.edu.cn organization: Wuhan University – sequence: 7 givenname: Ren-Xi surname: Zhuo fullname: Zhuo, Ren-Xi organization: Wuhan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25735191$$D View this record in MEDLINE/PubMed |
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SubjectTerms | acrylic acid chemical elements crosslinking Delayed-Action Preparations - chemical synthesis Diffusion esters glucosamine glucose Glucose - chemistry glycosylation Hydrogen-Ion Concentration hydrolysis Materials Testing Nanocapsules - chemistry Nanocapsules - ultrastructure nanoparticles Nanopores - ultrastructure Particle Size polyacrylic acid polymerization Polymers - chemistry Porosity porous media silica Silicon Dioxide - chemistry |
Title | Glucose- and pH-Responsive Nanogated Ensemble Based on Polymeric Network Capped Mesoporous Silica |
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