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Complex Assembly of Polymer Conjugated Mesoporous Silica Nanoparticles for Intracellular pH-Responsive Drug Delivery.
Yang, Yang; Achazi, Katharina; Jia, Yi; Wei, Qiang; Haag, Rainer; Li, Junbai.
Afiliação
  • Yang Y; CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology , Beijing 100190, China.
  • Achazi K; Department of Chemistry and Biochemistry, Freie Universität Berlin , Takustrasse 3, 14195 Berlin, Germany.
  • Jia Y; Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Colloid and Interface Science, Institute of Chemistry, Chinese Academy of Sciences (CAS) , Beijing 100190, China.
  • Wei Q; Department of Chemistry and Biochemistry, Freie Universität Berlin , Takustrasse 3, 14195 Berlin, Germany.
  • Haag R; Department of Chemistry and Biochemistry, Freie Universität Berlin , Takustrasse 3, 14195 Berlin, Germany.
  • Li J; CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology , Beijing 100190, China.
Langmuir ; 32(47): 12453-12460, 2016 11 29.
Article em En | MEDLINE | ID: mdl-27467698
ABSTRACT
There is a great challenge in constructing pH-responsive drug delivery systems in biomedical application research. Many nanocomposites are intended to be pH-responsive as drug carriers because of a tumorous or intracellular mildly acidic environment. However, it is always difficult to find an appropriate system for quick response and release before the carrier is excreted from the living system. In this work, hyperbranched polymer, hyperbranched polyglycerol (hPG), and conjugated mesoporous silica nanoparticles (MSNs) were assembled as complexes to serve as drug carriers. Herein, the conjugated polymer-MSNs interacted through the Schiff base bond, which possessed a mildly acidic responsive property. Interestingly, the assembled system could rapidly respond and release guest molecules inside cancer cells. This would make the entrapped drug released before the carriers escape from the endosome counterpart. The results show that the assembled composite complexes can be considered to be a drug delivery system for cancer therapy.
Assuntos
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Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Sistemas de Liberação de Medicamentos / Nanopartículas Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Sistemas de Liberação de Medicamentos / Nanopartículas Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article