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Fluorinated polymer emulsion systems: Construction and application in delivering genes and proteins.
Xiao, Ya-Ping; Zhang, Ji; Liu, Yan-Hong; Huang, Zheng; Yu, Xiao-Qi.
Afiliação
  • Xiao YP; Key Laboratory of Green Chemistry and Technology (Ministry of Education), College of Chemistry, Sichuan University, Chengdu, 610064, PR China.
  • Zhang J; Key Laboratory of Green Chemistry and Technology (Ministry of Education), College of Chemistry, Sichuan University, Chengdu, 610064, PR China. Electronic address: jzhang@scu.edu.cn.
  • Liu YH; Key Laboratory of Green Chemistry and Technology (Ministry of Education), College of Chemistry, Sichuan University, Chengdu, 610064, PR China.
  • Huang Z; Key Laboratory of Green Chemistry and Technology (Ministry of Education), College of Chemistry, Sichuan University, Chengdu, 610064, PR China.
  • Yu XQ; Key Laboratory of Green Chemistry and Technology (Ministry of Education), College of Chemistry, Sichuan University, Chengdu, 610064, PR China. Electronic address: xqyu@scu.edu.cn.
Eur J Med Chem ; 207: 112799, 2020 Dec 01.
Article em En | MEDLINE | ID: mdl-32980740
ABSTRACT
Emulsions have shown great potential in the delivery of various types of cargoes such as nucleic acids and proteins. In this study, fluorinated polymer emulsions (PFx@PFD-n) were prepared using fluorinated polymers with different structures as surfactant in PFD emulsions under ultrasound. These polymer emulsions gave comparable DNA binding ability compared with corresponding polymers. Heparin competition experiment showed that polymer emulsions could compact DNA or protein to form more stable complexes. In vitro gene transfection results showed that the polymer emulsions could induce higher gene expression than corresponding polymers and polyethyleneimine (PEI), and the transfection efficiency was enhanced with the increase of PFD amount in polymer emulsions. Flow cytometry studies revealed that the emulsions could mediate more efficient cellular uptake with stronger serum tolerance. Moreover, the polymer emulsion could deliver considerable amount of OVA into Raw 264.7 cells at low mass ratio, showing its potential in immunotherapy. The activities of ß-galactosidase delivered by the emulsions could also be well maintained after entering cells. This study provides a strategy to construct cationic gene and cytosolic protein vectors with high efficiency and low toxicity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polímeros / DNA / Portadores de Fármacos / Proteínas / Halogenação Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polímeros / DNA / Portadores de Fármacos / Proteínas / Halogenação Idioma: En Ano de publicação: 2020 Tipo de documento: Article