Your browser doesn't support javascript.
loading
Characterization and cytocompatibility of thermosensitive hydrogel embedded with chitosan nanoparticles for delivery of bone morphogenetic protein-2 plasmid DNA.
Li, Dan-Dan; Pan, Jian-Feng; Ji, Qiu-Xia; Yu, Xin-Bo; Liu, Ling-Shuang; Li, Hui; Jiao, Xiao-Ju; Wang, Lei.
Afiliação
  • Li DD; Stomatological Hospital of Zhengzhou, Zhengzhou, 450000, Henan Province, China.
  • Pan JF; The Affiliated Hospital of Qingdao University, Qingdao, 266001, Shandong Province, China.
  • Ji QX; School of Stomatology, Qingdao University, Qingdao, 266001, Shandong Province, China.
  • Yu XB; The Arrail Dental Hospital of Beijing, Beijing, 100107, Chaoyang Province, China.
  • Liu LS; The Affiliated Hospital of Qingdao University, Qingdao, 266001, Shandong Province, China. jiqx@qduhospital.cn.
  • Li H; School of Stomatology, Qingdao University, Qingdao, 266001, Shandong Province, China. jiqx@qduhospital.cn.
  • Jiao XJ; The Affiliated Hospital of Qingdao University, Qingdao, 266001, Shandong Province, China.
  • Wang L; School of Stomatology, Qingdao University, Qingdao, 266001, Shandong Province, China.
J Mater Sci Mater Med ; 27(8): 134, 2016 Aug.
Article em En | MEDLINE | ID: mdl-27405491
ABSTRACT
A novel injectable chitosan thermosensitive hydrogel was designed as a target multi-effect scaffold for endogenous repair of the periodontium. The hydrogel complex was designed by embedding chitosan nanoparticles (CSn) loaded with bone morphogenetic protein-2 plasmid DNA (pDNA-BMP2) into a chitosan (CS)-based hydrogel with α,ß-glycerophosphate (α,ß-GP), termed CS/CSn(pDNA-BMP2)-GP. Characterization, the in vitro release profile for pDNA-BMP2, and cytocompatibility to human periodontal ligament cells (HPDLCs), were then conducted. The average diameter of the CSn(pDNA-BMP2) was 270.1 nm with a polydispersity index (PDI) of 0.486 and zeta potential of +27.0 mv. A DNase I protection assay showed that CSn could protect the pDNA-BMP2 from nuclease degradation. Encapsulation efficiency and loading capacity of CSn(pDNA-BMP2) were more than 80 and 30 %, respectively. The sol-gel transition time was only 3 min when CSn(pDNA-BMP2) was added into the CS/α,ß-GP system. Scanning electron microscopy showed that CSn(pDNA-BMP2) was randomly dispersed in a network with regular holes and a porous structure. Weighting method showed the swelling ratio and degradation was faster in medium of pH 4.0 than pH 6.8. An in vitro pDNA-BMP2 release test showed that the cumulative release rate of pDNA-BMP2 was much slower from CS/CSn-GP than from CSn in identical release media. In release media with different pH, pDNA-BMP2 release was much slower at pH 6.8 than at pH 4.0. Three-dimensional culture with HPDLCs showed good cell proliferation and the Cell-Counting Kit-8 assay indicated improved cell growth with the addition of CSn(pDNA-BMP2) to CS/α,ß-GP. In summary, the CS/CSn(pDNA-BMP2)-GP complex system exhibited excellent biological properties and cytocompatibility, indicating great potential as a gene delivery carrier and tissue regeneration scaffold for endogenous repair of the periodontium.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Plasmídeos / DNA / Hidrogéis / Quitosana / Proteína Morfogenética Óssea 2 Limite: Humans Idioma: En Revista: J Mater Sci Mater Med Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Plasmídeos / DNA / Hidrogéis / Quitosana / Proteína Morfogenética Óssea 2 Limite: Humans Idioma: En Revista: J Mater Sci Mater Med Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China