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Biodegradable and biocompatible polyampholyte microgels derived from chitosan, carboxymethyl cellulose and modified methyl cellulose.
Dhar, Neha; Akhlaghi, Seyedeh Parinaz; Tam, Kam C.
Afiliação
  • Dhar N; Department of Chemical Engineering, Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, Canada N2L 3G1.
  • Akhlaghi SP; Department of Chemical Engineering, Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, Canada N2L 3G1.
  • Tam KC; Department of Chemical Engineering, Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, Canada N2L 3G1. Electronic address: mkctam@uwaterloo.ca.
Carbohydr Polym ; 87(1): 101-109, 2012 Jan 04.
Article em En | MEDLINE | ID: mdl-34662937
Two biocompatible and biodegradable polyampholyte microgels, namely chitosan-carboxymethyl cellulose (CS-CMC) and chitosan-modified methyl cellulose (CS-ModMC) were synthesized by an inverse microemulsion technique. The CS-CMC microgel system was pH-responsive while the CS-ModMC system possessed both pH and thermo-responsive properties. For CS-CMC system, the number of -OCH2COOH and -NH2 groups was determined to be 1.5 and 1.1meq/g of microgel, respectively. In the pH range of 4-9, the zeta potential values varied from +10 to -40mV, while the hydrodynamic radius varied from 160nm in the swollen state (acidic and basic pH) to 110nm in the "collapse" state (neutral pH). Furthermore, TEM micrographs confirmed the swelling/deswelling behaviour of CS-CMC microgel particles at acidic, neutral and basic conditions. For CS-ModMC system, the number of -OCH2COOH and -NH2 groups was determined to be 0.8 and 0.6meq/g microgel, respectively. In the pH range of 4-9, the surface charge on the microgels varied from +25 to -60mV and the hydrodynamic radii were 190nm at low pH, 80nm at neutral pH, to 120nm at a high pH. In vitro drug release studies confirmed that CS-CMC microgels could encapsulate and release a model drug, thus they could potentially be used as biocompatible and biodegradable drug carriers.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article