Preparation of chitosan self-aggregates as a gene delivery system

J Control Release. 1998 Feb 12;51(2-3):213-20. doi: 10.1016/s0168-3659(97)00173-9.

Abstract

Hydrophobically modified chitosan containing 5.1 deoxycholic acid groups per 100 anhydroglucose units was synthesized by an EDC-mediated coupling reaction. Formation and characteristics of self-aggregates of hydrophobically modified chitosan were studied by fluorescence spectroscopy and dynamic light scattering method. The critical aggregation concentration (cac) of the self-aggregate was determined by measuring the fluorescence intensity of pyrene as a fluorescent probe. The cac value in PBS solution (pH 7.2) was 1.7x10(-2) mg/ml. Mean diameter of self-aggregates in PBS solution (pH 7.2) was 162 +/- 18 nm with an unimodal size distribution. Charge complex formation between self-aggregates and plasmid DNA was confirmed by electrophoresis on an agarose gel. Migration of DNA on an agarose gel was completely retarded above a charge ratio ( +/-) of 4/1 at pH 7.2. The free DNA dissociated from the complexes was observed by electrophoresis above pH 8.0 at a fixed charge ratio of 4/1. An efficient of COS-1 cells was achieved by self-aggregates/DNA complexes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocompatible Materials / chemistry*
  • Cell Line
  • Chitin / analogs & derivatives*
  • Chitin / chemistry
  • Chitosan
  • Chloramphenicol O-Acetyltransferase / analysis
  • DNA, Bacterial / chemistry*
  • Deoxycholic Acid
  • Escherichia coli / enzymology
  • Fluorescent Dyes / analysis
  • Gene Transfer Techniques
  • Glucose
  • Hydrogen-Ion Concentration
  • Plasmids
  • Spectrometry, Fluorescence
  • Transfection

Substances

  • Biocompatible Materials
  • DNA, Bacterial
  • Fluorescent Dyes
  • Deoxycholic Acid
  • Chitin
  • Chitosan
  • Chloramphenicol O-Acetyltransferase
  • Glucose