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Characterization of polyelectrolyte complexes between chondroitin sulfate and chitosan in the solid state
Author(s) -
Chen WenBin,
Wang LiFang,
Chen JennShing,
Fan SuYun
Publication year - 2005
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.30393
Subject(s) - polyelectrolyte , chitosan , gel permeation chromatography , dissolution , stoichiometry , molar mass , materials science , fourier transform infrared spectroscopy , nuclear chemistry , polymer , analytical chemistry (journal) , polymer chemistry , chemistry , organic chemistry , chemical engineering , engineering , composite material
Chondroitin sulfate (ChS) was used to form polyelectrolyte complexes with chitosan (ChI), and its potential as a colon‐targeted drug carrier was investigated. In order to determine the optimal conditions for the formation of a stable polyelectrolyte complex, the formation of ChS/ChI complexes was examined at two different pH values with various weight ratios, or at a fixed molar ratio of ChS/ChI of 1/2 under various pH conditions. The molar compositions of the various ChS/ChI complexes were quantitated with the use of solid‐state 13 C CP MAS NMR. The equivalent molar ratios of the complexes ranged from 0.47 to 0.54, in agreement with the data determined by elemental analysis. The fact that these values were close to 0.5 suggests that most of the OSO 3 −and the COO − groups on ChS formed strong electrostatic interactions with the NH 3 +groups on ChI, obeying a simple stoichiometric reaction between two oppositely charged moieties. Similar compositions of the complexes were obtained under most conditions tested; however, different strengths of the interactions between the two polysaccharides were noted from measurements of the water‐associated transition and thermal degradation temperatures and the degree of ChS dissolution. FTIR and 13 C NMR clearly showed H‐bond formation at low pH, indicating that in addition to the varying degrees of electrostatic interaction, H bonding may be involved in complex formation. The highest degradation temperature, as determined by thermal gravimetric analysis, and the lowest ChS sol fraction, as measured by gel permeation chromatography, were observed with the complex prepared at pH 5, with a 1:1 mole ratio of the two opposite charges in feed. This complex also exhibited the highest water‐associated transition temperature, as determined by differential scanning calorimetry. Furthermore, the swelling behavior of these complexes was pH dependent; this is a property that can potentially be exploited to control drug release from these complexes under specific pH conditions. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005