Literature DB >> 17850110

Ionization and solubility of chitosan solutions related to thermosensitive chitosan/glycerol-phosphate systems.

Dominic Filion1, Marc Lavertu, Michael D Buschmann.   

Abstract

Chitosan is a linear cationic biopolymer composed of glucosamine and N-acetyl-glucosamine that is only soluble in acidic aqueous solutions and precipitates when neutralized. However, it was recently discovered that chitosan dissolved in solutions containing glycerol phosphate was soluble at near neutral pH and produced a sol-gel transition when heated. Understanding this unique thermogelling system requires improved characterization of the ionization and solubility behaviors of chitosan, in particular dependencies on temperature, salt, chitosan concentration, and fD, where fD is the fraction of glucosamine monomers (deacetylated monomers) in chitosan. In the current study we performed temperature-controlled titration and dilution experiments on chitosan solutions with fD of 0.72, 0.85, and 0.98 at concentrations ranging from 1.875 to 30 mM of its glucosamine monomer and with 0 to 150 mM added salt. Light transmittance measurements were performed during titration to indicate precipitation. We found the apparent proton dissociation constant of chitosan, pKap, to (1) decrease strongly with increased temperature, (2) increase strongly with increased salt, (3) increase strongly with increased chitosan concentration in low-salt conditions, and (4) decrease weakly with increasing fD. All of the above influences on chitosan pKap were accurately predicted using a mean-field Poisson-Boltzmann (PB) cylindrical cell model where the only adjustable parameter was the temperature-dependent chitosan intrinsic monomeric dissociation constant pK0(T). The resulting chitosan pK0 values at 25 degrees C were in the range from 6.63 to 6.78 for all chitosans and salt contents tested. The temperature dependence of chitosan ionization was found to strongly reduce pK0(T) by 0.023 units per degrees C, for example, resulting in a reduction of chitosan pK0(T) from 7.1 at 5 degrees C to 6.35 at 37 degrees C for fD of 0.72 in 150 mM salt. A similar temperature-dependent reduction of the pKa of the glucosamine monomer was found (-0.027 units per degrees C) while the pKa of glycerol phosphate did not change significantly with temperature. The latter result suggested that chitosan solutions heated in the presence of glycerol phosphate will become partly neutralized by transferring protons to glycerol phosphate and thereby allow attractive interchain forces to form a physically cross-linked gel under the appropriate conditions. Additionally, the degree of ionization of chitosan when it precipitates upon addition of a strong base was measured to be in the range from 0.25 to 0.55 and was found to (1) be insensitive to temperature, (2) increase strongly with increased salt, and (3) increase strongly with fD. The salt effect was accounted for by the PB model, while the influence of fD appeared to be due to acetyl groups impeding attractive chain-to-chain association to increase solubility and require reduced ionization levels to precipitate.

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Year:  2007        PMID: 17850110     DOI: 10.1021/bm700520m

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  11 in total

1.  What can we learn from the saga of chitosan gums in hyperphosphatemia therapy?

Authors:  Man S Oh; Jaime Uribarri
Journal:  Clin J Am Soc Nephrol       Date:  2014-01-09       Impact factor: 8.237

2.  pH-Responsive Self-Assembly of Polysaccharide through a Rugged Energy Landscape.

Authors:  Brian H Morrow; Gregory F Payne; Jana Shen
Journal:  J Am Chem Soc       Date:  2015-09-30       Impact factor: 15.419

3.  Release and activity of anti-TNFalpha therapeutics from injectable chitosan preparations for local drug delivery.

Authors:  Mohammed F Shamji; Priscilla Hwang; Robert W Bullock; Samuel B Adams; Dana L Nettles; Lori A Setton
Journal:  J Biomed Mater Res B Appl Biomater       Date:  2009-07       Impact factor: 3.368

4.  Enhanced gene delivery mediated by low molecular weight chitosan/DNA complexes: effect of pH and serum.

Authors:  Surendra Nimesh; Marc M Thibault; Marc Lavertu; Michael D Buschmann
Journal:  Mol Biotechnol       Date:  2010-10       Impact factor: 2.695

Review 5.  3D Cell Culture in a Self-Assembled Nanofiber Environment.

Authors:  Yi Wen Chai; Eu Han Lee; John D Gubbe; John H Brekke
Journal:  PLoS One       Date:  2016-09-15       Impact factor: 3.240

6.  Regioselective thioacetylation of chitosan end-groups for nanoparticle gene delivery systems.

Authors:  V D Pickenhahn; V Darras; F Dziopa; K Biniecki; G De Crescenzo; M Lavertu; M D Buschmann
Journal:  Chem Sci       Date:  2015-05-07       Impact factor: 9.825

7.  Nucleotide Interaction with a Chitosan Layer on a Silica Surface: Establishing the Mechanism at the Molecular Level.

Authors:  Tetyana M Budnyak; Nataliya N Vlasova; Lyudmila P Golovkova; Olga Markitan; Glib Baryshnikov; Hans Ågren; Adam Slabon
Journal:  Langmuir       Date:  2021-01-15       Impact factor: 3.882

Review 8.  Chitosans for delivery of nucleic acids.

Authors:  Michael D Buschmann; Abderrazzak Merzouki; Marc Lavertu; Marc Thibault; Myriam Jean; Vincent Darras
Journal:  Adv Drug Deliv Rev       Date:  2013-07-18       Impact factor: 15.470

9.  Intra-Articular Formulation of GE11-PLGA Conjugate-Based NPs for Dexamethasone Selective Targeting-In Vitro Evaluation.

Authors:  Enrica Chiesa; Silvia Pisani; Barbara Colzani; Rossella Dorati; Bice Conti; Tiziana Modena; Kevin Braekmans; Ida Genta
Journal:  Int J Mol Sci       Date:  2018-08-06       Impact factor: 5.923

10.  Chitosan rate of uptake in HEK293 cells is influenced by soluble versus microparticle state and enhanced by serum-induced cell metabolism and lactate-based media acidification.

Authors:  Caroline D Hoemann; Jessica Guzmán-Morales; Nicolas Tran-Khanh; Geneviève Lavallée; Mario Jolicoeur; Marc Lavertu
Journal:  Molecules       Date:  2013-01-15       Impact factor: 4.411

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