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2018 | 23 | 76 - 87

Article title

CHARACTERISTICS OF ASCORBIC ACID RELEASE FROM TPP-CROSSLINKED CHITOSAN/ALGINATE POLYELECTROLYTE COMPLEX MEMBRANES

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EN

Abstracts

EN
Chitosan/alginate polyelectrolyte complex membranes (Ch/Alg) additionally cross-linked with tripolyphosphate (TPP) and containing ascorbic acid (AA) were prepared. The dynamic swelling behaviour of Ch/Alg/TPP and ascorbic acid release from the membrane were characterised in different buffer solutions. It has been found that the pH of the buffer solution affects the swelling and release behaviour of AA. Ascorbic acid release, observed over a period of 360 min, exhibited a biphasic pattern, characterised by a fast initial burst release, followed by a slow, sustained release. Different mathematical models were used to study the kinetics and transport mechanism of AA from Ch/Alg/TPP hydrogels. Drug release data were fitted to the zero order kinetic model and first order kinetic model. To characterise the drug mechanism, the release data were fitted to the Higuchi and Korsmeyer-Peppas equations. The initial burst AA release followed zero order kinetics and was quasi-Fickian in nature. The second step of AA release followed first order kinetics.

Contributors

  • Faculty of Chemistry, Nicolaus Copernicus University in Toruń
  • Faculty of Chemistry, Nicolaus Copernicus University in Toruń
  • Faculty of Chemistry, Nicolaus Copernicus University in Toruń

References

  • [1] Peppas NA; (2004) Hydrogels. In: Ratner BD, Hoffman AS, Schoen FJ, Lemons JE (eds), Biomaterials Science: An Introduction to Materials in Medicine, 2nd edn. Academic Press, New York, 100-107.
  • [2] Hoffman AS; (2002) Hydrogels for biomedical applications. Adv Drug Deliver Rev 43, 3-12. DOI: 10.1016/j.addr.2012.09.010
  • [3] Thünemann AF, Müller M, Dautzenberg H, Joanny JF, Löwen H; (2004) Polyelectrolyte complexes. Adv Polym Sci 166, 113-171. DOI: 10.1007/b11350
  • [4] Struszczyk MH; (2002) Chitin and. chitosan, Part I. Properties and production. Polimery (Warsaw) 47, 316-325.
  • [5] Draget I, Smidsrřd O, Skjåk-Broek G; (2002) Alginates from algae. In: Vandamme EJ, De Baets S (eds), Biopolymers. Polysaccharides II. Polysaccharides from Eukaryotes. Wiley, Trondheim, 216-244.
  • [6] Berger J, Reist M, Mayer JM, Felt O, Gurny R; (2004) Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications. Eur J Pharm Biopharm 57, 35–52. DOI: 10.1016/S0939-6411(03)00160-7
  • [7] Krayukhina MA, Samoilova NA, Yamskov IA; (2008) Polyelectrolyte complexes of chitosan: formation, properties and applications. Russ Chem Rev 77, 799–813. DOI: 10.1070/RC2008v077n09ABEH003750
  • [8] Hamman JH; (2010) Chitosan based polyelectrolyte complexes as potential carrier materials in drug delivery systems. Mar Drugs 8, 1305–1322. DOI: 10.3390/md8041305
  • [9] Berger J, Reist M, Mayer JM, Felt O, Peppas NA, Gurny R; (2004) Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur J Pharm Biopharm 57, 19-34. DOI: 10.1016/S0939-6411(03)00161-9
  • [10] Tahtat D, Mahlous M, Benamer S, Khodja AN, Oussedik-Oumehdi H, Laraba-Djebari F; (2013) Oral delivery of insulin from alginate/chitosan crosslinked by glutaraldehyde. Int J Biol Macromol 58, 160-168. DOI: 10.1016/j.ijbiomac.2013.03.064
  • [11] Jiang C, Wang Z, Zhang X, Zhu X, Nie J, Ma G; (2014) Crosslinked polyelectrolyte complex fiber membrane based on chitosan-sodium alginate by freeze-drying. RSC Adv 4, 41551-41560. DOI: 10.1039/C4RA04208E
  • [12] Lee FL, Sung HW, Shyu SS; (2002) Drug release from chitosan-alginate complex beads reinforced by a naturally occurring cross-linking agent. Carbohyd Polym 48, 61-72. DOI:10.1016/S0144-8617(01)00212-0
  • [13] Ostrowska-Czubenko J, Gierszewska-Drużyńska M; (2009) Effect of ionic crosslinking on the water state in hydrogel chitosan membranes. Carbohyd Polym 77, 590-598. DOI: 10.1016/j.carbpol.2009.01.036
  • [14] Dash S, Murthy PN, Nath L, Chowdhury P; (2010) Kinetic modelling on drug release from controlled drug delivery systems. Acta Pol Pharm - Drug Res 67, 217-223.
  • [15] Rosu M-C, Bratu I; (2014) Promising psyllium-based composite containing TiO2 nanoparticles as aspirin-carrier matrix. Prog Nat Sci - Mater 24, 205-209. DOI: 10.1016/j.pnsc.2014.05.007
  • [16] Rao CNR; (1963) Chemical Application of Infrared Spectroscopy. Academic Press, New York.
  • [17] Huang X, Brazel CS; (2001) On the importance and mechanisms of burst release in matrix-controlled drug delivery systems. J Control Release 73, 121-136. DOI: 10.1016/S0168-3659(01)00248-6
  • [18] Gupta KC, Jabrail FH; (2006) Preparation and characterization of sodium hexameta phosphate cross-linked chitosan microspheres for controlled and sustained delivery of centchroman. Int J Biol Macromol 38, 272-283. DOI: 10.1016/j.ijbiomac.2006.03.013
  • [19] Gupta KC, Jabrail FH; (2007) Controlled-release formulations for hydroxy urea and rifampicin using polyphosphate-anion-crosslinked chitosan microspheres. J Appl Polym Sci 104, 1942-1956. DOI: 10.1002/app.25881
  • [20] Gupta KC, Jabrail FH; (2008) Effect of molecular weight and degree of deacetylation on controlled release of isoniazid from chitosan microspheres. Polym Advan Technol 19, 432–441. DOI:10.1002/pat.1035
  • [21] Gupta P, Vermani K, Garg S; (2002) Hydrogels: from controlled release to pH-responsive drug delivery. DDT 7, 569-579. DOI: 10.1016/S1359-6446(02)02255-9
  • [22] Lai F, Lin B, Mo F, Xu C, Lin M; (2017) Novel composite microparticles of alginate coated with chitosan for controlled release and protection of ascorbic acid. Adv Polym Tech 36, 21574. DOI: 10.1002/adv.21574
  • [23] Alishahi A, Mirvaghefi A, Tehrani MR, Farahmand H, Shojaosadati SA, Dorkoosh FA, Elsabee MZ; (2011) Shelf life and delivery enhancement of vitamin C using chitosan nanoparticles. Food Chem 126, 935-940. DOI: 10.1016/j.foodchem.2010.11.086
  • [24] Shu XZ, Zhu KJ; (2002) The influence of multivalent phosphate structure on the properties of ionically cross-linked chitosan films for controlled drug release. Eur J Pharm Biopharm 54, 235-243. DOI: 10.1016/S0939-6411(02)00052-8
  • [25] Shu XZ, Zhu KJ; (2002) Controlled drug release properties of ionically cross-linked chitosan beads: the influence of anion structure. Int J Pharm 233, 217-225. DOI: 10.1016/S0378-5173(01)00943-7
  • [26] Unagollaa JM,. Jayasuriyaa AC; (2018) Drug transport mechanisms and in vitro release kinetics of vancomycin encapsulated chitosan-alginate polyelectrolyte microparticles as a controlled drug delivery system. Eur J Pharm Sci 114, 199-209. DOI: 10.1016/j.ejps.2017.12.012

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article

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bwmeta1.element.psjd-26c0dd60-328b-4139-a23b-75e60325cdb9
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