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Wound healing, anti-ulcerogenic, anti-inflammatory and anti-proliferative properties of Chitosan

2009Journal article Open access
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dc.contributor.authorTavaria, F.
dc.contributor.authorJorge, M.
dc.contributor.authorMarchetti, G.
dc.contributor.authorSouza, V.
dc.contributor.authorRuíz, A. L.
dc.contributor.authorMalcata, F. Xavier
dc.contributor.authorPintado, M. E.
dc.contributor.authorCarvalho, J.
dc.date.accessioned2011-09-12T16:37:30Z
dc.date.available2011-09-12T16:37:30Z
dc.date.issued2009
dc.description.abstractChitosan, is one of the most abundant, renewable, nontoxic and biodegradable carbohydrate polymers, and is largely available in the exoskeletons of shellfish and insects. It has recently attracted great attention in the pharmaceutical, biomedical and food arenas, due to its favourable physico-chemical and biological properties. In this research effort, we have assessed wound healing, antiulcerogenic and antiinflammatory properties of chitosan in vivo, and the anti-proliferative activity in vitro.We used three chitosans differing in their molecular weight and degree of deacetylation. The wound healing study was performed using healthy adult (250—300 g) maleWistar rats (Rattus norvegicus), n = 5/group. After thiopental anaesthesia, excision wounds sized 1.5cm2 in average were made. Wounds were treated topically for ten days by applying 200_L/wound of each sample (0.2 mg/mL) and protected by a wound curative. On day 11, animals were sacrificed and tissue samples from wound site of each animal were removed for histopathological analysis and for total collagen determination. The anti-ulcerative assay was done in healthy adult (250—300 g) male Wistar rats (R. norvegicus), n = 5/group, using carbenoxolone as a positive control. Compounds were administered orally according to their body weight (1000 mg/kg). After 30 min, each animal received 1mL of absolute ethanol orally. After one hour, animals were sacrificed by cervical displacement and their stomachs were removed, opened along the greater curvature and the ulcerative lesion index was determined. Ear oedema was used to evaluate the anti-inflammatory effect of chitosans in Swiss adult mice (Mus musculus) weighing approximately 30—40 g. Croton oil was used as the inflammatory agent and dexamethazone as positive control. The oedema was measured by subtracting the weight of the ear receiving only acetone (vehicle) by that receiving the irritating agent. The oedema inhibition (%) was determined by the formula: [(wC − wT)/wC] × 100, where wC was the ear weight in the croton oil group and wT was the ear weight in the treatment groups. The anti-proliferative activity of chitosan was evaluated in vitro against eight human tumor cell lines. The Total Growth Inhibition (cytostatic activity) was determined for each compound. The in vitro cytotoxic activity of chitosan was found to be minimal, whereas it showed wound healing ability. The ear oedema assay showed no differences among the croton oil group and chitosan groups, demonstrating no anti-inflammatory activity. High molecular weight chitosan seems to render gut protection, but the medium molecular weight is the best anti-ulcerative compound.
dc.identifier.citation14TH EUROPEAN CONGRESS ON BIOTECHNOLOGY, Barcelona, Spain, 13-16 Setembro, 2009 - "New Biotechnology." ISSN 1871-6784. 25s (2009) S68por
dc.identifier.doi10.1016/j.nbt.2009.06.027
dc.identifier.urihttp://hdl.handle.net/10400.14/5382
dc.identifier.wos000281760100024
dc.language.isoengpor
dc.publisherElsevierpor
dc.titleWound healing, anti-ulcerogenic, anti-inflammatory and anti-proliferative properties of Chitosanpor
dc.typejournal article
dspace.entity.typePublication
person.familyNameKekhasharú Tavaria
person.familyNameMalcata
person.familyNamePintado
person.givenNameFreni
person.givenNameFrancisco
person.givenNameMaria Manuela
person.identifier456608
person.identifier.ciencia-id1B15-5DAD-7B27
person.identifier.ciencia-id1B13-38A5-35F5
person.identifier.ciencia-id2F13-AAE0-3405
person.identifier.orcid0000-0002-6273-6668
person.identifier.orcid0000-0003-3073-1659
person.identifier.orcid0000-0002-0760-3184
person.identifier.ridF-5696-2013
person.identifier.scopus-author-id6602645613
person.identifier.scopus-author-id7102542478
person.identifier.scopus-author-id7004483898
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicatione42f563a-5b1e-4586-b302-efabe7ce07da
relation.isAuthorOfPublicationa06c00da-0e2f-4434-8ede-4d7b22c0dfe9
relation.isAuthorOfPublicationba387c7d-27c9-4016-895c-b35597e91ebc
relation.isAuthorOfPublication.latestForDiscoveryba387c7d-27c9-4016-895c-b35597e91ebc

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