Cytotoxicity of the Calcium Alginate/ N,O-carboxymethylchitosan Hemostatic Sponge on Primary Human Gingival Fibroblasts
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Creator Marnisa Sricholpech
Title Cytotoxicity of the Calcium Alginate/ N,O-carboxymethylchitosan Hemostatic Sponge on Primary Human Gingival Fibroblasts
Contributor Tanawat Mahatchariyapong, Kaltimas Phaewpala, Wasana Kosorn, Wanida Janvikul, Kitwat Kitrueangphatchara
Publisher Faculty of Dentistry, Chiang Mai University
Publication Year 2565
Journal Title Chiang Mai Dental Journal
Journal Vol. 43
Journal No. 1
Page no. 19-28
Keyword CA/NOCC sponge, calcium ion, cell morphology, cell proliferation
URL Website http://www.dent.cmu.ac.th/cmdj/frontend/web/?r=site/index
Website title Chiang Mai Dental Journal
ISSN 2773-921X
Abstract To date, chitosan-based hemostatic agents have gained increasing interest from their biocompatibility, inexpensiveness and hemostatic capability, especially in coagulopathic conditions. We have developed a functionally improved Calcium Alginate/N,O-carboxymethylchitosan (CA/NOCC) hemostatic sponge, shown to be biocompatible and biodegradable.Objectives: To ensure its safe use with the gingival tissue, this study aimed to evaluate the cytotoxicity of CA/NOCC sponge on primary human gingival fibroblasts (GFs).Methods: Human GFs were cultured with or without the CA/NOCC sponge. Cell morphology was assessed by scanning electron microscopy. Cell viability and proliferation were determined by MTT assays. The levels of Ca2+ released into the culture medium were also measured.Results: Gingival fibroblasts cultured with the CA/NOCC sponge demonstrated lowered cell density, and significant ultrastructural changes of the cell membrane, by forming numerous blebs and fibrils. From MTT assays, approximately 30% decrease in the proliferation rate was observed. Moreover, the levels of Ca2+, up to 4.6 mM, were detected in the medium of GFs cultured with the CA/NOCC sponge.Conclusions: It could be implicated that the cytopathic effects on the morphology and proliferative ability of GFs may result from the high level of Ca2+ released from the CA/NOCC hemostatic sponge.
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