1989
DOI: 10.1016/0142-9612(89)90113-0
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Reconstruction of parodontal tissue with chitosan

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Cited by 178 publications
(99 citation statements)
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“…30,31,[38][39][40][41][42][43][44][45][46][47] Such ionogels have been found to be suitable for an array of electrochemical applications. 38,46 Therefore, in addition to the preparation of AG-CH composites, we have attempted to prepare AG-CH-IL composite ionogels using a high solvating ability IL, 3 ) with a purity of 98% mass fraction was purchased from SD FINE CHEM, Mumbai. The molecular structure of IL and repeating units of agarose and chitosan is shown in Fig.…”
Section: Introductionmentioning
confidence: 99%
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“…30,31,[38][39][40][41][42][43][44][45][46][47] Such ionogels have been found to be suitable for an array of electrochemical applications. 38,46 Therefore, in addition to the preparation of AG-CH composites, we have attempted to prepare AG-CH-IL composite ionogels using a high solvating ability IL, 3 ) with a purity of 98% mass fraction was purchased from SD FINE CHEM, Mumbai. The molecular structure of IL and repeating units of agarose and chitosan is shown in Fig.…”
Section: Introductionmentioning
confidence: 99%
“…Because of its biodegradable, biocompatible, non-toxic, antimicrobial and metal-binding properties, CH has been widely studied in chemical, biochemical and biomedical fields, and is extensively used in pharmaceutical and biomedical fields for controlled release of drugs, wound management, space filling implants, etc. [3][4][5] Since CH is a good interacting polymer having amine groups, it can combine or interact with an AG hydroxyl group to form an AG-CH complex, forming environmentally safe composite materials with combined advantages suitable for different applications. [6][7][8] However, the preparation of composites of these biopolymers in water or common organic solvents under mild conditions is not an easy process due to the presence of many hydroxyl groups, intra-and intermolecular hydrogen bonding and molecular close chain packing which creates difficulties in their effective solubilization.…”
Section: Introductionmentioning
confidence: 99%
“…İlk olarak 1811 yılında mantarlarda keşfedilmiş daha sonra 1830 lu yıllarda böceklerden izole edilmiştir ve 1859 yılında ise C. Rouget kitozanı keşfetmiştir. [1][2][3][4][5] Kitin (2-asetamid-2-deoksi-β-D-glukoz) doğada yaygın bulunan biyopolimer olup yapısal olarak selüloza benzerdir. Deniz eklem bacaklılarının dış iskeletlerinde, böceklerin epidermislerinde ve mantarların hücre duvarlarında bulunur.…”
unclassified
“…Kitozan cerrahi yaralarda iyileşmeyi hızlandırıp ve skar oluşumunu azaltarak yara iyileşmesine katkıda bulunur. 3,23,24 Yara iyileşmesini ve kapanmasını hızlandıran kitozan filmleri, hidrojelleri, süspansiyonları, çözeltileri ve yara örtüleri hazırlanmaktadır. 15 Kitozanın yara tedavisinde kullanılabilmesini sağlayan önemli özellikleri şunlardır: yara iyileşmesini hızlandırır, rahat ve ağrısız olarak yara yüzeyinin korunmasını sağlar, hijyenik olmayan koşullarda da kullanışlıdır, antibiyotik kullanımını gerektirmez ve operasyonları kolaylaştırır.…”
unclassified
“…The glucosamine backbone produced by the N-deacetylation process gives chitosan a polycationic character. Because of these positive charges, such derivatives have been receiving much attention as potential candidates for use as a stimulant for regenerating oral soft tissues 15) and some blood coagulant factors 6) . Our previous study demonstrated that five chitin derivatives reduced the adsorption of oral streptococci onto saliva-treated hydroxyapatite and detached these bacteria from hydroxyapatite beads 20) .…”
Section: Introductionmentioning
confidence: 99%