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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Mechanical property, degradation rate, and bone cell growth of chitosan coated titanium influenced by degree of deacetylation of chitosan.
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Mechanical property, degradation rate, and bone cell growth of chitosan coated titanium influenced by degree of deacetylation of chitosan.

机译:壳聚糖涂覆钛的机械性能,降解率和骨细胞生长受壳聚糖脱乙酰化程度的影响。

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Chitosan has shown promise as a coating for dental/craniofacial and orthopaedic implants. However, the effects of degree of deacetylation (DDA) of chitosan on coating bond strength, degradation, and biological performance is not known. The aim of this project was to evaluate bonding, degradation, and bone cell growth on titanium coated with chitosans of different DDA and from different manufacturers. Three different chitosans, 80.6%, 81.7%, and 92.3% DDA were covalently bonded to titanium coupons via silane-glutaraldehyde molecules. Bond strengths were evaluated in mechanical tensile tests, and degradation, over 5 weeks, was conducted in cell culture medium with and without 100 microg/mL lysozyme. Cytocompatibility was evaluated for 10 days using UMR 106 osteoblastic cells. Results showed that mean chitosan coating bond strengths ranged from 2.2-3.8 MPa, and that there was minimal affect of DDA on coating bond strengths. The coatings exhibited little dissolution over 5 weeks in medium with or without lysozyme. However, the molecular weight (MW) of the chitosan coatings remaining on the titanium samples after 5 weeks decreased by 69-85% with the higher DDA chitosan coatings exhibiting less percent change in MW than the lower DDA materials. The growth of the UMR 106 osteoblast cells on the 81.7% DDA chitosan coating was lower on days 3 and 5, as compared with the other two coatings, but by day 10, there were no differences in growth among three coatings or to the uncoated titanium controls. Differences in growth were attributed to differences in manufacturer source material, though all coatings were judged to be osteocompatible in vitro.
机译:壳聚糖已经显示为牙科/颅面和骨科植入物的涂层。然而,壳聚糖脱乙酰化(DDA)的效果尚不清楚壳聚糖对涂布粘合强度,降解和生物学性能的影响。该项目的目的是评估含有不同DDA壳聚糖的钛和不同制造商的钛的键合,降解和骨细胞生长。通过硅烷 - 戊二醛分子将三种不同的壳聚糖,80.6%,81.7%和92.3%DDA与钛试样共价键合。在机械拉伸试验中评估粘合强度,并在细胞培养基中,在细胞培养基中进行降解,在细胞培养基中,没有100μg/ mL溶菌酶。使用UMR 106骨细胞细胞评估细胞锁定性10天。结果表明,平均壳聚糖涂料粘合强度范围为2.2-3.8MPa,对DDA对涂布粘合强度的影响最小。涂层在有或没有溶菌酶的培养基中显示出少于5周的溶解。然而,5周后残留在钛样品上残留在钛样品上的壳聚糖涂层的分子量(MW)减少了69-85%,较高的DDA壳聚糖涂层比下部DDA材​​料更少的MW变化较少。与其他两种涂层相比,81.7%DDA壳聚糖涂层对81.7%的DDA壳聚糖涂层上的生长较低,但在第10天,在第10天,三种涂层或未涂层的钛生长没有差异控制。增长的差异归因于制造商来源材料的差异,尽管所有涂层都被判断为骨质化的体外腐蚀。

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