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首页> 外文期刊>Journal of biomedical materials research, Part A >A methodology based on the 'anterior chamber of rabbit eyes' model for noninvasively determining the biocompatibility of biomaterials in an immune privileged site
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A methodology based on the 'anterior chamber of rabbit eyes' model for noninvasively determining the biocompatibility of biomaterials in an immune privileged site

机译:基于“兔眼前房”模型的方法,可无创地确定免疫特权部位中生物材料的生物相容性

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摘要

In this study, a novel methodology based on the anterior chamber of rabbit eyes model was developed to evaluate the in vivo biocompatibility of biomaterials in an immune privileged site. The 7-mm-diameter membrane implants made from either a biological tissue material (amni-otic membrane, AM group) or a biomedical polymeric material (gelatin, GM group) were inserted in rabbit anterior chamber for 36 months and characterized by biomicroscopic examinations, intraocular pressure measurements, and cor-neal thickness measurements. The noninvasive ophthalmic parameters were scored to provide a quantitative grading system. In this animal model, both AM and GM implants were visible in an ocular immune privileged site during clinical observations. The implants of the AM group appeared as soft tissue patches and have undergone a slow dissolution process resulting in a partial reduction of their size. Additionally, the AM implants did not induce any foreign body reaction or change in ocular tissue response for the studied period. By contrast, in the GM groups, significant corneal edema, elevated intraocular pressure, and increased corneal thickness were noted in the early postoperative phase (within 3 days), but resolved rapidly with in vivo dissolution of the gelatin. The results from the ocular grading system showed that both implants had good long-term biocompatibility in an ocular immune privileged site for up to 3 years. It is concluded that the anterior chamber of rabbit eyes model is an efficient method for noninvasively determining the immune privileged tissue/biomaterial interactions.
机译:在这项研究中,开发了一种基于兔眼前房模型的新颖方法,用于评估免疫优先部位中生物材料的体内生物相容性。将由生物组织材料(羊膜,AM组)或生物医学聚合材料(明胶,GM组)制成的7毫米直径的膜植入物在兔前房中插入36个月,并进行生物显微镜检查,眼内压测量和角膜厚度测量。对非侵入性眼科参数评分,以提供定量分级系统。在这种动物模型中,在临床观察期间,AM和GM植入物均在眼部免疫特权部位可见。 AM组的植入物表现为软组织斑块,并经历了缓慢的溶出过程,导致其尺寸部分减小。此外,在研究期间,AM植入物未引起任何异物反应或眼组织反应的变化。相比之下,在GM组中,术后早期(3天内)注意到明显的角膜水肿,眼内压升高和角膜厚度增加,但随着明胶的体内溶解而迅速消失。眼部分级系统的结果表明,两种植入物在长达3年的眼部免疫特权部位均具有良好的长期生物相容性。结论是,兔眼模型的前房是非侵入性确定免疫特权组织/生物材料相互作用的有效方法。

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