CN108567994A - 一种改性胶原膜及其应用 - Google Patents
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Abstract
本发明提供了一种改性胶原膜,制备方法如下:由表没食子儿茶素没食子酸酯交联胶原膜;加载白细胞介素‑4至步骤A得到的胶原膜,清洗,干燥,即得。本发明的优点在于:本发明用白细胞介素‑4和表没食子儿茶素没食子酸酯改性胶原膜后,拥有更好的能力诱导颅顶骨缺损的修复。提高了以前胶原膜的生物性能,具有很好的应用前景,为引导再生术等相关增量手术提供了新选择。
Description
技术领域
本发明属于生物材料领域,具体涉及一种改性胶原膜及其应用。
背景技术
牙科手术中常需要应用引导骨再生手术进行骨增量。胶原是细胞外基质的一种成分,已 经广泛应用于引导骨再生术中。胶原膜有较好的生物兼容性,并能促进成骨细胞黏附、增殖、 迁移和分化,也能有阻挡成纤维细胞快速入侵骨组织生长位点、隔开软组织与硬组织的生长 等屏障功能。
然而,作为一种外源性移植物,胶原仍然会引起一定的炎症反应,同时也因为它的易降 解性而缺乏较好的机械性能。本领域常用采用戊二醛与胶原进行交联,从而提高它的机械性 能,但容易引发炎症和产生细胞毒性。因此,胶原膜长期的保存和使用,不仅仅需要提高机 械性能,更要抗炎和提高生物兼容性。
发明内容
本发明的目的是针对现有技术中存在的不足,提供一种改性胶原膜及其应用。
为了达到上述目的,本发明采用了下列技术方案:一种改性胶原膜,制备方法如下:
A.由表没食子儿茶素没食子酸酯交联胶原膜;
B.加载白细胞介素-4至步骤A得到的胶原膜,清洗,干燥,即得。
作为优选,所述的胶原膜为牛来源I型胶原制备得到。
作为优选,所述步骤A中,表没食子儿茶素没食子酸酯和胶原膜的重量比为1:100。
作为优选,所述步骤A中,交联是将胶原置于表没食子儿茶素没食子酸酯中改性60min, lX PBS缓冲液冲洗。
作为优选,所述步骤A中,胶原膜是在-26℃温度下冷冻过夜;在-53℃、1Pa条件下,真 空冷冻干得到。
作为优选,所述步骤B中,加载为按照100mg:1ml的比例,将胶原膜浸泡在浓度为500ng/ml的白细胞介素-4的水溶液中,浸泡时间为24小时。
作为优选,所述步骤B中,干燥为将制备好的改性胶原膜置于-20℃条件下冷冻干燥过夜。
所述改性胶原在医疗领域的应用。
表没食子儿茶素没食子酸酯是一种茶多酚,拥有抗癌、抗氧化、抗炎、抗纤维化和促骨 再生的作用。并且,表没食子儿茶素没食子酸酯能提高胶原的热稳定性,并保护胶原不被胶 原酶降解,因此它可以用于胶原膜的交联。
近年来,基于巨噬细胞极化的生物材料获得了广泛关注。近期研究表明,巨噬细胞大致 分为两类:促炎型(M1)巨噬细胞和促生长型(M2)巨噬细胞。M1型巨噬细胞由干扰素-γ和脂多糖诱导激活,分泌促炎因子,并参与细胞免疫和组织损伤。与之相反,M2型巨噬细胞由白细胞介素-4诱导激活,分泌抗炎因子白介素-10,并在体液免疫、过敏反应、抗寄生虫反应和组织修复中起到重要作用。
本发明的优点在于:本发明创造性用白细胞介素-4和表没食子儿茶素没食子酸酯改性胶 原膜后,拥有更好的能力诱导颅顶骨缺损的修复。提高了以前胶原膜的生物性能,具有很好 的应用前景,为引导再生术等相关增量手术提供了新选择。
具体实施方式
下面对本发明作详细的说明。
为了使本发明的目的、技术方案及优点更加清楚明白,以下结合实施例,对本发明进行 进一步详细说明。应当理解,此处所描述的具体实施例仅仅用以解释本发明,并不用于限定 本发明。
实施例1:一种改性胶原膜,包括如下制备步骤:
A.由表没食子儿茶素没食子酸酯交联胶原膜;
B.加载白细胞介素-4至步骤A得到的胶原膜,清洗,干燥,即得。
实施例2:一种改性胶原膜,制备方法如下:
A.由表没食子儿茶素没食子酸酯交联胶原膜;
B.加载白细胞介素-4至步骤A得到的胶原膜,清洗,干燥,即得。
所述的胶原膜为牛来源I型胶原制备得到。
所述步骤A中,表没食子儿茶素没食子酸酯和胶原膜的重量比为1:100。
所述步骤A中,交联是将胶原置于表没食子儿茶素没食子酸酯中改性60min,lXPBS缓 冲液冲洗。
所述步骤A中,胶原膜是在-26℃温度下冷冻过夜;在-53℃、1Pa条件下,真空冷冻干得 到。
所述步骤B中,加载为按照100mg:1ml的比例,将胶原膜浸泡在浓度为500ng/ml的白 细胞介素-4的水溶液中,浸泡时间为24小时。
所述步骤B中,干燥为将制备好的改性胶原膜置于-20℃条件下冷冻干燥过夜。
本发明并不局限于前述的具体实施方式。本发明扩展到任何在本说明书中披露的新特征 或任何新的组合,以及披露的任一新的方法或过程的步骤或任何新的组合。
Claims (8)
1.一种改性胶原膜,其特征在于制备方法如下:
A.由表没食子儿茶素没食子酸酯交联胶原膜;
B.加载白细胞介素-4至步骤A得到的胶原膜,清洗,干燥,即得。
2.根据权利要求1所述的一种改性胶原,其特征在于:所述的胶原膜为牛来源I型胶原制备得到。
3.根据权利要求1所述的一种改性胶原,其特征在于:所述步骤A中,表没食子儿茶素没食子酸酯和胶原膜的重量比为1:100。
4.根据权利要求1所述的一种改性胶原,其特征在于:所述步骤A中,交联是将胶原置于表没食子儿茶素没食子酸酯中改性60min,lX PBS缓冲液冲洗。
5.根据权利要求1所述的一种改性胶原,其特征在于:所述步骤A中,胶原膜是在-26℃温度下冷冻过夜;在-53℃、1Pa条件下,真空冷冻干得到。
6.根据权利要求1所述的一种改性胶原,其特征在于:所述步骤B中,加载为按照100mg:1ml的比例,将胶原膜浸泡在浓度为500ng/ml的白细胞介素-4的水溶液中,浸泡时间为24小时。
7.根据权利要求1所述的一种改性胶原,其特征在于:所述步骤B中,干燥为将制备好的改性胶原膜置于-20℃条件下冷冻干燥过夜。
8.根据权利要求1-7任一所述的一种改性胶原,其特征在于:所述改性胶原在医疗领域的应用。
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109331232A (zh) * | 2018-10-25 | 2019-02-15 | 四川大学华西医院 | 一种表没食子儿茶素没食子酸酯交联的小肠黏膜下层引导骨再生膜的制备方法 |
CN111888531A (zh) * | 2020-08-14 | 2020-11-06 | 广州润虹医药科技股份有限公司 | 一种引导性组织再生膜及其制备方法 |
Citations (2)
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CN101998862A (zh) * | 2008-02-12 | 2011-03-30 | 骨骼技术股份有限公司 | 人胶原产品和制备人胶原产品的方法 |
CN106390195A (zh) * | 2016-11-16 | 2017-02-15 | 四川大学 | 一种胶原膜的改性方法 |
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Patent Citations (2)
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CN101998862A (zh) * | 2008-02-12 | 2011-03-30 | 骨骼技术股份有限公司 | 人胶原产品和制备人胶原产品的方法 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109331232A (zh) * | 2018-10-25 | 2019-02-15 | 四川大学华西医院 | 一种表没食子儿茶素没食子酸酯交联的小肠黏膜下层引导骨再生膜的制备方法 |
CN111888531A (zh) * | 2020-08-14 | 2020-11-06 | 广州润虹医药科技股份有限公司 | 一种引导性组织再生膜及其制备方法 |
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