CN107802882A - 一种医用新材料 - Google Patents
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Abstract
本发明涉及一种医用新材料,由以下质量份的原料制备:α‑氰基丙烯酸甲酯16‑28份、对苯二酚0.03‑0.09份、芦荟纳米微粉10‑20份、大豆蛋白粉25‑45份、壳聚糖20‑30份、醋酸1‑5份、抗菌剂0.5‑1.5份、粘合剂1‑4份。本发明将几种组分按比例组合成一种新材料,极大的提高了其抗冲击能力,该新材料固化速度适中,粘合强度高,对皮肤刺激性小,固化后无疤痕。
Description
技术领域
本发明涉及新材料技术领域,尤其涉及一种医用新材料。
背景技术
医用胶水是代替缝针用的新兴医用产品,医用胶水的主要成分是a-氰基丙稀酸酯,其在生物体组织的聚合速度最快。医用胶水在创面血液和组织液中阴离子的作用下,能快速聚合固化成膜并与创面镶嵌紧密,可牢固地保持伤口的对合状态,且胶膜可阻止血球、血小板通过,在凝血酶和纤维蛋白原的共同作用下,封闭创面断裂的小血管可以有效止血,同时胶膜将组织和细菌隔离,还具有抗感染和保护创面的作用。聚合物中的醚链还具有止痛作用,因此医用胶水具有粘和、止血、止痛、消炎、护创、促进愈合等综合功效。
与传统的技术相比,医用胶水具有减少疼痛、缝合的伤口小以及降低术后复发率等优点,但是,现有的医用胶水还存在缺陷:抗冲击能力差、降解速度慢、黏结力强度不够的缺点。
发明内容
本发明所要解决的技术问题是提供一种医用新材料,旨在解决现用医用胶水的抗冲击能力差、降解速度慢、黏结力强度的问题。
本发明解决上述技术问题的技术方案如下:
一种医用新材料,由以下质量份的原料制备:α-氰基丙烯酸甲酯16-28 份、对苯二酚0.03-0.09份、芦荟纳米微粉10-20份、大豆蛋白粉25-45份、壳聚糖20-30份、醋酸1-5份、抗菌剂0.5-1.5份、粘合剂1-4份。
在上述技术方案的基础上,本发明还可以做如下改进。
进一步,所述的一种医用新材料,由以下质量份的原料制备:α-氰基丙烯酸甲酯20份、对苯二酚0.07份、芦荟纳米微粉15份、大豆蛋白粉37 份、壳聚糖25份、醋酸3份、抗菌剂1.0份、粘合剂2份。
进一步,所述芦荟纳米微粉的制备方法是:取新鲜芦荟,干燥至水分含量11~15%,粉碎至粒径350-450nm。
进一步,所述粘合剂为聚乙烯醇聚甲基纤维中的一种或两种。
进一步,所述医用新材料的制备方法,包括以下步骤:去离子水配置浓度25-35%的壳聚糖溶液,再加入壳聚糖溶液体积5-6倍的去离子水,加热至 45-55℃,依次加入α-氰基丙烯酸甲酯、对苯二酚、芦荟纳米微粉、大豆蛋白粉、醋酸、抗菌剂和粘合剂混合搅拌均匀,调整固含至生产要求,即可。
本发明的有益效果是:本发明配方简单,制作工艺简单,省时省力,降低了生产成本;本发明加入芦荟纳米微粉提高了其抗冲击能力,壳聚糖组分增加产品的抑制细菌活性,本发明产品固化速度适中,粘合强度高,对皮肤刺激性小,固化后无疤痕。
具体实施方式
以下结合具体实施例对本发明的原理和特征进行描述,所举实例只用于解释本发明,并非用于限定本发明的范围。
实施例1
本实施例提供一种医用新材料,由以下质量份的原料制备:α-氰基丙烯酸甲酯20份、对苯二酚0.07份、芦荟纳米微粉15份、大豆蛋白粉37份、壳聚糖25份、醋酸3份、抗菌剂1.0份、粘合剂2份。
上述新材料的制备方法包括以下步骤:去离子水配置浓度25-35%的壳聚糖溶液,再加入壳聚糖溶液体积5-6倍的去离子水,加热至45-55℃,依次加入α-氰基丙烯酸甲酯、对苯二酚、芦荟纳米微粉、大豆蛋白粉、醋酸、抗菌剂和粘合剂混合搅拌均匀,调整固含至生产要求,即可。
实施例2
本实施例提供一种医用新材料,由以下质量份的原料制备:α-氰基丙烯酸甲酯17份、对苯二酚0.04份、芦荟纳米微粉11份、大豆蛋白粉26份、壳聚糖20份、醋酸2份、抗菌剂0.6份、粘合剂1份。
上述新材料的制备方法包括以下步骤:去离子水配置浓度25-35%的壳聚糖溶液,再加入壳聚糖溶液体积5-6倍的去离子水,加热至45-55℃,依次加入α-氰基丙烯酸甲酯、对苯二酚、芦荟纳米微粉、大豆蛋白粉、醋酸、抗菌剂和粘合剂混合搅拌均匀,调整固含至生产要求,即可。
实施例3
本实施例提供一种医用新材料,由以下质量份的原料制备:α-氰基丙烯酸甲酯25份、对苯二酚0.09份、芦荟纳米微粉19份、大豆蛋白粉44份、壳聚糖30份、醋酸4份、抗菌剂1.4份、粘合剂4份。
上述新材料的制备方法包括以下步骤:去离子水配置浓度25-35%的壳聚糖溶液,再加入壳聚糖溶液体积5-6倍的去离子水,加热至45-55℃,依次加入α-氰基丙烯酸甲酯、对苯二酚、芦荟纳米微粉、大豆蛋白粉、醋酸、抗菌剂和粘合剂混合搅拌均匀,调整固含至生产要求,即可。
专利号为CN 105770980 A的专利公开了一种医用胶水及其制备方法,依照该专利制备的新材料,分别对该专利提供的五组实施例制备的新材料的性能进行测试,测试结果如下表:
实施例1 | 实施例2 | 实施例3 | 实施例4 | 实施例5 | |
粘结强度/MPa | 695 | 703 | 710 | 706 | 699 |
降解时间/d | 9 | 8 | 7 | 7 | 8 |
固化时间/s | 6 | 5 | 5 | 5 | 6 |
对本发明提供的三组实施例制备的新材料的性能进行测试,测试结果如下表:
实施例1 | 实施例2 | 实施例3 | |
粘结强度/MPa | 736 | 740 | 745 |
降解时间/d | 6 | 5 | 5 |
固化时间/s | 4 | 3 | 4 |
上述测量数据表明,本发明制备的材料具有良好的粘结强度,固化时间短,生产效率高,降解速度快,减少了环境污染,经济效益好。
以上所述仅为本发明的较佳实施例,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (5)
1.一种医用新材料,其特征在于,由以下质量份的原料制备:α-氰基丙烯酸甲酯16-28份、对苯二酚0.03-0.09份、芦荟纳米微粉10-20份、大豆蛋白粉25-45份、壳聚糖20-30份、醋酸1-5份、抗菌剂0.5-1.5份、粘合剂1-4份。
2.根据权利要求1所述的一种医用新材料,其特征在于,由以下质量份的原料制备:α-氰基丙烯酸甲酯20份、对苯二酚0.07份、芦荟纳米微粉15份、大豆蛋白粉37份、壳聚糖25份、醋酸3份、抗菌剂1.0份、粘合剂2份。
3.根据权利要求1所述的一种医用新材料,其特征在于:所述芦荟纳米微粉的制备方法是:取新鲜芦荟,干燥至水分含量11~15%,粉碎至粒径350-450nm。
4.根据权利要求1所述的一种医用新材料,其特征在于:所述粘合剂为聚乙烯醇聚甲基纤维中的一种或两种。
5.根据权利要求1或2所述的一种医用新材料的制备方法,其特征在于,包括以下步骤:去离子水配置浓度25-35%的壳聚糖溶液,再加入壳聚糖溶液体积5-6倍的去离子水,加热至45-55℃,依次加入α-氰基丙烯酸甲酯、对苯二酚、芦荟纳米微粉、大豆蛋白粉、醋酸、抗菌剂和粘合剂混合搅拌均匀,调整固含至生产要求,即可。
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CN105617452A (zh) * | 2015-12-31 | 2016-06-01 | 佛山铭乾科技有限公司 | 一种医用生物新材料 |
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