CN112546286A - 一种抗菌止血敷料 - Google Patents

一种抗菌止血敷料 Download PDF

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CN112546286A
CN112546286A CN202011459256.0A CN202011459256A CN112546286A CN 112546286 A CN112546286 A CN 112546286A CN 202011459256 A CN202011459256 A CN 202011459256A CN 112546286 A CN112546286 A CN 112546286A
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mxene
aqueous solution
chitosan
concentration
acetic acid
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马贵平
董慧丰
陈炎
杨小萍
王良玉
聂俊
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Changzhou Institute for Advanced Materials Beijing University of Chemical Technology
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Abstract

本发明涉及医用敷料技术领域,尤其涉及一种具有近红外光响应抗菌止血敷料及其制备方法。为了以壳聚糖、MXene作为主要原料制备一种具有光响应,抗菌性能优异的敷料,本发明提供一种抗菌止血敷料,以质量百分含量计,包括以下成分:壳聚糖9.1%‑90.9%、MXene 9.1%‑90.9%,本发明所制备的抗菌止血敷料柔韧性好,抗菌、止血性能优异,具有良好的商业应用前景。

Description

一种抗菌止血敷料
技术领域:
本发明涉及的是一种医疗用品领域的材料,具体是涉及一种具有红外光响应的抗菌止血敷料及其制备方法。
技术背景:
人体皮肤受到利器深度划伤时会造成局部出血,人体短时间内大量出血,会造成休克甚至死亡,因此止血是急症医疗的重要环节。快速,有效的止血对于急症创伤,尤其是复杂环境下的创伤至关重要。目前市场上有多种止血材料,虽然它们有着明显的止血功能,但都有着各自的缺点。例如,胶原敷料组织的粘附性差,多孔孔沸石吸收血液中的水后释放热量,这可能导致伤口炎症,羧甲基纱布不能在伤口表面降解,在去除后产生疤痕等。基于天然高分子壳聚糖的复合止血材料在兼具止血功能的同时,还具有良好的生物相容性,可降解性和抗菌活性。
止血过程主要是通过促进血液凝结来封闭破裂的血管,从而控制损伤部分出血。而血液凝结是一个相对复杂的过程,由多步紧密相关的级联反应构成,其中纤维蛋白交织成网,红细胞聚集与血小板粘附对促进血液凝结尤为重要。作为止血材料,壳聚糖分子链携带少量的正电荷,可以促进红细胞聚集和血小板粘附,从而表现出优良的止血效果。除此以外,在敷料粘附止血的同时还需保证必要的抗菌环境,以免引起体内的炎症反应。壳聚糖作为一种天然高分子,在具有良好生物活性和可降解性的同时,也已被证明其具有优良的抗菌功能。壳聚糖的抗菌作用主要有两种方式,一是通过干扰细胞膜阻碍细胞对营养物质的吸收,从而达到抑菌作用;二是壳聚糖对细胞壁的破坏作用,使得壳聚糖表现出优良的抗微生物活性。
MXene是一类二维无机化合物,由几个原子层厚度的过渡金属碳化物,氮化物或碳氮化物构成。MXene材料表面官能团通常是含有-OH,-F,=O的复合官能团,利用这些复合官能团可以实现MXene与不同聚合物的复合,制备一系列功能化的复合材料。同时MXene具有优异的稳定性能和光热响应特性,尤其是对其光热响应特性的利用尤为重要。
通过壳聚糖与MXene的混合,将壳聚糖包裹并嵌入MXene的片层之间,利用静电作用形成复合材料。在兼具壳聚糖优良的生物相容性,抗菌活性及止血功能的同时,利用MXene的光热响应特性,在一定频率的光照射下增强伤口敷料的抗菌能力,建立快速,高效的抗菌止血响应。
发明内容:
针对现有技术中存在的问题,本发明要解决的技术问题是:如何以壳聚糖,MXene为原料快速制备具有红外光响应的抗菌止血敷料。
本发明解决其技术问题所采用的技术方案是:本发明提供一种抗菌敷料,以质量百分含量计,包括以下成分:
壳聚糖:9.1%-90.9%
MXene:9.1%-90.9%
具体地,所述壳聚糖的脱乙酰度≥85%。
具体地,所述MXene为Ti3C2、V2C、Nb2C、或Ta4C3
具体地,抗菌止血敷料的制备方法,具体按照以下步骤制备:
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:10,1:5,1:3,1:1,3:1,5:1,10:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
具体地,所述MAX粉末为Ti3AlC2、V2SiC、Nb2SiC、或Ta4AlC3
附图说明:
图1为本发明实施例1中制得的抗菌止血敷料的实物图。
图2为本发明实施例1中制得的抗菌止血敷料的SEM图。
具体实施方式:
实施例1
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:10的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例2
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:5的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例3
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:3的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例4
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例5
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照3:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例6
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照5:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
实施例7
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照10:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
对比例1
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)将浓度为10mg/mL的MXene水溶液直接抽滤,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。

Claims (5)

1.一种抗菌止血敷料,其特征在于:所述抗菌止血敷料包括壳聚糖、MXene。
2.根据权利要求1所述的一种抗菌止血敷料,其特征在于,按抗菌止血敷料的总质量为100%计,所述壳聚糖在敷料中的质量百分比为9.1%-90.9%,所述MXene为9.1%-90.9%。
3.根据权利要求1或2所述的复合止血海绵,其特征在于,抗菌止血敷料具有近红外光热抗菌特性。
4.根据权利要求1~3中任一项所述的抗菌止血敷料,其特征在于,所述的制备方法包括以下步骤:
(1)制备MXene
将2g氟化锂溶解在40mL浓度为9mol/L的盐酸溶液中得到LiF/HCl混合溶液,室温下,将2g MAX粉末加入到上述配置好的LiF/HCl混合溶液中,搅拌刻蚀36h,水洗、干燥后,得到MXene粉末;
(2)配制MXene水溶液
将MXene加入到水溶液中,超声分散均匀,得到浓度为10mg/mL的MXene水溶液;
(3)配制壳聚糖的醋酸水溶液
将壳聚糖溶解在浓度为1wt%的醋酸水溶液中,得到浓度为10mg/mL的壳聚糖醋酸水溶液;
(4)将浓度为10mg/mL的MXene水溶液按照1:10,1:5,1:3,1:1,3:1,5:1,10:1的质量比逐滴加入到浓度为10mg/mL的壳聚糖醋酸水溶液中,磁力搅拌2h,利用真空抽滤机抽滤成膜,烘干,剥离,紫外杀菌处理后放入4°冰箱中密封保存。
5.根据权利要求4所述的制备方法,其特征在于,所述的所述MAX粉末为Ti3AlC2、V2SiC、Nb2SiC、或Ta4AlC3
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114225089A (zh) * 2021-12-16 2022-03-25 哈尔滨工业大学 一种电活性抗菌止血敷料的制备方法
CN115282327A (zh) * 2022-08-16 2022-11-04 北京化工大学常州先进材料研究院 一种湿性抗菌敷料

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CN111617309A (zh) * 2020-05-08 2020-09-04 北京化工大学常州先进材料研究院 一种抗菌止血海绵及其制备方法

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CN111617309A (zh) * 2020-05-08 2020-09-04 北京化工大学常州先进材料研究院 一种抗菌止血海绵及其制备方法

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114225089A (zh) * 2021-12-16 2022-03-25 哈尔滨工业大学 一种电活性抗菌止血敷料的制备方法
CN115282327A (zh) * 2022-08-16 2022-11-04 北京化工大学常州先进材料研究院 一种湿性抗菌敷料
CN115282327B (zh) * 2022-08-16 2023-11-10 常州华联医疗器械集团股份有限公司 一种湿性抗菌敷料

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