CN108498843B - 一种三维打印抗菌水凝胶敷料及其制备方法 - Google Patents

一种三维打印抗菌水凝胶敷料及其制备方法 Download PDF

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CN108498843B
CN108498843B CN201810606909.XA CN201810606909A CN108498843B CN 108498843 B CN108498843 B CN 108498843B CN 201810606909 A CN201810606909 A CN 201810606909A CN 108498843 B CN108498843 B CN 108498843B
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polyvinyl alcohol
hydrogel
sodium alginate
antibacterial
chitosan
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CN108498843A (zh
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敖宁建
林越威
张丽
叶开均
李洲
赖学旭
李日旺
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Jinan University
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Abstract

本发明属于生物材料的制备技术领域,具体涉及一种三维打印抗菌水凝胶敷料及其制备方法。该方法将可用于熔融沉积成型的聚乙烯醇和不能用于熔融沉积成型的海藻酸钠、壳聚糖及抗菌剂以溶胀吸附的方法进行分子复合,使产物可通过计算机辅助设计技术进行设计和成型的同时,具有多糖材料的生物活性。由于采用了三维打印技术成型聚乙烯醇,因此该制备方法简单、周期短且可随时随地按需生产,产品便于储存和运输。由此得到的伤口敷料同时达到对吸水性、透气性等物理性质和促进细胞生长、促进伤口愈合等生物学性质的要求。其对大肠杆菌、金黄葡萄球菌的抗菌率均超过99%。

Description

一种三维打印抗菌水凝胶敷料及其制备方法
技术领域
本发明属于生物材料的制备技术领域,具体涉及一种三维打印抗菌水凝胶敷料及其制备方法。
背景技术
由于战争、灾祸、疾病等缘故,皮肤出现严重且难以愈合的伤口,患者需要使用伤口敷料覆盖伤口,以保持伤口清洁卫生,并达到湿性愈合的效果,使伤口更快更好地愈合。水凝胶伤口敷料有吸水性好、不粘连、容易去除等优点,对于严重的伤患来说非常重要,一旦有重大灾难发生,成批伤者送医时经常供不应求,导致部分伤者延迟或无法得到合适的救治,造成严重的后遗症,需要截肢甚至死亡。
目前制备水凝胶伤口敷料的方法包括冻融法、静电纺丝法、共混法、接支共聚法、高能辐射交联法等,都需要复杂的生产成型设备,无法在灾难现场或医院里进行生产。
发明内容
为克服现有技术的缺点与不足,本发明的首要目的在于提供一种三维打印抗菌水凝胶敷料的制备方法。
本发明的另一目的在于提供由上述制备方法得到的三维打印抗菌水凝胶敷料。
为实现上述目的,本发明采用的技术方案如下:
一种三维打印抗菌水凝胶敷料的制备方法,包括以下步骤:
(1)聚乙烯醇的三维打印
将聚乙烯醇加入熔融沉积成型三维打印机,设置打印参数,按照AutoCAD设计的模型进行打印,得到三维打印的聚乙烯醇;
(2)水凝胶的制备
对三维打印的聚乙烯醇喷洒硼砂溶液,使聚乙烯醇分子链交联,得到三维打印的聚乙烯醇水凝胶;
(3)材料复合
将海藻酸钠溶液和壳聚糖溶液混合,得到海藻酸钠/壳聚糖复合溶液,将三维打印的聚乙烯醇水凝胶浸泡于海藻酸钠/壳聚糖复合溶液中进行吸附,得到吸附有海藻酸钠和壳聚糖的聚乙烯醇水凝胶,然后浸泡于氯化钙溶液中,干燥,得到聚乙烯醇/海藻酸钠/壳聚糖水凝胶,将聚乙烯醇/海藻酸钠/壳聚糖水凝胶浸泡在抗菌剂溶液中,干燥,即得到所述的三维打印抗菌水凝胶敷料。
优选的,步骤(1)中所述的聚乙烯醇的直径为1.75~3mm,熔点为180~220℃。
优选的,步骤(1)中所述的打印参数为打印温度180~220℃,热床温度20~100℃,打印速度100~150mm/min,挤出速度25~45rpm。
优选的,步骤(2)中所述的硼砂溶液的浓度为1~2wt.%。
优选的,步骤(3)中所述的海藻酸钠溶液的浓度为2wt.%。
优选的,步骤(3)中所述的壳聚糖溶液的浓度为1wt.%。
优选的,步骤(3)中所述的海藻酸钠/壳聚糖复合溶液中,海藻酸钠溶液的体积为壳聚糖溶液体积的5~8倍。
优选的,步骤(3)中所述的将三维打印的聚乙烯醇水凝胶浸泡于海藻酸钠/壳聚糖复合溶液中时,海藻酸钠/壳聚糖复合溶液的体积为三维打印的聚乙烯醇水凝胶的10~25倍。
优选的,步骤(3)中所述的吸附的条件为在室温20~40℃下吸附5~10min。
优选的,步骤(3)中所述的氯化钙溶液的浓度为2wt.%。
优选的,步骤(3)中所述的浸泡于氯化钙溶液中时,氯化钙溶液的体积为吸附有海藻酸钠和壳聚糖的聚乙烯醇水凝胶的体积的20~50倍。
优选的,步骤(3)中所述的浸泡于氯化钙溶液中和浸泡在抗菌剂溶液中的条件分别为在室温20~40℃下浸泡15~30min。
优选的,步骤(3)中所述的抗菌剂溶液中的抗菌剂为碘或聚二乙二醇单甲醚-三苯基膦对甲苯磺酸盐。
优选的,步骤(3)中所述的抗菌剂溶液的浓度为0.0125~0.05M。
优选的,步骤(3)中所述的将聚乙烯醇/海藻酸钠/壳聚糖水凝胶浸泡在抗菌剂溶液中时,抗菌剂溶液与聚乙烯醇/海藻酸钠/壳聚糖水凝胶的质量比为10:1~20:1。
优选的,步骤(3)中所述的干燥的温度为30~60℃。
本发明进一步提供由上述制备方法得到的三维打印抗菌水凝胶敷料,所述的三维打印抗菌水凝胶敷料的液体吸收性为10~20g/100cm2,水蒸气透过率为700~1000g/m2/24h,断裂强度为2~3MPa,断裂伸长率为200~300%,杨氏模量为2~3MPa。
本发明与现有技术相比,具有如下优点和有益效果:
(1)本发明使用三维打印技术制备伤口敷料,提供了一种较为简单、方便和快捷的伤口敷料生产方法,缩短了伤口敷料的生产周期,可随时随地按需生产伤口敷料。此外,通过计算机辅助设计技术,可根据患者伤口的需要,设计并制备出形状适合的伤口敷料。所得敷料便于储存和运输,方便使用。
(2)本发明将可用于熔融沉积成型的聚乙烯醇和不能用于熔融沉积成型的海藻酸钠、壳聚糖及抗菌剂以溶胀吸附的方法进行分子复合,使产物可通过计算机辅助设计技术进行设计和成型的同时,具有多糖材料的生物活性。利用海藻酸钠的吸水性,易于钙离子络合成水凝胶的特点,利用壳聚糖的抗菌性和凝血性的特点,使伤口敷料同时达到对吸水性、透气性等物理性质和促进细胞生长、促进伤口愈合等生物学性质的要求。
(3)本发明制作的三维打印技术制备伤口敷料对大肠杆菌、金黄葡萄球菌的抗菌率均超过99%。
附图说明
图1为实施例1~3中采用的三维打印抗菌敷料的AutoCAD设计图。
图2为实施例1制备的聚乙烯醇/海藻酸钠/壳聚糖水凝胶(未浸泡碘液)的实物图。
图3为实施例1制备的聚乙烯醇/海藻酸钠/壳聚糖水凝胶(未浸泡碘液)的红外光谱图。
图4为实施例1制备的三维打印抗菌水凝胶敷料的剖面扫描电镜图。
图5为实施例1~3制备的三维打印抗菌水凝胶敷料的实物图。
图6为实施例1~3中制备的三维打印抗菌水凝胶敷料的红外光谱图。
具体实施方式
下面结合实施例和附图对本发明作进一步的详细说明,但本发明的实施方式不限于此。对于未特别注明的工艺参数,可参照常规技术进行。
下列实施例中使用的材料均可从商业渠道获得。
实施例1
本实施例提供一种三维打印抗菌水凝胶敷料及其制备方法。
一种三维打印抗菌水凝胶敷料的制备方法,包括以下步骤:
(1)将直径为1.75毫米的聚乙烯醇三维打印耗材加入熔融沉积成型三维打印机中,设定打印参数为打印温度180℃,热床温度20℃,打印速度100mm/min,挤出速度25rpm,按照AutoCAD设计的模型(参见图1)进行打印,得到三维打印的聚乙烯醇。
(2)向三维打印的聚乙烯醇上喷洒1wt.%的硼砂溶液,使聚乙烯醇分子链交联,得到三维打印的聚乙烯醇水凝胶。
(3)将2wt.%海藻酸钠溶液和1wt.%壳聚糖溶液按体积比5:1的比例混合,得到海藻酸钠/壳聚糖复合溶液,将三维打印的聚乙烯醇水凝胶浸泡在海藻酸钠/壳聚糖复合溶液中5min,海藻酸钠/壳聚糖复合溶液的体积为三维打印的聚乙烯醇水凝胶的10倍,然后浸泡于2wt.%的氯化钙溶液中,在30℃下进行干燥,得到聚乙烯醇/海藻酸钠/壳聚糖水凝胶,再浸泡在0.0125M的碘液中15min,碘液的体积为聚乙烯醇/海藻酸钠/壳聚糖水凝胶的10倍,再在30℃下进行干燥,即得到所述的三维打印抗菌水凝胶敷料(含碘量为1.3±0.3mg/g,液体吸收性为10g/100cm2,水蒸气透过率为700g/m2/24h,断裂强度为2MPa,断裂伸长率为200%,杨氏模量为2MPa)。
图2为本实施例制备的聚乙烯醇/海藻酸钠/壳聚糖水凝胶(未浸泡碘液)的实物图,对其进行红外光谱分析,结果如图3所示,可见,在1590、1725和3300处出现了吸收峰,表明聚乙烯醇/海藻酸钠/壳聚糖水凝胶(未浸泡碘液)中存在能够剪切震动的酰胺基、能够剪切震动的酯基和具有氢键的羟基。对进一步浸泡碘液的三维打印抗菌水凝胶敷料进行红外光谱分析,结果如图5中的C所示,可见1590处吸收峰消失,1725和3300处的吸收峰减弱,表示酰胺基受到碘分子吸引无法进行剪切震动,酯基亦受到吸引使震动减弱,羟基之间的氢键受到阻隔,在3670出现自由羟基的震动峰。
采用扫面电镜对本实施例制备的三维打印抗菌水凝胶敷料的剖面进行微观形貌分析,结果如图4所示,由图可知,水凝胶内存在设计中的孔洞结构,该孔洞结构可极大增加敷料的吸收性和透气性。
实施例2
本实施例提供一种三维打印抗菌水凝胶敷料及其制备方法。
一种三维打印抗菌水凝胶敷料的制备方法,包括以下步骤:
(1)将直径为1.75毫米的聚乙烯醇三维打印耗材加入熔融沉积成型三维打印机中,设定打印参数为打印温度190℃,热床温度60℃,打印速度125mm/min,挤出速度35rpm,按照AutoCAD设计的模型(参见图1)进行打印,得到三维打印的聚乙烯醇。
(2)向三维打印的聚乙烯醇上喷洒1.5wt.%的硼砂溶液,使聚乙烯醇分子链交联,得到三维打印的聚乙烯醇水凝胶。
(3)将2wt.%海藻酸钠溶液和1wt.%壳聚糖溶液按体积比6:1的比例混合,得到海藻酸钠/壳聚糖复合溶液,将三维打印的聚乙烯醇水凝胶浸泡在海藻酸钠/壳聚糖复合溶液中5min,海藻酸钠/壳聚糖复合溶液的体积为三维打印的聚乙烯醇水凝胶的20倍,得到聚乙烯醇/海藻酸钠/壳聚糖水凝胶,然后浸泡于2wt.%的氯化钙溶液中,在40℃下进行干燥,再浸泡在0.025M的碘液中15min,碘液的体积为聚乙烯醇/海藻酸钠/壳聚糖水凝胶的15倍,再在40℃下进行干燥,即得到所述的三维打印抗菌水凝胶敷料(含碘量为3.6±0.9mg/g,液体吸收性为16g/100cm2,水蒸气透过率为800g/m2/24h,断裂强度为2MPa,断裂伸长率为222%,杨氏模量为2MPa)。
实施例3
本实施例提供一种三维打印抗菌水凝胶敷料及其制备方法。
一种三维打印抗菌水凝胶敷料的制备方法,包括以下步骤:
(1)将直径为3毫米的聚乙烯醇三维打印耗材加入熔融沉积成型三维打印机中,设定打印参数为打印温度220℃,热床温度100℃,打印速度150mm/min,挤出速度45rpm,按照AutoCAD设计的模型(参见图1)进行打印,得到三维打印的聚乙烯醇。
(2)向三维打印的聚乙烯醇上喷洒2wt.%的硼砂溶液,使聚乙烯醇分子链交联,得到三维打印的聚乙烯醇水凝胶。
(3)将2wt.%海藻酸钠溶液和1wt.%壳聚糖溶液按体积比8:1的比例混合,得到海藻酸钠/壳聚糖复合溶液,将三维打印的聚乙烯醇水凝胶浸泡在海藻酸钠/壳聚糖复合溶液中5min,海藻酸钠/壳聚糖复合溶液的体积为三维打印的聚乙烯醇水凝胶的25倍,得到聚乙烯醇/海藻酸钠/壳聚糖水凝胶,然后浸泡于2wt.%的氯化钙溶液中,在40℃下进行干燥,再浸泡在0.05M的碘液中15min,碘液的体积为聚乙烯醇/海藻酸钠/壳聚糖水凝胶的20倍,再在40℃下进行干燥,即得到所述的三维打印抗菌水凝胶敷料(含碘量为11.2±2.6mg/g,液体吸收性为20g/100cm2,水蒸气透过率为1000/m2/24h,断裂强度为3MPa,断裂伸长率为300%,杨氏模量为3MPa)。
图5为实施例1~3制备的三维打印抗菌水凝胶敷料的实物图,其中A、B、C分别对应实施例3、2、1的样品。
对实施例2和3制备的三维打印抗菌水凝胶敷料进行红外光谱分析,结果分别如图5中的图谱B和A所示,由图可知,图谱B中,1590吸收峰消失,1725和3300的吸收峰减弱,表示酰胺基受到碘分子吸引无法进行剪切震动,酯基亦受到吸引使震动减弱,羟基之间的氢键受到阻隔,在3670出现自由羟基的震动峰。图谱A中,三个吸收峰都消失,表示材料中所有的酰胺基和酯基都被碘分子吸附上,所有羟基之间的氢键都受到阻隔。
实施例4
本实施例提供实施例1~3得到的三维打印抗菌水凝胶敷料的抗菌应用效果。
采用大肠杆菌(8099)和金黄色葡萄球菌(ATCC 6538)作为革兰氏阴性菌和革兰氏阳性菌的代表菌种,使用吸收法测定样品的抗菌效果。将细菌接种于营养肉汤中,在37℃下培养24小时,将菌液浓度调整为
Figure BDA0001694548570000062
Figure BDA0001694548570000063
将0.2ml细菌液接种到锥形瓶内的三维打印抗菌水凝胶敷料中,在37℃下温育24小时。之后加入20ml大豆酪蛋白消化卵磷脂聚山梨酯(SCDLP)培养基冲洗样品,用平板计数法计算细菌数目。用纯棉纱布作对照样本。按照方程式确定抑菌值
抗菌值=lg C-lg T
其中C是来自对照样本的细菌数目,T是来自测试样本的细菌数目。
如方程式所示测定抗菌率
Figure BDA0001694548570000061
其中C是来自对照样本的细菌数目,T是来自测试样本的细菌数目。
从表1可看出,本发明制得的抗菌敷料具有良好的抗菌效果。
表1实施例1~3所得的三维打印抗菌水凝胶敷料的抗菌效果
Figure BDA0001694548570000071
上述实施例为本发明较佳的实施方式,但本发明的实施方式并不受上述实施例的限制,其他的任何未背离本发明的精神实质与原理下所作的改变、修饰、替代、组合、简化,均应为等效的置换方式,都包含在本发明的保护范围之内。

Claims (8)

1.一种三维打印抗菌水凝胶敷料的制备方法,其特征在于,包括以下步骤:
(1)聚乙烯醇的三维打印
将聚乙烯醇加入熔融沉积成型三维打印机,设置打印参数,按照AutoCAD设计的模型进行打印,得到三维打印的聚乙烯醇;
(2)水凝胶的制备
对三维打印的聚乙烯醇喷洒浓度为1~2wt.%的硼砂溶液,使聚乙烯醇分子链交联,得到三维打印的聚乙烯醇水凝胶;
(3)材料复合
将浓度为2wt.%的海藻酸钠溶液和浓度为1wt.%的壳聚糖溶液按照体积比5:1~8:1混合,得到海藻酸钠/壳聚糖复合溶液,将三维打印的聚乙烯醇水凝胶浸泡于海藻酸钠/壳聚糖复合溶液中进行吸附,得到吸附有海藻酸钠和壳聚糖的聚乙烯醇水凝胶,然后浸泡于浓度为2wt.%的氯化钙溶液中,干燥,得到聚乙烯醇/海藻酸钠/壳聚糖水凝胶,将聚乙烯醇/海藻酸钠/壳聚糖水凝胶浸泡在浓度为0.0125~0.05M的抗菌剂溶液中,干燥,即得到所述的三维打印抗菌水凝胶敷料;
所述的抗菌剂溶液中的抗菌剂为碘或聚二乙二醇单甲醚-三苯基膦对甲苯磺酸盐。
2.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:步骤(1)中所述的打印参数为打印温度180~220℃,热床温度20~100℃,打印速度100~150 mm/min,挤出速度25~45rpm。
3.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:
步骤(3)中所述的将三维打印的聚乙烯醇水凝胶浸泡于海藻酸钠/壳聚糖复合溶液中时,海藻酸钠/壳聚糖复合溶液的体积为三维打印的聚乙烯醇水凝胶的10~25倍;
所述的浸泡于氯化钙溶液中时,氯化钙溶液的体积为吸附有海藻酸钠和壳聚糖的聚乙烯醇水凝胶的体积的20~50倍;
所述的将聚乙烯醇/海藻酸钠/壳聚糖水凝胶浸泡在抗菌剂溶液中时,抗菌剂溶液与聚乙烯醇/海藻酸钠/壳聚糖水凝胶的质量比为10:1~20:1。
4.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:步骤(3)中所述的吸附的条件为在室温20~40℃下吸附5~10 min。
5.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:步骤(3)中所述的浸泡于氯化钙溶液中和浸泡在抗菌剂溶液中的条件分别为在室温20~40℃下浸泡15~30min。
6.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:步骤(3)中所述的干燥的温度为30~60℃。
7.根据权利要求1所述的三维打印抗菌水凝胶敷料的制备方法,其特征在于:步骤(1)中所述的聚乙烯醇的直径为1.75~3mm,熔点为180~220℃。
8.一种三维打印抗菌水凝胶敷料,其特征在于:由权利要求1~7任一项所述制备方法得到。
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