CN114984077A - 一种无醇免洗消毒凝胶及其制备方法 - Google Patents
一种无醇免洗消毒凝胶及其制备方法 Download PDFInfo
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Abstract
本发明公开了一种无醇免洗消毒凝胶,按质量份计,包括杀菌剂0.01‑0.2份、保湿剂0.05‑0.25份、增稠剂2‑25份、水20‑80份、植物提取物1‑20份、增溶剂1‑10份和pH调节剂制成。本发明针对醇类物质气味重、易燃且对皮肤有刺激作用的问题,以超支化聚赖氨酸替代乙醇作为抗菌剂,在保证抗菌效果的同时,可以解决上述含醇类免洗消毒凝胶的不足。选用特定的植物提取液不仅提高了消毒凝胶的亲肤润肤效果,并且与超支化聚赖氨酸可以产生协同抗菌的效果,进一步提升消毒凝胶的杀菌性能。本发明提供的一种无醇免洗消毒凝胶能快速杀灭皮肤表面上常见的致病菌,具有广谱、强大的杀菌效果,具有良好的持久力,可以对皮肤起到长效保护作用。
Description
技术领域
本发明涉及一种无醇免洗消毒凝胶及其制备方法,属于卫生保健领域。
背景技术
科学抗菌可以做到尽力预防和抑制病菌入侵人体,在后疫情时代,抗菌、消毒将成为必然趋势。
环境中存在着各种各样的细菌、真菌等致病菌。手部是我们日常生活中使用最多的部位,因此常会带有各种各样的病原微生物;这些微生物不仅可能使自己染病,还可能传播给他人。80%的病原微生物可以通过正确的洗手方式消除,而其余的20%则需要通过消毒药物除去。免洗手消毒凝胶作为一种高效、便捷的手消毒方法,相比消毒液等其他方式更加安全、便捷。
现有市面上的免洗洗手液以及免洗消毒凝胶的消毒抗菌作用主要来源于成分中60-80%的醇类物质,或是额外添加的抑菌剂如三氯生或葡萄糖酸氯己定。然而酒精属于易燃物品,不可带上火车、高铁和飞机,并且酒精在常温下易挥发,可通过皮肤、鼻腔或口腔吸入人体,不适用于酒精过敏人群。此外,对于儿童或是皮肤较为敏感的人群来说,含酒精的洗手液过于刺激,可能会引起肌肤干裂、过敏等症状,对于皮肤有伤口的人而言刺激作用更显著。此外,由于酒精的易挥发性导致酒精对真菌等真核致病菌的抑菌效果不强。
发明内容
本发明的目的在于针对现有技术的不足,提供一种杀菌性能优异、安全无醇免洗消毒凝胶及其制备方法。该凝胶可以解决含乙醇消毒制品无法带上火车、高铁、飞机等交通工具、气味刺激、对人体皮肤存在刺激性的问题。
本发明的目的是通过以下技术方案实现的:
一种无醇免洗消毒凝胶,包括杀菌剂、保湿剂、增稠剂、增溶剂、植物提取物、水和pH调节剂制成。所述杀菌剂包括分子量3000-6000Da的超支化聚赖氨酸,所述植物提取物包括芦荟提取液、仙人掌提取液中的至少一种。
各物料按重量份计为:超支化聚赖氨酸0.01-0.2份,保湿剂0.05-0.25份,增稠剂2-25份,水20-80份,植物提取物1-20份,增溶剂1-10份。
具体地,所述保湿剂为甘油。
具体地,所述增稠剂为羟丙甲基纤维素、羟乙基纤维素、羟丙基瓜尔胶、聚乙烯醇、羧甲基纤维素、羧甲基壳聚糖、卡波姆940中的至少一种。
具体地,所述增溶剂包括吐温20、吐温60、吐温80中的至少一种。
具体地,所述pH调节剂包括三乙醇胺、1mol/L的氢氧化钠水溶液、磷酸缓冲液、柠檬酸、柠檬酸钠中的至少一种。
进一步地,无醇免洗消毒凝胶按照以下步骤制备:
(1)将2-25份增稠剂、1-10份增溶剂加入到20-80份去离子水中,充分搅拌至混合均匀。
(2)将0.01-0.2份杀菌剂加入步骤(1)所得产物中,继续搅拌反应,充分搅拌至混合均匀。
(3)向步骤(2)所得产物中加入0.05-0.25份保湿剂、1-20份植物提取物,充分搅拌至混合均匀。
(4)向步骤(3)所得产物中加入适量pH调节剂调节溶液pH至7,持续搅拌至体系透明均匀,离心脱泡后获得均一凝胶,得到无醇免洗消毒凝胶。
本发明的有益效果是:
第一,本发明采用一种超支化聚赖氨酸替代乙醇作为杀菌剂,可以解决乙醇消毒凝胶无法带上火车、高铁、飞机的问题。
第二,本发明采用一种超支化聚赖氨酸替代乙醇作为杀菌剂,具有广谱、高效的杀菌效果,对大肠杆菌和金黄色葡萄球菌、绿脓杆菌及白色念珠菌都具有良好的杀灭作用,稳定性好,无刺激,可以解决乙醇消毒凝胶的刺激性气味以及对人体皮肤的刺激性。
第三,本发明添加的植物提取物可以和超支化聚赖氨酸一起协同灭菌,同时还可以促进肌肤保湿、滋润肌肤,不仅有消炎止痒的功效,还具有保湿护肤功效。
具体实施方式
以下结合实施例进一步说明本发明的技术方案,但这些实施例并不用于限制本发明。
实施例1:
将1份甘油与2份吐温80加入80份去离子水中充分搅拌溶解,再向其中加入0.02份分子量3000-6000的超支化聚赖氨酸,充分搅拌溶解;向其中加入5份芦荟提取液、5份仙人掌提取液、0.25份甘油,充分搅拌溶解,最后加入pH调节剂将pH调节至7,加入去离子水补齐质量分数到100份,离心脱泡。最后得到一种无醇免洗消毒凝胶。
实施例2:
将1份甘油与2份吐温80加入80份去离子水中充分搅拌溶解,再向其中加入0.01份分子量3000-6000的超支化聚赖氨酸,充分搅拌溶解;向其中加入5份芦荟提取液、5份仙人掌提取液、0.25份甘油,充分搅拌溶解,最后加入pH调节剂将pH调节至7,加入去离子水补齐质量分数到100份,离心脱泡。最后得到一种无乙醇免洗手消毒凝胶。
对比例1
将1份甘油与2份吐温80加入90份去离子水中充分搅拌溶解,再向其中加入0.01份分子量3000-6000的超支化聚赖氨酸,充分搅拌溶解;加入0.25份保湿剂,充分搅拌溶解,最后加入pH调节剂将pH调节至7,加入去离子水补齐质量分数到100份,离心脱泡。最后得到一种无醇免洗消毒凝胶。
对比例2
将1份甘油与2份吐温80加入80份去离子水中充分搅拌溶解,充分搅拌溶解,再向其中加入5份芦荟提取液、5份仙人掌提取液、0.25份甘油,充分搅拌溶解,最后加入pH调节剂将pH调节至7,加入去离子水补齐质量分数到100份,离心脱泡。最后得到一种无醇免洗消毒凝胶。
对比例3
CN 111714424A中制备的一种免洗手消毒凝胶,其主要杀菌成分为乙醇。
实施例1同实施例2,不同之处在于杀菌剂的质量分数分别为0.02%和0.01%。
实施例2同对比例1,不同之处在于对比例1中用等量去离子水替代了植物提取液。
实施例2同对比例2,不同之处在于对比例2中用等量去离子水替代了杀菌剂。
效果验证例
抗菌试验:
1、检测所有实施例和对比例中制备得到的无醇免洗手消毒凝胶对大肠杆菌、金黄色葡萄球菌、白色念珠菌的灭菌效果。具体检测方法参考15979-2002《一次性使用卫生用品卫生标准》附录C4进行试验,用样品原液,与细菌共培养16h,试验温度37℃。
2、试验菌株:大肠杆菌(ATCC25922),金黄色葡萄球菌(ATCC6538),白色念珠菌(ATCC10231),以上菌种代数为4代,并用含0.03mol/L的磷酸盐缓冲液(PBS)配制细菌悬液。
3、试验样品:以上各实施例样品1-4、对比例。
皮肤刺激性实验:
1、实验动物准备:实验前日,将家兔背部脊柱两侧毛剪掉,去毛范围左、右各约3cm*3cm。
2、实验与对照:正式实验时,将实施例样品0.2g涂抹于左侧去毛皮肤上,每天涂抹一次,连续涂抹14d。右侧皮肤作为对照。
3、实验观察:每天观察皮肤反映,按《化妆品安全性评价程序和方法》GB7919-87中表1评分,并根据评分结果按照GB7919-87中表2评价样品的皮肤刺激强度。
无醇免洗消毒凝胶对金黄色葡萄球菌、大肠杆菌、白色念珠菌的杀菌数据见表1,皮肤刺激性结果见表2:
表1杀菌实验结果
通过实施例2、对比例1、对比例2可见超支化聚赖氨酸与植物提取液存在协同抑菌作用。
表2皮肤刺激评分表
通过上表数据可见根据本发明的配方制备的无醇免洗消毒凝胶无皮肤刺激性。
Claims (7)
1.一种无醇免洗消毒凝胶,其特征在于,按质量份计,包括杀菌剂0.01-0.2份、保湿剂0.05-0.25份、增稠剂2-25份、水20-80份、植物提取物1-20份、增溶剂1-10份和pH调节剂制成;所述杀菌剂包括分子量3000-6000Da的超支化聚赖氨酸。
2.根据权利要求1所述的一种无醇免洗消毒凝胶,其特征在于,所述保湿剂为甘油。
3.根据权利要求1所述的一种无醇免洗消毒凝胶,其特征在于,所述的增稠剂包括羟丙甲基纤维素、羟乙基纤维素、羟丙基瓜尔胶、聚乙烯醇、羧甲基纤维素、羧甲基壳聚糖、卡波姆940中的至少一种。
4.根据权利要求1所述的一种无醇免洗消毒凝胶,其特征在于,所述的植物提取物包括芦荟提取液、仙人掌提取液中的至少一种。
5.根据权利要求1所述的一种无醇免洗消毒凝胶,其特征在于,所述的增溶剂包括吐温20、吐温60、吐温80中的至少一种。
6.根据权利要求1所述的一种无醇免洗消毒凝胶,其特征在于,所述的pH调节剂包括三乙醇胺、1mol/L的氢氧化钠水溶液、磷酸缓冲液、柠檬酸、柠檬酸钠中的至少一种。
7.权利要求1-6任一项所述的一种无醇免洗消毒凝胶的制备方法,其特征在于,所述方法包括以下步骤:
(1)将2-25份增稠剂、1-10份增溶剂加入到20-80份去离子水中,充分搅拌至混合均匀;
(2)将0.01-0.2份杀菌剂加入步骤(1)所得产物中,继续搅拌反应,充分搅拌至混合均匀;
(3)向步骤(2)所得产物中加入0.05-0.25份保湿剂、1-20份植物提取物,充分搅拌至混合均匀;
(4)向步骤(3)所得产物中加入适量pH调节剂调节溶液pH至7,持续搅拌至体系透明均匀,离心脱泡后获得均一凝胶,得到无醇免洗消毒凝胶。
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