CN110180032A - 一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用 - Google Patents

一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用 Download PDF

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CN110180032A
CN110180032A CN201910506538.2A CN201910506538A CN110180032A CN 110180032 A CN110180032 A CN 110180032A CN 201910506538 A CN201910506538 A CN 201910506538A CN 110180032 A CN110180032 A CN 110180032A
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pcl
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朱利民
郭敏
张红梅
郑永利
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Donghua University
National Dong Hwa University
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Abstract

本发明涉及一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用,所述支架为皮芯结构,芯层为五氟脲嘧啶5‑Fu和聚氧化乙烯PEO,皮层为聚己内酯PCL。本发明的支架生物相容性好,可降解,力学性能好,具有消炎和抗癌的作用,且能起到抗癌药的缓释效果,在组织工程支架方面具有巨大应用潜能。

Description

一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和 应用
技术领域
本发明属于载药纤维支架领域,特别涉及一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用。
背景技术
全球癌症负担继续增加,主要原因是世界人口的老龄化和增长,以及经济发展中国家越来越多地采用致癌行为,特别是吸烟。在许多经济发展中国家,女性乳腺癌、肺癌和结肠直肠癌的发病率很高,此外,与感染相关的癌症负担也高得不成比例。很大一部分的癌症是可以预防的全球负担通过现有的癌症控制的应用知识,并通过实施烟草控制项目,疫苗接种(肝癌和宫颈癌),早期发现和治疗,以及公共卫生运动促进身体活动和健康的饮食模式。关于包括前列腺癌和结肠直肠癌在内的几种主要癌症的病因,还有很多需要了解。
同轴静电纺,是在静电纺的基础上改造而成,其原理与静电纺丝原理基本一致,改变了原有的静电纺丝头,将静电纺丝头改为同心圆结构,芯层和壳层纺丝液被分割在两个不相通的容器中,使用两个推进器推进注射器,此方法解决了电纺时,纺丝液必须是均一体系的缺陷,所制备的同轴纤维在均匀性、连续性上都优于其它方法得到的纤维。
聚己内醋(PCL)是一种脂肪族聚酯共聚物。物相容性好,在体内可完全降解且无毒副作用,力学性能强,可纺性高,能较好的应用在软骨组织、骨组织、血管、尿路上皮组织、心脏组织等组织工程。
5-Fu对多种肿瘤如消化道肿瘤、乳腺癌、卵巢癌、绒毛膜上皮癌、子宫颈癌、肝癌、膀胱癌、皮肤癌(局部涂抹)外阴白斑(局部涂抹)等均有一定疗效。单独或与其他药物联合应用于乳腺癌和胃肠道肿瘤手术辅助治疗,也用于一些非手术恶性肿瘤的姑息治疗,尤其是那些胃肠道、乳腺、头颈部、肝、泌尿系统和胰腺的恶性肿瘤。以往经验表明5-Fu对转移性乳腺癌和胃肠道肉瘤部分反应率为10%~30%。5-Fu与某些其他药物联合应用常可获较高的反应率、存活率。如合用环磷酰胺和MTX(乳腺癌)、顺铂(卵巢和头颈部癌)、醛氢叶酸(结直肠癌)虽可提高5-UF活性,但也增加其毒性。5-Fu联合应用左旋咪唑(免疫兴奋、副作用弱)治疗结直肠癌可降低疾病的复发率,提高术后存活率。5-Fu局部外敷治疗皮肤基底细胞癌有效,对严重的难治性牛皮癣亦有效。
5-Fu作为治疗实体瘤的抗代谢类抗癌药物,已有40多年历史。然而5-Fu的半衰期短,且全身毒性大,目前还缺少一种可以有效缓释5-FU的载药纤维支架,因此本发明采用同轴静电纺丝的技术将5-Fu载在纳米纤维膜上,以改善半衰期短、毒性大的缺点。
发明内容
本发明所要解决的技术问题是提供一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用,该支架生物相容性好,可降解,力学性能好,具有消炎和抗癌的作用,且能起到抗癌药的缓释效果,在组织工程支架方面具有巨大应用潜能。
本发明提供了一种载药控释的同轴静电纺丝纳米纤维支架,所述支架为皮芯结构,芯层为五氟脲嘧啶5-Fu和聚氧化乙烯PEO,皮层为聚己内酯PCL,记为5-Fu/PEO@PCL。
本发明还提供了一种载药控释的同轴静电纺丝纳米纤维支架的制备方法,包括:
将聚己内酯PCL溶于溶剂A中,搅拌溶解,得到壳层纺丝液;将聚氧化乙烯PEO溶于溶剂B中,加入五氟脲嘧啶5-Fu,加入溶剂A搅拌溶解,得到芯层纺丝液;将壳层纺丝液和芯层纺丝液进行同轴静电纺丝,得到同轴静电纺丝纳米纤维支架。
所述溶剂A为六氟异丙醇HFIP;溶剂B为去离子水。
所述PCL的浓度为10-15%w/v。
所述PEO的浓度为3-4%w/v;5-Fu与PEO的质量比为1:5。
所述同轴静电纺丝的工艺参数为:注射器规格为5mL;同轴针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm;喷出流速壳层为0.8-1.0mL/h,芯层为0.4-0.6mL/h;电压为9-10kV,接收距离为15-20cm,纺丝时间为6-10h,铝箔收集,并在铝箔上放置40个圆形载玻片收集;环境温度为25℃,湿度为30-40%。
本发明还提供了一种载药控释的同轴静电纺丝纳米纤维支架的应用,用于组织工程支架。
有益效果
本发明支架PEO具有纺丝性能好、分子量变化范围广以及聚合物共混改性能够结合各种聚合物的优点,改善纤维的综合性能。PEO可以和有机低分子聚合物、无机电解质形成混合溶液,进而提高溶液的纺丝性能。PCL作为生物可降解性高分子,对人体无害,对许多药物有很好的渗透性,广泛用于各种药物制剂中,以PEO/PCL作为支架,具有良好的生物相容性和机械性能以及生物可降解性。此外,作为一种可以有效缓释5-Fu的载药纤维支架,具有消炎和能起到抗癌药的缓释效果,因而在组织工程支架方面具有巨大应用潜能。
附图说明
图1为PCL纳米纤维膜扫描电镜图;
图2为5-Fu/PEO@PCL的纳米纤维膜扫描电镜图;
图3为3天后PCL纳米纤维膜与5-Fu/PEO@PCL的纳米纤维膜的DAPI和鬼笔环肽荧光染色图及其合成图;
图4为实施例4在醋酸和磷酸盐缓冲液中的五氟脲嘧啶释药图。
具体实施方式
下面结合具体实施例,进一步阐述本发明。应理解,这些实施例仅用于说明本发明而不用于限制本发明的范围。此外应理解,在阅读了本发明讲授的内容之后,本领域技术人员可以对本发明作各种改动或修改,这些等价形式同样落于本申请所附权利要求书所限定的范围。
实施例1
(1)称取0.175g聚氧化乙烯(PEO)和0.035g五氟脲嘧啶(5-Fu)溶于5mL水中,磁力搅拌4h,得到芯层纺丝液。
(2)称取0.5g PCL溶于5mL六氟异丙醇(HFIP)中,用磁力搅拌器搅拌10h,直至溶质在溶剂中完全溶解,得到壳层PCL纺丝液。
(4)使用5mL医用注射器针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm分别吸取步骤(1)中芯层纺丝液和步骤(2)中壳层纺丝液,固定在同轴静电纺装置上,调节纺丝参数进行电纺,喷出流速壳层为0.8mL/h,芯层为0.4mL/h,静电压为10kV,接收距离为18cm,接收装置为铝箔,所处环境温度为25℃,湿度为30-40%,纺丝时间为10h。
(5)依照以上步骤将得到载药的同轴五氟脲嘧啶(5-Fu)/聚氧化乙烯(PEO)@聚己内酯(PCL)纳米纤维支架,放在真空干燥箱中干燥24h。
实施例2
((1)称取0.175g聚氧化乙烯(PEO)和0.035g五氟脲嘧啶(5-Fu)溶于5mL水中,磁力搅拌4h,制备芯层纺丝液。
(2)称取0.5g PCL溶于5mL六氟异丙醇(HFIP)中,用磁力搅拌器搅拌10h,直至溶质在溶剂中完全溶解,得到壳层PCL纺丝液;
(4)使用5mL医用注射器针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm分别吸取步骤(1)中芯层纺丝液和步骤(2)中壳层纺丝液,固定在同轴静电纺装置上,调节纺丝参数进行电纺,喷出流速壳层为0.9mL/h,芯层为0.5mL/h,静电压为10kV,接收距离为18cm,接收装置为铝箔,所处环境温度为25℃,湿度为30-40%,纺丝时间为10h。
(5)依照以上步骤将得到载药的同轴五氟脲嘧啶(5-Fu)/聚氧化乙烯(PEO)@聚己内酯(PCL)纳米纤维支架,放在真空干燥箱中干燥24h。
实施例3
(1)称取0.175g聚氧化乙烯(PEO)和0.035g五氟脲嘧啶(5-Fu)溶于5mL水中,磁力搅拌4h,制备芯层纺丝液。
(2)称取0.5g PCL溶于5mL六氟异丙醇(HFIP)中,用磁力搅拌器搅拌10h,直至溶质在溶剂中完全溶解,得到壳层PCL纺丝液;
(4)使用5mL医用注射器针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm分别吸取步骤(1)中芯层纺丝液和步骤(2)中壳层纺丝液,固定在同轴静电纺装置上,调节纺丝参数进行电纺,喷出流速壳层为1.0mL/h,芯层为0.6mL/h,静电压为10kV,接收距离为18cm,接收装置为铝箔,所处环境温度为25℃,湿度为30-40%,纺丝时间为10h。
(5)依照以上步骤将得到载药的同轴五氟脲嘧啶(5-Fu)/聚氧化乙烯(PEO)@聚己内酯(PCL)纳米纤维支架,放在真空干燥箱中干燥24h。
实施例4
(1)称取0.175g聚氧化乙烯(PEO)和0.035g五氟脲嘧啶(5-Fu)溶于5mL水中,磁力搅拌4h,制备芯层纺丝液。
(2)称取0.5g PCL溶于5mL六氟异丙醇(HFIP)中,用磁力搅拌器搅拌10h,直至溶质在溶剂中完全溶解,得到壳层PCL纺丝液;
(4)使用5mL医用注射器针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm分别吸取步骤(1)中芯层纺丝液和步骤(2)中壳层纺丝液,固定在同轴静电纺装置上,调节纺丝参数进行电纺,喷出流速壳层为1.1mL/h,芯层为0.7mL/h,静电压为10kV,接收距离为18cm,接收装置为铝箔,所处环境温度为25℃,湿度为30-40%,纺丝时间为10h。
(5)依照以上步骤将得到载药的同轴五氟脲嘧啶(5-Fu)/聚氧化乙烯(PEO)@聚己内酯(PCL)纳米纤维支架,放在真空干燥箱中干燥24h。
实施例1-4可以发现随着皮层和芯层纺丝液流速增大,纳米纤维膜的内外径也增大。但是流速过大会出现滴液现象。
由图3可知,单纯的PGL纳米纤维膜有着良好的细胞相容性,癌细胞生长良好,5-Fu/PEO@PCL纳米纤维膜抗癌效果明显。
由图4可知,5-Fu/PEO@PCL纳米纤维膜有一定的缓释效果。

Claims (8)

1.一种载药控释的同轴静电纺丝纳米纤维支架,其特征在于:所述支架为皮芯结构,芯层为五氟脲嘧啶5-Fu和聚氧化乙烯PEO,皮层为聚己内酯PCL。
2.一种载药控释的同轴静电纺丝纳米纤维支架的制备方法,包括:
将聚己内酯PCL溶于溶剂A中,搅拌溶解,得到壳层纺丝液;将聚氧化乙烯PEO溶于溶剂B中,加入五氟脲嘧啶5-Fu,加入溶剂A搅拌溶解,得到芯层纺丝液;将壳层纺丝液和芯层纺丝液进行同轴静电纺丝,得到同轴静电纺丝纳米纤维支架。
3.根据权利要求2所述的制备方法,其特征在于:所述溶剂A为六氟异丙醇HFIP;溶剂B为去离子水。
4.根据权利要求2所述的制备方法,其特征在于:所述PCL的浓度为10-15%w/v。
5.根据权利要求2所述的制备方法,其特征在于:所述PEO的浓度为3-4%w/v;5-Fu与PEO的质量比为1:5。
6.根据权利要求2所述的制备方法,其特征在于:所述同轴静电纺丝的工艺参数为:注射器规格为5mL;同轴针头内部直径约为0.6-0.7mm,外部直径约为1.4-1.4mm;喷出流速壳层为0.8-1.0mL/h,芯层为0.4-0.6mL/h;电压为9-10kV,接收距离为15-20cm,纺丝时间为6-10h,铝箔收集,并在铝箔上放置40个圆形载玻片收集;环境温度为25℃,湿度为30-40%。
7.一种如权利要求1所述的载药控释的同轴静电纺丝纳米纤维支架的应用。
8.根据权利要求7所述的应用,其特征在于:用于组织工程支架。
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