CN110051690A - 一种治疗足癣的复方药剂及其制备方法、应用 - Google Patents
一种治疗足癣的复方药剂及其制备方法、应用 Download PDFInfo
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Abstract
本发明公开了一种治疗足癣的复方药剂,由以下重量份的组分制成:0.5~1.5份明矾,3~5份水杨酸,3~5份苯甲酸,3~5份硼酸,0.3~0.5份呋喃西林,2~4份甲硝唑,2~4份苯甲酸钠。本发明的治疗足癣的复方药剂临床效果好,不含有机溶剂及强刺激物质,故刺激性小、无痛、不损伤正常皮肤。本发明还公开了一种治疗足癣的复方药剂制备方法,通过混合复配即可得到本发明的治疗足癣的复方药剂,工艺步骤简单,可操作性强,对设备无特殊要求。
Description
技术领域
本发明涉及一种复方药剂,尤其是涉及一种治疗足癣的复方药剂及其制备方法、应用。
背景技术
足癣是一种常见的皮肤病。临床表现为足底及趾间发生水泡、糜烂、鳞屑、剧痒等。尤其是军队官兵因训练常穿胶鞋,为真菌生长提供了适宜条件(温度、湿度),所以发病率高,加之部队医疗经费受限,不能及时就医,影响了官兵的身体健康。目前治疗的药物及方法很多,但疗效均不甚满意,且复发率高。
发明内容
本发明是为了解决现有技术的足癣治疗药物疗效均不甚满意,且复发率高的问题,提供了一种原料易得,疗效可靠,刺激性小,不损伤正常皮肤的治疗足癣的复方药剂。
本发明还提供了一种治疗足癣的复方药剂制备方法,工艺步骤简单,可操作性强,对设备无特殊要求。
为了实现上述目的,本发明采用以下技术方案:一种治疗足癣的复方药剂,由以下重量份的组分制成:0.5~1.5份明矾,3~5份水杨酸,3~5份苯甲酸,3~5份硼酸,0.3~0.5份呋喃西林,2~4份甲硝唑,2~4份苯甲酸钠。本发明的复方药剂又名“癣杀净”,其由中西药组成,使用低浓度、强渗透之药,使用之后在真菌表面不形成凝固膜,并缓慢渗透到真菌的细胞质,达到彻底杀灭真菌之目的,本发明不含有机溶剂及强刺激物质,故刺激性小、无痛、不损伤正常皮肤。
作为优选,所述治疗足癣的复方药剂由以下重量份的组分制成:1份明矾,4份水杨酸,4份苯甲酸,4份硼酸,0.4份呋喃西林,3份甲硝唑,3份苯甲酸钠。
一种治疗足癣的复方药剂制备方法,包括以下步骤:
(1)按上述重量份配比称取各组分后,取明矾粉碎,过筛;
(2)另取水杨酸、苯甲酸、硼酸、呋喃西林、苯甲酸钠、甲硝唑与明矾充分搅拌均匀,分装即可。通过混合复配即可得到本发明的治疗足癣的复方药剂,工艺步骤简单,可操作性强,对设备无特殊要求。
作为优选,步骤(1)中,明矾粉碎后过60目筛。
一种治疗足癣的复方药剂应用,具体应用方法为:将复方药剂用沸水溶解,降温后浸泡患处。
作为优选,复方药剂与沸水的质量比为1:(50~60)。
作为优选,降温至40±5℃。
作为优选,浸泡15~20min。
因此,本发明具有如下有益效果:
(1)渗透力强,使之在真菌表面不形成凝固膜,可缓慢渗透到真菌的细胞质,达到彻底消灭真菌之目的;
(2)不含有机溶剂及强刺激性物质,故刺激性小,无痛,不损伤正常皮肤;
(3)临床疗效好;
(4)制备方法的工艺步骤简单,可操作性强,对设备无特殊要求。
附图说明
图1是本发明在广州军区空军系统内的推广应用证明。
图2是本发明在空军广州医院的临床疗效证明。
图3是本发明在空军襄樊医院的临床疗效证明
图4是本发明在空军衡阳医院的临床疗效证明。
具体实施方式
下面结合附图和具体实施方式对本发明做进一步的描述。
本发明的治疗足癣的复方药剂(癣杀净)具有很好的疗效,已在广州军区空军系统内广泛应用,推广应用证明如图1所示,深受战员好评。
实施例
药物处方:明矾1克,水杨酸4克,苯甲酸4克,硼酸4克,呋喃西林0.4克,甲硝唑3克,苯甲酸钠3克,总重量19.4克/包。
制备方法:
(1)按药物处方称取各组分,取明矾粉碎,过60目筛;
(2)另取水杨酸、苯甲酸、硼酸、呋喃西林、苯甲酸钠、甲硝唑与明矾充分搅拌均匀,分装即可。
上述复方药剂(癣杀净),经发明人所在单位(空军桂林医院科研室)组织与中国人民解放军空军广州医院临床观察923例,其中男性408例,女性515例,年龄11~76岁;病程43天~37年。脱屑型196例;水泡型364例;糜烂性278例;角化型85例。
应用方法:取一包置盆内,用1100毫升沸水溶解,待水温降至40℃后浸泡患处15~20分钟,自然晾干,每日一次,连续三天,严重者5天。
疗效评定标准:①治愈:患处无瘙痒,皮肤光洁,追踪访查二年内无临床症状。②显效:患处无瘙痒,皮肤光洁,半年内无临床症状。③有效:患处无瘙痒,三个月后小水泡。④无效:症状无改变。
具体结果如表1所示:
表1临床观察疗效统计
类型 | 病例数 | 治愈 | 显效 | 有效 | 无效 | 有效率 |
脱屑型 | 196 | 168 | 17 | 8 | 3 | 98.6% |
水泡型 | 364 | 340 | 13 | 11 | 0 | 100% |
糜烂性 | 278 | 262 | 11 | 5 | 0 | 100% |
角化型 | 85 | 40 | 16 | 14 | 15 | 82.4% |
由表1可知,在与空军广州医院临床观察的病例中,治愈率(根治率)达87.8%,总有效率达98.1%,临床疗效证明如图2所示。
上述复方药剂(癣杀净)经发明人所在单位(空军桂林医院科研室)组织,在其他单位(空军襄樊医院、空军衡阳医院)也已推广应用,具体的临床观察疗效结果分别如图3、图4所示。
由此可知,本发明的治疗足癣的复方药剂的临床疗效好,适合推广应用。
以上所述的实施例只是本发明的一种较佳的方案,并非对本发明作任何形式上的限制,在不超出权利要求所记载的技术方案的前提下还有其它的变体及改型。
Claims (8)
1.一种治疗足癣的复方药剂,其特征在于,由以下重量份的组分制成:0.5~1.5份明矾,3~5份水杨酸,3~5份苯甲酸,3~5份硼酸,0.3~0.5份呋喃西林,2~4份甲硝唑,2~4份苯甲酸钠。
2.根据权利要求1所述的一种治疗足癣的复方药剂,其特征在于,所述治疗足癣的复方药剂由以下重量份的组分制成:1份明矾,4份水杨酸,4份苯甲酸,4份硼酸,0.4份呋喃西林,3份甲硝唑,3份苯甲酸钠。
3.一种如权利要求1或2所述的治疗足癣的复方药剂制备方法,其特征在于,包括以下步骤:
(1)按上述重量份配比称取各组分后,取明矾粉碎,过筛;
(2)另取水杨酸、苯甲酸、硼酸、呋喃西林、苯甲酸钠、甲硝唑与明矾充分搅拌均匀,分装即可。
4.根据权利要求3所述的治疗足癣的复方药剂制备方法,其特征在于,步骤(1)中,明矾粉碎后过60目筛。
5.一种如权利要求1或2所述的治疗足癣的复方药剂应用,其特征在于,具体应用方法为:将复方药剂用沸水溶解,降温后浸泡患处。
6.根据权利要求5所述的治疗足癣的复方药剂应用,其特征在于,复方药剂与沸水的质量比为1:(50~60)。
7.根据权利要求5所述的治疗足癣的复方药剂应用,其特征在于,降温至40±5℃。
8.根据权利要求5所述的治疗足癣的复方药剂应用,其特征在于,浸泡15~20min。
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