CN108096260A - 一种含有溶血磷脂酸的拮炎剂 - Google Patents
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Abstract
本发明提供一种含有溶血磷脂酸的拮炎剂,由以下原料构成:山梨糖醇、羟丙甲纤维素、甘氨酸、聚乙二醇、氧化锌、甘油、庆大霉素、氮卓斯汀、溶血磷脂酸,与现有技术相比,本发明具有如下的有益效果:多种药物集成发挥协同作用,药效显著,控制疾病迅速有效,不仅能对皮肤炎症有效果显著的治疗功效,而且不会给患者带来痛苦,同时具有存放不分层,容器底部药不结块。
Description
技术领域
本发明是一种含有溶血磷脂酸的拮炎剂,属于药剂领域。
背景技术
溶血磷脂酸(1-酰基-2-羟基-sn-丙三醇-3-磷酸酯,LPA)是通过涉及磷脂酶A2和溶血磷脂酶D的若干酶促反应的作用由膜脂衍生得到的生物活性脂质介质。LPA在若干种细胞功能中发挥作用,例如:细胞增殖、分化、存活、迁移和侵袭。这些功能影响包括血管新生、伤口修复、纤维化、炎症和癌形成在内的许多生理和病理过程。
现有技术中,对于过敏性炎症的用药品种比较单一,使用不是很方便,一种药只能针对一个环节,不足以完全有效的控制疾病。在大多数情况下,需要同时两种以上抗过敏制剂联合使用,才能见效,使用和携带起来很不方便。单一的药物通常使用时间比较长,药效降低,副作用明显,即便是联合用药,时间久了增加了感染机会,易患细菌性结膜炎,治疗效果不稳定。
发明内容
针对现有技术存在的不足,本发明目的是提供一种含有溶血磷脂酸的拮炎剂,以解决上述背景技术中提出的问题。
为了实现上述目的,本发明是通过如下的技术方案来实现:一种含有溶血磷脂酸的拮炎剂,由以下原料构成:山梨糖醇、羟丙甲纤维素、甘氨酸、聚乙二醇、氧化锌、甘油、庆大霉素、氮卓斯汀、溶血磷脂酸。
进一步地,将电解法制得的锌锭加热至600~700℃熔融后,置于耐高温坩埚内,使之1250~1300℃高温下熔融气化,导入热空气进行氧化,生成的氧化锌经冷却、旋风分离,将细粒子用布袋捕集,即制得原料中的氧化锌。
进一步地,将配制好的53%葡萄糖水溶液加入高压釜,加入葡萄糖重量0.1%的镍催化剂,经置换空气后,在3.5MPa、150℃、pH8.2-8.4条件下加氢,终点控制残糖在0.5%以下,沉淀5min后,将所得山梨糖醇溶液通过离子交换树脂精制即得原料中的山梨糖醇。
进一步地,将精制棉纤维素用碱液在35-40℃处理半小时,压榨,将纤维素粉碎,于35℃进行老化,使所得的碱纤平均聚合度在所需的范围内。将碱纤维投入醚化釜,依次加入环氧丙烷和氯甲烷,在50-80℃醚化5h,最高压力1.8MPa,然后在90℃的热水中加入盐酸及草酸洗涤物料,使体积膨大,用离心机脱水,洗涤至中性,当物料中含水量低于60%时,以130℃的热空气流干燥至含5%以下,最后粉碎过20目筛得原料中的羟丙甲纤维素。
进一步地,将三聚甲醛加入碳酸铵和腈化钠的水溶液中,室温下搅拌溶解后于80-85℃下反应3h。得到乙内酰脲水溶液。然后直接加入30%NaOH水溶液,于170℃下水解3h。最后以阳离子交换树脂处理,得到原料中的甘氨酸。
本发明的有益效果:本发明的一种含有溶血磷脂酸的拮炎剂,多种药物集成发挥协同作用,药效显著,控制疾病迅速有效,不仅能对皮肤炎症有效果显著的治疗功效,而且不会给患者带来痛苦,同时具有存放不分层,容器底部药不结块。
具体实施方式
为使本发明实现的技术手段、创作特征、达成目的与功效易于明白了解,下面结合具体实施方式,进一步阐述本发明。
本发明提供一种技术方案:一种含有溶血磷脂酸的拮炎剂,由以下原料构成:山梨糖醇、羟丙甲纤维素、甘氨酸、聚乙二醇、氧化锌、甘油、庆大霉素、氮卓斯汀、溶血磷脂酸。
将电解法制得的锌锭加热至600~700℃熔融后,置于耐高温坩埚内,使之1250~1300℃高温下熔融气化,导入热空气进行氧化,生成的氧化锌经冷却、旋风分离,将细粒子用布袋捕集,即制得原料中的氧化锌。
将配制好的53%葡萄糖水溶液加入高压釜,加入葡萄糖重量0.1%的镍催化剂,经置换空气后,在3.5MPa、150℃、pH8.2-8.4条件下加氢,终点控制残糖在0.5%以下,沉淀5min后,将所得山梨糖醇溶液通过离子交换树脂精制即得原料中的山梨糖醇。
将精制棉纤维素用碱液在35-40℃处理半小时,压榨,将纤维素粉碎,于35℃进行老化,使所得的碱纤平均聚合度在所需的范围内。将碱纤维投入醚化釜,依次加入环氧丙烷和氯甲烷,在50-80℃醚化5h,最高压力1.8MPa,然后在90℃的热水中加入盐酸及草酸洗涤物料,使体积膨大,用离心机脱水,洗涤至中性,当物料中含水量低于60%时,以130℃的热空气流干燥至含5%以下,最后粉碎过20目筛得原料中的羟丙甲纤维素。
将三聚甲醛加入碳酸铵和腈化钠的水溶液中,室温下搅拌溶解后于80-85℃下反应3h。得到乙内酰脲水溶液。然后直接加入30%NaOH水溶液,于170℃下水解3h。最后以阳离子交换树脂处理,得到原料中的甘氨酸。
作为本发明的一个实施例:本发明的一种含有溶血磷脂酸的拮炎剂,多种药物集成发挥协同作用,药效显著,控制疾病迅速有效,不仅能对皮肤炎症有效果显著的治疗功效,而且不会给患者带来痛苦,同时具有存放不分层,容器底部药不结块。
以上显示和描述了本发明的基本原理和主要特征和本发明的优点,对于本领域技术人员而言,显然本发明不限于上述示范性实施例的细节,而且在不背离本发明的精神或基本特征的情况下,能够以其他的具体形式实现本发明。因此,无论从哪一点来看,均应将实施例看作是示范性的,而且是非限制性的,本发明的范围由所附权利要求而不是上述说明限定,因此旨在将落在权利要求的等同要件的含义和范围内的所有变化囊括在本发明内。
此外,应当理解,虽然本说明书按照实施方式加以描述,但并非每个实施方式仅包含一个独立的技术方案,说明书的这种叙述方式仅仅是为清楚起见,本领域技术人员应当将说明书作为一个整体,各实施例中的技术方案也可以经适当组合,形成本领域技术人员可以理解的其他实施方式。
Claims (9)
1.一种含有溶血磷脂酸的拮炎剂,其特征在于:由以下原料构成:山梨糖醇、羟丙甲纤维素、甘氨酸、聚乙二醇、氧化锌、甘油、庆大霉素、氮卓斯汀、溶血磷脂酸。
2.根据权利要求1所述的一种含有溶血磷脂酸的拮炎剂,其特征在于:将电解法制得的锌锭加热至600~700℃熔融后,置于耐高温坩埚内,使之1250~1300℃高温下熔融气化,导入热空气进行氧化,生成的氧化锌经冷却、旋风分离,将细粒子用布袋捕集,即制得原料中的氧化锌。
3.根据权利要求1所述的一种含有溶血磷脂酸的拮炎剂,其特征在于:将配制好的53%葡萄糖水溶液加入高压釜,加入葡萄糖重量0.1%的镍催化剂,经置换空气后,在3.5MPa、150℃、pH8.2-8.4条件下加氢,终点控制残糖在0.5%以下,沉淀5min后,将所得山梨糖醇溶液通过离子交换树脂精制即得原料中的山梨糖醇。
4.根据权利要求1所述的一种含有溶血磷脂酸的拮炎剂,其特征在于:将精制棉纤维素用碱液在35-40℃处理半小时,压榨,将纤维素粉碎,于35℃进行老化,使所得的碱纤平均聚合度在所需的范围内。
5.将碱纤维投入醚化釜,依次加入环氧丙烷和氯甲烷,在50-80℃醚化5h,最高压力1.8MPa,然后在90℃的热水中加入盐酸及草酸洗涤物料,使体积膨大,用离心机脱水,洗涤至中性,当物料中含水量低于60%时,以130℃的热空气流干燥至含5%以下,最后粉碎过20目筛得原料中的羟丙甲纤维素。
6.根据权利要求1所述的一种含有溶血磷脂酸的拮炎剂,其特征在于:将三聚甲醛加入碳酸铵和腈化钠的水溶液中,室温下搅拌溶解后于80-85℃下反应3h。
7.得到乙内酰脲水溶液。
8.然后直接加入30%NaOH水溶液,于170℃下水解3h。
9.最后以阳离子交换树脂处理,得到原料中的甘氨酸。
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1068034A (zh) * | 1991-05-31 | 1993-01-20 | 普罗格特-甘布尔公司 | 用溶血磷脂酸调整皮肤皱纹的方法 |
| CN1509178A (zh) * | 2001-04-25 | 2004-06-30 | 碧欧塞根公司 | 一种包括溶血磷脂酸的药用组合物 |
| CN105816354A (zh) * | 2015-08-03 | 2016-08-03 | 杭州莱凡网络科技有限公司 | 一种添加有闪光片、镭射粉、人造钻石粉的指彩 |
| CN106721919A (zh) * | 2016-12-07 | 2017-05-31 | 紫花(广州)药业有限公司 | 一种口腔清洁口含片 |
-
2017
- 2017-12-28 CN CN201711450291.4A patent/CN108096260A/zh active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1068034A (zh) * | 1991-05-31 | 1993-01-20 | 普罗格特-甘布尔公司 | 用溶血磷脂酸调整皮肤皱纹的方法 |
| CN1509178A (zh) * | 2001-04-25 | 2004-06-30 | 碧欧塞根公司 | 一种包括溶血磷脂酸的药用组合物 |
| CN105816354A (zh) * | 2015-08-03 | 2016-08-03 | 杭州莱凡网络科技有限公司 | 一种添加有闪光片、镭射粉、人造钻石粉的指彩 |
| CN106721919A (zh) * | 2016-12-07 | 2017-05-31 | 紫花(广州)药业有限公司 | 一种口腔清洁口含片 |
Non-Patent Citations (2)
| Title |
|---|
| 周学良等: "《精细化学品大全 食品和饲料添加剂卷》", 31 December 2000, 浙江科学技术出版社 * |
| 张威: "山梨醇", 《小氮肥设计技术》 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109646443A (zh) * | 2019-02-22 | 2019-04-19 | 潍坊医学院 | 溶血磷脂酸的应用 |
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