CN109172522A - 银杏叶口服微乳及其制备方法 - Google Patents
银杏叶口服微乳及其制备方法 Download PDFInfo
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Abstract
本发明公开了一种银杏叶口服微乳,其各组分的重量百分比为:银杏总黄酮醇苷:24%~60%,按银杏叶提取物干燥品计;萜类内酯:6%~15%,按银杏叶提取物干燥品计;总银杏酸:0~10ppm;吐温‑80:0%~5%;甘油:0%~5%;木糖醇:0%~5%;维生素C:0%~2%;海藻酸钠:0%~3%;制备方法:取乳化剂、助乳化剂,搅拌混合,制得(I),备用;取银杏叶提取物,与(I)搅拌混合,使均匀,制得(II),备用;取调味剂、抗氧化剂、增稠剂,用去离子水溶解,制得(III),备用;将(III)缓慢加入(II)中,边加边搅拌混合微乳化,过滤制得微乳液(IV),备用;微乳液(IV)经检查合格后,罐装,加塞,压盖;灭菌即得。
Description
技术领域
本发明涉及一种微乳形式的银杏叶口服微乳及其制备方法。
背景技术
现代药理研究表明,银杏叶提取物具有抗血小板激活因子的作用,可降低血液粘稠度与红细胞聚集,改变血液的流动性;可增强心肌缺血预适应,改善冠脉循环;并具有抗自由基,提高机体免疫功能等作用。银杏叶提取物的剂型较多,有片剂、胶囊剂、软胶囊剂、注射剂、颗粒剂、口服液等。由于银杏叶提取物难溶于水,口味极苦,因此,口服液中含有15~20%乙醇和30%左右的蔗糖,但仍然存在口味极苦、辛辣、患者难于服用之不足。微乳化技术是指将油、水、乳化剂和助乳化剂按一定比例,在一定温度下,通过适当方法混合成外观透明的胶体分散系统的技术。微乳用作药物的胶体性载体,它的特点是增大水难溶性药物溶解性,提高易水解药物的稳定性,掩盖药物的不良口味,也可作为缓释或靶向给药的制剂。
发明内容
针对上述银杏叶口服液的缺陷,本发明的主要目的在于提供一种不含乙醇的微乳形式的银杏叶口服微乳,其不仅不含乙醇和蔗糖,口味较好,外观透明,性质稳定,制备方便,而且具有更好的疗效。
为了实现上述目的,本发明的技术方案如下:
一种银杏叶口服微乳,各组分含量是:银杏总黄酮醇苷:24%~60%,按银杏叶提取物干燥品计;萜类内酯:6%~15%,按银杏叶提取物干燥品计;总银杏酸:0~10ppm;吐温-80:0%~5%;甘油:0%~5%;木糖醇:0%~5%;维生素C:0%~2%;海藻酸钠:0%~3%;按如下步骤制备:
(1)取乳化剂、助乳化剂,搅拌混合,制得(I),备用;
(2)取银杏叶提取物,与(I)搅拌混合,使均匀,制得(II),备用;
(3)取调味剂、抗氧化剂、增稠剂,用去离子水溶解,制得(III),备用;
(4)将(III)缓慢加入(II)中,边加边搅拌混合微乳化,过滤制得微乳液(IV),备用;
(5)微乳液(IV)经检查合格后,罐装,加塞,压盖;
(6)100~121℃热压灭菌10~60分钟即得。
本发明不含乙醇和蔗糖,口味较好,外观透明,性质稳定,制备方便,而且具有更好的疗效。
具体实施方式
下面结合实施例对本发明作进一步说明。
实施例1:各组分含量是:银杏总黄酮醇苷:24%~60%,按银杏叶提取物干燥品计;萜类内酯:6%~15%,按银杏叶提取物干燥品计;总银杏酸:0~10ppm;吐温-80:0%~5%;甘油:0%~5%;木糖醇:0%~5%;维生素C:0%~2%;海藻酸钠:0%~3%;按如下步骤制备:
(1)取乳化剂、助乳化剂,搅拌混合,制得(I),备用;
(2)取银杏叶提取物,与(I)搅拌混合,使均匀,制得(II),备用;
(3)取调味剂、抗氧化剂、增稠剂,用去离子水溶解,制得(III),备用;
(4)将(III)缓慢加入(II)中,边加边搅拌混合微乳化,过滤制得微乳液(IV),备用;
(5)微乳液(IV)经检查合格后,罐装,加塞,压盖;
(6)100~121℃热压灭菌10~60分钟即得。
Claims (1)
1.一种银杏叶口服微乳,其特征是各组分含量是:银杏总黄酮醇苷:24%~60%,按银杏叶提取物干燥品计;萜类内酯:6%~15%,按银杏叶提取物干燥品计;总银杏酸:0~10ppm;吐温-80:0%~5%;甘油:0%~5%;木糖醇:0%~5%;维生素C:0%~2%;海藻酸钠:0%~3%;按如下步骤制备:
(1)取乳化剂、助乳化剂,搅拌混合,制得(I),备用;
(2)取银杏叶提取物,与(I)搅拌混合,使均匀,制得(II),备用;
(3)取调味剂、抗氧化剂、增稠剂,用去离子水溶解,制得(III),备用;
(4)将(III)缓慢加入(II)中,边加边搅拌混合微乳化,过滤制得微乳液(IV),备用;
(5)微乳液(IV)经检查合格后,罐装,加塞,压盖;
(6)100~121℃热压灭菌10~60分钟即得。
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