CN109091639A - 一种治疗白内障的中草药制剂及其制备方法 - Google Patents
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Abstract
本发明涉及一种治疗白内障的中草药制剂及其制备方法,包括以下重量组份的原料:决明子15‑25份、牛膝20‑30份、芙蓉叶20‑30份、北沙参10‑20份、生地黄1‑2份、枸杞子5‑10份、黄连10‑20份、益智仁10‑20份、当归15‑30份。制备方法包括以下步骤:S1、按本发明中药组方,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油1‑5份混合在一起,二次研磨,得药材细末。本发明中草药制剂的配伍合理,原料为多味中草药,之间具有明显的协同增效作用,能够明显提高白内障治疗的显效率和总有效率,在初、中期的白内障治疗过程中取得了显着效果,愈后不复发,本发明中草药制剂的制备方法简单,无毒副作用,疗效确切,具有良好的应用前景,适宜广泛推广。
Description
技术领域
本发明涉及治疗白内障技术领域,具体是指一种治疗白内障的中草药制剂及其制备方法。
背景技术
多种原因如老化、遗传、局部营养障碍、免疫与代谢异常,外伤、中毒、辐射等,都能引起晶状体代谢紊乱,导致晶状体蛋白质变性而发生混浊,称为白内障,此时光线被混浊晶状体阻扰无法投射在视网膜上,导致视物模糊。
目前临床上常用的白内障治疗药物有眼药水或口服的中西药。一些早期白内障,用药以后病情可能会减慢发展,视力也稍有提高;一些中期白内障患者,用药后视力和晶状体混浊程度未能改善;近成熟期的白内障,药物治疗无实际意义。白内障囊外摘除已成为目前白内障的常规手术方式,但患者痛苦较大。因此,开发一种对白内障疗效确切的中草药制剂,将具有重要的意义和应用价值。
发明内容
本发明要解决的技术问题是,提供一种一种治疗白内障的中草药制剂及其制备方法,对白内障的治疗总有效率高,疗效确切。
为解决上述技术问题,本发明提供的技术方案为:一种治疗白内障的中草药制剂,包括以下重量组份的原料:决明子15-25份、牛膝20-30份、芙蓉叶20-30份、北沙参10-20份、生地黄1-2份、枸杞子5-10份、黄连10-20份、益智仁10-20份、当归15-30份。
一种治疗白内障的中草药制剂的制备方法,包括以下步骤:
S1、按本发明中药组方决明子、牛膝、芙蓉叶、北沙参、生地黄、枸杞子、黄连、益智仁、当归,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油1-5份混合在一起,二次研磨,得药材细末;
S2、加8-10倍药材细末重量的纯净水,浸泡3-5小时后,加热水至沸腾,煎煮2-4小时,分离煎出液,过滤得滤液;在滤渣中加入药材细末5-7倍重量的纯净水,煎煮1-3小时,过滤得滤液;依法煎出滤渣2-4次,将各次滤液混合得混合液;对混合液进行减压浓缩,直到混合液的相对密度为1.1-1.3时停止浓缩,得中药水提液;
S3、将步骤S2的药渣置于有盖容器中,加入4-6倍重量的乙醇溶液后密封,搅拌或振荡,浸渍2-4天,使有效成分充分浸出,倾取上清液,滤过出残渣回流煎煮2-4小时,过滤得滤液,压榨残渣后,得压榨液,混合上清液、滤液和压榨液,蒸馏除去乙醇,即为中药醇提液;
S4、将中药水提液和中药醇提液混合,离心分离或沉降滤过后,减压,70-79℃下浓缩得稠膏;
S5、利用现代通用的制剂技术将稠膏做成临床需要的成品制剂。
作为改进,所述步骤S5中所述药物的成品制剂包括:散剂、片剂、丸剂、颗粒剂、软胶囊、硬胶囊或微胶囊。
作为改进,所述步骤S2中减压浓缩在温度为70-75℃下进行。
作为改进,所述步骤S3中采用浓度为55-75%的乙醇溶液。
本发明具有如下优点:本发明中草药制剂的配伍合理,原料为多味中草药,之间具有明显的协同增效作用,能够明显提高白内障治疗的显效率和总有效率,在初、中期的白内障治疗过程中取得了显着效果,愈后不复发,本发明中草药制剂的制备方法简单,无毒副作用,疗效确切,具有良好的应用前景,适宜广泛推广。
具体实施方式
下面结合实施例对本发明做进一步的详细说明。
实施例1
一种治疗白内障的中草药制剂,包括以下重量组份的原料:决明子15份、牛膝20份、芙蓉叶20份、北沙参10份、生地黄1份、枸杞子5份、黄连10份、益智仁10份、当归15份。
2、一种治疗白内障的中草药制剂的制备方法,其特征在于,包括以下步骤:
S1、按本发明中药组方决明子、牛膝、芙蓉叶、北沙参、生地黄、枸杞子、黄连、益智仁、当归,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油1份混合在一起,二次研磨,得药材细末;
S2、加8倍药材细末重量的纯净水,浸泡3小时后,加热水至沸腾,煎煮2小时,分离煎出液,过滤得滤液;在滤渣中加入药材细末5倍重量的纯净水,煎煮1小时,过滤得滤液;依法煎出滤渣2次,将各次滤液混合得混合液;对混合液进行减压浓缩,直到混合液的相对密度为1.1时停止浓缩,得中药水提液;
S3、将步骤S2的药渣置于有盖容器中,加入4倍重量的乙醇溶液后密封,搅拌或振荡,浸渍2天,使有效成分充分浸出,倾取上清液,滤过出残渣回流煎煮2小时,过滤得滤液,压榨残渣后,得压榨液,混合上清液、滤液和压榨液,蒸馏除去乙醇,即为中药醇提液;
S4、将中药水提液和中药醇提液混合,离心分离或沉降滤过后,减压,70℃下浓缩得稠膏;
S5、利用现代通用的制剂技术将稠膏做成临床需要的成品制剂。
所述步骤S5中所述药物的成品制剂包括:散剂、片剂、丸剂、颗粒剂、软胶囊、硬胶囊或微胶囊,所述步骤S2中减压浓缩在温度为70℃下进行,所述步骤S3中采用浓度为55%的乙醇溶液。
实施例2
一种治疗白内障的中草药制剂,包括以下重量组份的原料:决明子25份、牛膝30份、芙蓉叶30份、北沙参20份、生地黄2份、枸杞子10份、黄连20份、益智仁20份、当归30份。
2、一种治疗白内障的中草药制剂的制备方法,其特征在于,包括以下步骤:
S1、按本发明中药组方决明子、牛膝、芙蓉叶、北沙参、生地黄、枸杞子、黄连、益智仁、当归,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油5份混合在一起,二次研磨,得药材细末;
S2、加10倍药材细末重量的纯净水,浸泡5小时后,加热水至沸腾,煎煮4小时,分离煎出液,过滤得滤液;在滤渣中加入药材细末7倍重量的纯净水,煎煮3小时,过滤得滤液;依法煎出滤渣4次,将各次滤液混合得混合液;对混合液进行减压浓缩,直到混合液的相对密度为1.3时停止浓缩,得中药水提液;
S3、将步骤S2的药渣置于有盖容器中,加入6倍重量的乙醇溶液后密封,搅拌或振荡,浸渍4天,使有效成分充分浸出,倾取上清液,滤过出残渣回流煎煮4小时,过滤得滤液,压榨残渣后,得压榨液,混合上清液、滤液和压榨液,蒸馏除去乙醇,即为中药醇提液;
S4、将中药水提液和中药醇提液混合,离心分离或沉降滤过后,减压,79℃下浓缩得稠膏;
S5、利用现代通用的制剂技术将稠膏做成临床需要的成品制剂。
所述步骤S5中所述药物的成品制剂包括:散剂、片剂、丸剂、颗粒剂、软胶囊、硬胶囊或微胶囊,所述步骤S2中减压浓缩在温度为75℃下进行,所述步骤S3中采用浓度为75%的乙醇溶液。
实施例3
一种治疗白内障的中草药制剂,包括以下重量组份的原料:决明子20份、牛膝25份、芙蓉叶25份、北沙参15份、生地黄1.5份、枸杞子8份、黄连15份、益智仁15份、当归25份。
2、一种治疗白内障的中草药制剂的制备方法,其特征在于,包括以下步骤:
S1、按本发明中药组方决明子、牛膝、芙蓉叶、北沙参、生地黄、枸杞子、黄连、益智仁、当归,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油3份混合在一起,二次研磨,得药材细末;
S2、加8倍药材细末重量的纯净水,浸泡4小时后,加热水至沸腾,煎煮3小时,分离煎出液,过滤得滤液;在滤渣中加入药材细末6倍重量的纯净水,煎煮2小时,过滤得滤液;依法煎出滤渣3次,将各次滤液混合得混合液;对混合液进行减压浓缩,直到混合液的相对密度为1.2时停止浓缩,得中药水提液;
S3、将步骤S2的药渣置于有盖容器中,加入5倍重量的乙醇溶液后密封,搅拌或振荡,浸渍3天,使有效成分充分浸出,倾取上清液,滤过出残渣回流煎煮3小时,过滤得滤液,压榨残渣后,得压榨液,混合上清液、滤液和压榨液,蒸馏除去乙醇,即为中药醇提液;
S4、将中药水提液和中药醇提液混合,离心分离或沉降滤过后,减压,75℃下浓缩得稠膏;
S5、利用现代通用的制剂技术将稠膏做成临床需要的成品制剂。
所述步骤S5中所述药物的成品制剂包括:散剂、片剂、丸剂、颗粒剂、软胶囊、硬胶囊或微胶囊,所述步骤S2中减压浓缩在温度为73℃下进行,所述步骤S3中采用浓度为65%的乙醇溶液。
Claims (5)
1.一种治疗白内障的中草药制剂,其特征在于:包括以下重量组份的原料:决明子15-25份、牛膝20-30份、芙蓉叶20-30份、北沙参10-20份、生地黄1-2份、枸杞子5-10份、黄连10-20份、益智仁10-20份、当归15-30份。
2.一种治疗白内障的中草药制剂的制备方法,其特征在于,包括以下步骤:
S1、按本发明中药组方决明子、牛膝、芙蓉叶、北沙参、生地黄、枸杞子、黄连、益智仁、当归,按照重量组份比称好后,将药材粉碎成粗末,加以鱼肝油1-5份混合在一起,二次研磨,得药材细末;
S2、加8-10倍药材细末重量的纯净水,浸泡3-5小时后,加热水至沸腾,煎煮2-4小时,分离煎出液,过滤得滤液;在滤渣中加入药材细末5-7倍重量的纯净水,煎煮1-3小时,过滤得滤液;依法煎出滤渣2-4次,将各次滤液混合得混合液;对混合液进行减压浓缩,直到混合液的相对密度为1.1-1.3时停止浓缩,得中药水提液;
S3、将步骤S2的药渣置于有盖容器中,加入4-6倍重量的乙醇溶液后密封,搅拌或振荡,浸渍2-4天,使有效成分充分浸出,倾取上清液,滤过出残渣回流煎煮2-4小时,过滤得滤液,压榨残渣后,得压榨液,混合上清液、滤液和压榨液,蒸馏除去乙醇,即为中药醇提液;
S4、将中药水提液和中药醇提液混合,离心分离或沉降滤过后,减压,70-79℃下浓缩得稠膏;
S5、利用现代通用的制剂技术将稠膏做成临床需要的成品制剂。
3.根据权利要求2所述的一种治疗白内障的中草药制剂的制备方法,其特征在于:所述步骤S5中所述药物的成品制剂包括:散剂、片剂、丸剂、颗粒剂、软胶囊、硬胶囊或微胶囊。
4.根据权利要求2所述的一种治疗白内障的中草药制剂的制备方法,其特征在于:所述步骤S2中减压浓缩在温度为70-75℃下进行。
5.根据权利要求2所述的一种治疗白内障的中草药制剂的制备方法,其特征在于:所述步骤S3中采用浓度为55-75%的乙醇溶液。
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CN105920070A (zh) * | 2016-06-13 | 2016-09-07 | 张国显 | 治疗白内障的中药组合物及其制备方法 |
CN105998431A (zh) * | 2016-06-29 | 2016-10-12 | 曹蕊 | 一种用于治疗白内障的中药组合物及其制备方法 |
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