CN109528762A - 一种亮氨酸血液透析浓缩液及其制备方法 - Google Patents
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Abstract
本发明公开了一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液:所述血液透析浓缩A液由以下物质组成:氯化钠、氯化钾、氯化钙、氯化镁、亮氨酸和水;所述血液透析浓缩B液由以下物质组成:碳酸氢钠和水。本发明提供一种亮氨酸血液透析浓缩液及其制备方法,该亮氨酸血液透析浓缩液生产过程对人友好,对眼鼻无刺激性。
Description
技术领域
本发明涉及血液透析浓缩液领域。更具体地说,本发明涉及一种亮氨酸血液透析浓缩液及其制备方法。
背景技术
血液透析(HD)是急慢性肾功能衰竭患者肾脏替代治疗方式之一。它通过将体内血液引流至体外,经一个由无数根空心纤维组成的透析器中,血液与含机体浓度相似的电解质溶液(透析液)在一根根空心纤维内外,通过弥散、浓度梯度和对流原理进行电解质平衡,带走体内的代谢废物、维持电解质和酸碱平衡;同时清除体内过多的水分,整个过程称为血液透析。现有的血液透析浓缩液的配方是用冰醋酸作为Ph调节剂,冰醋酸本身对人体没有益处,水溶液中呈弱酸性且蚀性强,对眼和鼻有刺激性作用,生产过程冰醋酸强烈的刺激性气味会让人极度不适。
发明内容
本发明的目的是提供一种亮氨酸血液透析浓缩液及其制备方法,该亮氨酸血液透析浓缩液生产过程对人友好,对眼鼻无刺激性。
为了实现根据本发明的这些目的和其它优点,提供了一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液:
所述血液透析浓缩A液由以下物质组成:氯化钠、氯化钾、氯化钙、氯化镁、亮氨酸和水;
所述血液透析浓缩B液由以下物质组成:碳酸氢钠和水。
优选的是,所述的一种亮氨酸血液透析浓缩液中,所述血液透析浓缩A液和所述血液透析浓缩B液的质量比为1:1-2。
优选的是,所述的一种亮氨酸血液透析浓缩液中,所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠200-220g/L、氯化钾4-6g/L、氯化钙6-8g/L、氯化镁2-4g/L和亮氨酸12-16g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为80-90g/L。
优选的是,所述的一种亮氨酸血液透析浓缩液中,所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠210.7g/L、氯化钾5.21g/L、氯化钙7.718g/L、氯化镁3.558g/L和亮氨酸13.77g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为84.01g/L。
一种上述亮氨酸血液透析浓缩液的制备方法,包括以下步骤:
S1、配置氯化钠浓度为200-220g/L、氯化钾浓度为4-6g/L、氯化钙浓度为6-8g/L、氯化镁浓度为2-4g/L和亮氨酸浓度为12-16g/L的血液透析浓缩A液,备用;
S2、配置碳酸氢钠浓度为80-90g/L的血液透析浓缩B液,备用;
S3、将血液透析浓缩A液、血液透析浓缩B液和透析用水混合均匀后,即制得所述亮氨酸血液透析浓缩液。
本发明的有益效果是:
1、本发明的亮氨酸血液透析浓缩液的生产过程不会使人产生不适感,解决现有的冰醋酸对眼和鼻的刺激性。
2、本发明的亮氨酸血液透析浓缩液中用亮氨酸代替了冰醋酸:亮氨酸与异亮氨酸和缬氨酸一起合作修复肌肉,控制血糖,并给身体组织提供能量。
本发明的其它优点、目标和特征将部分通过下面的说明体现,部分还将通过对本发明的研究和实践而为本领域的技术人员所理解。
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,以令本领域技术人员参照说明书文字能够据以实施。
<实施例1>
一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液:
所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠200g/L、氯化钾4g/L、氯化钙6g/L、氯化镁2g/L和亮氨酸12g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为80g/L。
一种上述亮氨酸血液透析浓缩液的制备方法,包括以下步骤:
S1、配置氯化钠浓度为200g/L、氯化钾浓度为4g/L、氯化钙浓度为6g/L、氯化镁浓度为2g/L和亮氨酸浓度为12g/L的血液透析浓缩A液,备用;
S2、配置碳酸氢钠浓度为80g/L的血液透析浓缩B液,备用;
S3、将血液透析浓缩A液、血液透析浓缩B液和透析用水混合均匀后,即制得所述亮氨酸血液透析浓缩液。
<实施例2>
一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液:
所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠210.7g/L、氯化钾5.21g/L、氯化钙7.718g/L、氯化镁3.558g/L和亮氨酸13.77g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为84.01g/L。
一种上述亮氨酸血液透析浓缩液的制备方法,包括以下步骤:
S1、配置氯化钠浓度为210.7g/L、氯化钾浓度为5.21g/L、氯化钙浓度为7.718g/L、氯化镁浓度为3.558g/L和亮氨酸浓度为13.77g/L的血液透析浓缩A液,备用;
S2、配置碳酸氢钠浓度为84.01g/L的血液透析浓缩B液,备用;
S3、将血液透析浓缩A液、血液透析浓缩B液和透析用水混合均匀后,即制得所述亮氨酸血液透析浓缩液。
<实施例3>
一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液:
所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠220g/L、氯化钾6g/L、氯化钙8g/L、氯化镁4g/L和亮氨酸16g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为90g/L。
一种上述亮氨酸血液透析浓缩液的制备方法,包括以下步骤:
S1、配置氯化钠浓度为220g/L、氯化钾浓度为6g/L、氯化钙浓度为8g/L、氯化镁浓度为4g/L和亮氨酸浓度为12g/L的血液透析浓缩A液,备用;
S2、配置碳酸氢钠浓度为90g/L的血液透析浓缩B液,备用;
S3、将血液透析浓缩A液、血液透析浓缩B液和透析用水混合均匀后,即制得所述亮氨酸血液透析浓缩液。
上述实施例中所使用的水均为透析用水,所涉及化验方法均为本领域常规的离子检验法。
尽管本发明的实施方案已公开如上,但其并不仅仅限于说明书和实施方式中所列运用,它完全可以被适用于各种适合本发明的领域,对于熟悉本领域的人员而言,可容易地实现另外的修改,因此在不背离权利要求及等同范围所限定的一般概念下,本发明并不限于特定的细节和这里示出与描述的实施例。
Claims (5)
1.一种亮氨酸血液透析浓缩液,包括血液透析浓缩A液和血液透析浓缩B液,其特征在于:
所述血液透析浓缩A液由以下物质组成:氯化钠、氯化钾、氯化钙、氯化镁、亮氨酸和水;
所述血液透析浓缩B液由以下物质组成:碳酸氢钠和水。
2.如权利要求1所述的一种亮氨酸血液透析浓缩液,其特征在于,所述血液透析浓缩A液和所述血液透析浓缩B液的质量比为1:1-2。
3.如权利要求1或2所述的一种亮氨酸血液透析浓缩液,其特征在于,所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠200-220g/L、氯化钾4-6g/L、氯化钙6-8g/L、氯化镁2-4g/L和亮氨酸12-16g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为80-90g/L。
4.如权利要求3所述的一种亮氨酸血液透析浓缩液,其特征在于,所述血液透析浓缩A液包括以下质量浓度的各组分:氯化钠210.7g/L、氯化钾5.219g/L、氯化钙7.718g/L、氯化镁3.558g/L和亮氨酸13.77g/L,所述血液透析浓缩B液中碳酸氢钠的质量浓度为84.01g/L。
5.一种如权利要求3所述的亮氨酸血液透析浓缩液的制备方法,其特征在于,包括以下步骤:
S1、配置氯化钠浓度为200-220g/L、氯化钾浓度为4-6g/L、氯化钙浓度为6-8g/L、氯化镁浓度为2-4g/L和亮氨酸浓度为12-16g/L的血液透析浓缩A液,备用;
S2、配置碳酸氢钠浓度为80-90g/L的血液透析浓缩B液,备用;
S3、将血液透析浓缩A液、血液透析浓缩B液和透析用水混合均匀后,即制得所述亮氨酸血液透析浓缩液。
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003095937A (ja) * | 2001-07-17 | 2003-04-03 | Otsuka Pharmaceut Factory Inc | 末梢静脈用輸液 |
CN102370990A (zh) * | 2010-08-09 | 2012-03-14 | 俞黎黎 | 用苹果酸作为pH调节剂的血液净化用制剂及其制备方法和应用 |
CN104208020A (zh) * | 2014-09-05 | 2014-12-17 | 河北一品制药有限公司 | 一种盐酸罗哌卡因注射液及其制备方法 |
-
2018
- 2018-12-27 CN CN201811613342.5A patent/CN109528762A/zh active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003095937A (ja) * | 2001-07-17 | 2003-04-03 | Otsuka Pharmaceut Factory Inc | 末梢静脈用輸液 |
CN102370990A (zh) * | 2010-08-09 | 2012-03-14 | 俞黎黎 | 用苹果酸作为pH调节剂的血液净化用制剂及其制备方法和应用 |
CN104208020A (zh) * | 2014-09-05 | 2014-12-17 | 河北一品制药有限公司 | 一种盐酸罗哌卡因注射液及其制备方法 |
Non-Patent Citations (1)
Title |
---|
骆小丽: "《女人这样做吃不胖、晒不黑、人不老 超值白金典藏版》", 31 July 2016 * |
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