CN107854483A - 一种腹膜透析液的制备方法 - Google Patents
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- 239000000385 dialysis solution Substances 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims abstract description 26
- 239000008103 glucose Substances 0.000 claims abstract description 24
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims abstract description 18
- PNNNRSAQSRJVSB-SLPGGIOYSA-N Fucose Natural products C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C=O PNNNRSAQSRJVSB-SLPGGIOYSA-N 0.000 claims abstract description 18
- SHZGCJCMOBCMKK-DHVFOXMCSA-N L-fucopyranose Chemical compound C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O SHZGCJCMOBCMKK-DHVFOXMCSA-N 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 13
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims abstract description 9
- 238000001914 filtration Methods 0.000 claims abstract description 8
- 239000012456 homogeneous solution Substances 0.000 claims abstract description 8
- 230000001954 sterilising effect Effects 0.000 claims abstract description 5
- 238000004659 sterilization and disinfection Methods 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000012982 microporous membrane Substances 0.000 claims abstract description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 20
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 18
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 10
- 239000001110 calcium chloride Substances 0.000 claims description 10
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 10
- 239000001103 potassium chloride Substances 0.000 claims description 10
- 235000011164 potassium chloride Nutrition 0.000 claims description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 9
- 239000011780 sodium chloride Substances 0.000 claims description 9
- 239000012528 membrane Substances 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 238000005660 chlorination reaction Methods 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 230000008859 change Effects 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000012510 hollow fiber Substances 0.000 claims description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 2
- 229920001230 polyarylate Polymers 0.000 claims description 2
- 238000000502 dialysis Methods 0.000 abstract description 13
- 239000007788 liquid Substances 0.000 description 6
- 230000006872 improvement Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000007912 intraperitoneal administration Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 150000003384 small molecules Chemical class 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 238000001631 haemodialysis Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000003319 supportive effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/14—Alkali metal chlorides; Alkaline earth metal chlorides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7004—Monosaccharides having only carbon, hydrogen and oxygen atoms
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/06—Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/08—Solutions
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Abstract
本发明公开了一种腹膜透析液的制备方法,属于透析领域,包括如下步骤:步骤一、将除岩藻糖和葡萄糖之外的其他物质和水混合,形成均匀溶液;步骤二、在高温下进行灭菌处理;步骤三、加入岩藻糖和葡萄糖,形成均匀溶液;步骤四、用微孔滤膜过滤。
Description
技术领域
本发明涉及透析领域,具体来说是一种腹膜透析液的制备方法。
背景技术
透析(dialysis)是通过小分子经过半透膜扩散到水(或缓冲液)的原理,将小分子与生物大分子分开的一种分离纯化技术。透析疗法是使体液内的成分(溶质或水分)通过半透膜排出体外的治疗方法,一般可分为血液透析和腹膜透析两种。
腹膜透析(peritoneal dialysis,PD)是利用人体自身的腹膜作为透析膜的一种透析方式。通过灌入腹腔的透析液与腹膜另一侧的毛细血管内的血浆成分进行溶质和水分的交换,清除体内潴留的代谢产物和过多的水分,同时通过透析液补充机体所必需的物质。通过不断的更新腹透液,达到肾脏替代或支持治疗的目的。
现有腹膜透析主要通过葡萄糖作为渗透压剂,在透析的过程当中,部分葡萄糖会被体内吸收,使得血糖升高,代谢异常,以及灭菌过程当中葡萄糖产生的有害物质对人体都有非常大的影响,影响透析效果,同时脱水性能差。
发明内容
本发明的目的在于:针对上述存在的问题,提供一种腹膜透析液,其特征在于,包括氯化钠10-15% W/V、氯化钙为0.2-5%W/V、氯化钾为2-5%W/V、碳酸氢钠为2-5 %W/V,氯化镁2-5 %W/V,岩藻糖2-10 %W/V以及小于5%W/V的葡萄糖。
作为优选,所述的岩藻糖为5-8% W/V ,葡萄糖的浓度小于3%W/V。
作为优选,各物质的浓度为氯化钠为10% W/V、氯化钙为0.2%W/V、氯化钾为2%W/V、葡萄糖为2% W/V,碳酸氢钠为3 %W/V。
作为优选,各物质的浓度为氯化钠为12% W/V、氯化钙为2%W/V、氯化钾为3%W/V、葡萄糖为2% W/V,岩藻糖为8 %W/V碳酸氢钠为3 %W/V。
作为优选,透析液中的PH值为5-8。
作为优选,PH值为6-7.5。
本发明还公开了一种透析液的制备方法,包括如下步骤:
步骤一、将除岩藻糖和葡萄糖之外的其他物质和水混合,形成均匀溶液;
步骤二、在高温下进行灭菌处理;
步骤三、加入岩藻糖和葡萄糖,形成均匀溶液;
步骤四、用微孔滤膜过滤。
作为改进,所述的微孔滤膜的过滤粒径为0.2-0.4μm,优选0.3μm。
作为改进,所述的微孔滤膜是一种聚芳酯中空纤维过滤膜。
具体实施方式
为了使本发明的目的、技术方案及优点更加清楚明白,以下结合实施例,对本发明进行进一步详细说明。应当理解,此处所描述的具体实施例仅仅用以解释本发明,并不用于限定本发明。
具体实施例1:一种腹膜透析液,包括氯化钠10-15% W/V、氯化钙为0.2-5%W/V、氯化钾为2-5%W/V、碳酸氢钠为2-5 %W/V,氯化镁2-5 %W/V,岩藻糖2-10 %W/V以及小于5%W/V的葡萄糖。所述的岩藻糖为5-8% W/V ,葡萄糖的浓度小于3%W/V。
具体实施例2:各物质的浓度为氯化钠为10% W/V、氯化钙为0.2%W/V、氯化钾为2%W/V、葡萄糖为2% W/V,岩藻糖为8 %W/V,碳酸氢钠为3 %W/V,PH值调整为7.
具体实施例3各物质的浓度为氯化钠为12% W/V、氯化钙为2%W/V、氯化钾为3%W/V、葡萄糖为2% W/V,岩藻糖为8 %W/V碳酸氢钠为3 %W/V,PH调整成6
具体实施例4:步骤一、将除岩藻糖和葡萄糖之外的其他物质和水混合,形成均匀溶液;
步骤二、在高温下进行灭菌处理;
步骤三、加入岩藻糖和葡萄糖,形成均匀溶液;
步骤四、用微孔滤膜过滤。所述的微孔滤膜的过滤粒径为0.2-0.4μm。
具体实施例5;具体实施例5是相对于2的一个对比实施例:各物质的浓度为氯化钠为10% W/V、氯化钙为0.2%W/V、氯化钾为2%W/V、葡萄糖为10% W/V,碳酸氢钠为3 %W/V,PH值调整为7.
具体实施例6:是实施例3的一个对比实施例:各物质的浓度为氯化钠为12% W/V、氯化钙为2%W/V、氯化钾为3%W/V、葡萄糖为10% W/V,碳酸氢钠为3 %W/V,PH调整成6。
在实施例中,用麻醉的白鼠做实验,将10ml,实施例2-3,5-6,注入白鼠腹腔内,10小时后,回收腹腔内液体(减去立即麻醉回收液体的液体量),测得实施例5和实施例6的液体量分别为42和56,实施例2和3回收的液体量分别为64和78。
以上所述仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明的保护范围之内。
Claims (10)
1.一种腹膜透析液的制备方法,其特征在于,包括如下步骤:
步骤一、将除岩藻糖和葡萄糖之外的其他物质和水混合,形成均匀溶液;
步骤二、在高温下进行灭菌处理;
步骤三、加入岩藻糖和葡萄糖,形成均匀溶液;
步骤四、用微孔滤膜过滤。
2.根据权利要求1所述的腹膜透析液的制备方法,其特征在于,所制备的透析液包括氯化钠10-15% W/V、氯化钙为0.2-5%W/V、氯化钾为2-5%W/V、碳酸氢钠为2-5 %W/V,氯化镁2-5%W/V,岩藻糖2-10 %W/V以及小于5%W/V的葡萄糖。
3.根据权利要求2所述的腹膜透析液的制备方法,其特征在于,所述的岩藻糖为5-8%W/V ,葡萄糖的浓度小于3%W/V。
4.根据权利要求 3所述的腹膜透析液的制备方法,其特征在于,各物质的浓度为氯化钠为10% W/V、氯化钙为0.2%W/V、氯化钾为2%W/V、葡萄糖为2% W/V,碳酸氢钠为3 %W/V。
5.根据权利要求4所述的腹膜透析液的制备方法,其特征在于,各物质的浓度为
氯化钠为12% W/V、氯化钙为2%W/V、氯化钾为3%W/V、葡萄糖为2% W/V,岩藻糖为8 %W/V碳酸氢钠为3 %W/V。
6.根据权利要求5所述的腹膜透析液的制备方法,其特征在于,透析液中的PH值为5-8。
7.根据权利要求6所述的腹膜透析液的制备方法,其特征在于,PH值为6-7.5。
8.根据权利要求6所述的一种腹膜透析液的制备方法,其特征在于,所述的微孔滤膜的过滤粒径为0.2-0.4μm。
9.根据权利要求8所述的一种腹膜透析液的制备方法,其特征在于微孔滤膜的粒径为0.3μm。
10.根据权利要求9所述的一种腹膜透析液的制备方法,所述的微孔滤膜是一种聚芳酯中空纤维过滤膜。
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CN101890041A (zh) * | 2010-02-10 | 2010-11-24 | 上海蓝怡科技有限公司 | 腹膜透析液及其制备方法 |
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Non-Patent Citations (2)
Title |
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韩明亮,等: "《食品化学》", 30 September 2005, 延边大学出版社 * |
顾学裘,等: "《药物制剂注解》", 31 May 1983, 人民卫生出版社 * |
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