CN1114193A - 一种高效硬化剂及制备方法 - Google Patents
一种高效硬化剂及制备方法 Download PDFInfo
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- CN1114193A CN1114193A CN 94106757 CN94106757A CN1114193A CN 1114193 A CN1114193 A CN 1114193A CN 94106757 CN94106757 CN 94106757 CN 94106757 A CN94106757 A CN 94106757A CN 1114193 A CN1114193 A CN 1114193A
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- sclerosing agent
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- aluminum sulfate
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- 239000003229 sclerosing agent Substances 0.000 title claims description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 42
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000012153 distilled water Substances 0.000 claims abstract description 12
- 239000003589 local anesthetic agent Substances 0.000 claims abstract description 9
- 230000001954 sterilising effect Effects 0.000 claims description 14
- 238000004659 sterilization and disinfection Methods 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 6
- 229960004919 procaine Drugs 0.000 claims description 5
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 claims description 5
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 claims description 4
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims description 4
- 229960004194 lidocaine Drugs 0.000 claims description 4
- 238000012856 packing Methods 0.000 claims description 3
- 229960003920 cocaine Drugs 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 208000014617 hemorrhoid Diseases 0.000 abstract description 4
- 102000004169 proteins and genes Human genes 0.000 abstract description 3
- 108090000623 proteins and genes Proteins 0.000 abstract description 3
- 229910000329 aluminium sulfate Inorganic materials 0.000 abstract 1
- 235000011128 aluminium sulphate Nutrition 0.000 abstract 1
- 230000000903 blocking effect Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- 229960004756 ethanol Drugs 0.000 description 14
- 230000000694 effects Effects 0.000 description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000003708 ampul Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229940037003 alum Drugs 0.000 description 3
- 229960000935 dehydrated alcohol Drugs 0.000 description 3
- GRIXGZQULWMCLU-UHFFFAOYSA-L disodium;7-[[2-carboxylato-2-(4-hydroxyphenyl)acetyl]amino]-7-methoxy-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound [Na+].[Na+].C12OCC(CSC=3N(N=NN=3)C)=C(C([O-])=O)N2C(=O)C1(OC)NC(=O)C(C([O-])=O)C1=CC=C(O)C=C1 GRIXGZQULWMCLU-UHFFFAOYSA-L 0.000 description 3
- 229960005491 sodium morrhuate Drugs 0.000 description 3
- UUTKICFRNVKFRG-WDSKDSINSA-N (4R)-3-[oxo-[(2S)-5-oxo-2-pyrrolidinyl]methyl]-4-thiazolidinecarboxylic acid Chemical compound OC(=O)[C@@H]1CSCN1C(=O)[C@H]1NC(=O)CC1 UUTKICFRNVKFRG-WDSKDSINSA-N 0.000 description 2
- 208000035985 Body Odor Diseases 0.000 description 2
- 206010055000 Bromhidrosis Diseases 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 201000011066 hemangioma Diseases 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 210000002751 lymph Anatomy 0.000 description 2
- -1 10% alum steep Chemical compound 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 230000000680 avirulence Effects 0.000 description 1
- 108700004675 bleomycetin Proteins 0.000 description 1
- QYOAUOAXCQAEMW-UTXKDXHTSA-N bleomycin A5 Chemical compound N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC=C(N=1)C=1SC=C(N=1)C(=O)NCCCNCCCCN)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1N=CNC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C QYOAUOAXCQAEMW-UTXKDXHTSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229960000443 hydrochloric acid Drugs 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
本发明涉及一种药用硬化剂及其制备方法。现有常用于治疗血管瘤、痔疮等疾病的硬化剂存在疗效差、副作用大的缺点。本发明提供一种由硫酸铝0.1~10%、乙醇1~50%、局部麻醉剂及蒸馏水组成的高效硬化剂,它具有凝固蛋白速度快、结块力强、无毒性、副作用小、制备简单的优点,易在临床上推广应用。
Description
本发明涉及一种药用硬化剂及其制备方法。
硬化剂常用于治疗血管瘤、淋巴水瘤、痔疮、腋臭等疾病,现有的常用硬化剂有;5%鱼肝油酸钠、无水乙醇、10%明矾液、三氯化铁、脲素、盐酸、奎宁、平阳霉素。其中鱼肝油酸钠、无水乙醇、明矾液和脲素最常用,但存在下列缺点:
1、鱼肝油酸钠是一种脂肪酸的钠盐,用其5%高渗液,其缺点是凝血作用极差、细胞脱水作用强,注入瘤体后水肿明显。
2、无水乙醇虽具有极强的凝固的作用,但注射过多易引起大块组织溃烂坏死,如降低其浓度(低于80%)又会失去疗效。
3、用5~10%的明矾溶液作硬化剂,其凝固蛋白的作用较弱,因此速度幔且结块力不强,疗效差。
本发明的目的在于提供一种凝固蛋白的速度快、结块力强且疗效好、副作用小的硬化剂。
本发明的目的可以通过如下措施实现:
经反复试验,结果显示:硬化剂主要由硫酸铝、乙醇、蒸溜水组成,其含量范围为硫酸铝0.1~10%、乙醇1~50%,余量为蒸溜水。
上述硬化剂,它还含有局部麻醉剂,其含量范围为0.1~2%。
上述硬化剂中所含的局部麻醉剂为利多卡因或普鲁卡因或可卡因。
如上述硬化剂,硫酸铝2~8%、乙醇10~30%、普鲁卡因1~1.5%,余量为蒸馏水效果较佳。
如上述硬化剂,硫酸铝5%,乙醇20%,利多卡因1%,余量为蒸馏水,效果最佳。
上述配方中,硫酸铝可用较价廉的明矾替代,以降低成本。
上述硬化剂的制备方法是:先将硫酸铝加入到蒸馏水中,均匀搅拌,让其充分溶解,然后加入乙醇及局部麻醉剂,混匀之后加水至所要求的量,再经常规的高温高压灭菌之后,在无菌室内分装,即可制成不同剂量的硬化剂,直接在临床上应用。
本发明相比现有技术具有如下优点:
1、治疗效果好。由于该硬化剂能够在血管内凝固蛋白,速度快,结块力强,能有效地防止硬化剂和血凝块被血液冲走。
2、毒性极低。硬化剂中所含各种成份无毒性,故副作用小,安全性高。
3、制备简单,成本低廉,容易在临床上广泛推广应用。
本发明实施例:
实施例1:取硫酸铝(分析纯)1g,加入300ml蒸馏水,均匀搅拌,待完全溶解后加入乙醇10ml,混匀之后再加水至1000ml,经常规高温高压灭菌后,在无菌室内分装成2ml~10ml安瓿,即成为含硫酸铝0.1%,乙醇1%的硬化剂,可用于治疗轻症腋奥。
实施例2:取硫酸铝10g,加入蒸馏水500ml,普鲁卡因1g,混匀之后再加水至1000ml,经常规高温高压灭菌后,在无菌室内分装成2ml~10ml安瓿,即成为含硫酸铝1%,乙醇5%的硬化剂,可用于治疗腋臭。
实施例3:取硫酸铝20g,加入蒸馏水600ml,均匀搅拌、待完全溶解后加入乙醇100ml,利多卡因10g,混匀之后再加水至1000ml,经常规高温高压灭菌后,在无菌室内分装成2ml~10ml安瓿,即成为含硫酸铝2%,乙醇10%的硬化剂,可用于重症腋奥的治疗和轻证痔疮、血管瘤的治疗。
实施例4:取硫酸铝50g,加入蒸馏水700ml均匀搅拌、待完全溶解后加入乙醇200ml,普鲁卡因1g混匀之后再加水至1000ml,经常规高温高压灭菌后,在无菌室内分装成2ml~10ml安瓿,即制备成含硫酸铝5%、乙醇20%的硬化剂,可用于治疗痔疮、血管瘤、淋巴水瘤,疗效最好。
实施例5:取硫酸铝100g,加入蒸馏水750ml,均匀搅拌、待完全溶解后加入乙醇500ml、前卡因20g,混匀之后再加入水至1000ml,经常规高温高压灭菌后,可在无菌室内分装,即成为含硫酸铝10%,乙醇50%的硬化剂,临床上可用于恶性肿瘤的治疗。
Claims (7)
1、一种高效硬化剂,其特征在于它主要硫酸铝、乙醇、蒸溜水组成,其含量范围为硫酸铝0.1~10%、乙醇1~50%,余量为蒸溜水。
2、按权利要求1所述的硬化剂,其特征在于它还含有局部麻醉剂,其含量为0.5~2%。
3、按权利要求2所述的硬化剂,其特征在于为所用的局部麻醉剂为利多卡因、普鲁卡因或可卡因。
4、按权利要求1所述的硬化剂,其特征在于硫酸铝2~8%、乙醇10~30%、局部麻醉剂1~1.5%,余量为蒸馏水。
5、按权利要求4所述的硬化剂,其特征在于硫酸铝5%,乙醇20%,局部麻醉剂1%,余量为蒸馏水。
6、按权利要求1~5所述的硬化剂,其特征在于上述硫酸铝可用明矾替代。
7、按权利要求1所述的硬化剂,其特征在于先将硫酸铝加入到蒸馏水中,均匀搅拌,溶解后加入乙醇及局部麻醉剂,混匀之后加水至所要求的量,再经常规的高温高压灭菌之后,在无菌室内分装,即可制成不同剂量的硬化剂。
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 94106757 CN1114193A (zh) | 1994-06-28 | 1994-06-28 | 一种高效硬化剂及制备方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 94106757 CN1114193A (zh) | 1994-06-28 | 1994-06-28 | 一种高效硬化剂及制备方法 |
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| Publication Number | Publication Date |
|---|---|
| CN1114193A true CN1114193A (zh) | 1996-01-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 94106757 Pending CN1114193A (zh) | 1994-06-28 | 1994-06-28 | 一种高效硬化剂及制备方法 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7381419B2 (en) * | 2000-06-06 | 2008-06-03 | Lequio Pharma Co., Ltd. | Medical composition kit for treating lesioned abnormal tissue |
| WO2020238148A1 (zh) * | 2019-05-28 | 2020-12-03 | 山东大学齐鲁医院 | 一种应用于治疗脉管异常的乙醇泡沫硬化剂及制备方法 |
-
1994
- 1994-06-28 CN CN 94106757 patent/CN1114193A/zh active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7381419B2 (en) * | 2000-06-06 | 2008-06-03 | Lequio Pharma Co., Ltd. | Medical composition kit for treating lesioned abnormal tissue |
| WO2020238148A1 (zh) * | 2019-05-28 | 2020-12-03 | 山东大学齐鲁医院 | 一种应用于治疗脉管异常的乙醇泡沫硬化剂及制备方法 |
| US11975099B2 (en) | 2019-05-28 | 2024-05-07 | Qilu Hospital of Shandong University | Ethanol foam sclerosing agent for treating vascular anomalies and preparation method thereof |
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