CN1488352A - 一种用于儿科解热镇痛的药物组合物 - Google Patents
一种用于儿科解热镇痛的药物组合物 Download PDFInfo
- Publication number
- CN1488352A CN1488352A CNA021394725A CN02139472A CN1488352A CN 1488352 A CN1488352 A CN 1488352A CN A021394725 A CNA021394725 A CN A021394725A CN 02139472 A CN02139472 A CN 02139472A CN 1488352 A CN1488352 A CN 1488352A
- Authority
- CN
- China
- Prior art keywords
- pediatrics
- antipyretic
- department
- aspirin
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 6
- 239000003907 antipyretic analgesic agent Substances 0.000 title description 5
- 229960004277 benorilate Drugs 0.000 claims abstract description 9
- FEJKLNWAOXSSNR-UHFFFAOYSA-N benorilate Chemical compound C1=CC(NC(=O)C)=CC=C1OC(=O)C1=CC=CC=C1OC(C)=O FEJKLNWAOXSSNR-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000008187 granular material Substances 0.000 claims abstract description 9
- 239000002552 dosage form Substances 0.000 claims description 8
- 229930003270 Vitamin B Natural products 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 235000019156 vitamin B Nutrition 0.000 claims description 7
- 239000011720 vitamin B Substances 0.000 claims description 7
- 239000002671 adjuvant Substances 0.000 claims description 2
- 239000003814 drug Substances 0.000 abstract description 18
- 229940079593 drug Drugs 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 3
- 230000008901 benefit Effects 0.000 abstract description 2
- 235000019605 sweet taste sensations Nutrition 0.000 abstract description 2
- 231100000419 toxicity Toxicity 0.000 abstract description 2
- 230000001988 toxicity Effects 0.000 abstract description 2
- 229930003451 Vitamin B1 Natural products 0.000 abstract 1
- 239000000890 drug combination Substances 0.000 abstract 1
- 229960003495 thiamine Drugs 0.000 abstract 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 abstract 1
- 239000011691 vitamin B1 Substances 0.000 abstract 1
- 235000010374 vitamin B1 Nutrition 0.000 abstract 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 13
- 229960001138 acetylsalicylic acid Drugs 0.000 description 13
- 230000000694 effects Effects 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 8
- 239000003826 tablet Substances 0.000 description 7
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 6
- 239000000796 flavoring agent Substances 0.000 description 6
- 235000019634 flavors Nutrition 0.000 description 6
- 230000000202 analgesic effect Effects 0.000 description 4
- 229920002261 Corn starch Polymers 0.000 description 3
- 206010037660 Pyrexia Diseases 0.000 description 3
- 230000001754 anti-pyretic effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 210000003734 kidney Anatomy 0.000 description 3
- 210000004185 liver Anatomy 0.000 description 3
- 229960005489 paracetamol Drugs 0.000 description 3
- -1 aspirin compound Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007910 chewable tablet Substances 0.000 description 2
- 229940068682 chewable tablet Drugs 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- ONJSZLXSECQROL-UHFFFAOYSA-N salicyluric acid Chemical compound OC(=O)CNC(=O)C1=CC=CC=C1O ONJSZLXSECQROL-UHFFFAOYSA-N 0.000 description 2
- 230000009967 tasteless effect Effects 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- AEMOLEFTQBMNLQ-AQKNRBDQSA-N D-glucopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-AQKNRBDQSA-N 0.000 description 1
- 208000004232 Enteritis Diseases 0.000 description 1
- 208000002091 Febrile Seizures Diseases 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 206010020741 Hyperpyrexia Diseases 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 206010057190 Respiratory tract infections Diseases 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- 206010046306 Upper respiratory tract infection Diseases 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 150000004716 alpha keto acids Chemical class 0.000 description 1
- XRTUHVPNMDUOBJ-UHFFFAOYSA-N azane sulfane hydrochloride Chemical compound S.[Cl-].[NH4+] XRTUHVPNMDUOBJ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000019636 bitter flavor Nutrition 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 206010006451 bronchitis Diseases 0.000 description 1
- 230000023852 carbohydrate metabolic process Effects 0.000 description 1
- 235000021256 carbohydrate metabolism Nutrition 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006606 decarbonylation reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 206010016284 febrile convulsion Diseases 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 210000003811 finger Anatomy 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002510 pyrogen Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229940032021 tetramune Drugs 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 206010044008 tonsillitis Diseases 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
本发明属一种于儿科解热镇痛的复方制剂,它是由贝诺酯、维生素B1、辅料配伍制成,剂型为片剂或颗粒剂。本发明经药理、毒性、临床试验证实,具有安全程度高,副作用小,药性稳定,无臭的优点,其加味咀嚼片或加味颗粒剂有香甜味,咀嚼易碎,患儿乐于服用,解决我国儿科临床使用的解热镇痛药品单调、制剂剂型规格少的状况,从而对满足日益增长的儿科临床需要和市场需求具有一定的积极意义。
Description
技术领域
本发明属一种用于解热镇痛的制剂,尤其是适宜儿科临床使用及一般家庭婴幼儿服用的制剂。
背景技术
发热是儿科疾病中最常见的一种临床表现,虽然发热本身对机体具有一定的保护作用,但高热或超高热对小儿健康影响极大并可导致生命危险,即便是轻度发热,对某些患儿也会引起热性惊厥。根据致热原因和程度不同,常需采取退热措施,而药物降温是简便易行的有效方法,多数情况是将成人服用的复方阿斯匹林(APC)及去痛片掰成几份或碾成细粉给小儿灌服。在服用过程中因阿斯匹林(APC)有酸苦味,小儿不乐于服用,其次,阿斯匹林(APC)刺激胃肠道及肝、肾有副作用。另一方面剂型不适合小儿服用,剂量也不易准确,使用极感不便,造成了儿科用药“三难”,即医生开药难,家长喂药难,患儿吃药难的状况。
本发明的内容
解热镇痛药物在儿科医疗上具有十分重要的地位。本发明的目的旨在研制一种安全范围大,副作用小,药性稳定,无臭无味,适宜于婴幼儿,加味咀嚼片及加味颗粒解热镇痛药物,改变我国儿科临床使用的解热镇痛药物制品单调,制剂剂型规格较少的局面。
本发明的目的是这样实现的
一种用于儿科解热镇痛的药物组合物,在已定剂型数下,其成份及含量为贝诺酯200-300g,维生素B12-3g、辅料适量组成。
贝诺酯(Benorylatum)是目前非甾体类解热镇痛药中的优良品种之一,具有效果好,毒副作用轻微,治疗剂量安全范围较大以及无味、无臭、化学性质稳定等十分适合儿科临床使用及一般家庭成药使用的特点,故作为制剂的主体药物是十分适宜的。
盐酸硫铵(Tyiamine Hd;维生素B1 VitaminB1)是机体维持正常代谢和机能所必需的一类低分子有机化合物,当人体(尤其是儿童)处于发热状态时,维生素B1的充分供给可免于糖代谢中α酮酸的氧化脱羰反应受阻。从而消除和减轻神经系统和心血管系统的各种症状,对机体进行保护,遴选为制剂的辅药,对小儿来说也是十分合理的。
药物的剂型为颗粒剂或片剂。
本发明与现用药物阿斯匹林(APC)相比照优点和产生的有益效果是
1、以本发明和阿斯匹林(见表1)比照,本发明退热镇痛效应及作用强度优于阿斯匹林
表1 本发明和阿斯匹林疗效对照
组别 | 例数 | 显效例数(%) | 有效例数(%) | 无效例数(%) | 总有效率(%) |
本发明 | 693 | 455(65.65) | 190(27.41) | 48(6.92) | 93.07 |
阿斯匹林组 | 241 | 111(46.05) | 85(35.26) | 45(18.67) | 81.32 |
2、本发明与阿斯匹林不良反应发生情况(见表2)相比照,本发明服用后对胃、肠道及肝肾副作用较阿斯匹林低微。
表2 本发明与阿斯匹林不良反应发生情况
反应 | 本发明 | 阿斯匹林 | ||
例次 | % | 例次 | % | |
恶心 | 10 | 1.4 | 13 | 5.39 |
呕吐 | 3 | 0.43 | 3 | 1.24 |
嗜睡 | 1 | 0,14 | 0 | 0 |
液汗淋漓 | 33 | 4.76 | 33 | 13.69 |
3、本发明制成的加味咀嚼片和小儿复方贝诺酯加味颗粒剂具有良好的解热镇痛作用,尤其对小儿急性发热,如上呼吸道感染化脓性扁桃体炎、支气管炎、肠炎等发热疾病,其退热作用稳定疗效佳,未发现副作用,使用安全、片剂在口腔中很容易嚼碎吞咽,易被患儿接受,颗粒剂经冲溶后幼儿口服较易,是一个受临床欢迎的新型儿科解热镇痛制剂。
4、以贝诺酯为主体药物,并辅以维生素B1而组成的复方制剂,贝诺酯为阿斯匹林与扑热息痛的酯化产物,具有较强的解热镇痛作用。该药进入血液后,即分为阿斯匹林及扑热息痛而显效,然后在肝内代谢成扑热息痛葡萄糖醛酸或水杨尿酸等产物,由尿中排泄,对白细胞无抑制作用,对肝、肾、胃肠无不良影响。
5、本发明制成的加味可嚼片及加味颗粒剂经药理、毒性、临床试验,确定为一高效低毒的解热镇痛药复方新制剂。具有适于儿科临床应用,新型新颖,服用方便,适应症范围广,副作用轻微,用药安全程度高,价格低廉,药源充足等特点,它的研制和生产对加速我国解热镇痛的多剂型、多品种化、特别是儿童解热镇痛药及其剂型的更新换代,从而满足日益增长的儿科临床需要和市场需求具有一定的积极意义。
具体实施方式
结合上述,本发明再作进一步的详述:
实施例1,一种用于儿科解热镇痛的药物组合物,制成1000片片剂,其成份及含量为:
贝诺酯 200g 维生素B1 2g 辅料:适量
片剂所含的辅药及其它的赋形剂,以选择蒸馏水和5%(玉米)淀粉浆作为湿润剂和粘合剂,选择(玉米)淀粉、(甜菜)糖粉为填充剂(稀释剂),选择(玉米)淀粉、甘露醇为崩解剂,考虑到盐酸胺当PH在5以上时很容易破坏,为了使制剂的PH值得到适量的调整,故应选择硼酸为润滑剂并同时作调整剂,其用量不得超过0.5%。
为了吸引患儿乐于服用,片剂应具有适宜的甜味,为了达到这一要求,片剂中应包括足量的(甜菜)糖份,但其比例应以不影响剂型的适宜硬度、粘合为宜。
实施例2,一种用于儿科解热镇痛的药物组合物,制成1000袋(每袋3g)颗粒剂,其中,贝诺酯300g、维生素B13g、辅料适量与实施例1相同。
Claims (3)
1、一种用于儿科解热镇痛的药物组合物,在已定的剂型数下,其成份及含量为:
贝诺酯 200g-300g 维生素B1 2g-3g 辅料:适量
2、如权利要求1所述的一种用于儿科解热镇痛的药物组合物,其特征在于所述的剂型为片剂。
3、如权利要求1所述的一种用于儿科解热镇痛的药物组合物,其特征在于所述的剂型为颗粒剂。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNA021394725A CN1488352A (zh) | 2002-10-09 | 2002-10-09 | 一种用于儿科解热镇痛的药物组合物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNA021394725A CN1488352A (zh) | 2002-10-09 | 2002-10-09 | 一种用于儿科解热镇痛的药物组合物 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1488352A true CN1488352A (zh) | 2004-04-14 |
Family
ID=34147459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA021394725A Pending CN1488352A (zh) | 2002-10-09 | 2002-10-09 | 一种用于儿科解热镇痛的药物组合物 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1488352A (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103230568A (zh) * | 2013-04-18 | 2013-08-07 | 林凡友 | 一种小儿贝诺酯维b1颗粒及其制备工艺 |
CN104274712A (zh) * | 2014-09-30 | 2015-01-14 | 孟庆军 | 一种用于儿科解热镇痛的药物组合物 |
CN105727011A (zh) * | 2015-12-23 | 2016-07-06 | 马敬斌 | 一种用于儿科解热镇痛的中药组合物 |
-
2002
- 2002-10-09 CN CNA021394725A patent/CN1488352A/zh active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103230568A (zh) * | 2013-04-18 | 2013-08-07 | 林凡友 | 一种小儿贝诺酯维b1颗粒及其制备工艺 |
CN104274712A (zh) * | 2014-09-30 | 2015-01-14 | 孟庆军 | 一种用于儿科解热镇痛的药物组合物 |
CN105727011A (zh) * | 2015-12-23 | 2016-07-06 | 马敬斌 | 一种用于儿科解热镇痛的中药组合物 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101396466A (zh) | 一种药食两用感冒药茶组合物及其制备方法和用途 | |
WO2015003478A2 (zh) | 一种适用于婴幼儿及儿童的口腔崩解片及其制备方法 | |
Pattanayak et al. | Formulation development and optimization of medicated lozenges for pediatric use | |
CN1840044A (zh) | 治疗失眠的药物及其制备方法 | |
CN101085045B (zh) | 治疗口腔溃疡的纯中药制剂 | |
CN101270072A (zh) | 右旋吲哚布芬及其用于制备药物的用途 | |
US6509035B1 (en) | Oral preparation of coenzyme a useful for lowering blood lipid and a method producing for same | |
CN1488352A (zh) | 一种用于儿科解热镇痛的药物组合物 | |
CA2906060A1 (en) | Method of treating vitamin b12 deficiency | |
Rudinskas et al. | Poor clinical response to enteric-coated iron preparations | |
JP4634589B2 (ja) | 食品又は医薬品易服用化剤 | |
CN103877533B (zh) | 一种含有二甲双胍的治疗糖尿病的药物组合物及其制备方法 | |
CN102525979B (zh) | 一种小儿布洛芬组合物 | |
Chowdary et al. | Preparation and evaluation of fast dissolving tablets of Paracetamol employing super disintegrants | |
CN101301350A (zh) | 一种独一味提取物口服冻干片及其制备方法 | |
CN104721808A (zh) | 用于治疗新生儿黄疸的药物组合物 | |
CN115721614B (zh) | 一种α-KG缓释制剂及用途 | |
WO2025046047A1 (en) | Pharmaceutical composition of combination of a non-steroidal anti-inflammatory drugs (nsaids) and decongestant in the form of a powder or granules for preparing a hot drink | |
CN1850243A (zh) | 新型口炎制剂及其制备方法 | |
TWI703989B (zh) | 口腔內保持型崩解性固形製劑、其製造方法、及用於該製造方法之粉體組成物 | |
JP2000229853A (ja) | 生理痛改善用組成物 | |
CN104490926A (zh) | 一种碳酸钙组合物咀嚼片及其制备方法 | |
Patel | Formulation Development and Evaluation of Orally Disintegrating Antiretroviral Pediatric Tablet | |
CN1314391C (zh) | 保妇康阴道泡腾片及其制法 | |
PHARMACEUTICS | FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF LAMIVUDINE |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |