CN107789621A - 一种治疗头痛的药物及其配制方法 - Google Patents
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Abstract
本发明公开了一种治疗头痛的药物及其配制方法,其主要是由灯盏花素、安基比林、糜蛋白酶按一定比例配制而成,本发明药物具有调节骨内外压力平衡的作用,用于治疗头痛疗效快,治愈率高。
Description
技术领域
本发明涉及一种药物,尤其是一种治疗头痛的药物。
背景技术
头痛是一种临床常见的症状,可由多种原因引起,近期研究发现,骨减压对治疗头痛有效,头痛患者因受外界感染后全身发热,血流增加,造成骨内压增高,又因骨膜的屏障,使内外形成压力差,故而导致头痛。
发明内容
本发明的目的就是提供一种骨减压的药物。
本发明的药物包括局注药物及再注药物。
局注药物由利多卡因、地塞米松、维生素B1组成,再注药物由灯盏花素、安基比林、头孢哌酮、糜蛋白酶组成,选用利多卡因(Lidocaine),主要作用于浦肯野纤维和心室肌,抑制Na+内流而降低心肌自律性,促进心肌细胞内K+外流而引起超极化,消除折返激动,抑制心室应激性,提高心室颤动阈值。但对心房及窦房结作用很轻;在治疗剂量时,对心肌细胞的电活动具有抗室性心律失常作用,但对房室传导和心肌的收缩无明显影响;血药浓度进一步升高,可引起心脏传导速度减慢,房室传导阻滞,抑制心肌收缩力和使心排血量下降,主要用于阻滞麻醉及硬膜外麻醉。也用于室性心律失常,如室性心动过速及频发室性早搏。地塞米松(Dexamethasone,简称DXMS),地塞米松是一种人工合成的皮质类固醇,可用于治疗多种症状,包含风湿性疾病,某些皮肤病、严重过敏、哮喘、慢性阻塞性肺病、义膜性喉炎、脑水肿,也可能与抗生素合并用于结核病患者。地塞米松是糖皮质类激素。其衍生物有氢化可地松、泼尼松等,其药理作用主要是抗炎、抗毒、抗过敏、抗风湿,临床使用较广泛。极易自消化道吸收,其血浆T1/2为190分钟,组织T1/2为3日,肌注地塞米松磷酸钠或地塞米松醋酸酯后分别于l小时和8小时达血药浓度峰值。该品血浆蛋白结合率较其他皮质激素类药物为低.该品0.75mg的抗炎活性相当于5mg泼尼松龙。肾上腺皮质激素类药,抗炎、抗过敏和抗毒作用较泼尼松更强,水钠潴留和促进排钾作用很轻,可肌注或静滴对垂体-肾上腺抑制作用较强。1.抗炎作用:可减轻和防止组织对炎症的反应,从而减轻炎症的表现。激素抑制炎症细胞,包括巨噬细胞和白细胞在炎症部位的集聚,并抑制吞噬作用、溶酶体酶的释放以及炎症化学中介物的合成和释放。2.免疫抑制作用:包括防止或抑制细胞介导的免疫反应,延迟性的过敏反应,减少T淋巴细胞、单核细胞、嗜酸性细胞的数目,降低免疫球蛋白与细胞表面受体的结合能力,并抑制白介素的合成与释放,从而降低T淋巴细胞向淋巴母细胞转化,并减轻原发免疫反应的扩展。可降低免疫复合物通过基底膜,并能减少补体成份及免疫球蛋白的浓度。维生素B1,维生素B1又称硫胺素或抗神经炎维生素或抗脚气病维生素,为白色晶体,在有氧化剂存在时容易被氧化产生脱氢硫胺素,后者在有紫外光照射时呈现蓝色荧光。由嘧啶环和噻唑环通过亚甲基结合而成的一种B族维生素。为白色结晶或结晶性粉末;有微弱的特臭,味苦,有引湿性,露置在空气中,易吸收水分。在碱性溶液中容易分解变质。酸碱度在3.5时可耐100℃高温,酸碱大于5时易失效。遇光和热效价下降。故应置于遮光,凉处保存,不宜久贮。在酸性溶液中很稳定,在碱性溶液中不稳定,易被氧化和受热破坏。还原性物质亚硫酸盐、二氧化硫等能使维生素B1失活。作用用途:促进成长;帮助消化,特别是碳水化合物的消化;改善精神状况;维持神经组织、肌肉、心脏活动的正常;减轻晕机、晕船;可缓解有关牙科手术后的痛苦;有助于对带状疱疹(herpes zoster)的治疗。灯盏花素,为中药提取制剂,其剂型有片剂、注射剂、滴丸剂等。具有扩张脑血管,抗血凝的作用。临床上用于治疗脑供血不足、脑出血所致后遗症、高粘脂血症、脑血栓、冠心病、心绞痛等疾病。灯盏花素具有扩张脑血管的作用,能降低脑血管阻力,增加脑血流量,改善微循环,并有对抗血小板聚集作用。故可用于治疗缺血性脑血管疾病,如脑血栓形成,脑栓塞、脑溢血等所致后遗症瘫痪病人,具有较好疗效,对病程在6个月以内的疗效比6个月以上者好。安基比林(aminophenazone),化学名为1-苯基-2,3-二甲基-4-二甲氨基吡唑酮,白色或几乎白色的结晶性粉末;无臭,味微苦;遇光可变质;水溶液显碱性反应,用于缓解感冒、上呼吸道感染引起发热、头痛等症状,亦可用于神经痛、风湿痛、牙痛。头孢哌酮(Cefoperazone sodium)头孢哌酮为第三代头孢菌素,对大肠埃希菌、克雷白菌属、变形杆菌属、伤寒沙门菌、志贺菌属、枸橼酸杆菌属等肠杆菌科细菌和铜绿假单胞菌有良好抗菌作用,对产气肠杆菌、阴沟肠杆菌、鼠伤寒杆菌和不动杆菌属等的作用较差。流感嗜血杆菌、淋病奈瑟菌和脑膜炎奈瑟菌对本品高度敏感。本品对各组链球菌、肺炎球菌亦有良好作用,对葡萄球菌(甲氧西林敏感株)仅具中度作用,肠球菌属耐药。头孢哌酮对多数革兰阳性厌氧菌和某些革兰阴性厌氧菌有良好作用,脆弱拟杆菌对本品耐药。在脑膜发炎时,可进入脑脊液,用于各种敏感菌所致的呼吸道、泌尿道、腹膜、胸膜、皮肤和软组织、骨和关节、五官等部位的感染,还可用于败血症和脑膜炎等。糜蛋白酶(Chymotrypsin)系蛋白水解酶,尚有脂酶作用,使某些脂水解。因此可消化脓液、积血、坏死组织,起创面净化、消炎、消肿作用。主要用于创伤或手术后创伤愈合、抗炎及防止局部水肿、积血、扭伤血肿、乳房手术后水肿、中耳炎、鼻炎、角膜溃疡、泪道疾病、眼外伤、眼睑水肿、出血和玻璃体积血、慢性支气管炎、支气管扩张、肺脓肿以及毒蛇咬伤等。
具体实施方式
本发明药物包括局注药物及再注药物,其中各组分原料药的用量也是发明人经过大量的摸索总结取得的。
局注药物的用量为:利多卡因5ml、地塞米松1ml、维生素B1 0.1g。
再注药物的用量为:灯盏花素0.1ml、安基比林0.1ml、头孢哌酮0.1ml、糜蛋白酶0.1ml。
使用方法:
1、用注射器抽取利多卡因、地塞米松、维生素B1混合液中的0.5ml为麻醉剂,取太阳穴,将麻醉剂注入太阳穴中实施麻醉;
2、退去麻醉针,用负压吸引罐盖住太阳穴位负压0.1kp抽吸3分钟;
3、用穿刺针抽取灯盏花素、安基比林、头孢哌酮、糜蛋白酶混合后作为治疗剂,延太阳穴位刺入至骨板夹层的骨质部注入治疗剂,退出穿刺针,用无菌创可贴封贴针眼。
本发明将灯盏花素、安基比林、头孢哌酮、糜蛋白酶组合,使其功效产生协同作用,从而能够调节骨内外的压力平衡,达到治疗头痛的效果。
下面结合试验例进一步阐述本发明药物的有益效果。
测试头痛患者46人,用上述方法用药,其中31人一侧用药即愈,12人再由另一侧太阳穴位用药后痊愈,3人效果不明显,总有效率为93.47%。
Claims (2)
1.一种治疗头痛的药物,其特征在于:它包括局注药物及再注药物,其中:局注药物的用量为:利多卡因5ml、地塞米松1ml、维生素B1 0.1g;再注药物的用量为:灯盏花素0.1ml、安基比林0.1ml、头孢哌酮0.1ml、糜蛋白酶0.1ml。
2.一种治疗头痛药物的使用方法,其特征在于:它包括下列步骤:
(1)用注射器抽取利多卡因、地塞米松、维生素B1混合液中的0.5ml为麻醉剂,取太阳穴,将麻醉剂注入太阳穴中实施麻醉;
(2)退去麻醉针,用负压吸引罐盖住太阳穴位负压0.1kp抽吸3分钟;
(3)用穿刺针抽取灯盏花素、安基比林、头孢哌酮、糜蛋白酶混合后作为治疗剂,延太阳穴位刺入至骨板夹层的骨质部注入治疗剂,退出穿刺针,用无菌创可贴封贴针眼。
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CN106943340A (zh) * | 2017-04-28 | 2017-07-14 | 北京茗泽中和药物研究有限公司 | 一种盐酸利多卡因凝胶 |
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