麻醉学精品ppt课件_第1页
麻醉学精品ppt课件_第2页
麻醉学精品ppt课件_第3页
麻醉学精品ppt课件_第4页
麻醉学精品ppt课件_第5页
已阅读5页,还剩17页未读 继续免费阅读

下载本文档

版权说明:本文档由用户提供并上传,收益归属内容提供方,若内容存在侵权,请进行举报或认领

文档简介

Chapter 1 Anesthetics,Anesthetic is a drug that causes reversible anesthesia and a loss of consciousness (including the feeling of pain). This allows patients to undergo surgery and other procedures without the distress and pain they would otherwise experience.,Local anesthetics General anesthetics,Local anesthetic is used on specific nerve pathways , has effect of a loss of awareness of a part of the body. Whreas general anesthetic is used on central nervous system, has effect of a total unconsciousness.,1.1.1 Discovery and development of local anesthetics,Peruvian were known chewing coca leaves from South America for pain in 1532. An alkaloid was extracted from the leaves of coca and named Cocaine in 1860. Cocaine was used as a local anesthetic in clinic in 1884. Chemical structure was modified because of severe side-effect such as addiction, allergy, tissue irritating and unstable in aqueous solution,1.1 Local anesthetics,Cocaine,Studying results showed that benzoate fraction played the important role but methoxy carbonyl is not necessary for the activity of anesthesia. On the other hand, simplification of ecgonine led to the discovery of synthetic compounds -Eucaine and -Eucaine. This resulted that tropine was not necessary for the activity.,ecgonine,-Eucaine,-Eucaine,According to the obtained results, researchers begun to study the synthetic benzoic acid esters as the local anesthetics. First of all, Benzocaine was discovered in 1890. Shortly after, Orthoform and Orthoform New were found with strong local anesthesia effect. At last,Procaine was discovered in 1904.,Benzocaine,Procaine,Orthoform,Orthoform New,Procaine hydrochloride,4-氨基苯甲酸-2-(二乙氨基)乙酯盐酸盐,又名盐酸奴佛卡因 4-Aminobenzoic acid 2-(diethylamino)ethyl ester monohydrochloride, or Novocaine hydrochloride),Physical properties: white crystal or crystalline powder, odorless, bitter taste and then a sense of paralysis. Mp.154 157 . Soluble in water (1:1), slightly soluble in ethanol (1:30) and chloroform, hardly soluble in ether.,Chemical properties: Hydrolysis: 酸、碱及体内酶均使其水解。pH3-3.5最稳定,在碱性、中性及强酸性条件下易水解。 Oxidization:含芳伯氨基,易被氧化变色。,Activity and clinical application: Procaine 具有良好的局麻作用,毒性低,无成瘾性,是国内外临床广泛应用的局麻药之一,主要用于浸润麻醉,传导麻醉和封闭疗法。 With good local anesthesia, low toxicity and non-addiction Used for infiltration anesthesia, conduction anesthesia and closed treatment.,Synthesis of Procaine,Aromatic acid esters-Procaine and its derivatives,1.1.2 Classifications of local anesthetic,procaine,chloroprocaine,hydroxyprocaine,(1) Procaine的苯环上引入取代基,增加空间位阻使水解速率减慢,从而增加局麻作用。 Introduction of substituents on benzene ring of Procaine lead to increasing of the steric hindrance so slow down the hydrolysis to increase anesthesia.,parethoxycaine,tetracaine,(2) Procaine的苯环对位氨基被烷氨基或烷氧基取代,局麻作用增强,但毒性也增强。,(3) 侧链碳链改变可使稳定性增加,麻醉作用时间延长。,tutocaine,dimethocaine,thiocaine,(3) 羧酸酯中,以电子等排体S代替O,脂溶性增大,显效迅速。,1.1.2.2 Amides,lidocaine,prilocaine,trimecaine,盐酸利多卡因 Lidocaine Hydrochloride,N-(2,6-二甲苯基)-2-(二乙胺基)乙酰胺盐酸盐一水合物 2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide hydrochloride monohydrate,Properties: white crystalline powder, odorless, bitter taste then a sense of numbness. Mp.75 79 , anhydrous complex mp.127 129 . soluble in water and ethanol, slightly soluable in chloroform (1:40), insoluble in ether. pH of 0.5% aqueous solution is 4.0 to 5.5.,Lidocaine was firstly synthesized in 1943, used as a local anesthetic with anesthesia 2 9 times stronger than procaine and two times enduration time but also severe toxicity than procaine. Lidocaine also was found the effect of anti-arrhythmia.,Metabolism of Lidocaine,Synthesis of Lidocaine,1.1.2.3 Amino ketones,以电子等排体-CH2-代替酯基中的-O-,形成酮类化合物,不少氨基酮类化合物具有局麻作用。,Dyclonine,Falicaine,盐酸达克罗宁 Dyclonine hydrochloride,1-(4-丁氧苯基)-3-(1-哌啶基)-1-丙酮盐酸盐 1-(4-Butoxyphenyl)-3-(1-piperidinyl)-1-propanone hydrochloride,Dyclonine 具有强的麻醉作用和穿透力,作用快且持久,临床用作表面麻醉(surface anesthesi

温馨提示

  • 1. 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。图纸软件为CAD,CAXA,PROE,UG,SolidWorks等.压缩文件请下载最新的WinRAR软件解压。
  • 2. 本站的文档不包含任何第三方提供的附件图纸等,如果需要附件,请联系上传者。文件的所有权益归上传用户所有。
  • 3. 本站RAR压缩包中若带图纸,网页内容里面会有图纸预览,若没有图纸预览就没有图纸。
  • 4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
  • 5. 人人文库网仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对用户上传分享的文档内容本身不做任何修改或编辑,并不能对任何下载内容负责。
  • 6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
  • 7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

评论

0/150

提交评论