{"title":"葡萄球菌感染","authors":"---WITH Methicillin, J. W. Harding","doi":"10.1542/9781581107951-ch123","DOIUrl":null,"url":null,"abstract":"MrrHICILLIN (sodium 6-[2,6 dimethoxybenzamido] penicillinate .monohydrate) has been the first compound of major importance resulting from the isolation of pure 6-amino penicillanic acid by Batchelor, Doyle, Nayler and Rolinson (1959). This new penicillin compound is of great therapeutic importance on account of several valuable properties which it, possesses. It is bactericidal (Knox, I960), virtually non-toxic (Brown and Acred, 1960), is unaffected by staphylococcal penicillinase (Knox, I960; Rolinson, Stevens, Batchelor, Wood and Chain, i960) and is effective against all isolated strains of staphylococci in vitro (Thompson, Harding and Simon, I960). Furthermore, it is effective against staphylococci in vivo (Douthwaite and Trafford, I960; Stewart, Nixon, Coles, Kesson, Lawson, Thomas,. Mishra, Mitchell, Semmens and: Wade, i960). Most of these findings have been confirmed by workers in Canada (Branch, Rodger, Lee'and'Power, I966). We have had the opportunit of observing the results of treatment with this compound of a number of patients infected with penicillinresistant staphylococci'in this hospital.","PeriodicalId":109465,"journal":{"name":"Red Book Atlas of Pediatric Infectious Diseases","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Staphylococcal Infections\",\"authors\":\"---WITH Methicillin, J. W. Harding\",\"doi\":\"10.1542/9781581107951-ch123\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"MrrHICILLIN (sodium 6-[2,6 dimethoxybenzamido] penicillinate .monohydrate) has been the first compound of major importance resulting from the isolation of pure 6-amino penicillanic acid by Batchelor, Doyle, Nayler and Rolinson (1959). This new penicillin compound is of great therapeutic importance on account of several valuable properties which it, possesses. It is bactericidal (Knox, I960), virtually non-toxic (Brown and Acred, 1960), is unaffected by staphylococcal penicillinase (Knox, I960; Rolinson, Stevens, Batchelor, Wood and Chain, i960) and is effective against all isolated strains of staphylococci in vitro (Thompson, Harding and Simon, I960). Furthermore, it is effective against staphylococci in vivo (Douthwaite and Trafford, I960; Stewart, Nixon, Coles, Kesson, Lawson, Thomas,. Mishra, Mitchell, Semmens and: Wade, i960). Most of these findings have been confirmed by workers in Canada (Branch, Rodger, Lee'and'Power, I966). We have had the opportunit of observing the results of treatment with this compound of a number of patients infected with penicillinresistant staphylococci'in this hospital.\",\"PeriodicalId\":109465,\"journal\":{\"name\":\"Red Book Atlas of Pediatric Infectious Diseases\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Red Book Atlas of Pediatric Infectious Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1542/9781581107951-ch123\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Red Book Atlas of Pediatric Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1542/9781581107951-ch123","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
MrrHICILLIN(6-[2,6二甲氧基苄胺]一水合青霉酸钠)是Batchelor, Doyle, Nayler和rollinson(1959)从纯6-氨基青霉酸中分离出来的第一个重要化合物。由于这种新的青霉素化合物具有几种有价值的性质,它具有重要的治疗意义。它具有杀菌作用(Knox, 1960),几乎无毒(Brown和Acred, 1960),不受葡萄球菌青霉素酶的影响(Knox, 1960;Rolinson, Stevens, Batchelor, Wood and Chain, 1960),并且对所有葡萄球菌的体外分离菌株都有效(Thompson, Harding和Simon, 1960)。此外,它在体内对葡萄球菌有效(Douthwaite and Trafford, 1960;斯图尔特,尼克松,科尔斯,凯森,劳森,托马斯。米什拉,米切尔,塞门斯和:韦德,1960)。这些发现大部分已被加拿大的工人证实(Branch, Rodger, Lee'and'Power, 1966)。我们有机会在这家医院观察了一些感染青霉素耐药葡萄球菌的患者使用这种化合物治疗的结果。
MrrHICILLIN (sodium 6-[2,6 dimethoxybenzamido] penicillinate .monohydrate) has been the first compound of major importance resulting from the isolation of pure 6-amino penicillanic acid by Batchelor, Doyle, Nayler and Rolinson (1959). This new penicillin compound is of great therapeutic importance on account of several valuable properties which it, possesses. It is bactericidal (Knox, I960), virtually non-toxic (Brown and Acred, 1960), is unaffected by staphylococcal penicillinase (Knox, I960; Rolinson, Stevens, Batchelor, Wood and Chain, i960) and is effective against all isolated strains of staphylococci in vitro (Thompson, Harding and Simon, I960). Furthermore, it is effective against staphylococci in vivo (Douthwaite and Trafford, I960; Stewart, Nixon, Coles, Kesson, Lawson, Thomas,. Mishra, Mitchell, Semmens and: Wade, i960). Most of these findings have been confirmed by workers in Canada (Branch, Rodger, Lee'and'Power, I966). We have had the opportunit of observing the results of treatment with this compound of a number of patients infected with penicillinresistant staphylococci'in this hospital.