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伊康唑治疗皮肤癣菌病疗效观察
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作者 廖万清 李竹青 +1 位作者 蔡剑飞 邵经政 《中国人兽共患病杂志》 CSCD 北大核心 1991年第2期57-58,共2页
伊康唑是一种新的广谱。强效口服抗真菌药。我们应用伊康唑胶囊,以每天100mg的剂量治疗皮肤癣菌病患者120例,随访观察113例,分为A(30天)及B(15天)两组,结果两均有明显效果,但对手足癣的治疗,A组的治愈率明显高于B组,两者经统计学处理P&l... 伊康唑是一种新的广谱。强效口服抗真菌药。我们应用伊康唑胶囊,以每天100mg的剂量治疗皮肤癣菌病患者120例,随访观察113例,分为A(30天)及B(15天)两组,结果两均有明显效果,但对手足癣的治疗,A组的治愈率明显高于B组,两者经统计学处理P<0.001,有非常显著的差异,说明对手、足癣的治疗以30天为一疗程较为合适;体、股癣的治愈率B组为81.25%,有效率为100%。可见对体、股癣的治疗一般15天可治愈,对少数较广泛病例继续治疗1~2周亦可达到治愈目的。 伊康唑(Itracouazole,R51211)是比利时杨森公司研制的一种新的口服抗真菌药。从1982年以来已于欧洲、美洲、非洲、澳洲等27个国家应用40万胶囊(50mg)进行临床验证,表明对浅部真菌病及系统性真菌病均有明显效果,但在我国尚无临床应用的报告,我们于1987年12月~1988年6月应用2700胶囊(100mg)对120例皮肤癣菌病患者进行临床治疗观察,获得满意效果,兹报告如下。 展开更多
关键词 皮肤癣菌病 伊康唑 疗效
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三种唑类抗真菌药——酮康唑、伊康唑和氟康唑 被引量:1
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作者 虞瑞尧 《药学情报通讯》 1991年第2期10-13,共4页
随着医学的发展临床上大量应用广谱抗生素、皮质类固醇激素;恶性肿瘤病人大量应用抗肿瘤药;脏器移植病人、自家免疫性疾病病人大量应用免疫抑制剂以及世界上出现了获得性免疫缺陷综合症—艾滋病使真菌病的发病率显著地增长,由于深部真... 随着医学的发展临床上大量应用广谱抗生素、皮质类固醇激素;恶性肿瘤病人大量应用抗肿瘤药;脏器移植病人、自家免疫性疾病病人大量应用免疫抑制剂以及世界上出现了获得性免疫缺陷综合症—艾滋病使真菌病的发病率显著地增长,由于深部真菌病发病率的剧增。 展开更多
关键词 抗真菌药 酮康 伊康唑 氟康
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伊康唑与酮康唑治疗甲癣临床疗效比较
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作者 虞瑞尧 《解放军医学杂志》 CAS CSCD 北大核心 1990年第5期379-381,共3页
伊康唑(Itraconzole)是唑类第3代三唑类最新口服广谱抗真菌药。由比利时Janssen药厂生产。作者于1988年4月至9月用口服伊康唑治疗11例甲癣,采用随机酮康唑疗效对照,初步证明伊康唑治疗甲癣的疗效优于酮康唑。现报告如下。
关键词 伊康唑 酮康 甲癣 疗效
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伊康唑在真菌感染的临床应用
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作者 滕传远 顾有守 《国外医学(皮肤性病学分册)》 北大核心 1991年第4期198-202,共5页
本文综合了J Am Acad Dermatol 1990,23(3)上的部分文章,报道了一种新的口服抗真菌药伊康唑(itraconazole,ICZ)治疗花斑癣,表皮癣菌病,头癣,口腔、阴道念珠菌病,暗色丝孢霉病,孢子丝菌病,隐球菌病和曲霉菌病的临床疗效.结果表明:ICZ与... 本文综合了J Am Acad Dermatol 1990,23(3)上的部分文章,报道了一种新的口服抗真菌药伊康唑(itraconazole,ICZ)治疗花斑癣,表皮癣菌病,头癣,口腔、阴道念珠菌病,暗色丝孢霉病,孢子丝菌病,隐球菌病和曲霉菌病的临床疗效.结果表明:ICZ与其它抗真菌制剂相比具有疗效高、毒副作用少、口服方便、对角蛋白亲和力高,停药后继续有效等特点,值得在临床上推广应用. 展开更多
关键词 伊康唑 抗真菌感染
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伊康唑在深部真菌病的临床应用
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作者 虞瑞尧 《北京医学》 CAS 北大核心 1989年第2期101-104,共4页
由于临床上广泛的应用抗生素免疫抑制剂,皮质类固醇激素以及抗肿瘤药等使浅部真菌病,特别是致命性条件致病菌引起的深部真菌病发病率明显增高。为了挽救病人的生命,人们积极寻找各种新的高效抗真菌药。
关键词 伊康唑 真菌病 药理 杀真菌药
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伊康唑治疗皮肤癣菌病疗效观察
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作者 廖万清 李竹青 《临床皮肤科杂志》 CAS CSCD 北大核心 1989年第5期243-245,共3页
关键词 伊康唑 皮肤 真菌病
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治疗动物真菌性皮肤病的新药——伊康唑
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作者 程远国 《中国兽医科技》 CSCD 1991年第12期39-40,共2页
50年代,二性霉素B(amphotericin B)和灰黄霉素(griseofulvin)的发现,为治疗全身性霉菌病和真菌性皮肤疾病开创了一个新的里程碑。在80年代初又开发了第二代咪唑类全身抗真菌药——酮康唑(ketoconazole)。酮康唑是一种高效的治疗许多种... 50年代,二性霉素B(amphotericin B)和灰黄霉素(griseofulvin)的发现,为治疗全身性霉菌病和真菌性皮肤疾病开创了一个新的里程碑。在80年代初又开发了第二代咪唑类全身抗真菌药——酮康唑(ketoconazole)。酮康唑是一种高效的治疗许多种全身性霉菌病和真菌性皮肤病的药物。与二性霉素B相比,它的优点是能口服且副作用较小。随后,通过修饰吡咯环,产生了第三代氮杂茂系全身性抗真菌药——伊康唑(itracona-zole)。与酮康唑相比,伊康唑具有抗菌谱广、有效浓度低、副作用更小等优点。咪唑类药物与氮杂茂类药物的结构的不同点在于吡咯环上氮原子的数目不同。 展开更多
关键词 动物 真菌性 皮肤病 药物 伊康唑
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伊曲康唑和氟康唑治疗甲真菌病疗效及安全性观察 被引量:4
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作者 黄亚华 《皮肤病与性病》 2006年第2期8-9,共2页
目的研究伊曲康唑和氟康唑治疗甲真菌病的疗效和安全性。方法采用随机、双盲对照的临床研究方法,对98例甲真菌病患者进行随机分组,治疗组给予斯皮仁诺口服,对照组采用氟康唑口服,观察治疗3m和6m的临床疗效和不良反应。结果服药后3m、6m... 目的研究伊曲康唑和氟康唑治疗甲真菌病的疗效和安全性。方法采用随机、双盲对照的临床研究方法,对98例甲真菌病患者进行随机分组,治疗组给予斯皮仁诺口服,对照组采用氟康唑口服,观察治疗3m和6m的临床疗效和不良反应。结果服药后3m、6m治疗组和对照组的有效率分别为77.5%和75.5%,75.5%和85.4%试验中没有发生严重不良反应。结论斯皮仁诺和氟康唑治疗甲真菌病疗效显著,差异无显著性。 展开更多
关键词 伊康唑 氟康 甲真菌病 治疗
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孢子丝菌病的新老治疗药物
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作者 李军 《传染病信息》 1996年第1期31-31,共1页
治疗孢子丝菌病的老药SSKI和两性霉素B已经被伊康唑大量取代。SSKI对于皮淋巴孢子丝菌病很有效,但给药困难并常产生副作用,而伊康唑对该病的有效率为90%以上。骨关节孢子丝菌病患者极少有系统性症状,采用延长疗程伊康唑治疗是很有效的... 治疗孢子丝菌病的老药SSKI和两性霉素B已经被伊康唑大量取代。SSKI对于皮淋巴孢子丝菌病很有效,但给药困难并常产生副作用,而伊康唑对该病的有效率为90%以上。骨关节孢子丝菌病患者极少有系统性症状,采用延长疗程伊康唑治疗是很有效的,而静脉内两性霉素B会引起副作用。 展开更多
关键词 孢子丝菌病 两性霉素 副作用 伊康唑 有效率 长疗程 骨关节 系统性 治疗药物 静脉内
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Isolation,identification,and antifungal susceptibility test for Kodamaea ohmeri:a case report on endocarditis 被引量:2
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作者 Qin Yanghua Wang Weiwei +2 位作者 Liu Yang Xiao Jian Shen Qian 《Journal of Medical Colleges of PLA(China)》 CAS 2010年第4期252-256,共5页
A 43-year-old man with a history of rheumatoid heart disease developed endocarditis.Blood culture showed endocarditis was caused by Kodamaea ohmeri and the susceptibility test showed the yeast species were susceptible... A 43-year-old man with a history of rheumatoid heart disease developed endocarditis.Blood culture showed endocarditis was caused by Kodamaea ohmeri and the susceptibility test showed the yeast species were susceptible to itraconazole,amphotericin B,and voriconazole,but susceptible-dose dependent to fluconazole,and resistant to 5-flucytosine.Treated with surgery and anti-fungi agents,the patient recovered from endocarditis.This is the first case of K.ohmeri fungemia found in Chinese from mainland.More and more evidence indicate that K.ohmeri is an important opportunistic pathogen for human beings. 展开更多
关键词 ENDOCARDITIS Kodamaea Ohmeri FUNGEMIA
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Expression Variability of Carbohydrates at the Cell Wall Surface of Aspergillus Species and in Vitro Susceptibility to Amphotericin B, Voriconazole and Itraconazole
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作者 André Ferraz Goiana Leal Eduardo Isidoro Cameiro Beltrao +1 位作者 Almir Goncalves Wanderley Rejane Pereira Neves 《Journal of Life Sciences》 2014年第4期358-363,共6页
This study evaluated the expression of N-acetyl-D-glucosamine, L-fucose, D-galactose and glucose/mannose on the cell wall surface of Aspergillus species using lectins and the in vitro antifungal activity of AMB (amph... This study evaluated the expression of N-acetyl-D-glucosamine, L-fucose, D-galactose and glucose/mannose on the cell wall surface of Aspergillus species using lectins and the in vitro antifungal activity of AMB (amphotericin B), VOR (voriconazole) and ITC (itraconazole). Con A (Concanavalin A), WGA (wheat germ agglutinin), UEA-I (Ulex europeus agglutinin I) and PNA (peanut agglutinin), all conjugated with horseradish peroxidase, were used. For the susceptibility tests, sterilized fiat-bottomed 96-well microtitre plates were used and the procedures were followed of the Clinical and Laboratory Standard Institute. The inoculum was added to the wells with the tested drugs and the plates were incubated at 25 ℃ for 48 h before reading the results to determine the MIC (minimal inhibitory concentration) of AMB, VOR and ITC. All Aspergillus strains showed low MIC for AMB (0.031-1 μg/mL) and ITC (0.031-0.25μg/mL). However, the isolates were less susceptible to VOR, for which the MIC ranged from 4 to 16 μg/mL. The results of this study indicate that the expression of N-acetyl-D-glucosamine and glucose/mannose on the cell wall surface of the Aspergillus species evaluated showed greater stability of expression in the fungal growth both in vitro and in parasitism. 展开更多
关键词 Cell wall carbohydrates LECTINS ASPERGILLUS antifungal activity.
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Clinical efficacy and safety of intravenous itraconazole in patients with invasive fungal infections in emergency intensive care unit 被引量:1
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作者 罗晓 邵宏 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2015年第10期678-682,共5页
This study aimed to analyze the clinical efficacy and safety of itraconazole. We investigated 68 patients with invasive fungal infections(IFI) in emergency intensive care unit(EICU). A retrospective analysis was p... This study aimed to analyze the clinical efficacy and safety of itraconazole. We investigated 68 patients with invasive fungal infections(IFI) in emergency intensive care unit(EICU). A retrospective analysis was performed in patients with IFI who were treated in the authors' institution, a grade III first class hospital in Beijing, China, between Feb. 2013 and Feb. 2015. The age of patients ranged from 35 to 90 years old with the mean age of(75.1±11.1) years old. The study population comprised 36 male and 32 female patients. Total response rate was 60.3%. The response rates in definitive diagnosis, clinical diagnosis and presumed diagnosis were 33.3%, 59.5% and 65.2%, respectively(P〈0.05). The empirical treatment should be provided for patients with presumed diagnosis as earlier as possible. Eleven(16.2%) cases had adverse drug event(ADE) during treatment. The main signs were hepatic functional impairment and hypokalemia of ADE. The clinical efficacy and safety of intravenous itraconazole were precisely assessed. To reduce the adverse drug reaction(ADR), hepatic and renal function and other biochemical criterion should be closely monitored. 展开更多
关键词 ITRACONAZOLE Invasive fungal infections EFFICACY SAFETY Adverse drug reaction
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Enhanced release of the poorly soluble drug itraconazole loaded in ordered mesoporous silica 被引量:3
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作者 Xiao Liu Shunai Che 《Science China Chemistry》 SCIE EI CAS CSCD 2015年第3期400-410,共11页
It is known that the energy of the amorphous state of itraconazole loaded in ordered mesoporous materials is high relative to that of the crystalline state and is responsible for enhanced solubility and dissolution ra... It is known that the energy of the amorphous state of itraconazole loaded in ordered mesoporous materials is high relative to that of the crystalline state and is responsible for enhanced solubility and dissolution rate. We investigated the effects of particle size(0.7–5μm), mesostructure(2D p6 mm, cubic Ia-3d and cubic Fm-3m) and pore size(2.2–15.4 nm) of mesoporous silicas on the release performance of itraconazole. Results indicated that the release performance was not influenced by the particle sizes tested here, that the release performance increased with increasing pore diameter due to the lower probability of drug molecules colliding to recrystallize in large pores, and that the release performance was decreased in the cage-type pore structure(Fm-3m) compared to that in the cylindrical pore structures(p6mm and Ia-3d) because of the small entrance to the cagelike pores that retards the drug release. 展开更多
关键词 ITRACONAZOLE poorly soluble enhanced release mesoporous silica
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