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[Polyvalent antibiotics in ambulatory practice]. 多价抗生素在门诊的应用
Pub Date : 1993-08-01
A Blahútová, J Majtás

The present paper analyzes the consumption of antibiotics from the viewpoint of the diagnosis, specialization of the prescribing physician, and the age and sex of the out-patients. The analysis concerns the prescription within two months in a pharmacy at a policlinic. The results are presented according to the frequency of diagnosis, polyvalence of the antibiotics and the specialization of the prescribing physician.

从抗菌药物的诊断情况、处方医师的专业程度、门诊患者的年龄和性别等方面分析抗菌药物的使用情况。该分析涉及两个月内在一家诊所药房开出的处方。结果是根据诊断频率,抗生素的多价和处方医师的专业化提出的。
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引用次数: 0
[The effect of calcium channel blockers in experimental myocardial infarct in rats]. [钙通道阻滞剂对实验性大鼠心肌梗死的影响]。
Pub Date : 1993-06-01
M Kuzelová, P Svec

The effect of the blockers of calcium channels on the development of myocardial ischaemia in rats with an occlusion of the coronary artery was examined. An occlusion of the coronary artery was carried out in rats anaesthetized with pentobarbital by tightening the ends of the ligature freely placed under the left coronary artery - ramus interventricularis seven days prior to ligation. The ischaemia-induced changes in the R-wave and ST-segment were recorded using ECG. The occlusion of the coronary artery produced arrhythmias, a significant elevation of the ST-segment and a slight increase in the heart rate. The blockers of calcium channels with different pharmacological properties - verapamil, nifedipine and diltiazem influenced the ischaemia-induced changes with different intensity. Nifedipine (0.02 mg.kg-1, i.v., 30 min prior to occlusion), verapamil (0.2 mg.kg-1, i.v., 10 mins prior to ischaemia), and diltiazem (0.3 mg.kg-1, i.v., 10 mins prior to ischemia) significantly reduced the increased elevation of the ST-segment. The highest effect on the above-mentioned model was shown by verapamil.

观察钙通道阻滞剂对冠状动脉闭塞大鼠心肌缺血发展的影响。用戊巴比妥麻醉大鼠,在结扎前7天将游离于左冠状动脉室支下的结扎末端收紧,对冠状动脉进行封堵。用心电图记录缺血后r波和st段的变化。冠状动脉闭塞导致心律失常,st段明显升高,心率轻微增加。不同药理学性质的钙通道阻滞剂维拉帕米、硝苯地平和地尔硫卓对缺血的影响程度不同。硝苯地平(0.02 mg。Kg-1,静脉注射,闭塞前30分钟),维拉帕米(0.2 mg。Kg-1,缺血前10分钟静脉注射),地尔硫卓(0.3 mg。kg-1, i.v.,缺血前10分钟)显著降低st段升高。维拉帕米对上述模型的影响最大。
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引用次数: 0
[The past and the future of the Czech Pharmaceutical Society]. [捷克药学会的过去和未来]。
Pub Date : 1993-06-01
J Solich

The main features of development of the Pharmaceutical Society as the only scientific, specialist and professional organization in the years 1950-1990 are surveyed. Increasing activities of the Society, extenvicity of the arranged actions and increasing interest of pharmacists to participate are stressed. Attention is drawn to the regular changes in the activity of the Society in the present time which result from the establishment and activity of the Pharmaceutical Chamber and the need to intensity the trade union movement. The Czech Pharmaceutical Society must continue tu guarantee the scientific standard of Czech pharmacy and appropriate foreign co-operation. Pharmacists working in the individual pharmaceutical sciences should assume positions in the management of the Society and its journal.

作为唯一的科学、专业和专业组织,药学会在1950-1990年间的主要发展特点进行了调查。强调社会活动的增加,安排行动的广泛性和药剂师参与的兴趣的增加。由于制药商会的建立和活动以及加强工会运动的需要,目前协会活动的定期变化引起了人们的注意。捷克药学会必须继续保证捷克药学的科学标准和适当的对外合作。在个别药学领域工作的药剂师应担任该学会及其期刊的管理职位。
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引用次数: 0
[Preparation of the first peroral antibiotic, Anginol-tablet]. [制备第一种经口抗生素,anginol片]。
Pub Date : 1993-06-01
L Novácek

In 1892-1896 Ivan Honl and Jaroslav Bukovský successfully tested pyocyaneoprotein (pyocynase), later used as the pharmaceutical preparation Tonsilan, in the therapy of crural ulcers and other bacterial diseases. In 1911 Honl prepared pyocyaneoprotein as the first antibiotic in the form of tablets called Anginol-tablets. Anginol was used in the Czech Lands in infectious diseases of the pharynx and larynx, particularly in tonsillitis, until the end of the Second World War. The present paper reports the procedure of compounding Anginol-tablets and their composition.

1892-1896年,Ivan Honl和Jaroslav Bukovský成功地测试了pyocyaneoprotein (pypyynase),后来被用作药物制剂扁桃体兰,用于治疗脚溃疡和其他细菌性疾病。1911年,Honl以片剂的形式制备了pyocyaneoprotein作为第一种抗生素,称为anginol片剂。直到第二次世界大战结束,在捷克土地上,Anginol被用于咽喉传染病,特别是扁桃体炎。本文报道了anginol片剂的合成工艺及组成。
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引用次数: 0
[Anti-inflammatory activity of aqua-(aryloxyacetate) copper complexes]. [水-(芳氧乙酸)铜配合物的抗炎活性]。
Pub Date : 1993-06-01
J Sokolík, S Sedlácková, E Racanská, M Blahová, P Svec

The anti-inflammatory activity of selected mononuclear Aqua(aryloxyacetato)copper(II) complexes with the composition [Cu(R-O-CH2COO)2(H2O)n].mH2O (R = phenyl, n = 3; m = 0), 4-chlorophenyl (2; 0), 4-chloro-2-methylphenyl (2; 0) and naphthyl (2; 2) was examined using rat paw dextrano edema. The antiphlogistic effects of the tested complexes were compared to those for corresponding aryloxyacetic acids and salicylic acid and its Cu(II) salt. The compounds were administered i.p. in a single effective dose of 10 mg/kg. The complexes with R = phenyl, 4-chlorophenyl and 4-chloro-2-methylphenyl exhibited a biological activity comparable to that of copper(II) salicylate tetrahydrate.

[Cu(R-O-CH2COO)2(H2O)n]单核水(芳基乙酸)铜(II)配合物的抗炎活性。mH2O (R =苯基,n = 3;M = 0), 4-氯苯基(2;0), 4-氯-2-甲基苯基(2;0)和萘基(2;2)采用大鼠足跖右旋糖酐水肿法检测。并与相应的芳氧乙酸、水杨酸及其Cu(II)盐的抗炎作用进行了比较。这些化合物以10mg /kg的单有效剂量单次给药。与R =苯基、4-氯苯基和4-氯-2-甲基苯基配合物的生物活性与四水水杨酸铜相当。
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引用次数: 0
[Antimicrobial activity of diazole-(N-salicylidene-L-alpha- alaninato)-copper complexes]. [二唑-(n -水杨基- l - α -丙氨酸)-铜配合物的抗菌活性]。
Pub Date : 1993-06-01
M Blahová, J Sokolík, S Sedlácková, E Burianová, D Mlynarcík

The antimicrobial activities of a group of copper(II) chelates with the composition [Cu(TSB)(L)] or [Cu(TSB)(L')]. (TSB = N-salicylidene-L-alpha-alaninate dianion, L = imidazole and its alkyl derivatives, L' = pyrazole and 3,5-dimethylpyrazole) were studied. Bis-diazole complexes with L' = pyrazole and 3,5-dimethylpyrazole were found to be the most active against S. aureus (MIC = 78 and 20 micrograms.cm-3), less effective against C. albicans (156 micrograms.cm-3), T. terrestre and M. gypseum (100 micrograms.cm-3). The observed biological properties of complexes are discussed in relation to their proposed structures.

[Cu(TSB)(L)]或[Cu(TSB)(L’)]组成的铜(II)螯合物的抗菌活性。(TSB = n -水杨基-L- α -丙氨酸钠离子,L =咪唑及其烷基衍生物,L' =吡唑和3,5-二甲基吡唑)。双二唑与L′=吡唑和3,5-二甲基吡唑配合物对金黄色葡萄球菌(MIC分别为78和20 μ g .cm-3)的抑制作用最强,对白色念珠菌(MIC分别为156 μ g .cm-3)、地霉和石膏分枝杆菌(MIC分别为100 μ g .cm-3)的抑制作用较弱。对观察到的配合物的生物学性质及其提出的结构进行了讨论。
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引用次数: 0
[Local anesthetics. VXII. Preparation and effectiveness of dibasic alkylesters of 2-, and 3-alkoxy-substituted phenylcarbamic acids]. (局部麻醉剂。VXII。2-和3-烷氧基取代苯氨基甲酸二碱式烷基酯的制备及其有效性。
Pub Date : 1993-06-01
J Csöllei, L Búciová, J Cizmárik, L Kopácová

In a series of 24 compounds of the type of dibasic alkylesters of 2-, and 3-alkoxy substituted phenylcarbamic acids, esterified alcohols 1-dipropylamino-3-pyrrolidino (piperidino or perhydroazepino)-2-propanol were used. It follows from the results of pharmacological evaluation that these compounds possess a high index of effectiveness in surface and infiltration anaesthesia compared to the standards of cocaine and procaine. Maximum effectiveness in surface anaesthesia was shown by [1-dipropylaminomethyl)-2- (piperidino)ethyl]-ester of 3-butoxyphenylcarbamic acids whose activity is as much as 180 times higher than that of cocaine. Maximum effectiveness in infiltration anaesthesia was shown by [1-dipropylaminomethyl)-2-(pyrrolidino)ethyl] ester of pentyloxyphenylcarbamic acid achieving an activity 250 times higher than that of standard procaine. The prepared compounds are more effective in the case of infiltration than in the case of surface anaesthesia.

在一系列24种2-和3-烷氧基取代苯氨基甲酸的二碱式烷基酯化合物中,使用了1-二丙基氨基-3-吡咯里迪诺(胡椒或过氢氮化氨基)-2-丙醇酯化醇。从药理学评价的结果可以看出,与可卡因和普鲁卡因的标准相比,这些化合物在表面和浸润麻醉方面具有很高的有效性指数。3-丁氧基苯基氨基甲酸的[1-二丙基氨基甲基]- 2-(胡椒碱)乙基]-酯在表面麻醉中显示出最大的效果,其活性比可卡因高180倍。[1-二丙基氨基甲基)-2-(吡咯烷酮)乙酯]戊氧基苯基氨基甲酸酯在浸润麻醉中的效果最好,其活性比标准普鲁卡因高250倍。所制备的化合物在浸润情况下比在表面麻醉情况下更有效。
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引用次数: 0
[Salvia officinalis l. I. Botanic characteristics, composition, use and cultivation]. [鼠尾草. 1 .植物特性、组成、利用与栽培]。
Pub Date : 1993-06-01
T Daniela

Salvia officinalis L. is an essential oil containing plant, which does not wildly grow in the territories of the Czech and Slovak Republics but it can be successfully cultivated. It is a perennial half-shrub, from which non-flowering herbaceous sprouts or leaves are collected for pharmaceutical purposes. After drying at a temperature not exceeding 35 degrees C they are the plant drugs Herba salviae or Folium salviae. In PhBs, Herba salviae is official. The drug contains mainly ethereal oil (1-2%), diterpenes, triterpenes and tannin. The pharmacopoeial criterion of quality is the content of essential oil, which is produced in an increased amount in the plant in warm summer months. Herba salviae and the extracts prepared from it are used as an antiseptic agent, an antiphlogistic agent, in the inflammations of the oral cavity and gingivitis and also as a stomachic and an antihydrotic agent. Its utilization in cosmetics and food industry is also of importance.

鼠尾草(Salvia officinalis L.)是一种含精油的植物,在捷克和斯洛伐克共和国境内没有广泛生长,但可以成功栽培。它是一种多年生半灌木,从中收集不开花的草本芽或叶子用于制药目的。在不超过35摄氏度的温度下干燥后,它们就是植物药物鼠尾草或鼠尾草叶。在ph中,草药是官方的。该药主要含有乙醚油(1-2%)、二萜、三萜和单宁。药典质量标准是精油的含量,在温暖的夏季,植物会产生更多的精油。鼠尾草及其提取物在口腔和牙龈炎的炎症中用作防腐剂、消炎剂,也用作胃药和抗水剂。它在化妆品和食品工业中的应用也很重要。
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引用次数: 0
[Problems at the hospital pharmacy in Kladno]. [克拉迪诺医院药房的问题]。
Pub Date : 1993-06-01
Z Cecrdlová
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引用次数: 0
[Problems in receiving and dispensing in Czech pharmacies]. 【捷克药房收货和配药存在的问题】。
Pub Date : 1993-04-01
M Pancová
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引用次数: 0
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Ceskoslovenska farmacie
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