화학공학소재연구정보센터

Przemysl Chemiczny

Przemysl Chemiczny, Vol.91, No.3 Entire volume, number list
ISSN: 0033-2496 (Print) 

In this Issue (28 articles)

242 - 243 60 Years of the Pharmaceutical Institute in Warsaw
Szyprowski AJ
245 - 251 Interview with Mr Janusz Obukowicz, director of the Pharmaceutical Institute of Warsaw
Szyprowski AJ, Obukowicz J
253 - 254 Study on the drug at the Institute of Pharmacy - introduction to a series of articles from the Pharmaceutical Institute
Kutner A
255 - 262 Innovation in drug development
Szelejewski W, Kutner A
264 - 270 Synthesis of amino acid derivatives of 6H-indolo[2,3-b]quinoline
Sidoryk K, Szczepek WJ, Kaczmarek L
272 - 275 Use of NMR technique to study process and the reaction products in synthesis of Exemestane
Kubiszewski M, Cybulski M, Kaczmarek L
276 - 281 Application of Suzuki reaction for manufacturing an intermediate in synthesis of the pharmaceutical ingredient lapatinib. Use of palladium catalyst without any phosphine ligands
Luniewski W, Krzeczynski P, Klos K, Trzcinska K
283 - 287 Novel strategy of synthesis of paricalcitol
Chodynski M, Dzikowska J, Gutowska R, Krajewski K, Kubiszewski M, Krupa M, Pietraszek A, Winiarski J, Kutner A
289 - 294 Ezetimibe, the drug for lowering the cholesterol level. The development of process for the preparation of a product with high stereochemical purity
Bankowski K, Sidoryk K, Flip K, Chmielowiec U
296 - 301 Advantages and disadvantages syntheses of loteprednol etabonate
Bodziachowska-Panfil M, Groman A, Kubiszewski M, Stopa A, Witkowska AB, Szczepek WJ
303 - 305 Efficient synthesis of nepafenac via modified Gassman reaction
Cybulski M, Formela A, Mucha M, Klos K
307 - 312 Exploration of reaction parameter space of brinzolamide synthesis
Kaczmarek L, Les A, Mucha L, Badowska-Roslonek K, Rosa A
314 - 318 Application of accelerator mass spectrometry (AMS) in early drug development. Part 1. Background and procedures
Lipner G, Grynkiewicz G
320 - 325 Application of accelerator mass spectrometry (AMS) in early drug development. Part 2. Synthesis and certification of C-14-labelled compounds
Lipner G, Luniewski W, Maruszak W, Grynkiewicz G
327 - 331 Measurements of paricle size and shape distribution. Essential elements of modern pharmaceutical analysis
Maruszak W
333 - 341 Analysis of pharmaceutical hydrates
Laszcz M, Witkowska AB, Trzcinska K, Kubiszewski M, Kuziak K
343 - 350 Use of mass spectrometry for identification of impurities in pharmaceutical substances and products
Giller T, Stolarczyk EU, Eksanow K, Groman A, Luniewski W
352 - 357 Use of gas chromatography for impurities analysis in pharmaceutical products
Stolarczyk EU, Groman A, Eksanow K
358 - 364 Determination of the enantiomeric purity and the in-process control by HPLC in the technology for production of optically active ingredients on an example of tolterodine tartrate
Puchalska M, Zagrodzka J, Czerniec-Michalik E, Zezula M, Chmiel J, Luniewski W, Zagrodzki B
365 - 371 High performance electrophoretic separations in pharmaceutical analysis
Czerniec-Michalik E, Maruszak W, Puchalska M
372 - 375 Manufacturing of modified release tablets
Gluch M, Huszcza G
376 - 380 Semisolid formulations of the drugs. Methods for studying the pharmaceutical availability
Pesta-Dynda E, Zielinska A, Zagrodzka J, Dworzynska A
381 - 386 Selectivity control in pharmacokinetic studies
Musijowski J, Gilant E, Rudzki PJ
387 - 389 The importance of polymorphism in pharmaceutical research
Laszcz M, Trzcinska K, Bodziachowska-Panfil M, Maruszak W
389 - 392 Validation of bioanalytical methods. The new guideline of the European Medicines Agency
Rudzki PJ, Szlagowska A, Kaza M
392 - 395 Validation of the manufacturing process of pharmaceutical substances. Help in hindrance?
Zagrodzki B
396 - 398 Eye drops. Requirements for product and manufacturing process characteristics
Zdeb A, Melissa M
399 - 403 From Beilstein to Reaxys
Gryta A, Bajda A