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 |