Zobrazeno 1 - 10
of 11
pro vyhledávání: '"F A, Chrzanowski"'
Autor:
F. A. Chrzanowski, Kaleem Ahmad
Publikováno v:
Drug Development and Industrial Pharmacy. 43:421-431
Salts of linogliride with reduced solubilities were prepared and evaluated as potential candidates for extended-release oral dosage forms. A once-daily dose of 300-800 mg was intended. Seven acids were selected: p-acetamidobenzoic, benzoic, p-hydroxy
Autor:
F. A. Chrzanowski
Publikováno v:
AAPS PharmSciTech. 9:646-650
Two numerical methods, Decision Analysis (DA) and Potential Problem Analysis (PPA) are presented as alternative selection methods to the logical method presented in Part I. In DA properties are weighted and outcomes are scored. The weighted scores fo
Autor:
F. A. Chrzanowski
Publikováno v:
AAPS PharmSciTech. 9:635-638
The physical-chemical properties of interest for controlled release (CR) dosage form development presented are based on the author's experience. Part I addresses selection of the final form based on a logical progression of physical-chemical properti
Autor:
F. A. Chrzanowski
Publikováno v:
AAPS PharmSciTech. 9(2)
Practical examples of preformulation support of the form selected for formulation development are provided using several drug substances (DSs). The examples include determination of the solubilities vs. pH particularly for the range pH 1 to 8 because
Publikováno v:
The Journal of burn carerehabilitation. 21(1 Pt 1)
The cellular mechanisms by which topical cyclosporine A (tCsA) induces site-specific immunosuppression were investigated. Experiments were designed to elucidate how cyclosporine A (CsA) suppresses activated immunocytes in animals that are undergoing
Publikováno v:
Biochemical Medicine. 11:26-31
A method is presented for the analysis of theophylline in human serum. The method is specific with no interference from theophylline metabolites, ephedrine, hydrocortisone, or caffeine and their metabolites. It is sensitive to approximately 1 μg/ml
Autor:
F. A. Chrzanowski, J. E. Mills, C. Y. Ko, V. Paragamian, Walkling Wd, J. N. Plampin, R. S. Egan
Publikováno v:
Drug Development and Industrial Pharmacy. 10:241-258
Fenoctimine sulfate was demonstrated to exist in two distinct crystalline forms, i.e., form A (low melting, 0.5 mole water of hydration), and form B (high melting, anhydrous). These forms can exist separately, in crystalline mixtures with each other,
Publikováno v:
Journal of parenteral science and technology : a publication of the Parenteral Drug Association. 39(1)
Publikováno v:
Journal of parenteral science and technology : a publication of the Parenteral Drug Association. 36(5)
Publikováno v:
Chemischer Informationsdienst. 16
The pKa values for butaclamol (1), 1,2,3,5,6,10b beta-hexahydro-6 alpha-phenylpyrrolo[2,1-alpha]isoquinoline (2, McN-4612-Y), and 2-tert-butyl-1,3,4,6,7,11b beta-hexahydro-7 beta-phenyl-2H-benzo[alpha]quinolizin-2 alpha-ol (3, McN-4171) were determin