Zobrazeno 1 - 10
of 217
pro vyhledávání: '"R. Cadorniga"'
Publikováno v:
Chirality. 11:611-615
Crystalline characteristics of racemic, pure R and S enantiomers and physical mixtures of Ketoprofen (KET) have been studied by DSC and X-ray diffractometry. Aqueous solubilities were 182.6 +/- 9.1 microg/ml for racemic KET, 259.6 +/- 6.6 microg/ml f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17470052c411f4ba49f5842b417e0b06
https://doi.org/10.1002/(sici)1520-636x(1999)11:8<611::aid-chir1>3.0.co
https://doi.org/10.1002/(sici)1520-636x(1999)11:8<611::aid-chir1>3.0.co
Publikováno v:
International Journal of Pharmaceutics. 156:181-187
To improve the oral bioavailability of albendazole, a poorly water-soluble drug, a new liquid formulation was investigated in mice. The liquid formulation studied was a solvent system of Transcutol® (40% w/w) in 1.2 pH buffer. A significant (p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49e9a5a93609c656ca96dff48a7627c5
https://doi.org/10.1016/s0378-5173(97)00204-4
https://doi.org/10.1016/s0378-5173(97)00204-4
Publikováno v:
International Journal of Pharmaceutics. 140:247-250
In this study, solid dispersion systems of the sparingly water soluble drug, albendazole (ABZ), were mixed with varying concentrations of polyvinylpyrrolidone (PVP K 12) in an attempt to improve the solubility and dissolution rate of ABZ. Physical ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbf88664bda90001fb34b5542e46edfb
https://doi.org/10.1016/0378-5173(96)04586-3
https://doi.org/10.1016/0378-5173(96)04586-3
Publikováno v:
International Journal of Pharmaceutics. 140:45-50
The solubility of albendazole, a poorly water-soluble drug was evaluated. The effect of cosolvents and pH on the aqueous solubility of albendazole are described here. Albendazole aqueous solubility was tested over the pH range of 1.2–7.5. Albendazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb515413627bf9b03e5c3209c4ee8230
https://doi.org/10.1016/0378-5173(96)04545-0
https://doi.org/10.1016/0378-5173(96)04545-0
Publikováno v:
International Journal of Pharmaceutics. 133:65-70
The relationship between in vitro dissolution and in vivo characteristics of acetylsalicylic acid (ASA) from six different types of sustained-release tablet was evaluated. ASA pellets coated by Eudragit RS or L were tableted with different proportion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d82ed46fb4a7a32f180b499bc2badca3
https://doi.org/10.1016/0378-5173(95)04411-6
https://doi.org/10.1016/0378-5173(95)04411-6
Autor:
Susana Torrado, F. J. López-rodríguez, C. Escamilla, Juan J. Torrado, R. Cadorniga, Larry L. Augsburger
Publikováno v:
Drug Development and Industrial Pharmacy. 19:1369-1377
An instrumented tablet press was used to study the compression behavior of different acetylsalicylic acid (AAS) formulations. Formulations of AAS crystals and uncoated AAS pellets have compression behavior similar to formulations of AAS pellets coate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2712449fc3ea5bb0bf0b79d5c59a3cd0
https://doi.org/10.3109/03639049309047180
https://doi.org/10.3109/03639049309047180
Publikováno v:
International Journal of Pharmaceutics. 86:147-152
Egg albumin microspheres containing vitamin A (15.7 ± 0.8% w/w; size 222 ± 25 μm) were produced by an emulsion method. These particles were used to prepare O/W creams of vitamin A. The in vitro and in vivo drug release of a microencapsulated vitam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73979a8244857ac8c2c3821ba13c6ce2
https://doi.org/10.1016/0378-5173(92)90191-4
https://doi.org/10.1016/0378-5173(92)90191-4
Publikováno v:
International Journal of Pharmaceutics. 77:193-198
Thermomicroscopy and DSC were employed to study ciprofloxacin/PEG 6000 binary systems in the form of solid dispersions and physical mixtures. The dissolution processes of ciprofloxacin from the binary systems and pure ciprofloxacin were also studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96f0434d3885fd11d2767fcf1c08b130
https://doi.org/10.1016/0378-5173(91)90317-h
https://doi.org/10.1016/0378-5173(91)90317-h
Publikováno v:
Drug Development and Industrial Pharmacy. 17:1305-1323
Microaggregated egg albumin particles containing paracetamol were prepared by a new microencapsulation method. Thus, paracetamol was suspended into an ovalbumin solution and then heated to coagulate the protein. The paracetamol crystals were entrappe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::257548cb0a7b30feff16d888532e169b
https://doi.org/10.3109/03639049109057299
https://doi.org/10.3109/03639049109057299
Publikováno v:
Journal of Microencapsulation. 7:463-470
Different egg albumin microsphere systems for oral administration of paracetamol were prepared by the emulsion and capillary extrusion methods. The size of the microspheres depended on the method used to produce the microcapsules and also the size of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11ba4d7a11283f807d76ecde276e4bad
https://doi.org/10.3109/02652049009040468
https://doi.org/10.3109/02652049009040468