Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Judit, Dredán"'
Autor:
Judit, Turmezei, Eszter, Jávorszky, Eszter, Szabó, Judit, Dredán, Barnabás, Kállai-Szabó, Romána, Zelkó
Publikováno v:
Acta poloniae pharmaceutica. 72(5)
Physical, chemical and microbiological stability of total parenteral nutrient (TPN) admixtures was studied as a function of storage time and temperature. Particle size analysis and zeta potential measurements were carried out to evaluate the possible
Publikováno v:
Acta pharmaceutica Hungarica. 81(4)
Surface active agents can be classified 60 years ago with the introduction of the HLB system. The characterization of emulgents allowed their common use in the practice. The objective of the review is to summarize the research in the field of surface
Publikováno v:
Acta pharmaceutica Hungarica. 77(2)
The aim of stability testing lies in its possibility of revealing all the effects that may influence the quality, efficacy and safety of a pharmaceutical preparation. The stability of a dosage form means that the release of the active ingredients rem
Autor:
Emese, Balogh, Nikolett, Kállai, Judit, Dredán, Miléna, Lengyel, Imre, Klebovich, István, Antal
Publikováno v:
Acta pharmaceutica Hungarica. 77(2)
The morphological characteristics of pellets are critical parameters, because of their physico-chemical features depend on the size, shape and surface geometric of the particles. To ensure the spherical shape and required particle of pharmaceutical p
Autor:
Judit, Balogh, Júlia, Bubenik, Judit, Dredán, Ferenc, Csempesz, Dorottya, Kiss, Romána, Zelkó
Publikováno v:
Journal of pharmacypharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques. 8(3)
The physical stability of two types of total parenteral nutrient (TPN) admixtures was studied as a function of storage time and temperature. One of them contained only structured triglycerides and the other exclusively long-chain triglycerides as lip
Publikováno v:
Acta pharmaceutica Hungarica. 73(3)
Since drug release from the dosage forms has priority to absorption from the gastrointestinal system, physico-chemical characterisation of pharmaceutical systems is essential during the development of an optimal formulation with high efficacy and qua
Publikováno v:
Macromolecular Symposia; Jun2006, Vol. 239 Issue 1, p105-113, 9p