42 research outputs found
Metabolic, productive and reproductive responses to postpartum short-term supplementation in primiparous beef cows
Desempenho reprodutivo de cabras alpinas tratadas com hCG cinco dias após o acasalamento
Inovulação de embriões bovinos recém-colhidos em receptoras tratadas com rbST no dia do estro
Toxic effects of different doses of cyclophosphamide on the reproductive parameters of male mice
The Relationship between Maternal and Fetal Effects following Maternal Organophosphate Exposure during Gestation in the Rat
Simulation evaluation of three models for correlated binary data with covariates specific to each binary observation
An Evaluation of the Developmental Toxicity of 2,4-Pentanedione in the Fischer 344 Rat by Vapour Exposure
Prolonged Drug Release from Gels, using Catanionic Mixtures
The use of catanionic drug-surfactant mixtures was proven to be an efficient novel method of obtaining prolonged drug release from gels. It was shown that various commonly used drug compounds are able to form catanionic mixtures together with oppositely charged surfactants. These mixtures exhibited interesting phase behaviour, where, among other structures, vesicles and large worm-like or branched micelles were found. The size of these aggregates makes them a potential means of prolonging the drug release from gels, as only monomer drugs in equilibrium with larger aggregates were readily able to diffuse through the gel. When the diffusion coefficient for drug release from the formulation based upon a catanionic mixture was compared to that obtained for the drug substance and gel alone, the coefficient was some 10 to 100 times smaller. The effects of changes in the pH and ionic strength on the catanionic aggregates was also investigated, and this method of prolonging the release was found to be quite resilient to variations in both. Although the phase behaviour was somewhat affected, large micelles and vesicles were still readily found. The drug release was significantly prolonged even under physiological conditions, that is, at a pH of 7.4 and an osmolality corresponding to 0.9% NaCl. Surfactants of low irritancy, capric and lauric acid, may successfully be used instead of the more traditional surfactants, such as sodium lauryl sulfate (SDS), and prolonged release can still be obtained with ease. Some attempts to deduce the release mechanism from the proposed systems have also been made using transient current measurements, dielectric spectroscopy, and modelling of the release using the regular solution theory. In these studies, the previous assumptions made concerning the mechanism responsible for the release were confirmed to a large extent. Only small amounts of the drug existed in monomer form, and most seemed to form large catanionic aggregates with the oppositely charged surfactant