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Biomedical subjects

J Pálinkás

Publications and source records attributed to J Pálinkás.

16 recordsLinked to original sources

Structure and drug release of lamellar liquid crystals containing glycerol.

Lamellar lyotropic liquid crystalline (LLC) systems are thermodynamically stable, optically isotropic systems, which are formed with low energy input. New possibilities for the development of controlled drug delivery systems are inherent in these systems due to their stability and special skin-similarly structure. The present aim was to formulate multicomponent LLC systems with a relatively low surfactant content, composed of materials official in the European Pharmacopoeia 4th. Polarizing light microscopic examination of the samples was carried out, together with TEM observation of replicas produced by freeze-fractured technique for the purpose of demonstrating the presence of lamellar LC domains. Our LLC samples contained: Brij 96 (poly-oxyethylene-10-oleyl ether) with water, liquid petrolatum (LP) and glycerol in a given concentration range. The interlamellar repeated distance (d(L)) confirming the existence of a regular structure was determined by means of X-ray diffraction. The d(L) and G'values of the samples changed according to a maximum curve with increasing glycerol concentration up to 40% (w/w). A prolonged drug release was observed in case of the very water-soluble ephedrine hydrochloride and the same phenomena was observed in the case of tenoxicam, which is practically insoluble in water.

Delayed-Action Preparations↗

The effect of liquid crystalline structure on chlorhexidine diacetate release.

The aim of this study was to examine different liquid crystalline preparations containing chlorhexidine diacetate and to find connection between their structure and the kinetic of drug release. Nonionic surfactant, Synperonic A7 (PEG(7)-C(13-15)) was selected for the preparation of the examined liquid crystalline systems. Mixtures of different ratios of Synperonic A7 and water were produced. By increasing the water content of the systems, lamellar and hexagonal liquid crystal structures were observed. For the analysis of the prepared liquid crystalline systems polarising microscopy, rheology study, differential scanning calorimetry and dynamic swelling tests were carried out. The chlorhexidine diacetate release was examined by Franz-type vertical diffusion cell apparatus. The chlorhexidine diacetate release from hexagonal liquid crystalline preparations was characterised by zero-order release kinetics, while the drug release from lamellar liquid crystalline systems was described by anomalous (non-Fickian) transport. The results indicate that the drug release kinetic is strongly dependent on the liquid crystalline structure.

Anti-Infective Agents, Local↗

[Positron emission tomography: foundations and applications].

Positron emission tomography (PET) is a non-invasive biomedical imaging technique whereby the distribution of biological tracer molecules, labelled by positron emitting isotopes, in the living body can be studied quantitatively. As theoretically an metabolically active molecule can be labelled, the technique is applicable to the measurement of any biochemical or physiological process in proper anatomical context. The introduction of PET has revolutionised the exploration of normal physiological functions. With the help of technique, among others, anatomical structures underlying mental functions can be localised in the human brain, the receptor architecture of the nervous system can be mapped, or the kinetics of pharmacons can be properly measured and modelled. In the clinical practice, PET has proven to be a uniquely useful diagnostic technique in neurology, psychiatry, cardiology, and oncology in establishing primary diagnosis and differential diagnosis, designing therapeutic interventions as well as assessing their efficacy. Hungary's and Central European region's first PET center has been established at the University Medical School in Debrecen.

Humans↗