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rok 2007 - Fakulta chemickej a potravinárskej technológie

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signal transducers are investigated. Application of the electrochemical biosensors allows also in vitro generation<br />

and testing of potential metabolites and an investigation of mechanisms of risk species effects. This leads to the<br />

methodical development of new screening tools based on biosensors and bioelectronic chips. Possibilities of the<br />

biopolymers protection against a structural damage by environmental carcinogens using natural and synthetic<br />

antioxidants are studied too.<br />

Project duration: from 01.01.2005 to 31.12.<strong>2007</strong><br />

F. APVV Project 20-015904: New Biomaterials and Biosensors for Clinical Use (Ján Labuda).<br />

Preparation of new biomaterials based on biopolymers and bioinorganic materials for clinical application as well<br />

as biosensors based on deoxyribonucleic acid (DNA) and lipoproteins (LDL) for direct use in clinical medicine.<br />

Project duration: from 01.01.2005 to 31.12.<strong>2007</strong><br />

G. APVT Project 27-010304: Development of Sensitive Indicator-free Method for the Detection<br />

of DNA Damage Caused by Lipid Oxidation Products Using DNA/SPE Biosensor (Adriana<br />

Ferancová).<br />

The project aims at the study and evaluation of the activity of selected oxidation products of lipids on the DNA<br />

using new detection system based on carbon nanotubes modified DNA biosensor. Specific primary<br />

(hydroperoxides) and secondary lipid oxidation products can play an important role in the damage to DNA<br />

resulting in faster ageing process, neurodegeneraitve, carcinogenic or cardiovascular diseases.<br />

Project duration: from 15.06.<strong>2007</strong> to 15.11.<strong>2007</strong><br />

H. APVT Project 20-002904: Identification of Suitable Authentication Markers and<br />

Development of Optimal Analytical Methods for their Determination in Selected Food<br />

Commodities (Ivan Špánik).<br />

The major objective of project is identification of potential authentication markers and development of suitable<br />

analytical methods and sample treatment procedures for their determination. The first part of project covers<br />

determination of qualitative and quantitative data about selected authentication markers (including enantiomeric<br />

composition of optically active compounds) in selected food commodities, mainly for those that are most<br />

frequently distributed in Slovakian market (juices, ketchup and honey). Obtained data will be summarized in<br />

authentication markers database, which will be tested on unknown samples of food commodities commonly<br />

distributed on Slovakian market. The second part of project is aimed on detailed mapping of chemical composition<br />

of food commodities that are included in Slovak Republic claim on Protected Denomination of Origin, Protected<br />

Geographical Indication or Traditional Speciality Guaranteed (mainly beverages) by available single-,<br />

multidimensional and hyphenated chromatographic systems.<br />

Project duration: from 01.01.2005 to 31.12.<strong>2007</strong><br />

CH. VEGA Project NATO Project No 2/7074/07: Evaluation of Activity Parameters of Potential<br />

Inhibitors of Aldose Reductase - a Contribution to Therapy of Chronic Diabetic Complications<br />

(Pavel Májek).<br />

Inhibitors of the aldose reductase enzyme (ALR2) are drugs capable to prevent a tissue injure caused by<br />

diabetes, prevalently by type II, which is insulin-resistant and it is being spread epidemiologically. 3D structure of<br />

the ALR2 enzyme was already estimated from various biological sources and in complexes with different adducts.<br />

In this project we wish utilize connectivity with existing international and Slovak projects solved at IEPh SAS<br />

which are targeted to the projection of new ALR2 inhibitors missing in clinical praxis. We will use the experimental<br />

results on the inhibition activity for the pyridoindole-like (PyInd) substances which have been already synthesized<br />

and tested at Institute. First off, we will determine the best theoretical way of estimation of activity by means of the<br />

methods of computational chemistry. Then we will create a database of potential PyInd ALR2 inhibitors which<br />

shall fulfill the foregoing theoretical criteria as well as other conditions made for pharmacologically active<br />

substances. The most attractive derivatives will be proposed for synthesis and use in the connecting projects.<br />

Project duration: from 01.01.<strong>2007</strong> to 31.12.2009<br />

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