Express detection of Escherichia coli and bacteria of the Escherichia coli group at the oral cavity.

Currently, in the diagnosis of diseases, a decisive place is given to laboratory methods, which should be informative, relatively simple to perform and rapid. The article describes the approbation of a method for rapid detection of Escherichia coli and bacteria of Escherichia coli group in the oral cavity. Research involved 44 volunteers, who were sampled from the oral cavity, followed by incubation in Koda's medium.

Solid-state synthesis, magnetic and structural properties of interfacial B2-FeRh(001) layers in Rh/Fe(001) films.

Here we first report results of the start of the solid-state reaction at the Rh/Fe(001) interface and the structural and magnetic phase transformations in 52Rh/48Fe(001), 45Rh/55Fe(001), 68Rh/32Fe(001) bilayers from room temperature to 800 °C. For all bilayers the non-magnetic nanocrystalline phase with a B2 structure (nfm-B2) is the first phase that is formed on the Rh/Fe(001) interface near 100 °C. Above 300 °C, without changing the nanocrystalline B2 structure, the phase grows into the low-magnetization modification α' (M ~ 825 emu/cm) of the ferromagnetic α phase which has a reversible α' ↔ α" transition.

Cavitation treatment as a means of modifying the antibacterial activity of various feed additives.

The quality of feed, including its microbiological characteristics, is important for the organization of full-value feeding of animals in agriculture. So, the means of non-reagent processing of feeds, including cavitation treatment, are becoming more widespread. In our study, it was shown that the amount of mesophilic aerobic and facultative anaerobic microorganisms (QMAFAnM) decreases after a 5-min treatment of the test samples (chalk, fuz, bran, and zeolite) (1.

Steroid determination in fish plasma using capillary electrophoresis.

A capillary separation method that incorporates pH-mediated stacking is employed for the simultaneous determination of circulating steroid hormones in plasma from Perca flavescens (yellow perch) collected from natural aquatic environments. The method can be applied to separate eight steroid standards: progesterone, 17alpha,20beta-dihydroxypregn-4-en-3-one, 17alpha-hydroxyprogesterone, testosterone, estrone, 11-ketotestosterone, ethynyl estradiol, and 17beta-estradiol. Based on screening of plasma, the performance of the analytical method was determined for 17alpha,20beta-dihydroxypregn-4-en-3-one, testosterone, 11-ketotestosterone, and 17beta-estradiol.

Stacking enhanced determination of steroids by CE.

This study outlines a simple method for pH-mediated stacking of natural and synthetic steroids facilitated with carboxymethyl-beta-CD. Sample stacking (10 kV, 60 s) is accomplished with 23 mM carboxymethyl-beta-CD in 50 mM 3-[cyclohexylamino]-1-propanesulfonic acid buffered at pH 10. Following stacking, steroidal compounds are separated in less than 5 min with a running buffer of 13 mM hydroxypropyl-beta-CD, 30 mM SDS in 200 mM phosphate buffered at pH 2.