Radioactivity measurement of 85Kr by using anti-cosmic HPGe γ spectrometer.

In order to improve the detection sensitivity of 85Kr, an anti-cosmic HPGe γ spectrometer was established and a specific Marinelli beaker was designed for 85Kr measurement. Comparing to the non-anticoincidence γ spectrum, the integral background counts rate range from 20 to 2400 keV was reduced by a factor of 5.17 using anticoincidence shielding. The minimum detectable activity of 85Kr was 10.5 Bq within 24 h measurement in standard mode and that of 3.99 Bq in anticoincidence mode. The activity concentration of atmospheric 85Kr was preliminarily measured to be an average of 1.30 Bq/m3 in Beijing and corresponding minimum detectable concentration was 0.2 Bq/m3.

Determination of 226Ra Activity Using Gamma Spectrometry with 226Ra-222Rn Disequilibrium.

Radium-226 (Ra) activity is normally determined indirectly by gamma spectrometry, in particular by measuring the characteristic γ-ray emitted from its progeny (Pb and Bi) when Ra-Rn secular equilibrium is reached. This article describes a measurement method involving the measurement of Pb ingrowth. The activity of Ra determined by this method agrees with that measured after Ra-Rn equilibrium. The method of Pb ingrowth allows rapid and sufficiently accurate determination of Ra activity without the need to wait for Ra-Rn equilibrium.

A proteome-scale identification of novel antigenic proteins in Mycobacterium tuberculosis toward diagnostic and vaccine development.

Tuberculosis (TB) remains to be a major infectious disease throughout the world. However, the current vaccine for TB has variable protective efficacy, and there is no commercially available serodiagnostic test for this disease with acceptable sensitivity and specificity for routine laboratory use. One of the potential strategies in developing a new diagnostic method and in improving the TB vaccine involves the identification of novel antigenic candidates. This paper aims to identify systematically the novel antigenic proteins with the greatest potential as protective or diagnostic antigens by using the differential response of Mycobacterium tuberculosis proteins to serum from TB patients and healthy individuals. Approximately 87% of the open reading frames of M. tuberculosis were successfully cloned into IPTG-inducible expression vectors. The clone sets were expressed in Escherichia coli, purified under denatured conditions, and tested for antigenicity using a mixture of sera from 15 TB patients. Out of the 3480 proteins screened, 249 proteins had significant reactions with the serum samples. Among the 249 proteins, 20 proteins were identified as most reactive. Compared with the commercial test kits, 3 novel antigens from the top 20 proteins, namely, Rv1987, Rv3807c, and Rv3887c, provided better sensitivity and accuracy. These newly identified antigenic proteins may be used as candidates for serodiagnostic application and vaccine development. Overall, this study's findings may serve as an essential reference for developing new TB diagnostic methods and more effective tuberculosis vaccines.