Excitation energy dependence of the life time of orange emission from Mn-doped ZnS nanocrystals

Mn-doped ZnS nanocrystals were prepared by co-precipitation method. X-ray diffraction analysis indicates pure cubic zinc blende structure. We report for the first time experimental observation of the dependence of the decay time of Mn2+ emission from Mn-doped ZnS nanocrystals on excitation energy. Photon energy smaller than the ZnS bandgap induces faster decay time compared to the one equal to the bandgap energy. In addition, while the decay spectra of orange emission indicate both sub mu s and ms, the time-resolved luminescence measurement suggests that the sub mu s component belongs to the tail of the blue emission

The validation and utility of a quantitative one-step multiplex RT real-time PCR targeting Rotavirus A and Norovirus

Rotavirus (RoV) and Norovirus (NoV) are the main causes of viral gastroenteritis. Currently, there is no validated multiplex real-time PCR that can detect and quantify RoV and NoV simultaneously. The aim of the study was to develop, validate, and internally control a multiplex one-step RT real-time PCR to detect and quantify RoV and NoV in stool samples. PCR sensitivity was assessed by comparing amplification against the current gold standard, enzyme immunoassay (EIA), on stool samples from 94 individuals with diarrhea and 94 individuals without diarrhea. PCR detected 10% more RoV positive samples than EIA in stools samples from patients with diarrhea. PCR detected 23% more NoV genogroup II positive samples from individuals with diarrhea and 9% more from individuals without diarrhea than EIA, respectively. Genotyping of the PCR positive/EIA negative samples suggested the higher rate of PCR positivity, in comparison to EIA, was due to increased sensitivity, rather than nonspecific hybridization. Quantitation demonstrated that the viral loads of RoV and NoV in the stools of diarrheal patients were an order of magnitude greater than in individuals without diarrhea. This internally controlled real-time PCR method is robust, exhibits a high degree of reproducibility, and may have a greater utility and sensitivity than commercial EIA kits. </p