Objective To Evaluate the environment quality in underground construction site based on the measurement of atmosphere composition and microclimate. Method Concentrations and composition of gases were analyzed by combined detection with mass spectrometer and gas chromatograph. Microbial content was detected by striking method. A microclimate model was built based on the measurements of temperature, humidity and wind speed in two years. Result Concentrations of inorganic gas was higher than national standard. Total volatile organic compounds were in the range of 4～6 mg/m3, which highly exceeded the national standard. Concentration of O2 descended obviously at the time when personnel went into the construction site, and was lower than the national standard of 299 mg/m3 after continuous working for 3 h. When an aerator was started, the average noise level was in the range of 70～93 dB, which was higher than the national standard(55～70 dB). In the course of working, the average microbial content reached 4 000 cfu/m3 which was 3 times as high as the background level. The microclimate characteristic with high humidity, low temperature and inadequate sunshine was unsuitable for dwelling. Conclusion Environment in the underground construction site is unfavorable as compared with that on the ground. The physiological function of working staff may be influenced obviously due to cumulative effect of the above mentioned factors, and may lead to aprosexia, hypomnesis, fatigue, etc. Six kinds of protection means are suggested in the paper.

Objective:To study the interaction between the SARS-S1 protein and the SARS-sensitive cells.Methods:The SARS-S1 expression in the E.coli was purified and the anti-SARS-S1 was produced.After incubate with the SARS-S1 protein,cells was staining by the mouse-anti-SARS-S1 antibody and the anti-mouse antibody labeled by FITC.The result was determined by FACS.Results:After incubate with the SARS-S1 protein,different cell line have a different reaction to the SARS-S1 antibody.Conclusion:The SARS-S1 protein expressed by E.coli has a specific binding ability to the SARS-sensitive cells.

Aptamers are DNA or RNA fragments that can specifically bind to target substances.Because of the excellent properties such as strong binding force,high specificity,small physical size,chemical synthesis and modification,good biocompatibility,and low immunogenicity aptamers show wide application propects in biomedical researches.Aptamers can also bind specifically to receptors on the surface of cell membranes,and mediate the endocytosis of nanoparticles into cells,making them ideal drug targeting ligands.Organic nanomaterials have excellent application value in nanodrug delivery system because of their good biocompatibility and degradability.In this paper,the recent research progress of aptamers and organic nanomaterials drug delivery systems was reviewed.

Objective To investigate the risk factors of cognitive impairment associated with early post－acute stroke seizures (EPASS). Methods One hundred and sixty－eight eligible patients were recruited in the study. Patients were divided into cognitive impairment group and non－cognitive disorder group according to MMSE. General clinical data, severity of the stroke, location and extent of infarction, characteristics of epileptic seizures were compared between the two groups. Multivariate Logistic regression analysis was utilized to investigate the independent risk factors of EPASS related cognitive impairment. Results Multivariate logistic regression analysis showed that moderate to severe stroke (OR=4.386, P=0.006), cortical infarction (OR=6.430, P=0.012), general tonic clonic seizure (OR=8.189, P=0.004), seizure frequency≥1 time per day (OR=12.818, P＜0.001) were the independent risk factors for cognitive impairment in EPASS. Conclusions Patients with moderate to severe stroke, cortical infarction, general tonic clonic seizure and seizure frequency≥1 time per day may have a higher risk of cognitive impairment.

Humans ; Mental Retardation, X-Linked/genetics* ; Methyl-CpG-Binding Protein 2/genetics* ; Gene Duplication