ABSTRACT
Simulation-based ultrasound training provides repeated practice and promptly feedback, which has a great advantage in improving the safety of the patient, the professional operation skill and confidence of the trai-nees,and the standardization of education. In this review,we discuss the classification of currently available simu-lation-based medical education for ultrasound teaching, its role in"diagnostic"and"interventional"ultrasound practice training,as well as current deficits pertain in validation process.
ABSTRACT
Simulation-based ultrasound training provides repeated practice and promptly feedback, which has a great advantage in improving the safety of the patient, the professional operation skill and confidence of the trai-nees,and the standardization of education. In this review,we discuss the classification of currently available simu-lation-based medical education for ultrasound teaching, its role in"diagnostic"and"interventional"ultrasound practice training,as well as current deficits pertain in validation process.
ABSTRACT
OBJECTIVES@#To detect the changes of microbial community functional diversity of corpses with different postmortem interval （PMI） and to evaluate forensic application value for estimating PMI.@*METHODS@#The cultivation of microbial community from the anal swabs of a Sus scrofa and a human corpse placed in field environment from 0 to 240 h after death was performed using the Biolog-Eco Microplate and the variations of the absorbance values were also monitored. Combined with the technology of forensic pathology and flies succession, the metabolic characteristics and changes of microbial community on the decomposed corpse under natural environment were also observed.@*RESULTS@#The diversity of microbial metabolism function was found to be negatively correlated with the number of maggots in the corpses. The freezing processing had the greatest impact on average well color development value at 0 h and the impact almost disappeared after 48 h. The diversity of microbial metabolism of the samples became relatively unstable after 192 h. The principal component analysis showed that 31 carbon sources could be consolidated for 5 principal components （accumulative contribution ratio >90%）.The carbon source tsquare-analysis showed that N-acetyl-D-glucosamine and L-serine were the dominant carbon sources for estimating the PMI （0=240 h） of the Sus scrofa and human corpse.@*CONCLUSIONS@#The Biolog-Eco method can be used to reveal the metabolic differences of the carbon resources utilization of the microbial community on the corpses during 0-240 h after death, which could provide a new basis for estimating the PMI.
Subject(s)
Humans , Biodiversity , Cadaver , Carbon , Postmortem Changes , Principal Component Analysis , Soil Microbiology , Time FactorsABSTRACT
This paper described a rapid and sensitive HPLC method to analyze (E)-3,5,4'-trimethoxystilbene (BTM-0512) in rat plasma and tissues. The analysis used a BDS Hypersil C18 analytical column (250 mm x 4.6 mm ID, 5 microm) and acetonitrile/water as the mobile phase. The UV detection wavelength was 319 nm. Proteins were precipitated with acetonitrile and diethylstilbestrol as internal standard. The method was validated according to State Food and Drug Administration of China and ICH of Technical Requirements for Registration of Pharmaceuticals for Human Use Guidelines. The limit of detection (S/N: 3/1) for BTM-0512 was 0.005 microg x mL(-1) for plasma. The method performances were shown to be selective for BTM-0512 and the linearity of the assay method was up to 10.0 microg x mL(-1) and 40.0 microg x g(-1) for plasma and tissues, respectively. At 0.1, 1 and 5 microg x mL(-1) (n=5), intraday and interday precision values (% RSD) were in the range of 2.6% - 5.1% and 2.4% - 4.8%, respectively. Mean accuracy and absolute recoveries of BTM-0512 ranged from 95.3% - 100.1% and 95.9% - 100.9% for plasma and tissues, respectively. This method can be quite useful for BTM-0512 pharmacokinetic and tissue distribution studies, for purpose which multiple plasma and tissue samples can be analyzed quickly with high reproducibility.
Subject(s)
Animals , Male , Rats , Angiogenesis Inhibitors , Blood , Pharmacokinetics , Anti-Allergic Agents , Blood , Pharmacokinetics , Antineoplastic Agents , Blood , Pharmacokinetics , Chromatography, High Pressure Liquid , Methods , Rats, Sprague-Dawley , Reproducibility of Results , Spectrophotometry, Ultraviolet , Methods , Stilbenes , Blood , Pharmacokinetics , Tissue DistributionABSTRACT
17-allylamino-17-demethoxygeldanamycin (17-AAG) is a heat shock protein 90 ( HSP90) inhibitor. It is capable of target-inhibiting tumor-derived HSP90, leading to the depletion of on-cogenic client proteins which play key roles in several signal transduction pathways. Then cell growth and differetiation are inhibited. 17-AAG results in cytostasis and apoptosis. A lot of trials have indicated that 17-AAG is a selective target drug for cancer therapy. It can efficiently inhibit multiple signal transduction pathways involved in tumor cell proliferation and survival. Clinical phaseⅠand phaseⅡtrials have shown that 17-AAG has good pharmacokinetic-pharmacodynamic profile. Moreover, it can combine with radiation and the traditional chemotherapeutics and increase the therapeutic efficacy.