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国家科技支撑计划(2012BAK02B02-2)

作品数:3 被引量:1H指数:1
相关作者:贠克明王玉瑾王晋涛尉志文曹洁更多>>
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发文基金:国家科技支撑计划山西省科技攻关计划项目国家自然科学基金更多>>
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溴氰菊酯在家兔中死后弥散研究被引量:1
2014年
目的通过对溴氰菊酯死后弥散现象的研究,观察不受死后再分布现象影响的组织脏器,为溴氰菊酯的法医学检材采取提供实验依据。方法家兔处死半小时后分别经口给予4LD50溴氰菊酯,室温下分别放置24 h和48 h解剖,检测心血、股动脉血、尿液、胆汁、心、肝、脾、肺、肾、脑、左下肢肌肉中溴氰菊酯的浓度,比较其变化规律。结果家兔处死半小时后经口给予4LD50溴氰菊酯,灌胃24 h后溴氰菊酯就可以从胃弥散至其他组织器官,心血、周围血、尿液和胆汁中的浓度均高于其他脏器。与24 h组相比,48 h家兔尿液、胆汁、心、脾、肾和左下肢肌肉中溴氰菊酯浓度的变化没有统计学意义。结论溴氰菊酯在尿液、胆汁、心、脾、肾和肌肉中的浓度比较稳定,不受死后弥散的影响,在对溴氰菊酯中毒的法医学鉴定可以采取上述检材进行毒物检验和浓度确定。
肖昆王晋涛尉志文王玉瑾贾娟曹洁贠克明
关键词:死后再分布溴氰菊酯中毒
苯巴比妥在中毒大鼠体内死后分布研究
2014年
目的建立大鼠苯巴比妥灌胃给药致死模型,研究苯巴比妥中毒大鼠体内的死后分布规律。方法雄性Wistar大鼠随机分LD50组和2LD50组,分别经胃匀速注入LD50(0.66 mg/kg)和2LD50(1.32 mg/kg)苯巴比妥。观察从给药到死亡时的生命体征变化及中毒症状,待呼吸和心跳全部消失时,迅速解剖动物,取心血、心、肝、脾、肺、肾、脑、胃等,酸性乙醚提取,气相色谱质谱法定性、气相色谱定量检测其中苯巴比妥浓度。结果苯巴比妥灌胃后大鼠活动明显减少,出现嗜睡症状,LD50组大鼠平均死亡时间为7.24 h±3.17 h,2LD50组大鼠平均死亡时间为1.33 h±0.25 h。苯巴比妥在组织脏器中的分布规律为,LD50组:胃(1261.34μg/g±591.83μg/g)>心(332.12μg/g±70.87μg/g)、脑(289.81μg/g±71.43μg/g)、肝(284.68μg/g±79.44μg/g)、肺(284.41μg/g±67.47μg/g)、脾(272.56μg/g±31.53μg/g)、心血(269.52μg/g±44.62μg/g)>肾(167.76μg/g±43.72μg/g);2LD50组:胃(1 649.21μg/g±1 212.82μg/g)>肝(357.83μg/g±138.67μg/g)、脑(323.19μg/g±159.92μg/g)、心(310.95μg/g±130.73μg/g)、心血(309.93μg/g±135.60μg/g)、肺(308.28μg/g±134.48μg/g)、脾(299.77μg/g±104.58μg/g)>肾(233.24μg/g±91.92μg/g)。结论苯巴比妥死后分布不均匀,含血丰富和脂质含量高的器官如肝、肺、心、脑较其他组织及血液中苯巴比妥的含量高,在疑似苯巴比妥中毒致死案件进行法医学鉴定时应全面正确的采取检材进行毒物分析。
王晋涛郭建军尉志文万东方王勇王玉瑾贠克明
关键词:法医毒物分析苯巴比妥死后分布气相色谱
Comparison of the Concentrations of Lidocaine in Different Body Fluids/Tissues after Subarachnoid Space and Intravenous Administration of a Lethal Dose of Lidocaine
2015年
The objective of the study was to compare the concentration of lidocaine in different body fluids/tissues after subarachnoid space and intravenous administrations of a lethal dose of lidocaine.Totally 18 dogs were used in the experiment.Six dogs were given subarachnoid anesthesia,another were given an intravenous injection of a dose of 75 mg/kg weight of lidocaine hydrochloride in 5 min and the last 6 dogs were used as the blank control dogs and given a subarachnoid space injection or a femoral artery injection of the same volume of sodium chloride.As soon as its vital signs disappeared,each dog was dissected and the specimen,such as brain,cerebrospinal fluid(CSF)in lateral ventricle,CSF in subarachnoid space,spinal cord(cervical spinal cord,thoracic spinal cord,lumbar spinal cord,and waist spinal cord),heart,lung,liver,spleen,kidney,bile,urine,heart blood,peripheral blood,muscle in injection location,and muscle in no injection location,were collected for analysis of lidocaine immediately.Analysis was performed with gas chromatography‑mass spectrometry(GC‑MS).From the maximum to the minimum,the order of lidocaine concentration detected in the subarachnoid space‑administered dogs was as follows:CSF in subarachnoid space,waist spinal cord,thoracic spinal cord,CSF in lateral ventricle,lumbar spinal cord,cervical spinal cord,lung,kidney,muscle in injection location,heart,brain,spleen,heart blood,liver,peripheral blood,bile,muscle in no injection location,and urine.The order of lidocaine concentration detected in the intravenously administered dogs was as followed:Kidney,heart,lung,spleen,brain,liver,peripheral blood,bile,heart blood,cervical spinal cord,thoracic spinal cord,muscle in injection location,lumbar spinal cord,muscle in no injection location,CSF in subarachnoid space,urine,and CSF in lateral ventricle.The maximum concentration of lidocaine was detected in the subarachnoid space CSF of subarachnoid space‑administered dead dogs,while in intravenously injected dead dogs,the maximum concentration of li
Nan ZhangJunHong SunZhiwen WeiWenyan HeGuohua JinXiaohong ZhangPengxiang GaoLongmei WangKeming Yun
关键词:LIDOCAINE
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