基于深度学习的中医古文献临床经验抽取

中医古文献蕴藏着丰富的临床经验，是古代中医在行医过程中对临床诊疗的经验性总结，体现了中医学形成和发展的理论框架和思想基础.然而这些宝贵的临床经验不仅量大，而且分散在不同的文献中，使得中医从业者手工很难快速全面地获取它们，文献检索工具也只能提供文档级别的信息筛选，无法为这种细粒度的信息获取提供支持.此外，古汉语相对于现代汉语的不同特点也限制了主流文本分析工具的使用效果.为此本文提出面向临床经验获取的中医古文献信息抽取任务，用于识别古文献中描述临床经验的文本片段，手工标注了样本数据用于这种抽取模型的训练和测试，并设计了基于深度学习的序列标注器用于完成该任务.考虑到标注数据量小可能带来的过度拟合问题，本文引入对抗训练和虚拟对抗训练来增强模型的泛化能力.一系列充分的实验验证了模型的有效性，表明利用信息抽取技术从古文献获取中医临床经验具有可行性，为这一新的信息抽取任务提供了有希望的研究基线和可复用的标注数据集.     

基于DNA-AuNCs的荧光传感新方法灵敏检测胰蛋白酶活性

以DNA模板金纳米簇(DNA-AuNCs)作为荧光探针,发展了一种灵敏检测胰蛋白酶活性的荧光分析新方法.在胰蛋白酶存在条件下,牛血清白蛋白水解成多肽片段,释放出游离的半胱氨酸残基.半胱氨酸残基与金纳米簇通过Au-S键形成非荧光的配合物,导致金纳米簇的荧光强度显著降低.该方法对胰蛋白酶的线性检测范围为0.1～2.0mg/L,检出限为20μg/L(R_(SN)=3).此外,该方法被成功应用于人血清样品中胰蛋白酶含量的测定.     

高速实时可见光通信技术研究及应用

 介绍了可见光通信技术的发展历史及研究现状。基于带宽拓展技术搭建了1 W荧光型LED做光源、PIN光电二极管做探测器、单路速率610 Mb/s的实时传输演示系统，该系统在传输距离为6.2 m时的误码率为3.48×10^-5。在此基础上搭建了荧光型LED为光源、PIN光电二极管做探测器的、双向100 Mb/s无线光上网演示系统。     

利用Wittig反应合成荧光增白剂DX.EB

基于Wittig反应原理,利用(邻氰基苄基)膦酸二甲酯、(对氰基苄基)膦酸二甲酯、对苯二甲醛和甲醇钠合成了荧光增白剂DX.EB,研究了合成工艺.当原料(邻氰基苄基)膦酸二甲酯∶(对氰基苄基)膦酸二甲酯=1∶1.5,40℃滴加甲醇钠时,收率为最佳,可达74.72%.     

Synthesis and Photophysical Properties of Novel Rod-shaped and Star Shaped Fluorescent Phosphane Derivatives

1 Results Over the past few years significant research has been directed toward the development of organic materials for potential application in molecular photonic devices[1] and the development of sensors[2].Interest in these materials is primarily due to the infinite numbers of possible molecular structures with the desired properties,by virtue of the tremendous capabilities of organic synthesis.For the development of a new fluorescent molecular sensor consisting of a recognition moiety linked to a f...     

检验唐氏综合症的法医学方法研究

利用荧光标记的PCR法，对唐氏综合症的检验进行研究．采用法医学检验常用试剂盒AmpFe STR^TM Profiler Plus^TM对唐氏综合症病例进行PCR扩增，扩增产物用ABIPRISMT”310型DNA全自动测序仪分型判断．结果表明，该检验方法具有简便、快速、直接、准确的特点，检验效果非常好，而且可用于产前诊断．该方法用于检验唐氏综合症是一种理想的方法．     

时变条件下有宵禁限制的最短路问题

在组合优化过程中,往往需要获得从起点到终点之间的最短路,而其所考虑的目标可能是一个与时间相关的变量.同时,对于网络中的节点往往有宵禁的限制(curfews).给出时变条件下有软、硬宵禁限制的最短路模型,设计了求解时变条件下有宵禁限制最短路的算法,并对算法的复杂性进行了分析.最后给出了一个应用算例.     

In vitro amiodarone protein binding and its interaction with warfarin

Summary The binding of amiodarone to human plasma protein and to bovine serum, albumin was studied by three different methods, ultracentrifugation, equilibrium dialysis and fluorescence spectroscopy. The fraction of amiodarone bound to plasma protein amounted to 96.3%. The changes in the binding properties of 1-anilino-naphthalene-8-sulfonate for bovine serum albumin using warfarin and amiodarone as independent inhibitors were analyzed in terms of binding site specificity. The findings indicated that amiodarone and warfarin have two different binding sites on bovine serum albumin, so a noncompetitive inhibition mechanism was indicated. On the basis of our data we cannot exclude other mechanisms of interaction besides direct displacement of one drug by another; nevertheless, metabolite interference between amiodarone and coagulation cofactors may better explain the enhancement of warfarin's pharmacological action in association with amiodarone.This work was partially funded by the CNR (National Research Council, Rome, Italy), Program on Clinical Pharmacology and Rare Diseases. The authors would like to thanks Drs E. Marzi and E. riva for their help.     

AnAnolis skin melanophore assay suitable for photoaffinity labeling studies with α-MSH

Summary Visual determination of MSH-induced pigment migration in melanophores of small pieces ofAnolis carolinensis skin is standardized by first measuring photoelectrometrically the change in reflection/transmission of the whole dorsal skin in response to different hormone concentrations. This method allows the rapid and precise recording of time-response curves after photoaffinity labeling of MSH receptors or of dose-response curves of large series of synthetic compounds.Acknowledgments. We wish to thank Ms V. Jäggin, Ms C. Schulthess and Ms G. van Hees for excellent technical assistance, Dr. R. Andreatta, Ciba-Geigy AG, Basel, for his generous gift of -MSH and Prof. A Pletscher for his continuous interest. This work was supported by the Swiss National Science Foundation.     

胰腺腺泡细胞胞浆游离钙浓度的测定及药物作用的研究

本文建立了用荧光指示利Fura－2测定胰腺腺泡细胞胞浆游离Ca2＋浓度（［Ca2＋］i）的实验技术,包括：胰腺腺泡的分离制备;Fura—2／AM的负载;腺泡悬液的荧光光谱测量等．测定了胰腺腺泡细胞［Ca2＋］i。的静息值和卡巴可促腺泡细胞［Ca2＋］i升高的剂量—效应关系及动力学过程,并研究了柴胡总皂甙对胰腺腺泡细胞［Ca2＋i］的影响．发现0．01mg／ml浓度的柴胡总皂甙使胰腺腺泡细胞［Ca2＋］。明显升高,0．1mg／ml浓度时可使［Ca2＋］。升高到静息值的3倍,提示柴胡总皂甙的促酶分泌作用是通过胞内［Ca2＋］i升高介导的．