前缘弯掠斜流转子叶顶间隙流动特性数值分析

本文对前缘弯掠斜流转子叶顶间隙内的流动特性进行了数值分析。结果表明:叶顶间隙气流与主流发生卷吸而生成泄漏涡。泄漏涡作用的区域具有较低的压力分布。在叶片通道内,泄漏涡沿着与转子旋向相反的方向朝相邻叶片的压力面移动。大间隙时的泄漏涡比小间隙时强烈。低流量时泄漏涡的作用区域比高流量时大。在各种流量特性下,叶顶尾缘近吸力面区域都存在着二次间隙流。     

某轴流压气机叶尖间隙效应实验研究

本文对某低速轴流压气机叶尖间隙尺度对性能的影响进行了实验研究,并通过不同的机匣结构情况研究一种叶尖漏流不敏感机匣。实验表明,不同的间隙尺度对叶轮机总体性能存在十分明显的影响。对绝大部分运行状态,小间隙下的压升和效率均明显高于大间隙的情况。另外,所采用的毛刷式和篦齿式的机匣实验结果表明,不论毛刷式还是篦齿式机匣,在大流量负攻角情况下对性能的影响不大,但毛刷式机匣并不能达到提高失速裕度的目的,而篦齿式机匣在小流量情况下对压升有所提高,但对效率影响不大。     

轴流泵端壁区域流动三维粘性数值计算

本文采用通用流场分析软件FLUENT,基于N-S方程,选用RNG κ—ε湍流模型与SIMPLEC算法,对轴流泵叶轮内部(及端壁间隙)流动进行了三维粘性数值计算。通过实验验证,表明数值计算结果和实测数据吻合较好。详细分析了叶顶附近流场形态以及叶轮出口轴向、周向速度分布,进行了性能预估。并给出了实验装置图。     

压气机非定常叶顶间隙流的数值模拟研究

利用数值方法研究了某低速轴流孤立压气机转子中非定常叶顶间隙流的流动特征和频率特性。结果显示转子顶部区域的压力脉动主要来源于叶顶泄漏涡的非定常波动。波动的具体形式表现为泄漏涡瞬态空间位置、尺度和形态的周期性变化,波动频率为1266 Hz。     

动叶顶部间隙对1+1/2对转涡轮性能的影响

本文对1+1／2对转涡轮中动叶顶部间隙大小对涡轮性能的影响进行了详细的数值模拟。对涡轮总体性能参数、节距平均出口气流角、出口节距平均相对马赫数以及不同叶高的负荷进行了对照,发现间隙对1+1／2对转涡轮性能影响明显,尤其是当间隙较大时。当低压动叶间隙宽度达到高压动叶前缘叶高的4．5％时,低压动叶间隙中流动普遍超音,在设计1+1／2对转涡轮时需要加以重点考虑。     

Optimum Gas Journal Bearing with the Flexible Surface

The optimum shape of the cylindrical internal deformable (flexible) surface of a gas journal bearing of infinite length is designed. The variational problem of determining the clearance shape giving the maximum bearing load capacity is formulated and solved.     

Lipophilicity in PK design: methyl, ethyl, futile

Lipophilicity, often expressed as distribution coefficients (log D) in octanol/water, is an important physicochemical parameter influencing processes such as oral absorption, brain uptake and various pharmacokinetic (PK) properties. Increasing log D values increases oral absorption, plasma protein binding and volume of distribution. However, more lipophilic compounds also become more vulnerable to P450 metabolism, leading to higher clearance. Molecular size and hydrogen bonding capacity are two other properties often considered as important for membrane permeation and pharmacokinetics. Interrelationships among these physicochemical properties are discussed. Increasing size (molecular weight) often gives higher potency, but inevitably also leads to either higher lipophilicity, and hence poorer dissolution/solubility, or to more hydrogen bonding capacity, which limits oral absorption. Differences in optimal properties between gastrointestinal absorption and uptake into the brain are addressed. Special attention is given to the desired lipophilicity of CNS drugs. In examples using -blockers, Ca channel antagonists and peptidic renin inhibitors we will demonstrate how potency and pharmacokinetic properties need to be balanced.     

Hepatobiliary excretion and brain distribution of caffeine in rats using microdialysis

To investigate the pharmacokinetic mechanism of hepatobiliary excretion and brain distribution of caffeine, this study uses a method based on microdialysis technique and liquid chromatography that allows continuous and concurrent in vivo monitoring of extracellular caffeine in the blood, brain and bile of anesthetized rats following the administration of caffeine (3 or 10 mg/kg, i.v.) through the femoral vein. Dialysates of the blood, brain and bile were directly injected onto the liquid chromatographic system and no further clean-up procedures were required. The study design consisted of two groups of six rats in parallel: the rats of the control group received caffeine (3 or 10 mg/kg, i.v.) alone and those of the cyclosporine treated-group were injected cyclosporine (10 mg/kg, i.v.) 10 min prior to caffeine administration (3 or 10 mg/kg, i.v.). The decline of caffeine in the blood, brain striatum and bile suggested that caffeine had rapid exchange and equilibration between the peripheral compartment and the central nervous system. In addition, the results indicated that caffeine underwent hepatobiliary excretion and was distributed into brain. When cyclosporine was co-administered, the pharmacokinetic parameters were not significantly altered. The results of this study reveal that the pharmacokinetic mechanism of hepatobiliary excretion and brain distribution of caffeine might not relate to P-glycoprotein.     

Quantification of furosemide in camel plasma by high resolution mass spectrometry,application on pharmacokinetics

We developed and validated a high‐resolution liquid chromatography mass spectrometry method for the quantification of furosemide in camel plasma which was used for a pharmacokinetic study in camels. Plasma samples were extracted by supported liquid extraction and furosemide and internal standard (furosemide‐D5) were separated on a an Agilent Zorbax XDB C₁₈ column (50 × 2.1 mm i.d., 3.5 μm). Data was acquired in full‐scan mode over a mass range of 200–400 Da in negative electrospray mode at a resolution of 70,000. Linear calibration curves were obtained over the concentration ranges of 1.0–10,000 ng/mL. The validated method was then successfully applied in evaluating the pharmacokinetics and metabolites of furosemide in six camels (Camelus dromedarus ) and we were able to advice on a withdrawal time of furosemide treatment before racing.     

明日叶黄酮类化合物清除羟基自由基活性研究

为了研究明日叶黄酮类化合物对羟基自由基的清除作用,以明日叶（主要取叶片）为原料,用体积分数为65％乙醇提取明日叶总黄酮,测定其总黄酮含量.通过Fenton反应体系产生羟基自由基,利用明日叶提取液中的功能成分黄酮类化合物对羟基自由基的清除作用进行研究.结果表明：明日叶提取物总黄酮质量分数为10.18％,且黄酮类化合物对羟基自由基有较强清除效力,当提取物总黄酮浓度在0.1～1.0 mg/mL范围内,其与清除率呈正相关.明日叶中黄酮类化合物对羟基自由基有较强清除效力,作为天然抗氧化产品开发具有一定价值.