Database-assisted global metabolomics profiling of pleural effusion induced by tuberculosis and malignancy

Database-assisted global metabolomics has received growing attention due to its capability for unbiased identification of metabolites in various biological samples. Herein, we established a mass spectrometry (MS)-based database-assisted global metabolomics method and investigated metabolic distance between pleural effusion induced by tuberculosis and malignancy, which are difficult to be distinguished due to their similar clinical symptoms. The present method utilized a liquid chromatography (LC) system coupled with high resolution mass spectrometry (MS) working on full scan and data dependent mode for data acquisition. Unbiased identification of metabolites was performed through mass spectral searching and then confirmed by using authentic standards. As a result, a total of 194 endogenous metabolites were identified and 33 metabolites were found to be differentiated between tuberculous and malignant pleural effusions. These metabolites involved in tryptophan catabolism, bile acid biosynthesis, and β-oxidation of fatty acids, provided non-invasive biomarkers for differentiation of the pleural effusion samples with high sensitivity and specificity.     

低渗温热腹腔灌注化疗治疗恶性腹腔积液的临床研究

目的 评价低渗温热腹腔灌注化疗治疗恶性腹腔积液的疗效及不良反应。方法 行腹腔穿刺置单腔中心静脉导管,外接引流袋,记录腹水引流量,当日排放腹水1 500ml 后,予加热至43~45℃注射用双蒸馏水1 000ml 行腹腔灌注,次日重复放液1 500ml,再予加热至43~45℃注射用双蒸馏水1 000ml 行腹腔灌注,并于灌注后腹腔注入顺铂60mg、氟尿嘧啶500mg 并封管,治疗期间常规给予简单水化、对症止吐等治疗。结果 31 例恶性腹腔积液患者共完成低渗温热腹腔灌注化疗42 周期,完全缓解7例,部分缓解15,稳定5 例,进展4 例,完全缓解+ 部分缓解占70.97%。中位进展时间（TTP）3.6个月（2～9 个月）, 中位生存期（MST）5.6 个月。毒副反应以消化道反应为主。结论 低渗温热腹腔灌注化疗治疗恶性腹腔积,在延长患者的生存期、提高生活质量方面效果较好,临床上可推荐应用。     

致密微孔壁绝热冷却效果研究

本文采用经热电偶标定的红外热像表面温度测量技术,实验研究了吹风比M(M=0．30-1．59)对致密微孔壁热侧壁面上绝热冷却效果ηaw的影响,并与数值模拟结果进行了比较。实验与数值模拟的结果都表明:与常规气膜冷却在M≥1．0时ηaw随着M增大而减小的现象不同,致密微孔壁的ηaw随着M增大逐渐增加的,但随着M的增大,ηaw增加的幅度越来越小。在相同的吹风比M下,致密微孔壁的绝热冷却效果ηaw明显高于常规气膜冷却的ηaw。     

Thermodynamic properties of gaseous cerium phosphate studied by Knudsen effusion mass spectrometry

Gaseous CePO₂ has been identified by Knudsen effusion mass spectrometry during vaporization of CeO₂ and magnesium diphosphate from tungsten double, two‐temperature effusion cell. Structure and molecular parameters of gaseous cerium phosphate under study were determined using quantum chemical calculations. On the basis of equilibrium constants measured for gas‐phase reaction, standard formation enthalpy of CePO₂ was determined to be ?508 ± 41 kJ ? mol^?1 at the temperature 298 K.     

致密微孔壁复合冷却对流换热系数研究

本文采用数值模拟的方法研究了吹风比M和孔阵排列偏转角γ对致密微孔壁复合冷却热侧壁面上对流换热系数的影响。分析比较了在M=0.50-2.0、γ=10°-35°几种情况下的对流换热系数。结果表明:M越大,对流换热系数越低。在气膜孔区内的上游部分γ对斜排对流换热系数影响不很明显,在中下游部分斜排模型的对流换热系数比常规错排模型低。     

Structural studies of cyclic ureas: 3. Enthalpy of formation of barbital

A thermochemical and thermophysical study has been carried out for crystalline barbital [5,5′-diethylbarbituric acid]. The thermochemical study was made by static bomb combustion calorimetry, from which the standard () molar enthalpy of formation of the crystalline barbital, at T = 298.15 K, was derived as −(753.0 ± 1.8) kJ · mol⁻¹. The thermophysical study was made by differential scanning calorimetry over the temperature interval (265 to 470) K. A solid–solid phase transition was found at T = 413.3 K. The vapour pressures of the crystalline barbital were measured at several temperatures between T = (355 and 377) K, by the Knudsen mass-loss effusion technique, from which the standard molar enthalpy of sublimation, at T = 298.15 K was derived as (117.3 ± 0.6) kJ · mol⁻¹. The combination of the experimental results yielded the standard molar enthalpy of formation of barbital in the gaseous phase, at T = 298.15 K, as −(635.8 ± 1.9) kJ · mol⁻¹. This value is compared and discussed with our theoretical calculations by several methods (Gaussian-n theories G2 and G3, complete basis set CBS-QB3, density functional B3P86 and B3LYP) by means of atomization and isodesmic reaction schemes.     

对四类泻流问题的深入研究

对热学中的4类泻流问题进行了详细的计算,并对结果进行了分析讨论.恒温的泻流问题有解析的解,而绝热泻流问题往往受限于数学知识只能得到数值的结果;同时本文也对泻流的近平衡态条件进行了大致的分析.这些将有助于广大师生对于泻流问题的全面认识.     

Using 1 MHz pulse-echo ultrasound externally applied to detect mastoid effusion: cadaver experiments

The objective of this study is to explore the feasibility of using ultrasound to detect mastoid effusion (ME). In the past, ultrasound has been used to measure middle ear effusion (MEE) by injecting water into the external ear canal to measure echoes from the tympanic membrane, which is uncomfortable for the patient. It has been shown that air cells in the mastoid of patients with MEE are filled with fluid, which implies that ME could be a useful indicator of MEE. This study suggests using ultrasound to detect ME as a potentially noninvasive approach for MEE detection. In vitro experiments were performed on ten cadaver samples of the human ear. A single-element 1 MHz transducer was used to measure the mastoid of each cadaver before and after injecting water into the mastoid. The experimental results showed that the relative amplitudes of ultrasonic signals differed significantly between before (0.24 ± 0.09, mean ± standard deviation) and after (0.15 ± 0.03) the water injection (p < 0.05, t-test), demonstrating that the ultrasonic reflection can be used to detect ME. The location of the human mastoid under the skin behind the ear allows external measurements, and hence ultrasound-based ME detection may be an alternative, noninvasive diagnostic approach to detecting MEE in the future, providing an examination that avoids discomfort.     

Determination of thermodynamic stability of CdMoO4 by knudsen effusion vapor pressure measurement method

Thermodynamic stability of CdMoO₄ was determined by measuring the vapor pressures of Cd and MoO₃ bearing gaseous species. Th vaporization reaction could be described as CdMoO₄(s)+MoO₂(s) =Cd(g)+2/n(MoO₃)_n (n=3, 4 and 5). The vapor pressures of the cadmium (p _Cd) and trimer (p _(MoO3)3) measured in the temperature range 987≤T/K≤1111 could be expressed, respectively, as ln (p _Cd/Pa) = –32643.9/T+29.46±0.08 and ln(p _(MoO3)3/Pa) = –32289.6/T+29.28±0.08. The standard molar Gibbs free energy of formation of CdMoO₄(s), derived from the vaporization results could be expressed by the equations: °_f G _{CdMoO4 (s)} ⁰= –1002.0+0.267T±14.5 kJ mol^–1 (987≤T/K≤1033) and °_f G _{CdMoO4 (s)} ⁰ = –1101.9+0.363T±14.4 kJ mol^–1 (1044≤T/K≤1111). The standard enthalpy of formation of CdMoO₄(s) was found to be –1015.4±14.5 kJ mol^–1 .