顶空气相色谱法测定全血中乙醇的含量

【目的】建立顶空气相色谱法内标法测定全血中乙醇浓度。【方法】分析柱为FFAP 30m×0.53mmID色谱柱,载气为N2,检测器为FID;0.4mL全血样品以小瓶密封,40℃下平衡40min,用气体进样器取顶空进样0.6mL,内标法定量。【结果】本法日内精密度〈2.74%,日间精密度〈2.69%,回收率96.53%-100.35%。【结论】本法操作简便快速,灵敏度高,结果准确可靠。

黄芪药渣发酵液中乙醇含量测定方法的研究

【目的】建立黄芪药渣发酵液中乙醇含量的测定方法。【方法】采用顶空气相色谱法,以正丙醇为内标物,采用安捷伦HP-5色谱柱(30 mm×0.25 mm×0.25μm),程序升温(起始温度40℃,保留6 min;以3℃·min^(-1)的升温速率升至55℃,保留2 min;再以7℃·min^(-1)的升温速率升至120℃,保留2 min);进样口温度180℃;FDI检测温度为200℃;载气为氮气,流速1 m L·min^(-1)。【结果】黄芪药渣发酵液中乙醇得到有效分离,乙醇在所考察的浓度范围内线性关系良好(r=0.999 1),平均回收率为98.12%。【结论】顶空气相色谱法可用于黄芪药渣发酵液中乙醇含量的测定;该方法操作简便,准确度和灵敏度高。

Systematic review and meta-analysis of colon cleansing preparations in patients with inflammatory bowel disease

AIM To performed a systematic review and meta-analysis to determine any possible differences in terms of effectiveness, safety and tolerability between existing colon-cleansing products in patients with inflammatory bowel disease.METHODS Systematic searches were performed( January 1980-September 2016) using MEDLINE, EMBASE, Scopus, CENTRAL and ISI Web of knowledge for randomized trials assessing preparations with or without adjuvants, given in split and non-split dosing, and in high(> 3 L) or low-volume(2 L or less) regimens. Bowel cleansing quality was the primary outcome. Secondary outcomes included patient willingness-torepeat the procedure and side effects/complications.RESULTS Out of 439 citations, 4 trials fulfilled our inclusion criteria(n = 449 patients). One trial assessed the impact of adding simethicone to polyethylene glycol(PEG) 4 L with no effect on bowel cleansing quality, but a better tolerance. Another trial compared senna to castor oil, again without any differences in term of bowel cleansing. Two trials compared the efficacy of PEG high-volume vs PEG low-volume associated to an adjuvant in split-dose regimens: PEG low-dose efficacy was not different to PEG high-dose; OR = 0.84(0.37-1.92). A higher proportion of patients were willing to repeat low-volume preparations vs high-volume; OR = 5.11(1.31-20.0). CONCLUSION In inflammatory bowel disease population, PEG lowvolume regimen seems not inferior to PEG high-volume to clean the colon, and yields improved willingness-torepeat. Further additional research is urgently required to compare contemporary products in this population.

Analysis of Ethanol Dehydration Products by Gas Chromatography

An accurate reliable analysis method for dehydration of ethanol to ethylene was established using chromatographic separation technique and the principle of carbon balance, and the activivity of HZSM-5 molecular seive was evaluated. The results showed that at an ethanol mass concentration of 50%, a mass space velocity of 2.0/h and a temperature of 280 ℃, the activity of catalyst was ideal, and the conversion rate of ethanol and the selectivity of ethylene were up to 99.60% and98.10%, respectively. The selectively of ethylene decreased notably with further increase of reaction temperature.

Multiplicity Analysis in Reactive Distillation Column Using ASPEN PLUS

Reactive distillation processes for synthesis of ethylene glycol （EG） and ethyl tert-butyl ether （ETBE） were modeled with the simulation package ASPEN PLUS. The input multiplicity and output multiplicity were discussed with the method of sensitivity analysis for both cases. In EG production process, steady state multiplicities were studied in terms of effective liquid holdup volume and boil-up ratio. In ETBE synthesis process, the user kinetic subroutine was supplied into ASPEN PLUS firstly, and then the composition, temperature and reaction-rate profiles within the reactive distillation column were presented in detail. A set of stable solution branches based on distinct initial guesses for a range of boil-up ratio were found in EG synthesis. Input multiplicities were observed for a range of reboiler duty at several values of reflux ratio for ETBE synthesis process. These results can be used to avoid excessive energy consumption and achieve optimum design of reactive distillation column.

cDNA Cloning and Sequence Analysis of ADH Gene in Delia antiqua

[Objective] This study aims to conduct cloning and sequence analysis of ADH gene in D. Antiqua. [Method] Full-length cDNA of ADH gene in D. antiqua was cloned by using RACE technology （GenBank access number： JQ666006）. Analysis of the homology, characteristics and functional domains of ADH sequence and the phy- Iogenetic relationship to other dipteran ADH were conducted. [Result] The full length of ADH cDNA is 1 088 bp containing a 771 bp of ORF, encoding 256 amino acids, with a calculated relative molecular weight of 30.80 kDa and a theoretical isoelectric point of 8.22. The deduced amino acid sequence shares the highest homology with Glossina morsitans morsitans based on homological analysis and phylogenetic analysis. [Conclusion] This study provides basis for further research of ADH gene.

Ethanol injection is highly effective for hepatocellular carcinoma smaller than 2cm

AIM： To analyze the long-term prognosis in a cohort of western cirrhotic patients with single hepatocellular carcinoma treated with ethanol injection.METHODS： One-hundred forty-eight patients with solitan/hepatocellular carcinoma were enrolled. The tumor diameter was lower than 2 cm in 47 patients but larger in the remaining 101 patients. The impact of some pre- treatment clinical and laboratory parameters and of tu- mor recurrence on patients＇ survival was assessed.RESULTS： Among the pre-treatment parameters, only a tumor diameter of less than 2 cm was an independent prognostic factor of survival. The occurrence of new nodules in other liver segments and the neoplastic portal invasion were linked to a poorer prognosis at univariate analysis. Patients with a single hepatocellular carcinoma smaller than 2 cm showed a better 5-year cumulative survival （73.0% vs 47.9%） （P = 0.009）, 3-year local re- currence rate （29.1% vs 51.5%） （P = 0.011）, and 5-year distant intrahepatic recurrence rate （52.g% vs 62.8%） （P = 0.054） compared to patients with a larger tumor. CONCLUSION： The 5-year survival rate of patients with single hepatocellular carcinoma 〈 2 cm undergoing ethanol injection is excellent and comparable to that achieved using radiofrequency ablation.

Isothermal Crystallization Kinetics of Microencapsulated Polyethylene Glycol Particles

The microenapsulated polyethylene glycol （PEG） with different molecular weight by a fluidized coating method has been prepared and the crystallization behaviors of PEG particles in three-dimensional confined vohume were investigated by using differential scanning calorimetry （DSC） measurement. The results showed that the width of the crystallization peak of PEG increases and its height gradually diminishes in case that the PEG particles are microencapsulated. Compared with the non-microencapsulated PEG particles, the proportion of the first crystallization peak of microencapsulated PEG particle increases, and that of the second one decreases. The reason for the difference maybe is that the crystallization process of microencapsulated PEG particles is uniform and the crystallization ends when the spherulites touch the wall, thus the opportunity of producing the second crystallization peak was relatively reduced.

Low-Grade and High-Grade Invasive Ductal Carcinomas of the Breast Follow Divergent routes of Progression

Low-grade invasive ductal carcinoma is almost diploid, and has frequent losses of chromosome 16q, which is shared by other precancerous lesions of the mammary gland such as flat epithelial atypia （FEA）, atypical ductal hyperplasia （ADH）, and lownuclear grade ductal carcinoma in situ （DCIS）. The genetic alterations accumulate in a stepwise fashion as the precancerous lesions progress to invasve ductal carcinoma. This supports the linear progression model of breast cancer from FEA, through ADH, to low- nuclear grade DCIS as non-obligate early events in low-grade IDC evolution. In contrast, high-grade carcinoma tends to aneuploidy with complex genetic alterations--most importantly, frequent gains at chromosome 16q. Frequent losses at chromosome 16q in low-grade IDC and gains in the same arm of the same chromosome in high-grade IDC imply that these lesions are two end outcomes of different disease processes and that they do not lie in the same continuum of a process. Therefore, low-grade and high-grade IDC are two distinct diseases with a divergent route of progression.

Photodissociation Dynamics of Methanol and Ethanol at 157 nm

157 nm photodissociation of jet-cooled CH3OH and C2HsOH was studied using the high-n Rydberg atom time-of-flight （TOF） technique. TOF spectra of nascent H atom products were measured. Simulation of these spectra reveals three different atomic H loss processes： one from hydroxyl H elimination, one from methyl （ethyl） H elimination, and one from secondary dissociation of the methoxy （ethoxy） radical. The relative branching ratio indicates secondary dissociation of ethoxy is less important than that of methoxy. The average angular anisotropy parameter of methanol is negative （with β≈-0.3）, indicating the transition dipole moment is perpendicular to the C-O-H plane. The slightly more negative β value of ethanol （with β≈-0.4） implies that ethanol has a longer rotational period. These experimental results indicate that both systems undergo fast internal conversion to the 3s surface after it is excited to the 3px surface, and then dissociate on the 3s surface. The translational energy distribution of the CH3O＋H products reveals extensive CH3 rocking or CH3 umbrella excitation in the CH30 radical. However the vibrational structures are not resolved in the C2H5O radical.

Electron Momentum Spectroscopy of Ethanethiol Complete Valence Shell

The binding energy spectra and electron momentum distributions for the complete valence orbitals of ethanethiol were measured for the first time by binary （e, 2e） electron momentum spectroscopy employing non-coplanar symmetric kinematics at an impact energy of 1200 eV plus binding energy. The experimental results are generally consistent with the theoretical calculations using density functional theory and Hartree-Fock methods with various basis sets. A possible satellite line at 17.8 eV in binding energy spectrum was observed and studied by electron momentum spectroscopy.

Study of Synthesis of Copoly (lactic acid/glycolic acid) by Direct Melt Polycondensation

A two steps direct copolymerisation process was developed. The first step is to produce oligomer and then the oligomer of lactic acid/glycolic acid (90/10) is polymerized with binary catalyst tin chloride dihydrate/p-toluenesulfonic acid. In this way, the direct synthesis of copoly (lactic acid/glycolic acid) without any organic solvent was investigated. The properties and structures of products were characterized by nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), X-ray diffraction and so on. The results show that comparatively high molecular weight copolymer of lactic acid and glycolic acid can be prepared by direct processing under appropriate technological conditions.

Investigation of Propoxylation and Ethoxylation of 2-Ethylhexanol in the Presence of an Alkaline and DMC Type Catalyst at Initial Stages of the Syntheses

This paper reports the results of monopropoxylation and monoethoxylation of ethylhexyl alcohol performed in the presence of KOH and a DMC type catalyst, respectively. The existing differences are discussed in terms of kinetic performance of the syntheses, as well as the obtained products＇ compositions. The investigated DMC type catalyst showed 60 to 70 times as high conversion rates, narrower homolog distributions and higher selectivity, in comparison with KOH. Interpretation of the experimental results was performed using kinetic parameters of the WeibulI-Nycander-Gold model and the Natta Mantica relationships. In spite of any differences between the reactivity of the investigated catalysts and alkylene oxides, a significant contribution ofpolymerisation parallel to the target polyaddition was determined, absorbing a major part of the converted adducts, both in the presence of DMC and KOH.

A population-based case-crossover study of polyethylene glycol use and acute renal failure risk in the elderly

AIM:To evaluate the possibility of an association between polyethylene glycol(PEG) and acute renal failure(ARF) in elderly patients using a health insurance claims database.METHODS:We conducted a population-based casecrossover study using information obtained from Korean Health Insurance Review and Assessment Service(HIRA) claims from January 1,2005 to December 31,2005(Seoul,Korea).The study population consisted of elderly patients who received PEG prior to experiencing their first ARF-related hospitalization from April 1,2005 to December 31,2005.For each patient,one case and two control periods were matched.PEG use in a 2-or 4-wk window period prior to hospitalization for ARF was compared with PEG use in two earlier 2-or 4-wk control window periods.Conditional logistic regression analysis was used to estimate odds ratios(ORs) and 95% CI,adjusting for concomitant uses of diuretics,angiotensin converting enzyme inhibitors,non-steroidal anti-inflammatory drugs,antibiotics,anti-cancer drugs,and contrast media.RESULTS:Within the HIRA database which contained 1 093 262 elderly patients,1156 hospitalized ARF cases were identified.Among these cases,PEG was prescribed to 17(1.5%) patients before hospitalization.The adjusted ORs when applying the 2-and 4-wk window periods were 0.4(95% CI:0.03-5.24) and 2.1(95% CI:0.16-27.78),respectively.CONCLUSION:No increased risk of ARF was found in elderly PEG users.However,based on the limited number of study subjects,further analysis should be performed to confirm these results.

HPLC法测定注射用奈达铂中水解杂质乙醇酸的含量

目的建立一种注射用奈达铂中水解杂质乙醇酸测定的HPLC方法。方法采用Shimpack VP-ODS C18（250 mm×4.6 mm,5μm）为色谱柱,以磷酸盐缓冲液（p H6.0）-乙腈（80：20）为流动相;流速为1.0m L/min;柱温：25℃;检测波长为205 nm。结果本法线性范围为0.9822～19.64μg/m L（r=0.9995）,精密度RSD为4.5%（n=5）,重复性RSD为4.0%（n=6）,回收率为94.67%～105.7%,RSD为3.2%（n=9）。结论本方法准确、专属、耐用,可以很好的控制水解杂质乙醇酸的含量。

Carbon Balance of Cassava-based Ethanol Fuel in China

Considering energy security and greenhouse gas emission, many governments are developing bio-liquid fuel industries. The Chinese Government advocates the development of a fuel ethanol industry with non-food crops such as cassava. However, scientists debate the carbon emission of these bio-liquid fuels. The focuses are the influence of soil carbon pool destruction and by-product utilization. This study built a carbon balance analysis model, and assessed carbon emission of cassava fuel ethanol across its life cycle. The results show that the carbon emission of cassava fuel ethanol per kilogram in its life cycle was 0.457 kg under new technical conditions and 0.647 kg under old technical conditions. Carbon emission mainly came from the use of nitrogen fertilizer （9% of total emissions）, the destruction of the soil carbon pool （29%） and fossil energy inputs （50%）. Taking gasoline as a reference, the carbon emission of cassava fuel ethanol was 90% of that of gasoline. This percentage would drop to 64% if soil carbon pool destruction was avoided. Therefore, in order to promote the development of cassava fuel ethanol in China, farms should apply fertilizer properly, grow cassava on marginal land, and not alter land use patterns of woodland, grassland and other environments. In addition, we should exploit efficient fuel ethanol conversion technologies and strengthen the use of by-products.

Structural analysis of [Bmim]_2CuCl_4 ionic liquids in the presence of water and ethanol by XAFS technique

The structure of [Bmim]2CuCl4 ionic liquids （Bmim： 1-butyl-3-methylimidazolium） with different ratios of H2O and C2H5OH was investigated using X-ray absorption fine structure （XAFS） technique. In this study, XAFS was employed to directly probe the conformational variations of copper ions in [Bmim]2CuCl4 with the addition of either water or ethanol. XAFS analysis confirmed that the structure of ionic liquids gradually transformed from tetrahedral to octahedral configuration with the increase in ratio of H2O. Our results also showed that water molecules coordinated with the copper ions of [Bmim]2CuCl4, leading to the conformational change in ionic liquids. However, the XAFS spectra of [Bmim]zCuCIa/C2H5OH indicated no coordination of anhydrous ethanol with the copper ions of [Bmim]2CuC14. The structure of [Bmim]2CuCl4 ionic liquids is maintained as the tetrahedral configuration in presence of ethanol. Therefore, anhydrous ethanol causes little variation in the structure of ionic liquids and it is a good solvent for the dilution of ionic liquids.