程控电流示波计时电位法

使用计算机产生极化电流具有纯度高，稳定性好和波形形状种类多等优点。研究了极化电流的频率，波形和相角对示波图的影响。对Ｃｄ＾２＋的测定的线性范围为２×１０＾－５～２×１０＾－４ｍｏｌ／Ｌ，相关系数为０．９９７，该方法可且希望用于分析测试和动力学方面的研究。     

凝胶过滤色谱法测定泥鳅多糖的组成及分子量

从泥鳅粘液中分离提取到中性的粗多糖 ,采用凝胶过滤色谱柱在高效液相色谱仪上进行分离和测定 ,结果表明 ,该多糖由一个高聚糖 (MAP ,19 1% )和一个寡糖 (MAO ,80 9% )组成。用标准的Pullulan(P 112 0 0 0 ,P 4 730 0 ,P 2 2 80 0 ,P 5 90 0 ,P 2 70 0 )作标准曲线 ,测得其重均分子量分别为 130 2 5 2 (约 72 3个糖基 )和 15 39(约 9个糖基 )。粗多糖经SephadexG 10 0凝胶柱 (1cm× 5 0cm)过滤 ,分离得到纯化的MAP和MAO。     

Determination of flurazepam and its hydroxyethyl and dealkyl metabolites by some packed and capillary ECD-GLC methods: Application to pharmacokinetic studies

A sensitive gas-liquid chromatographic assay was developed for plasma determinations of flurazepam (F), N1-desalkylflurazepam (DF), and N1-hydroxyethylflurazepam (HF). The internal standards used were delorazepam for F and DF and 1 ã-hydroxymidazolam for HF. Following extraction and derivatization for HF, these compounds were analyzed by ECD-GLC, using either glass packed columns (poly A 103 for F and DF, OV 225 for HF) or CP-Sil 5 capillary columns for DF and HF. The detection limit of the packed-column assay was approximately 3ng/ml for HF and DF, and 5ng/ml for F; with capillary GLC analysis, the sensitivity limit for HF and DF was lower than 1 ng/ml. These methods were used for pharmacokinetic investigations after i. v. administration of these compunds.     

神经网络与紫外光谱法同时测定芳香类化合物

测定了苯酚、苯胺、α萘胺、间二硝基苯及对氧基苯甲醛混合体系的紫外光谱，用神经网络法直接对混合体系紫外光谱数据进行处理，成功地测定了混合体系各组分含量，结果良好     

Isotopenverdünnungsanalyse mit der Funkenquellen-Massenspektrometrie

Es wird über Untersuchungen zur massenspektrometrischen Isotopenverdünnungsanalyse mit stabilen Nukliden unter Verwendung von Hochfrequenzfunken- Ionenquellen berichtet. Die Analysenmethode zeichnet sich durch eine gute Richtigkeit und Reproduzierbarkeit der Analysenergebnisse mit durchschnittlichen Standardabweichungen von 5% bis 10% im ppm- Bereich aus. Durch die Anwendung des elektrischen Ionennachweises und der Ionenstromverstärkung mittels Sekundärionenvervielfacher konnten die Analysenzeiten gegen über der Isotopenverdünnungsanalyse mit photographischer Ionenstromregistrierung wesentlich gesenkt werden.     

The crystal structure of a Terbium(III) complex with 1,1-Cyclobutanedicarboxylic acid

A complex of 1,1-cyclobutanedicarboxylic acid with terbium was obtained as a pentahydrate. The salt crystallizes in the monoclinic system, space group P2₁/n with a = 15.885(3), b = 8.489(2), c = 19.189(4)?Å, β = 106.02(3)° and Z = 4. The structure was solved by direct methods and refined to R = 0.0537. The complex forms polymeric chains in which terbium(III) ions are linked by carboxylate bridges. Each terbium cation is surrounded by carboxylate oxygen atoms and two or three water oxygen atoms, giving coordination number 9. The structure is stabilized by a system of hydrogen bonds.     

多元统计分析方法在大鼠肾病疗效分析中的应用

本文根据河北医科大学运用中药青风藤提取物青藤碱治疗患系膜增生性肾小球肾炎的SD大鼠的最新实验数据,采用多元统计分析的Fisher判别法,对该实验制模过程、治疗效果进行判别分析.从统计意义上讲,该实验制模是成功的,青藤碱的治疗效果与常用药物雷公藤多苷一样比较显著.     

迭代目标因子分析-紫外分光光度法测定克感敏片三组分

本文应用迭代目标因子分析－紫外分光光度法不经分离同时测定克感敏 片中非那西丁、氨基比林、咖啡因三组分含量,其回收率和相对标准偏差分别为100．4％,0．83％,99．2％,0．77％,99．4％,0．69％。     

Synthesis of 3-amino-4-methyl-6-trifluoromethylthieno[2,3-b]pyridine-2-carboxanilide and its crystal and molecular structure

4-Methoxy-1,1,1-trifluoropent-3-en-2-one reacts with cyanothioacetamide to give 3-cyano-4-methyl-6-trifluoromethylpyridine-2(1H)-thione, which was transformed into 3-amino-4-methyl-6-trifluoromethylthieno[2,3-b]pyridine-2-carboxanilide by the reaction with chloroacetanilide. The crystal and molecular structure of the amide obtained was studied by X-ray analysis. Translated fromIzvestiya Akademii Nauk Seriya Khimicheskaya, No. 4, pp. 701–703, April, 1998.     

Biosorption of lead from aqueous solution by seed powder of Strychnos potatorum L.

In the present study, Pb(II) removal efficiency of Strychnos potatorum seed powder (SPSP) from aqueous solution has been investigated. Batch mode adsorption experiments have been conducted by varying pH, contact time, adsorbent dose and Pb(II) concentration. Pb(II) removal was pH dependent and found to be maximum at pH 5.0. The maximum removal of Pb(II) was achieved within 360 min. The Lagergren first-order model was less applicable than pseudo-second-order reaction model. The equilibrium adsorption data was fitted to Langmuir and Freundlich adsorption isotherm models to evaluate the model parameters. Both models represented the experimental data satisfactorily. The monolayer adsorption capacities of SPSP as obtained from Langmuir isotherm was found to be 16.420 mg/g. The FTIR study revealed the presence of various functional groups which are responsible for the adsorption process.