流动注射分析法测定醋酸泼尼松片含量均匀度的研究

根据蓝四氮唑与泼尼松生成蓝色产物,并于525nm 波长处测定吸光度。测定条件为:反应管长度为3.8m(0.5mm id);流速为1.6ml/min;反应温度为55±0.5℃;注射样品溶液为100μl;本测定系统的测定速度可达100次/h;线性范围可达0.09mg/ml;检测限量为1.54μg/ml;测定结果的变异系数小于1%。     

曲肘式机构的优化设计

以功效系数为目标函数,相应地确定了设计变量和约束函数,对塑料注塑机合模机构的参数进行优化计算,提高了机构的综合性能。     

黄芪注射液治疗充血性心力衰竭的临床观察

目的 :观察黄芪注射液对充血性心力衰竭 (CHF)的治疗效果。方法 :将 12 7例心衰病人随机分为 2组。对照组 5 5例 ,给予传统治疗心衰药物洋地黄、利尿剂及休息、低盐饮食、吸氧等治疗 ;治疗组 72例 ,在对照组病人用药的基础上加黄芪注射液 40ml ,静脉滴注 ,每日 1次 ,2组均连续用药 15天。结果 :总有效率治疗组 91 7%,对照组 6 7 3%,治疗组效果明显优于对照组 (P <0 0 1) ,且 2组自身对照 ,治疗后好转程度 ,治疗组优于对照组 ,左室射血分数 (LVEF)明显好于对照组。结论 :在常规治疗CHF的同时加用黄芪注射液可显著提高疗效。     

Measurement of free and total hydroxyproline by automated flow injection of serum or urine samples from maintenance hemodialysis patients with renal osteodystrophy

An automated measurement of total and free hydroxyproline in serum or urine is presented that uses flow injection analysis. After exclusion of nonspecific substances, hydroxyproline was oxidized by chloramine- T and L-cysteine with Ehrlich's reagent. The linearity obtained was from 3.8μmole/ L to 1.22 mmole/L with good precision (CV <3%). Comparison of the proposed method with HPLC yielded r = 0.939 as the correlation coefficient. Reference intervals of free and total hydroxyproline are 1.4–9.7 μmole/L, 3.8–27.2 μmole/L for serum, and 10.0–72.5 μmole/L, 25.2–303.6 μmole/L for urine, respectively. Serum free and total hydroxyproline levels in renal osteodystrophy patients on maintenance hemodialysis (N = 71) were significantly higher than in controls (P<0.0001). This method is superior to the use of HPLC with regard to stability of the color reaction. The measurement of serum free and total hydroxyproline is a useful marker for therapeutic observation of renal osteodystrophy patients. © 1994 Wiley-Liss, Inc.     

A Study of the Mechanism of Yinzhihuang（菌栀黄）Injection in the Treatment of Infantile Hepatitis Syndrome

ＡＳｔｕｄｙｏｆｔｈｅＭｅｃｈａｎｉｓｍｏｆＹｉｎｚｈｉｈｕａｎｇ（菌栀黄）ＩｎｊｅｃｔｉｏｎｉｎｔｈｅＴｒｅａｔｍｅｎｔｏｆＩｎｆａｎｔｉｌｅＨｅｐａｔｉｔｉｓＳｙｎｄｒｏｍｅＤｏｎｇＹｏｎｇ－ｓｕｉ（董永绥）；ＨｕａｎｇＺｈｉ－ｈｕａ（黄志华）；...     

病人自控硬膜外镇痛泵治疗难治性腰椎间盘突出症临床观察

目的观察病人自控硬膜外镇痛（PCEA）泵治疗难治性腰椎间盘突出症的临床疗效。方法采用临床随机对照的方法，观察组和对照组分别应用病人自控硬膜外镇痛（PCEA）泵和用传统硬膜外注射术进行治疗，并对治疗结果进行统计分析。结果观察组痊愈31例（治愈率68．89％），好转11例（有效率93．33％），对照组痊愈18例（治愈率43．90％），好转16例（有效率82．93％）。两组治愈率比较P=0．019〈0．05，差异有显著性意义，有效率比较P=0．243〉0．05，差异无显著性意义。结论病人自控硬膜外镇痛（PCEA）泵治疗难治性腰椎间盘突出症治愈率要高于传统硬膜外注射术，在药物效应的基础上起液体剥离和持续给药的效果是其可能的作用机制。     

参芪扶正注射液对淋巴细胞的作用

目的:观察参芪扶正注射液对淋巴细胞的作用.方法:用参芪扶正注射液处理Jurkat淋巴细胞,通过台盘兰染色计数和流式细胞计观察其对淋巴细胞的作用,用参芪处理过的淋巴细胞分别加入化疗药和肝癌细胞,观察两种细胞的反应.结果:参芪扶正注射液处理过的淋巴细胞,细胞增殖快,有较强的抵抗化疗药诱导凋亡的能力,杀伤肝癌细胞的能力增强.结论:参芪扶正注射液具有多方面的免疫调节作用.     

小牛血清去蛋白注射液细菌内毒素检测方法的研究

目的：建立小牛血清去蛋白注射液的细菌内毒素检查方法。方法：根据2000年版《中国药典》进行试验。结果：小牛血清去蛋白注射液在2mg/ml浓度下进行细菌内毒素检查干扰现象，获得了可靠的数据和结果。结论：本品所采用的细菌内毒素检查方法灵敏、可靠。     

水蛭注射液对大白鼠血小板粘附和血小板聚集功能的影响

目的　探讨水蛭注射液对大白鼠血小板粘附性和聚集性的影响。方法　采用大白鼠 2 4只 ,随机分成两组 ,实验组给药 ,对照组以实验组同样的方法和剂量给予生理盐水 ,5d后由颈总动脉取血 ,做血小板粘附性和聚集性试验。结果　水蛭注射液对大鼠血小板粘附性和聚集性具有显著的抑制作用 ,实验组与对照组抑制率有显著的统计学意义 (P <0 0 0 1)。结论　水蛭注射液能够抑制大白鼠血小板的粘附和聚集。     

Action of intravenously administered talipexole on the rat striatal neurons receiving excitatory input from nigral dopamine neurons

Electrophysiological studies using rats anesthetized with chloral hydrate were performed to elucidate whether or not intravenously injected talipexole acted as a D₂ receptor agonist on the striatal neurons in comparison with the action of bromocriptine. The activities of the striatal neurons were extracellularly recorded using a glass microelectrode attached along a seven-barreled micropipette, each barrel of which was filled with talipexole, bromocriptine, SCH23390 (D₁ antagonist), domperidone (D₂ antagonist), glutamate or 2 M NaCl. These drugs were iontophoretically applied to the immediate vicinity of the target neuron being recorded. The effects of talipexole and bromocriptine were examined on the neurons, whose spikes (induced by the stimulation of the substantia nigra pars compacta) were inhibited by the iontophoretic application of domperidone. Iontophoretic application of talipexole or bromocriptine increased spontaneous firing of these neurons and this increase in firing was also inhibited by iontophoretically applied domperidone. In the same neurons, intravenously administered talipexole (0.01, 0.02 and 0.04 mg/kg) dose-dependently increased firing, and this increase was inhibited by microiontophoretically applied domperidone, but not by SCH23390. On the other hand, the intravenous injection of bromocriptine (0.1, 0.2 and 0.4 mg/kg) also increased the firing rate. However, the increase was not dose-dependent and fluctuated; the firing transiently decreased during the increase in firing with intravenously administered bromocriptine. However, the bromocriptine-induced increase in firing was also suppressed by domperidone, and decrease in firing was inhibited by SCH23390. These findings suggest that talipexole acts as a D₂ agonist on the striatal neurons receiving input from substantia nigra pars compacta and increases firing when intravenously applied. However, intravenously administered bromocriptine appears to act as both a D₂ agonist and probably as a D₁ agonist on the striatal neurons to increase and decrease firing, respectively.