目的探讨加兰他敏原料药、制剂市场的发展前景。
OBJECTIVE: To analyze the market prospect of the raw material and the preparations of galantamine.
采用溶剂萃取法和上行硅胶柱层析法分离加兰他敏。
The solvent extraction and upstream silica gel column chromatography are combined to separate galanthamine.
目的研究氢溴酸加兰他敏分散片的处方组成及制备工艺。
Objective To investigate the composition and preparation method of galanthamine hydrobromide dispersion tablets.
目的：研究氢溴酸加兰他敏及其分散片的处方和制备工艺。
Objective: To instigate both prescription and stability of galanthamine hydrobromide dispersion tablets.
目的建立一种光纤传感快速测定氢溴酸加兰他敏注射液光谱和含量的方法。
OBJECTIVE To develop a rapid analysis method by fiber-optic sensor for determining galanthamine hydrobromide injection spectrum and content rapidly.
加兰他敏是从雪片莲中提取的一种生物碱，具有可逆性胆碱酯酶抑制活性。
Galantamine is an alkaloid originally extracted from the bulbs of the plant Leucojum aestivum and shows reversible acetylcholinesterase(AChE) inhibitory activity.
芬兰科学家们发现加兰他敏药物可以对老年性痴呆患者提供有效的对症治疗。
Scientists in Finland found that the drug galanthamine provides an effective symptomatic treatment for patients with dementia.
根据客户的不同要求采用CP 2000、BP98、USP标准生产氢溴酸加兰他敏。
According to the requirements from different clients, we have adopted CP2000, BP98, USP standards to produce Galanthamine Hydrobromide.
方法分析加兰他敏野生资源分布与人工栽培，及其外消旋体与对映体的化学合成进展状况。
METHODS: Comprehensivelly analyzing the status of the wildlife and the planting herb resource of galantamine, and the progress of synthesizing racemized galantamine and it's enantiomer.
同一地区样品中总生物碱与加兰他敏的含量呈一定的正相关，相关系数为0.601，但并不显著。
Correlation analysis showed that the relationship between the contents of total alkaloids and galanthamine was positive in the same place, the correlation coefficient was 0.601.
目的：建立加兰他敏血浆药物浓度的HPLC - UV检测法，研究其在人体的药代动力学和相对生物利用度。
OBJECTIVE: to develop a HPLC-UV method to determine the concentration of galanthamine in human plasma and study its pharmacokinetic profiles and bioequivalence.
目的：建立加兰他敏血浆药物浓度的HPLC - UV检测法，研究其在人体的药代动力学和相对生物利用度。
OBJECTIVE: to develop a HPLC-UV method to determine the concentration of galanthamine in human plasma and study its pharmacokinetic profiles and bioequivalence.
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