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1.
Chinese Traditional and Herbal Drugs ; (24): 3261-3269, 2018.
Article in Chinese | WPRIM | ID: wpr-851828

ABSTRACT

Objective: To evaluate the pilot technological process of Compound Banlangen Liyan Granules (CBLG). Methods: According to the indexes of six effective ingredients loss amount, accumulated loss rate, and HPLC characteristic spectrum similarity, the process quality of four key processes was evaluated and compared, such as microfiltration of ceramic membrane, vacuum concentration of extract, vacuum drying of concrete, and atmospheric drying of granules. Results: It was found that the total loss rates of glycyrrhizic acid, harpagoside, (R,S)-epigoitrin, liquiritin in two batches were 50.06%—66.99%, and angoroside C, adenosine were 35.49%—41.90%. The total content of the six effective ingredients of each material within the same batch of the two pilot batches from high to low were as follows: extract solution before membrane filtration > extract solution after membrane filtration > concentrate extract solution > dried concrete powder > granules of finished product. The comparison among four key processes loss rates was as follows: vacuum drying of concrete > ceramic membrane microfiltration > vacuum concentration of extract, atmospheric drying of granules. Loss amount of concrete vacuum drying process of the two pilot batches were 0.545 9 and 0.737 5 mg/g, and the process was the major loss process. The total loss rates of the two pilot batches were 48.15%, 50.85%, respectively. The HPLC characteristic spectrum similarity of each material within the same batch of the two pilot batches decreased from 0.998 to 0.818 with increasing process. The HPLC characteristic between the two batches of finished products was good (the similarity was 0.999). Conclusion: The consistency of the finished product quality between two batches was good. The study provided a basis for pilot production process control of CBLG. In the modernization and standardization study of traditional Chinese medicine preparation process, mild process of low temperature and short time heating should be applied as far as possible. It can reduce the effective components loss of original extract (decoction of herbal medicine) in the preparation process and maintain the quality and efficacy consistency of traditional Chinese medicine preparation and original extract (decoction of herbal medicine).

2.
Chinese Traditional and Herbal Drugs ; (24): 1161-1166, 2015.
Article in Chinese | WPRIM | ID: wpr-854223

ABSTRACT

Objective: Through studying the rationalization of alcohol precipitation process of Liuwei Dihuang Prescription to obtain the stability alcohol precipitation process which could be used to promote industrialization. Methods: It screens the most reasonable alcohol precipitation process taking the contents, the relative molecular weight distribution, and the extract of loganin, peoniflorin, morroniside, manninotriose, and polysaccharide as the evaluation index to investigate the way of adding ethanol, centrifugation,, and whether to carry out the ethanol washing process. Results: The alcohol precipitation process is reasonable by calculating the alcohol volume method. The polysaccharides and alcohol precipitation supernatant could be efficiently separated by ethanol washing method. The polysaccharide extract and the contents of glycosides and manninotriose were up to the standard after the process improved. Conclusion: The optimized alcohol precipitation process is easy operation with good controllability and repeatability. It is worthy of popularization and application of industrialization.

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