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1.
China Pharmacy ; (12): 1914-1919, 2019.
Article in Chinese | WPRIM | ID: wpr-817205

ABSTRACT

OBJECTIVE:  To improve the method for the content determination of astragaloside Ⅳ in Xiangju granules, and to evaluate the consistency of relevant preparations with the components of original formulation, so as to provide evidence for the modern preparation of TCM compound. METHODS: HPLC-ELSD method was established for the content determination of astragaloside Ⅳ in Xiangju granules, and compared with original standard TLC scanning. Using critrinin, ferulic acid, calycosin glucoside, liquiritin, glycyrrhizic acid, rosmarinic acid, buddleoside and magnoline as control, HPLC method was used to determine the release components of self-made Xiangju granules, Xiangju capsules, Xiangju tablets in water. Fingerprint characteristics chromatogram of different Xiangju preparations and original formulation extract were compared by using Similarity Evaluation System for Chromatographic Fingerprint of TCM (2012 version). At the same time, HPLC-ELSD method was used to determine and compare the release rate of astragaloside Ⅳ from different Xiangju preparations and original formulation extract in water. RESULTS: Established HPLC-ELSD method was specific. The linear range of astragaloside Ⅳ was 0.13-2.10 mg/mL. RSDs of precision, repeatability and stability tests were all lower than 3% (n=6), and average recovery was 97.66% (RSD=1.01%,n=6). Average content of astragaloside Ⅳ by this method was 0.398 mg/g (RSD=1.01%, n=3), which had better reproducibility than TLC scanning. The comparative results of characteristic fingerprints showed that the similarity among Xiangju granules, Xiangju capsules, Xiangju tablets and the original formulation dry extract powder was more than 0.850. Average release rates of astragaloside Ⅳ in Xiangju granules, Xiangju capsules, Xiangju tablets and the original formulation extract were 0.392, 0.358, 0.349, 0.389 mg, respectively. Compared with original formulation extract, there was no statistical significance in release rate of astragaloside Ⅳ in Xiangju granules (P>0.05), while there was statistical significance in Xiangju capsules and Xiangju tablets (P<0.01). CONCLU- SIONS: Established HPLC-ELSD method is accurate and feasible, and is suitable for the content determination of astragaloside Ⅳ in Xiangju granules. The main components of Xiangju granules are consistent with original formulation.

2.
Chinese Traditional and Herbal Drugs ; (24): 308-310, 2001.
Article in Chinese | WPRIM | ID: wpr-410630

ABSTRACT

Object To determine the amount of acacetin-7-O-β-D-glucoside and apigenin-7-O-β-D-glucoside in Chrysanthemum morifolium Ramat. from different localities. Methods By the use of HPLC. Results The contents of acacetin-7-O-β-D-glucoside in Boju1, Chuju2, Gongju3 and Hangju4 were 0.082 6%~0.124 9%, 0.015 7% and 0.033 5% respectively; the contents of apigenin-7-O-β-D-glucoside in Chuju, Boju, Gongju and Hangju were 0.012 6%, 0.027 4%, 0.117 7% and 0.587 7% respectively. Conclusion The contents of the two flavone glycoside in C. morifolium from different localities were markedly different.

3.
Chinese Traditional Patent Medicine ; (12)1992.
Article in Chinese | WPRIM | ID: wpr-680966

ABSTRACT

Objective: To determine luteolin 7 O ? D glucoside in Chrysanthemum morirolium Ramat. Methods: The content of luteolin 7 O ? D glucoside was determined by HPLC on Symmetry Shield TM RP S column with MeoH H 2O(49∶51) as a mobile phase and detection wavelength at 348nm. Results: The liuear relationship of this method was well and the average recovery of the added sample is 99.74%. Conclusion: The analytical time is short, separating degree is good and results are accurate when luteolin 7 O ? D glucoside is determined by this method.

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