1.Analysis of Dual-wavelength Fingerprint Chromatogram of Buzhong Yiqi Decoction
Rufeng HUA ; Keer HUANG ; Xuehong KE ; Jinfu CHEN
Traditional Chinese Drug Research & Clinical Pharmacology 1993;0(01):-
Objective To establish the fingerprint chromatogram of Buzhong Yiqi Decoction(BYD) by multiple wavelength method,and to analyze the substance of formulas as a whole.Methods HPLC-PDA method was adopted.The chromatographic conditions were as follows:Hypersil ODS2 analytical column,the mobile phase consisting of 0.05 %phosphate acid and acetonitrile with gradient elution,detecting wavelength at 254 and 280 nm,the flow rate being 1.0 mL/min and the temperature of the column at 30 ℃.Results The methodological results were good.The results of dual-wavelength fingerprint chromatogram showed the all-around information of the fingerprints at 254 and 280 nm.The similarity of 10 batches of BuzhongYiqi Decoction was over 0.98.Conclusion Dual-wavelength fingerprint chromatogram can realize the analysis of a formulas as a whole,which supplies references for improving the quality control of BuzhongYiqi Decoction.
2.Fingerprint of Xiasangju Granules and its application in quality control
Xuehong KE ; Weiguang SUN ; Jiangxiong YAO ; Rufeng HUA ; Jinfu CHEN
Chinese Traditional Patent Medicine 1992;0(07):-
AIM: To establish an effective and convenient method for applying HPLC fingerprints to quality control in the production of Xiasangju Granules(Spica prunellae,Folium mori,Flos chrysanthemi). METHODS: Komasil Sunfrie C_(18)(150 mm?4.6 mm,5 ?m) analytical column was used and eluted with a gradient program consisted of phase A(1% acetic acid) and phase B(methanol) and detected at 290 nm.The fingerprints of aqueous extract,alcohol-precipitated extract,concentrate and finished product were compared with. RESULTS: The fingerprint method for Xiasangju Granules was established.The similarity among 10 batches of Xiasangju Granules was no less than 0.970.The difference between extracts and finished product of Xiasangju Granules was obvious. CONCLUSION: This validated method is available for quality evaluation and quality control in Xiasangju Granule's production.
3.Determination of Hesperidin in Separated Prescriptions of Buzhong Yiqi Decoction
Yuan LI ; Xuehong KE ; Wei CHEN ; Rufeng HUA ; Jinfu CHEN ; Xiaocui YANG
Traditional Chinese Drug Research & Clinical Pharmacology 1993;0(03):-
Objective To study the change of Hesperidin content in various combinations of medicine from Buzhong Yiqi Decoction(BYD) by RP-HPLC.Methods The hesperidin content was determined by HPLC and analyzed by L8(27) orthogonal design and statistic analysis(SPSS).Results Principal herbs and ministerial herbs of BYD had a significant effect on the hesperidin content of adjunctive herbs(P
4.Study on preparation process for Xuesaitong Dropping Pills
Jiaming ZHOU ; Jinfu KE ; Xiuming CUI ; Chaoliang WANG ; Hualong YUANG ; Chen LIANG ;
Chinese Traditional Patent Medicine 1992;0(10):-
Objective: To establish the optimum preparation process for Xuesaitong Dropping Pills(total saponin of Radix Notoginseng). Methods: On the basis of orthogonal design, preparation conditions were selected among sort of polyglycol (as substance), consumption of polyglycol and processing temperature of usoline (as cooling agent). Results: Under the condition of using polyglycol 6000, and processing temperature at 10~15 ?C , the quality of Xuesaitong Dropping Pills is good.