OBJECTIVE: To establish the method for the determination of emodin, resveratrol, polydatin and gentiopicrin in the Compound Polygonum cuspidatum semisolid matrix capsule in order to provide basis of its quality control. METHODS: TLC scanning method was used to determine emodin and resveratrol at same plate and the developer was petroleum ether-butyl acetate-methanol-glacial acetic acid(4∶1∶0.7∶0.03) with determination wavelength of 285 nm and 293 nm respectively. Polydatin and gentiopicrin were determined at same plate and the developer was chloroform-methanol(7 ∶ 2)with determination wavelength of 313 nm and 270 nm respectively. RESULTS: All target components were separated and the standard curves of emodin, resveratrol, polydatin and gentiopicrin showed good linearity. Average recoveries of them were 100.1%(RSD=0.86%),99.6%(RSD=2.86%), 101.4%(RSD=0.99%),98.5%(RSD=2.89%),respectively. CONCLUSION: Established method is rapid, simple for the quality control of Compound P. cuspidatum semisolid matrix capsule.

AIM: To establish the method of determining ginsenoside Rg1 and notoginsenoside R1,and control the quality of Yiqi Gushen Dialysis Liquid(Radix et Rhizoma Notoginseng,Radix Astragali,etc.) METHODS: Sample was pretreated with solid phase extraction using ODS C_13 cartridges.Ginsenoside Rg1 and Notoginsenoside R1 were separated with TLC method.The mobile phase was chloroform-methanol-water(3∶0.8∶0.1),developed twice.The coloration was 10% sulphuric acid ethanol solution.The detection wavelength was 560 nm. RESULTS: The calibration curves for ginsenoside Rg1 and notoginsenoside R1 were A=113.4 C-34.976,(r=0.997),A=92.14 C-13.597,(r=0.997),respectively,the linear ranges were between 2.64-13.2 mg and 0.85-8.5 mg,and the detection limit was 0.88 mg and 0.65 mg,respectively.The average recoveries were 100.31% and 98.72%,respectively.The contents of the sample were between 5.683-5.764mg,1.528-1.599 mg per 10 mL,respectively. CONCLUSION: The proposed method for estimating ginsenoside Rg1 and notoginsenoside R1 is simple,precise,specific,sensitive and accurate and can be used for quality control of Yiqi Gushen Dialysis Liquid.

OBJECTIVE:To optimize the extraction craft of gentiopicrin from gentian.METHODS:The extraction craft was optimized by orthogonal test with gentiopicrin as an index,and the content of gentiopicroside was determined by TLC scanning method.RESTLUTS:The quantity of menstruum and the extraction times of gentiopicrin had significant influence in the gentiopicrin extraction(P

OBJECTIVE: To optimize the extraction conditions of plumula nelumbinis. METHODS: The semi - bionic extraction (SBE) conditions were optimized by homogeneous design while total alkaloids and dry extract were adopted as markers. Factors of extraction time, solute quantity and the pH values were evaluated for their effects on extraction process. RESULTS: Optimal parameters were as follows: plumula nelumbinis was extracted in water 8 times as much as it for 3 times; the pH values of the water for the 1st, 2nd and 3rd decoctions were 5.0,6.0 and 8.0, respectively; the boiling lasted 4 hours. CONCLUSION: The method prouides theoretical reference for the extraction plumula nelumbinis.

OBJECTIVE:To establish a HPLC method for determination of anthraquinone free derivatives from Chinese herbal in dog serum METHODS:With Hypersil BDS C18 column,the mobile phase was methanol-0 5% acetic acid(80∶20) The sample was extracted with methanol and dried at room temperature The residue was reconstituted by methanol and analyzed at 430nm RESULTS:The five components can be separated well The linear ranges were Aloe-emodin(0 15～6 0?g/ml,r=0 9 996) Rhein(0 14～5 6?g/ml,r=0 9 982);Emodin(0 13～5 2?g/ml,r=0 9 990);Chrysophanol(0 2～8 0?g/ml,r=0 9 991);Physcion(0 1～4 0?g/ml,r=0 9 994) CONCLUSION:This method can provide the basis for vivo analysis of anthraquinone free derivatives and bioavailability study of Rheum palmatum preparations

AIM: To establish an effective and economical processing method for high quality of Calcinatum Alumen with microwave heating. METHODS: A certain amount of Alumen was placed into microwave oven and heated, and its weight was determined by electronic balance every one or five minutes. The quality (appearance, aqueous solubility, water content) of Calcined Alum by microwave was compared with those of products prepared by traditional method, far IR, and electric oven. Moreover, the stability of Calcined Alum in several kinds of package were investigated at room temperature. RESULTS: The microwave for the processing of Alumen has the advantage of rapidness, low cost, and less water content, and its product could be dissolved completely in water. CONCLUSION: Microwave is a practical technique for Alumen processing.

Phe) polymorphism and GD in Han population of Chongqing area.

AIM:To establish a new processing method for Borax with microwave technique. METHODS: A certain amount of Borax was placed into microwave oven and heated, and its weight loss was determined by electronic balance. The optimum processing parameters were obtained through orthogonal design. Water content of Calcined Borax was determined by far IR, microwave oven, and electric oven(at (400 ?C)),respectively. In addition, the stability of Calcined Borax was studied at room temperature. RESULTS: Calcined Borax will be available (within) 30 min with microwave treatment. The total water content can be determined by electric oven(at (400 ?C)). Calcined Borax should be powdered and packed as soosn as possible after processing. CONCLUSION: Microwave is a kind of excellent method for preparation of Calcined Borax in laboratory, with advantages of rapidness and simplicity.

Object To study the difference of phenylethanoid glycoside between the cultured cells of Cistanche salsa (C. A. Mey.) Benth. et Hook. f. and Herba Cistanche. Methods Making comparison by means of FTIR and HPLC technique. Results Using the FTIR technique, the infrared spectrum of cutured cell of C. salsa was similar to that of native Herba Cistanche at a certain extent. The HPLC analysis indicated that the main chemical constituents in cultured cells of C. salsa were similar to that of native Herba Cistanche while considerable difference of constituents was found between them. Conclusion On the whole, there are much more constituents in the cultured cells of C. salsa comparing with the native Herba Cistanche. The content of echinacoside and acteoside in the cultured cells is much higher than that in the native Herba Cistanche.