1.Enrichment process of paeoniflorin from Kunyining Granules with macroreticular resin.
Jiancheng TANG ; Rongrong WANG ; Ying FENG
Chinese Traditional Patent Medicine 1992;0(06):-
AIM: To study the optimal condition and parameters for the enrichment process of paeoniflorin in Kunyining Granules (Radix Paeoniae Rubra, etc.) with macroreticular resin. METHODS: With the enrichment degree of paeoniflorin in Kunyining Granules as an index, the optimal conditions of the enrichment process were investigated. RESULTS: The optimal condition showed that the aqueous extract was taken into the macroporous resin column, and kept for 30 min, then the resin was washed by water to get rid of impurity and then we used six times as much 50% ethanol as aqueous extract to elute paeoniflorin. CONCLUSION: The process is feasible to enrich paeoniflorin from Kunyining Granules.
3.Study on the Preparation Technology of Tangzu Granula
Jiancheng TANG ; Rongrong WANG ; Danfei CHEN ; Jianming PAN
Traditional Chinese Drug Research & Clinical Pharmacology 2009;20(4):383-385
Objective To optimize the preparation process of Tangzu Granula. Methods With the paste-forming rate and total content of paeoniflorin as the indexes, the optimal water-extraction condition was screened by orthogonal design. With hydroscopicity, fluidity and formability as the indexes, the appropriate ratio of the excipient and the formula were selected. Results The optimum water-extraction condition was as follows: 10-fold water, decoction for 2 times and 1.5 hour for each time. The optimal ratio of the excipient and the formula for preparation of Tangzu granules were two proportions of the extract and three proportions of the excipient which consisted of lactose and dextrin(2 : 1, w/ w). Conclusion The technology is effec-tive, scientific, reasonable, and practical.
4.Effects of Cell-wall-broken Extraction Process on Total Flavones of Pollen Typhae
Rongrong WANG ; Danfei CHENG ; Xusheng WU ; Jiancheng TANG
Traditional Chinese Drug Research & Clinical Pharmacology 2000;0(05):-
Alcohol-infusion. Conclusion: With the cell-wall-broken extraction process, a higher content of total flavones was obtained from Pollen Typhae .
5.Comparative Study on Dissolution of the Total Flavones in Pollen Typhae Before and After Wall Breaking
Rongrong WANG ; Danfei CHEN ; Jiancheng TANG ; Xushen WU
Traditional Chinese Drug Research & Clinical Pharmacology 1993;0(01):-
Objective Dissolution test was applied to study the dissolution rates of total flav ones from Pollen Typhae before and after wall breaking.Methods The content of total flavones was determined by UV -spectrophotometry an d Basket -Stirring Method.Results Using total flavones as the index,T 50 was 29.57min and T d was 41.28min before wall break-ing,and 41.27min and 54.26min respectively after wall breaking,the dif ference being very significant.Conclusion The dissolution rate of the total fla vones from Pollen Typhae is faster after wall -breaking treatment than th at before treat-ment.
6.Comparison of the mucin 7 mRNA test and urine cytology for detection bladder cancer
Rongrong ZHANG ; Hong LIAO ; Guomin TANG ; Yiping LU ; Lin ZHANG
Chinese Journal of Urology 2008;29(12):826-828
Objective To compare the sensitivity and specificity of mucin 7(Muc7) mRNA test with urine cytology in detection bladder cancer.Methods In 86 patients suspected with bladder cancer,RT-PCR for Muc7 mRNA and urine cytology were conducted in the same urine samples.Fif-ty-two patients with bladder transitional cell carcinoma were confirmed histologically.The sensitivity and specificity of Muc7 mRNA and urine cytology were analyzed.Results The overall sensitivity,specificity and false positive of Mue7 mRNA test were 84.6%,85.2% and 14.7% respectively.Those of urine cytology were 34.6%,91.2% and 8.8% respectively.There were no significant differences between urine cytology and Muc7 mRNA test in the specificity and false positive; however,Muc7 mRNA had significantly higher sensitivity than urine cytology in detection of bladder cancer.Conclusion The sensitivity of Muc7 mRNA test is superior to urine cytology in detection of bladder cancer.
7.Intervention of BCG Polysaccharide and Nucleic Acid in Hypersusceptibility in Guinea Pigs
He TANG ; Ruilian LI ; Zishan LI ; Jiehu OUYANG ; Rongrong WANG
China Pharmacist 2015;(3):394-396,397
Objective:To study the effect and underlying mechanism of BCG polysaccharide and nucleic acid ( BCG-PSN) in hy-persusceptibility in guinea pigs to explore the improvement method for the quality control model of BCG-PSN. Methods:The ovalbumin induced hypersusceptibility animal model was established, the effect of BCG-PSN on hypersusceptibility in guinea pigs was observed. According to the guideline for immunity toxicity study on Chinese traditional medicine and natural medicine, the hypersusceptibility tests were carried out. Serum IgE and histamine were determined by ELISA. Results:The guinea pigs in the model group and the low dosage BCG-PSN group showed strong anaphylactic symptoms, while the middle and high dosage BCG-PNS groups showed fewer symp-toms. The level of IgE in the model group was (1. 673 0 ± 0. 158 6) μg·ml-1 and (1. 683 1 ± 0. 228 1)μg·ml-1 before and after the attacking, respectively, which was higher than that in the control group(P<0. 01). The levels of IgE in the middle and high dos-age BCG-PNS groups were decreased compared with those in the model group before and after the attacking(P<0. 01). The same re-sults were observed in the levels of histamine. Before and after the attacking, the levels of histamine in the model group was (1. 499 7 ± 0. 133 1) ng·ml-1 and (1. 512 1 ± 0. 050 6) ng·ml-1 , respectively, while the levels of histamine in low, middle and high dos-age BCG-PNS groups were decreased compared with those in the model group before and after the attacking(P<0. 01). Conclusion:BCG-PSN can dose-dependently inhibit the anaphylactic reaction induced by ovalbumin.
8.Self-microemulsifying drug delivery system of Acanthopanax senticosus total saponin
Haiyan ZHAO ; Jianping LIU ; Rongrong TANG ; Bo PAN
Chinese Traditional and Herbal Drugs 1994;0(04):-
Objective To develop self-microemulsifying drug delivery system(SMEDDS) of Acanthopanax senticosus total saponins(ASTS) and the determination method.Methods The equilibrium solubility of ASTS in different compositions of oils,emulsifier and assistant emulsifier was investigated.The self-microemulsion formula was optimized by constructing the pseudo-ternary phase diagrams of blank SMEDDS and the studying the self-microemulsifying efficiency and the stability of drug-loaded SMEDDS.Taking isofraxidin,an effective component of A.senticosus,as the content determination index,the content was determined by HPLC.Results The optimal self-microemulsion formula was composed of Caf,propanediol,and ethyl linolenate.The ratio of them was 16∶4∶5.The average particle size was 40 nm.The average content of isofraxidin was 92.6 ?g/mL.Conclusion The acquired microemulsion with small particle size is stable.The content determination method of taking isofraxidin as the quality control index is accurate and reliable.
9.Effects of Levofloxacin on QTcd Interval in Elderly Patients Hospitalized with Acute Exacerbations of COPD
Qian GUI ; Jie CHEN ; Rongrong TANG ; Changqing ZHU ; Yi CHEN
Chinese Journal of Nosocomiology 2006;0(06):-
OBJECTIVE To study the effects of levofloxacin on QT correction dispersion(QTcd) interval in elderly patients hospitalized with acute exacerbations of COPD(AECOPD).METHODS Totally 124 patients received IV levofloxacin(500 mg qd) for 10-14 days.Evaluations included of 12-lead ECGs at baseline and blood examination before treatment,day 5 and after treatment.RESULTS QT correction(QTc) interval was no significant changes,but the QTcd interval was with significant prolongation.CONCLUSIONS IV levofloxacin could not cause QTc interval prolongation,but could make QTcd interval prolongation,which is a potential risk of arrhythmia in elderly patients with AECOPD.
10.Alpinetin down-regulating Bcl-2 promotes apoptosis of human hepatic cancer Hep3B cells
Bo TANG ; Yang LI ; Fang TANG ; Zhenran WANG ; Rongrong NIE ; Shuiping YU ; Bo LI
Chinese Journal of General Surgery 2013;28(7):542-545
Objective To study the effects of alpinetin on apoptosis of Hep3B cells and explore the related mechanism.Methods Hep3B cells were cultured in vitro,treated with alpinetin; RT-PCR and Western blot was used to detect the mRNA and protein levels of Bcl-2; MTT assay was used to detect the cellular growth inhibitory rate; Annexin V-FITC/PI double staining was used to detect the apoptosis rate of cells; Mitochondrial membrane potential was analyzed by flow cytometry; Western blot was used to detect protein expression of Caspase-3,9 and Cytochrome C ; the experiment was carried out in four groups:control group,high dosage of alpinetin group,middle dosage of alpinetin group and low dosage of alpinetin group.Results The expression of Bcl-2 in Hep3B cells were decreased by alpinetin.After treated with different dosages of alpinetin (40,80,120 μmol/L),the apoptotic inhibitory rate detected by MTT were 6.38% ± 1.32%,21.58% ± 1.97% and 43.18% ± 3.89%,significantly higher than those in control group (tlowdose =13.01,tmiddle dose =15.12,thighdose =14.79,average P < 0.01) ; the expression of mitochondrial membrane potential green fluorescence protein (GFP) were 18.93% ± 2.3%,31.11% ± 2.67% and46.06% ± 2.95%,significantly higher than those in control group (tlow dose =16.70,tmiddle dose =31.38,thigh dose =48.15,average P < 0.01).Western blot analysis showed that the expression of Caspase-3,9 andCytochrome C in cytoplasm significantly was higher than those in control group(Caspase-3:llow dose =11.94,tmiddle dose =10.18,thigh dose =18.82,average P <0.01; Caspase-9:tlow dose =15.11,tmiddle dose =20.41,thish dose =21.25,average P <0.01; Cytochrome C:tlow dose =15.11,tmiddle dose =28.47,thigh dose =16.01,average P < 0.01).while that Cytochrome C in mitochondria significantly lower than those in control group (tlow dose =16.70,tmiddle dose =12.00,thighdose =27.61,average P < 0.01).Conclusions Alpinetin promotes apoptosis of human hepatic cancer cells Hep3B by down-regulating Bcl-2,probably through mitochondrial pathway.