1.Determination of Scutellarin in Brevisapin Tablets by HPLC
Traditional Chinese Drug Research & Clinical Pharmacology 1993;0(03):-
Objective To develop a HPLC method for the determination of scutellarin in Brevisapin Tablets.Methods C18 column with temperature of 40 ℃ was used.The mobile phase was the mixed solution of methanol-water-phosphoric acid(40 ∶ 60 ∶ 0.5) with the flow rate of 1.0 mL? min-1.Determination wavelength was 335 nm and the sample injected volume was 10 ? L.Results A good linearity of scutellarin was in the rang of 0.161 5~ 0.807 5 ? g.The average recovery of scutellarin was 98.7 % with RSD=1.26 %.Conclusion The method is simple,accurate,and can be used for the quality control of Brevisapin Tablets.
2.Design and development of institutional scientific research management information system
Changqin LI ; Jinghui WEI ; Dong WU
Chinese Journal of Medical Library and Information Science 2014;(11):65-67,74
After the institutional scientific research management at present was analyzed according to the literature investigation, expert consultation, comparative and comprehensive analysis, the following were advanced, including the principles, target, function module and structure module for institutional scientific research management infor-mation system , and realization of its functions using the J2 EE technology-based B/S framework .
3.STUDY ON EXTRACORPOREAL CIRCULATION IN 1286 PEDIATRIC PATIENTS
Jiali WANG ; Jiachun LI ; Changqin GAO
Medical Journal of Chinese People's Liberation Army 1981;0(04):-
To study retrospectively on extracorporeal circulation (ECC) in pediatric patients with congenital heart diseases. 1286 cases were divided into two groups. In groupⅠ( n =883) ECC were performed with nonpatterned tubing system, and in group Ⅱ( n =403) patterned tubing system was used. GroupⅠandⅡwere both primed with Ringer′s solastion and colloid. There were no stastistically significant difference in age or body weight between groupⅠand Ⅱ. The crystalloid priming volume in group Ⅱ was less than that in groupⅠ( P
4.The correlation between DWI and DCE MR of normal sacroiliac joint
Jian QIN ; Luping ZHAO ; Jianzhong ZHU ; Xiaoqian LI ; Changqin LI
Journal of Practical Radiology 2015;(5):805-809
Objective To study the correlation between the ADC value and Fenh value,Senh value based on DWI and DCE-MRI, by measuring them in sacroiliac joint bone marrow of healthy volunteers.Methods 21 healthy volunteers performing the sacroiliac joint MR were involved.ADC value based on DWI,and TIC based on DCE-MRI were measured.The relationship of ADC values with Fenh,Senh values and peak to time,Tmax values were analyzed.Results The differences of the measured ADC values on both sides of the sacroiliac joint bone marrow region were not statistically significant (P>0.05).There were three types of TIC curve,8.3% (7/84)Ⅰ type,8.3% (7/84)Ⅱ type,83.3% (70/84)Ⅲtype;Fenh,Senh average values were within 20%
5.Development and application of reference materials containing mixed degradation products of amoxicillin and ampicillin.
Wei LI ; Weiqing ZHANG ; Xiang LI ; Changqin HU
Acta Pharmaceutica Sinica 2014;49(9):1310-4
Reference materials containing mixed degradation products of amoxicillin and ampicillin were developed after optimization of preparation processes. The target impurities were obtained by controlled stress testing, and each major component was identified with HPLC-MS and compared with single traceable reference standard each. The developed reference materials were applied to system suitability test for verifying HPLC system performed in accordance with set forth in China Pharmacopeia and identification of major impurities in samples based on retention and spectra information, which have advantages over the methods put forth in foreign pharmacopoeias. The development and application of the reference materials offer an effective way for rapid identification of impurities in chromatograms, and provide references for analyzing source of impurities and evaluation of drug quality.
6.Current studies on assessment of scientific research capability in domestic and foreign medical institutions:A review
Ling YI ; Weitao ZONG ; Lijuan LI ; Changqin LI ; Lei XU
Chinese Journal of Medical Library and Information Science 2015;(4):15-20
After the systems, methods and criteria for assessment of scientific research capability in USA, Germany, Britain and Japan were described, the advances in studies on assessment of scientific research capability in China were summarized, their characteristics were compared, and the enlightenments to perform assessment of medical research institution capability were elaborated.
7.Subtype classification of ceftriaxone sodium and its influence on the quality of product.
Jing XUE ; Yanhua JIA ; Jin LI ; Lihui YIN ; Changqin HU
Acta Pharmaceutica Sinica 2014;49(7):1034-8
Powder X-ray diffraction (PXRD) technology combined with cluster analysis method was used to classify 75 batches of crystalline ceftriaxone sodium into subtypes, the crystalline characteristics of each subtype were measured with scanning electron microscope (SEM). By comparing some parameters of these subtypes correlated to crystallization process of ceftriaxone sodium, such as salification rate, water content in different subtypes, as well as by studying different lattice stabilities, different compatibilities with rubber closures during accelerated stability tests, the key point to improve the quality of domestic ceftriaxone sodium was disclosed. The results of this paper indicated that the fine structure of the products could be controlled well by improving the salification and crystallization process. As a result, the subtype II of ceftriaxone sodium with high stability can be produced.
8.Dissolution testing combined with computer simulation technology to evaluate the bioequivalence of domestic amoxicillin capsule.
Ruixue PAN ; Yuan GAO ; Wanli CHEN ; Yulan LI ; Changqin HU
Acta Pharmaceutica Sinica 2014;49(8):1155-61
Re-evaluation of bioequivalence of generic drugs is one of the key research focus currently. As a means to ensure consistency of the therapeutic effectiveness of drug products, clinical bioequivalence has been widely accepted as a gold standard test. In vitro dissolution testing based on the theory of the BCS is the best alternative to in vivo bioequivalence study. In this article, the conventional dissolution method and flow-through cell method were used to investigate the dissolution profiles of domestic amoxicillin capsules in different dissolution media, and the absorption behavior of the drugs with different release rates (t85% = 15-180 min) in the gastrointestinal tract was predicted by Gastro Plus. The flow-through cell method was thought better to reflect the release characteristics in vivo, and amoxicillin capsules with regard to the release rates up to 45 min (t85% = 45 min) were having a satisfied bioequivalence with the oral solution according to the C(max) and AUC. Although two different dissolution profiles of domestic amoxicillin capsules were found by flow-through cell methods, prediction results revealed that domestic capsules were probably bioequivalent to each other.
9.Clinical value of secondary ERCP with difficult intubation
Li YU ; Changqin XU ; Yongjun WANG ; Ming JI ; Shutian ZHANG
Chinese Journal of Digestive Endoscopy 2014;31(6):321-323
Objective To determine the safety and clinical value of secondary ERCP to a failed intubation procedure.Methods A total of 212 patients with difficult intubation during ERCP procedures were enrolled.Patients with failed conventional intubation accepted precut sphincterotomy.The operation stopped after one hour of effort.A secondary selective ERCP was performed at a appropriate time.The operation success rate and complication rate of first ERCP and secondary ERCP were compared.Results The success rate of first ERCP was 67.0% (142/212),and the total success rate was 90.6% (192/212).The total success rate is significantly higher than that of first ERCP operation(x2 =35.263,P <0.05).The complication rate of first ERCP,secondary ERCP and total complication rate was 8.96% (19/212),4.29% (3/70),10.38% (22/212),respectively.Complication rates of total ERCP and secondary ERCP were not significantly different from the first ERCP (P > 0.05).Conclusion It is safe and effective for patients with failed ERCP intubations after precut to receive a secondary ERCP at a appropriate time.
10.Study on the effect of the five pre-triage for infectious diseases in general hospitals
Changqin LI ; Chuanping HAN ; Song GAO ; Hua KONG ; Junying WANG
Chinese Journal of Hospital Administration 2011;27(8):585-588
Objective To investigate effective methodology for preventing infectious diseases from spreading within general hospitals at all levels. Methods Six hospitals at three levels in the city were made into two groups and investigated for their treatment of infectious diseases. The group of A1, A2 and A3 hospitals employs the five pre-triage, while the group of B2, B2 and B3 employs the routine pretriage. Results Comparison of undetected infectious cases between group A1, A2, A3 and group B1,B2,B3 identified significant difference with x2 testing, P<0. 005. Conclusion Five pre-triage method can screen, identify and pinpoint confirmed or suspected infectious disease patients from all outpatients in the first time, thus preventing and controlling the nosocornial transmission of epidemic or even an outbreak of nosocomial infection effectively.