1.Determination of Osthole and Columbianadin in Wangbi Tablets by HPLC
Leibing XUE ; Yan ZHOU ; Peifen JIN
China Pharmacist 2014;(4):697-699
Objective:To establish an HPLC method for the determination of osthole and columbianadin in Wangbi tablets. Meth-ods:The column was an Agilent XDB C18(150 mm ×4.6 mm, 5 μm). The mobile phase consisted of acetonitrile-water(49∶51)with gradient elution. The flow rate was 1. 0 ml·min-1 and the detection wavelength was at 330 nm. Results: The calibration curve was linear within the range of 0. 060-0. 597 μg(r=0. 999 9) for osthole and 0. 010-0. 102 μg(r=0. 999 9) for columbianadin. The aver-age recovery was 99. 12% and 98. 98%, respectively. Conclusion:The method is simple, practicable, accurate and rapid. It can be applied in the content determination of osthole and columbianadin in Wangbi tablets.
3.Effects of propofol on ATP sensitive K~+ currents in human atrial myocytes
Yi-Nan ZHANG ; Feng-Xue WANG ; Jin ZHOU ; Al ET
Chinese Journal of Anesthesiology 1995;0(12):-
Objective To investigate the effects of different doses of propofor on ATP-sensitive K~+currents(I_KATP)in human atrial myocytes and the underlying mechsnism.Methods A small piece of myocardiumwas obtained from right atrium in patients undergoing atrial septal defect or ventricular septal defect surgery.Themyocardium specimen was placed in cold Ca~(2+)-free cardioplegic solution aerated with 100% oxygen.Themyocardium specimen was cut into small chunks(1 mm~3).Atrial myocytes were isolated by enzymatic dissociationtechnique.The effects of propofol on I_KATP in atrial myocytes were studied using the whole-cell configuration ofpatch-clamp technique.Results The outward currents were recorded with a pipitte solution containing 0.3mmol?L~(-1) ATP.The currents were inhibited by glibendamide 10 ?mol?L~(-1),a specific K_ATP channel inhibitor,suggesting that the outward currents were I_KATP.I_KATP aws activited by propofol in a dose-dependent manner.Conclusion Propefol can activate the I_KATP in human myocytes in a concentration-dependent manner and themechanism of its myocardial depressant action may be partly explained.
4.Tiamcinolone acetonide and indocyanine green-assisted vitrectomy combined with inner limiting membrane peeling for idiopathic macular hole
Bo, JIN ; Xue-min, JIN ; Hai-yan, ZHU ; Peng-yi, ZHOU ; Xian-guo, ZENG
Chinese Journal of Experimental Ophthalmology 2012;30(3):239-241
BackgroundWhether the peeling of the inner limiting membrane (ILMP) increase the closure rate of idiopathic macular hole is still in controversy.Some ophthalmologist recommend vitrectomy combined with inner limiting membrane peeling for the treatment of idiopathic macular hole.However,the removal of ILMP is difficult because of its similar appearance to adjacent tissues.Objective This study was to investigate the efficacy of triamcinolone acetonide(TA) and indocyanine green(ICG) double staining-assisted vitrectomy combined with ILM peeling during the surgery.Methods A consecutive case- observational study was designed.The standardized vitrectomy was performed in 25 eye of 23 cases with IMH.During the vitrectomy,TA and ICG were injected into posterior pole vitreous to visualize and assist the ILM peeling.The dying effectiveness was observed,and the closure rate of macular hole,visual acuity,intraocular pressure and complications were evaluated after surgery.Written informed consent was obtained from each patient prior to operation.Results Posterior vitreous cortex and ILM were visible and the residual vitreous and cortex were removed clearly after dying of TA and ICG in all the 25 eyes.During the following-up duration of 3-8 months,the completely anatomical reattachment of the macular area was in 22 eyes ( 88.0% ) and partially reattachment in 3 eyes( 12.0% ).The best corrected vision was 0.07-0.60 in all of the operated eyes 2 months after surgery.Conclusions TA and ICG- assisted vitrectomy combined with ILM peeling appears to be a safe and effective method for IMH repair.
5.Lead acetate induced DNA damage in blood lymphocytes of rats.
Jian-hua ZHOU ; Lian XUE ; Xi-jin SHI ; Liu-ming PENG ; Chen BIAN
Chinese Journal of Industrial Hygiene and Occupational Diseases 2006;24(5):290-292
Animals
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Comet Assay
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DNA Damage
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drug effects
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Lymphocytes
;
drug effects
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Male
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Organometallic Compounds
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toxicity
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Rats
7.Facial skin nodules.
Jian-lan XIE ; Xiao-ge ZHOU ; Yan JIN ; Xiao-dan ZHENG ; Xue-jing WEI
Chinese Journal of Pathology 2010;39(6):410-411
Adult
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Antigens, CD20
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metabolism
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CD3 Complex
;
metabolism
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Diagnosis, Differential
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Facial Dermatoses
;
metabolism
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pathology
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surgery
;
Follow-Up Studies
;
Humans
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Lymphoma, B-Cell, Marginal Zone
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metabolism
;
pathology
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Lymphoma, Large-Cell, Anaplastic
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metabolism
;
pathology
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Male
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Pseudolymphoma
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metabolism
;
pathology
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surgery
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Skin Neoplasms
;
metabolism
;
pathology
8.Spindle cell variant of anaplastic large cell lymphoma.
Jian-lan XIE ; Xiao-ge ZHOU ; Yan JIN ; Xiao-dan ZHENG ; Xue-jing WEI
Chinese Journal of Pathology 2010;39(5):340-342
Actins
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metabolism
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Adult
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Diagnosis, Differential
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Granzymes
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metabolism
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Histiocytic Sarcoma
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metabolism
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pathology
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Humans
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Ki-1 Antigen
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metabolism
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Lymph Nodes
;
metabolism
;
pathology
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Lymphoma, Large-Cell, Anaplastic
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metabolism
;
pathology
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Male
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Neoplasms, Muscle Tissue
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metabolism
;
pathology
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Protein-Tyrosine Kinases
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metabolism
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Receptor Protein-Tyrosine Kinases
9.Left cervical mass.
Jian-lan XIE ; Xiao-ge ZHOU ; Yan JIN ; Xiao-dan ZHENG ; Xue-jing WEI
Chinese Journal of Pathology 2012;41(3):195-196
Adult
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Diagnosis, Differential
;
Female
;
Granulomatous Disease, Chronic
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metabolism
;
pathology
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Hodgkin Disease
;
metabolism
;
pathology
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Humans
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Ki-1 Antigen
;
metabolism
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Lewis X Antigen
;
metabolism
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Lymphoma, Large B-Cell, Diffuse
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metabolism
;
pathology
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Lymphoma, Large-Cell, Anaplastic
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metabolism
;
pathology
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Young Adult
10.Microscopic measurement of intercellular space of squamous epithelium in lower part esophagus of patients with gastro-esophageal reflux disease
Rongli CUI ; Liya ZHOU ; Sanren LIN ; Yan XUE ; Liping DUAN ; Zhiwei XIA ; Zhu JIN ; Hejun ZHANG
Chinese Journal of Digestive Endoscopy 2011;28(1):1-4
Objective To evaluate the clinical significance of intercellular space diameters (ISD)of squamous epithelium by light microscopy (LM) in lower esophagus of erosive reflux esophagitis (ERD),non-erosive reflux disease ( NERD), Barrett esophagus (BE) and healthy controls. Methods A total of 21 ERD and 21 NERD patients with reflux symptoms and confirmed with 24-hour esophageal pH monitoring, 13 BE patients diagnosed by gastroscopy and biopsy, and 20 other healthy controls were enrolled in the study.Samples of ERD, NERD and control group were collected at 2 cm above dentate line, and made HE slides in the conventional way. Images for measurement of ICS were acquired with oil lens ( × 1000). ICS of squamous epithelium was quantitatively measured by computer-assisted morphometry. Ten cells were taken for each sample, 10 consecutive ISD for each cell, i.e. 100 ISD for each subject. Mean ISD was calculated.Results Mean ISDs by LM in control, BE, ERD, and NERD groups were 0. 59, 0. 99, 1.29 and 1.06 μm, respectively. The mean ISDs in BE, ERD, and NERD group were much greater than that in control (P<0. 05). The mean, maximal and minimal ISDs of group ERD were greater than those of NERD and BE (P = 0. 000). However, the ISDs of NERD and BE are of no significant difference ( P > 0. 05 ). The cut-off value of mean ISD for diagnosis of gastro-esophageal reflux disease (GERD) was 0. 85 μm. Diagnostic sensitivity and specificity for ERD, NERD and BE were 89. 1% and 100. 0%, with reference to clinical symptoms, endoscopy and ISDs above the cut-off value. Conclusion Larger ISDs in lower esophagus by using LM will be found in all subgroups of GERD, including ERD, NERD and BE. Increased ISDs may be one of the markers for diagnosis of ERD, NERD and BE.