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1.
Journal of Pharmaceutical Analysis ; (6): 174-179, 2012.
Article in Chinese | WPRIM | ID: wpr-473353

ABSTRACT

A new modification method for glass slides was developed and applied to make ThinPrep Pap smears,in order to increase the adhesion ability of cervical exfoliative cells.3-glycidyloxypropyl trimethoxysilane (GOPS) was coated on the glass slides firstly on the slides,then poly-L-lysine (PLL)was covalently modified onto the above epoxy-terminated slides to form GOPS-PLL double decorated slides.The modified slides were characterized using X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM).The cell adhesion ability effect was tested and compared with traditional PLL coated slides by fixing the cervical exfoliative cells on the double adorned slides.The control test was conducted by the bare glass slides unmodified.The cell morphology of cervical exfoliative cells adhered on different slides was observed under the microscope after Papanicolaou staining.The number of cervical exfoliative cells on the unmodified slides,PLL coated slides and GOPS-PLL coated slides was 1030±300,3283±226 and 4119±280 (n=12),respectively.The data among the three different modification methods showed significant differences (one-way analysis of variance,ANOVA test,P< 0.05).The cell capturing effect of the GOPS-PLL slide was the best among the three different modified slides.In addition,the GOPS-PLL slide could enhance the uniformity of the adhered cells and be widely applied to the ThinPrep system for cervical carcinoma screening to increase the accuracy rate of diagnosis.

2.
Journal of Zhejiang University. Medical sciences ; (6): 203-207, 2008.
Article in Chinese | WPRIM | ID: wpr-344350

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate three dimensional dynamic contrast-enhanced magnetic resonance angiography (3D-DCE MRA) in diagnosis of cavernous transformation of portal vein (CTPV).</p><p><b>METHODS</b>Twenty-four patients with CTPV underwent 3D-DCE MRA examinations and the reconstructed images were retrospectively analyzed. A series of clinical, laboratory and imaging studies were performed on all these cases. Among all cases 14 underwent operations and 2 with hepatocellular carcinoma complicated portal thrombosis received transhepatic artery chemoembolization.</p><p><b>RESULT</b>The CTPA was located in the main trunk in 10 cases, in both the main trunk and left/right branches in 8, and in left or right branches of the portal vein in 4. In the remaining 2 cases CTPA was located at the level of superior mesenteric vein. MRA revealed multiple circuitous collateral veins striding over obstruction to extend into the liver in 9 cases,and in 7 it simultaneously showed streaky or dot-like low signal intensities representing thrombi in the extensively dilated network of portal system. MRA did not clearly demonstrate the structure of the portal vein but only showed multiple sinuous network of venous collaterals strangling together in 6 cases. In 15 cases it also showed the route and distribution of multiple hepatofugal venous collaterals.</p><p><b>CONCLUSION</b>3D-DCE MRA can provide adequate information about the site and severity of CTPA.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Contrast Media , Hemangioma, Cavernous , Diagnosis , Pathology , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Liver Neoplasms , Magnetic Resonance Angiography , Methods , Portal Vein , Pathology , Retrospective Studies , Venous Thrombosis , Diagnosis , Pathology
3.
Journal of Zhejiang University. Medical sciences ; (6): 88-92, 2007.
Article in Chinese | WPRIM | ID: wpr-271570

ABSTRACT

<p><b>OBJECTIVE</b>To discuss CT and MRI characteristics of hepatic angiomyolipoma based on pathological findings.</p><p><b>METHODS</b>The CT and MRI appearances with related pathohistological subtypes of 11 hepatic angiomyolipomas from 10 patients were retrospectively analyzed.</p><p><b>RESULT</b>Ten patients with hepatic angiomyolipomas were subcategorized into lipomatous (3 cases), angiomatous (1 case), myomatous (1 case) and mixed (5 cases) subtypes. Lesions of the lipomatous type were mainly composed of adipocytes which could be easily recognized on both CT and MRI. Abnormal vessels were commonly seen in the angiomatous lesions, which showed pronounced enhancement in the early arterial phase and remained higher than or isodense with the normal parenchyma in the portal phase. The myomatous type was predominantly composed of leiomyoid cells mixed with small amount of adipocytes. The mixed type was the most frequent,evenly comprising sheets of epithelioid muscle cells admixed with islands of adipocytes and abnormal vessels, and showing homogeneously low density on plain CT and low signal intensity on T1-weighted,intermediately high signal intensity on T2-weighted MRI scans. On dynamic study with both CT and MRI, the mixed type exhibited obvious enhancement, which retained to some degree during the portal phase.</p><p><b>CONCLUSION</b>The discrete CT and MRI appearances of hepatic angiomyolipomas with different pathological subtypes depend on the components of the tumor.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Angiomyolipoma , Pathology , Liver Neoplasms , Pathology , Magnetic Resonance Imaging , Methods , Neovascularization, Pathologic , Diagnostic Imaging , Retrospective Studies , Tomography, X-Ray Computed , Methods
4.
Acta Pharmaceutica Sinica ; (12): 346-351, 2006.
Article in Chinese | WPRIM | ID: wpr-271429

ABSTRACT

<p><b>AIM</b>A series of new 1,4-pentadien-3-one derivatives were synthesized to search for new Eight novel hydroxylated non-steroidal anti-inflammatory drugs (NSAIDs) with potent activity.</p><p><b>METHODS</b>E,E-1-(3'-indolyl)-5-( substituted phenyl)-1,4-pentadien-3-one derivatives were synthesized by means of aldol condensation and characterized by 1H NMR, ESI-MS and element analysis. Their anti-inflammatory activity in vitro were evaluated.</p><p><b>RESULTS</b>Preliminary in vitro pharmacological tests showed that all compounds exhibited anti-inflammatory activity.</p><p><b>CONCLUSION</b>Compounds 4d and 4e exhibited potent anti-inflammatory activity and their anti-inflammatory activity was comparable to resveratrol, and were worthy of further study.</p>


Subject(s)
Animals , Male , Mice , Alkadienes , Pharmacology , Anti-Inflammatory Agents , Pharmacology , Indoles , Pharmacology , Macrophages, Peritoneal , Cell Biology , Metabolism , Tumor Necrosis Factor-alpha , Bodily Secretions
5.
Journal of Zhejiang University. Medical sciences ; (6): 239-244, 2004.
Article in Chinese | WPRIM | ID: wpr-341898

ABSTRACT

<p><b>OBJECTIVE</b>To study the enhancing effect of isoflavonoid genistein in irradiation (IR) on prostate DU145 cancer cells.</p><p><b>METHODS</b>Prostate cancer cell line DU145 was used in this experiment. Clonogenic assay was applied to compare the survival fractions of DU145 cells after treatments with genistein alone and/or graded IR. DNA electrophoresis and TUNEL method were applied to detect cell apoptosis. Cell cycle was observed using flow cytometry and related protein expressions by immunoblotting.</p><p><b>RESULT</b>Clonogenic assay demonstrated that genistein, even at low to medium concentrations, enhanced the radiosensitivity of DU145 cells. After treatments with IR and/or genistein for 24 h, apoptosis was mainly seen with genistein at high concentration and was minimally dependent on IR. Apoptosis also occurred after treatments for 72 h with lower concentrations of genistein, especially when combined with IR. While IR or genistein led to a G2/M cell cycle arrest, combination of them could further increase DU145 cells at G2/M phase. This G2/M arrest was largely maintained at 72 h, and accompanied by increasing apoptosis and hyperdiploid cell populations. Cell-cycle related protein analysis disclosed biphasic changes in cyclin B1, less markedly increased cdc-2 and stably elevated p21(cip1) levels with increasing genistein concentrations.</p><p><b>CONCLUSION</b>Genistein could enhance the radiosensitivity of DU145 prostate cancer cells. The mechanisms might be involved in the increased apoptosis, prolonged cell cycle arrest and impaired damage repair induced by the combined treatment.</p>


Subject(s)
Humans , Male , Apoptosis , Radiation Effects , CDC2 Protein Kinase , Cell Line, Tumor , Cell Survival , Radiation Effects , Cyclin B , Cyclin B1 , G2 Phase , Radiation Effects , Genistein , Pharmacology , Prostatic Neoplasms , Pathology , Radiotherapy , Radiation-Sensitizing Agents , Pharmacology , S Phase , Radiation Effects
6.
Asian Journal of Andrology ; (6): 285-290, 2004.
Article in English | WPRIM | ID: wpr-270893

ABSTRACT

<p><b>AIM</b>To study the effect of the combined use of genistein and ionizing radiation (IR) on prostate DU145 cancer cells.</p><p><b>METHODS</b>DU145, an androgen-independent human prostate cancer cell line, was used in the experiment. Clonogenic assay was used to compare the survival of DU145 cells after treatments with genistein alone and in combination with graded IR. Apoptosis was assayed by DNA ladder and TUNEL stain. Cell cycle alterations were observed by flow cytometry and related protein expressions by immunoblotting.</p><p><b>RESULTS</b>Clonogenic assay demonstrated that genistein, even at low to medium concentrations, enhanced the radiosensitivity of DU145 cells. Twenty-four hours after treatment with IR and/or genistein, apoptosis was mainly seen with genistein at high concentrations and was minimally related to IR. At 72 h, apoptosis also occurred in treatment with lower concentration of genistein, especially when combined with IR. While both IR and genistein led to G2/M cell cycle arrest, combination of them further increased the DU145 cells at G2/M phase. This G2/M arrest was largely maintained at 72 h, accompanied by increasing apoptosis and hyperdiploid cell population. Cell-cycle related protein analysis disclosed biphasic changes in cyclin B1 and less dramatically cdc-2, but stably elevated p21 cip1 levels with increasing genistein concentrations.</p><p><b>CONCLUSION</b>Genistein enhanced the radiosensitivity of DU145 prostate cancer cells. The mechanisms might be involved in the increased apoptosis, prolonged cell cycle arrest and impaired damage repair.</p>


Subject(s)
Humans , Male , Androgens , Physiology , Anticarcinogenic Agents , Pharmacology , Apoptosis , Cell Cycle , Cell Line, Tumor , DNA, Neoplasm , Genetics , Flow Cytometry , Genistein , Pharmacology , Immunoblotting , In Situ Nick-End Labeling , Prostatic Neoplasms , Drug Therapy , Radiotherapy , Tumor Stem Cell Assay
7.
Acta Pharmaceutica Sinica ; (12): 264-267, 2003.
Article in Chinese | WPRIM | ID: wpr-251128

ABSTRACT

<p><b>AIM</b>To synthesize new fluoroquinolone analogues as antibacterial compounds.</p><p><b>METHODS AND RESULTS</b>By reaction of acryl chloride(chloro-carbonic ester) with sodium sulfocyanate, acyl isosulfocyanic ester were easily obtained. Twelve 7-(4-acylamino-thiocarbamoyl-1-piperazinyl) fluoroquinolone analogues (1-12) were synthesized through modifying the 7-piperazine of norflorxacin and ciprofloxacin with isosulfocyanic ester synthesized above. The structures of synthesized compounds were characterized by 1HNMR, IR and elemental analysis.</p><p><b>CONCLUSION</b>Antibacterial activities of the new compounds were evaluated in vitro compared with norflorxacin. Compounds 5, 7, 10 and 12 showed antibacterial activities.</p>


Subject(s)
Anti-Infective Agents , Chemistry , Pharmacology , Bacillus subtilis , Ciprofloxacin , Chemistry , Pharmacology , Combinatorial Chemistry Techniques , Methods , Escherichia coli , Fluoroquinolones , Chemistry , Pharmacology , Microbial Sensitivity Tests , Molecular Structure , Norfloxacin , Chemistry , Pharmacology
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