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1.
Chinese Journal of Medical Instrumentation ; (6): 88-91, 2020.
Article in Chinese | WPRIM | ID: wpr-942705

ABSTRACT

By analyzing the main problems existing in the current management of medical devices for clinical trials, this study proposes a feasible management model and specific requirements for acceptance, distribution, storage and recovery combining with the characteristics of medical consumable equipment and diagnostic reagent, which provides a favorable guarantee for the authenticity and reliability of clinical trials.


Subject(s)
Clinical Trials as Topic , Equipment and Supplies/standards , Indicators and Reagents/standards , Reproducibility of Results , Research Design/standards
2.
Braz. j. med. biol. res ; 47(4): 307-3015, 8/4/2014. graf
Article in English | LILACS | ID: lil-705765

ABSTRACT

Dye exclusion tests are used to determine the number of live and dead cells. These assays are based on the principle that intact plasma membranes in live cells exclude specific dyes, whereas dead cells do not. Although widely used, the trypan blue (TB) exclusion assay has limitations. The dye can be incorporated by live cells after a short exposure time, and personal reliability, related to the expertise of the analyst, can affect the results. We propose an alternative assay for evaluating cell viability that combines the TB exclusion test and the high sensitivity of the flow cytometry technique. Previous studies have demonstrated the ability of TB to emit fluorescence when complexed with proteins. According to our results, TB/bovine serum albumin and TB/cytoplasmic protein complexes emit fluorescence at 660 nm, which is detectable by flow cytometry using a 650-nm low-pass band filter. TB at 0.002% (w/v) was defined as the optimum concentration for distinguishing unstained living cells from fluorescent dead cells, and fluorescence emission was stable for 30 min after cell treatment. Although previous studies have shown that TB promotes green fluorescence quenching, TB at 0.002% did not interfere with green fluorescence in human live T-cells stained with anti-CD3/fluorescein isothiocyanate (FITC) monoclonal antibody. We observed a high correlation between the percentage of propidium iodide+CD3/FITC+ and TB+CD3/FITC+ cells, as well as similar double-stained cell profiles in flow cytometry dot-plot graphs. Taken together, the results indicate that a TB exclusion assay by flow cytometry can be employed as an alternative tool for quick and reliable cell viability analysis.


Subject(s)
Humans , Young Adult , /blood , Flow Cytometry/standards , Leukocytes, Mononuclear/metabolism , Trypan Blue , Cell Count , Cell Separation , Cell Survival , Cell Membrane/physiology , Fluorescence , Immunophenotyping , Indicators and Reagents/standards , Multiprotein Complexes/standards , Professional Competence , Propidium/standards , Staining and Labeling , Serum Albumin, Bovine/standards
3.
Southeast Asian J Trop Med Public Health ; 1999 ; 30 Suppl 3(): 136-48
Article in English | IMSEAR | ID: sea-34020

ABSTRACT

Quality control (QC) has been introduced in laboratories, and QC surveys in urinalysis have been performed by College of American Pathologist, by Japanese Association of Medical Technologists, by Osaka Medical Association and by manufacturers. QC survey in urinalysis for synthetic urine by the reagent strip and instrument made in same manufacturer, and by an automated urine cell analyser provided satisfactory results among laboratories. QC survey in urinalysis for synthetic urine by the reagent strips and instruments made by various manufacturers indicated differences in the determination values among manufacturers, and between manual and automated methods because the reagent strips and instruments have different characteristics, respectively. QC photo survey in urinalysis on the microscopic photos of urine sediment constituents indicated differences in the identification of cells among laboratories. From the results, it is necessary to standardize a reagent strip method, manual and automated methods, and synthetic urine.


Subject(s)
Automation , Humans , Indicators and Reagents/standards , Japan , Quality Assurance, Health Care , Quality Control , Reference Standards , Reproducibility of Results , Urinalysis/standards
4.
Acta bioquím. clín. latinoam ; 33(3): 297-329, sept. 1999. ilus, tab
Article in Spanish | LILACS | ID: lil-258457

ABSTRACT

En el presente trabajo se detallan los principios físico-químicos básicos que rigen la separación de sustancias en la electroforesis capilar. Se destaca el aporte que ha significado el desarrollo de los capilares de 20 a 50 µm de diámetro, de los detectores con arreglos de diodos y la operativa computacional para la interpretación gráfica de los datos obtenidos. Se detallan los principios que rigen la electroforesis libre, zonal, isotacoferesis, isoelectroenfoque y cromatografía micelar con surfactantes y ciclodextrinas, y distintos ejemplos sobre sus aplicaciones


Subject(s)
Electrophoresis, Capillary , In Vitro Techniques , Cyclodextrins , Electrophoresis , Electrophoresis, Capillary/instrumentation , Electrophoresis/history , Electrophoresis/instrumentation , Indicators and Reagents/standards , Surface-Active Agents
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