ISO 20776 PDF

ISO. First edition. Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation. ISO () Clinical laboratory testing and in vitro diagnostic test systems – Susceptibility testing of infectious agents and evaluation of performance of. Buy ISO , Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices, Part 1, at CLSI.

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Susceptibility testing of pathogenic fungi with itraconazole: Evaluation of performance of antimicrobial susceptibility test devices. Fifty microliters of the resultant mix was injected directly into the HPLC system.

Considering only data for dilution series prepared in Spain, no systematic difference was detected between ISO dilution and serial dilution. By using this website, you agree to its use of cookies. Susceptibility testing of yeasts ISO Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: When there are no breakpoints?

General Committee to 207776 article has been cited by other articles in PMC. Projects and data submission ITC precipitation after thaw-freeze cycles during transport is the most probable explanation.

Reference method for broth dilution antifungal susceptibility testing of yeast, 3rd ed. Simultaneous quantification of voriconazole and posaconazole in human plasma by high-performance liquid chromatography with ultra-violet detection.

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Sensitive determination of itraconazole and its active metabolite in isoo plasma by column-switching high-performance liquid chromatography with ultraviolet detection. Published online Mar Single-step extraction of fluconazole from plasma by ultra-filtration for the measurement of its free concentration by high performance liquid chromatography.

Relevant external documents

200776 Open in a separate window. Thus, serial dilution, which is attractive due to its simplicity, may be appropriate. Thus, ITC data obtained from trays prepared by the Inn Austria participant were excluded from the analysis since tray wrappings showed evidence of defrosting and spillage; also, concentrations of dilutions prepared in Denmark were unacceptably different from the target concentrations. Sitemap Search close sitemap.

Bioanalytical method validation-a revisit with a decade of progress. Itraconazole formulation studies of the melt-extrusion process with mixture design.

Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases. In this multicenter study we address this issue by comparing the concentrations of hydrophilic and hydrophobic antifungal agents, represented by fluconazole FLC and itraconazole ITCrespectively, in broth microdilution plates prepared according to the ISO standard as well as by serial dilution procedures.

Precision of fluconazole dilution series by dilution procedure and laboratory a. Use of cookies By using this website, you agree to its use of cookies. Regarding serial 2-fold dilution procedures, better results were detected when FLC plates were prepared according to the hydrophilic rather than the hydrophobic way.

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Support Center Support Center. All statistical analyses were done with the statistical package PAWS statistics Steering Committee to Presentations and statistics First indications of improved capability and capacity of public health microbiology laboratories in the European Union http: ISO Clinical laboratory testing and in vitro diagnostic test systems – Susceptibility testing of infectious agents and evaluation of performance of ixo susceptibility test devices – Part 1: Clinical and Laboratory Standards Institute.

Meetings, Minutes and Reports International Organization for Standards. Development and validation of a high-performance liquid chromatography assay for posaconazole utilizing solid-phase extraction.

EUCAST: External documents

Since the hydrophilic growth medium RPMI-G at pH 7 has been selected is testing in vitro antifungal susceptibility, it was important to describe the lack of proper solubility of this compound.

Reference method for testing the in vitro activity ixo antimicrobial agents against rapidly growing anaerobic bacteria involved in infectious diseases. Notably, although relative errors were greater for the lowest concentrations, we did not observe an increasing inaccuracy when performing serial dilutions compared to dilutions performed following the ISO procedure as would have been expected if the precision of modern pipettes had been insufficient.