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Voriconazole



Cat. # Description Qty. Unit
232202 Voriconazole
1 EA1

Intended Use:

These discs are used for semi-quantitative in vitro susceptibility testing by the agar disc diffusion test procedure of fungal pathogens.


Catalog # Description Code Conc. Quantity Unit
232202 Voriconazole
VOR-1 1 mcg 1 EA1

BD BBL™ Sensi-Disc™ Antimicrobial Susceptibility Test Discs
Revision: 2010/07     Revision Date: 07/01/2010    

Intended Use:

These discs are used for semi-quantitative in vitro susceptibility testing by the agar disc diffusion test procedure of fungal pathogens.



Product Summary:

Agar diffusion methods employing dried filter paper discs impregnated with specific concentrations of antimicrobial agents were developed in the 1940s. In order to eliminate or minimize variability in this testing, Bauer et al. developed a standardized procedure in which Mueller Hinton Agar was selected as the test medium.1,2

Various regulatory agencies and standards-writing organizations subsequently published standardized reference procedures based on the Bauer-Kirby method. Among the earliest and most widely accepted of these standardized procedures were those published by the U.S. Food and Drug Administration (FDA)3 and the World Health Organization (WHO).4,5 The procedure was adopted as a consensus standard by the Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) and is periodically updated.6,7

A disk diffusion method for testing Candida species was developed and in 2004, CLSI Approved Guideline M44-A, Method for Antifungal Disk Diffusion Susceptibility Testing of Yeasts, was released.8 The disk diffusion method often provides qualitative results 24 hours sooner than broth dilution, making antifungal susceptibility testing more readily available to some clinical laboratories and providing a reduced cost alternative. The latest CLSI documents should be consulted for current recommendations.



User Quality Control:



Reagents:

Sensi-Disc™ brand discs are 6-mm discs prepared by impregnating high quality absorbent paper with accurately determined amounts of antibiotic or other chemotherapeutic agents. Discs are clearly marked on both sides with letters and numbers designating the agent and the drug content. (See chart containing concentrations of reactive ingredients). The drug content of discs is assayed by the methods established by the FDA or by methods similar or comparable to those published in the United States Federal Register.

Sensi-Disc agents are furnished in cartridges containing 50 discs each. The last disc in each cartridge is marked "X" and contains the drug as coded. Cartridges are for use in BBL™ Sensi-Disc™ Dispensers; these include a Single Disc Dispenser, an 8-Place Dispenser for 100 mm-style Petri dishes, 6- and 8-Place Self-Tamping Dispensers for 100 mm-style dishes and a Self-Tamping 12-Place Dispenser for 150 mm-style plates.



Warnings and Precautions:

For in vitro Diagnostic Use.

Follow directions for use; disc performance depends not only on disc potency, but on use of proper inoculum and control cultures, functional pretested plates, proper storage temperature and other factors.

Observe aseptic techniques and established precautions against microbiological hazards throughout all procedures. Sterilize cultures, containers and other contaminated materials after use.



Information shown on this page is a short summary extracted from the Package Insert, available as a PDF under the Related Documents section of this page.