| Technology
MicroPhage
is engaging in the business of making diagnostics better. Faster
results. Expanded menus. Easy to use formats. MicroPhage is
in the business of delivering high value bacterial diagnostics
(identification and antibiotic testing) to the markets that
need it most.
MicroPhages
proprietary technology now allows for specific identification
bacteria - directly from samples and cultures. Our platform
technology also allows for direct antibiotic susceptibility
and resistance testing. Whether your need is rapid determination
of MRSA from blood cultures or clindamycin susceptibility in
S. aureus from skin and soft tissue infections, the MicroPhage
platform technology can
Up until
now, most immunoassay infectious disease menus have been comprised
of viruses (HIV 1/2, CMV, HSV, influenza A/B, etc.) with few
bacterial exceptions (Chlamydia, Gonorrhea, Groups A and B Streptococcus,
etc.). The MicroPhage technology increases immunoassay sensitivity
and specificity in particular, delivering tests with molecular
or culture level performance in an easy-to use format.
Phage
Amplification
MicroPhages
proprietary technology offers the ability to increase specificity
and decrease time to results on existing immunodiagnostic platforms.
The MicroPhage Amplification System allows for better results
with little or no extra effort or retraining required of the
end user.
MicroPhage's
technology represents a well-defined and novel approach to rapidly
identifying pathogens. Specific bacteriophage are introduced
to the processed sample, where they find, infect, and amplify
their target pathogen(s) providing a very specific, highly amplified
surrogate marker for rapid detection.
Bacteriophage
selectively infect targeted bacteria and rapidly multiply. The
system can generate as much as a 5-log amplification of signal.
This allows for reduced incubation times, resulting in complete
assay times of one to four hours compared with traditional culture
assays of twenty-four to forty-eight hours.
This system
represents a well-defined, yet novel approach to the non-PCR-based
amplification and identification of many pathogens. Specific
bacteriophages are used on the processed sample, infecting only
their targets and thus provide a very selective method for bacterial
identification.
Phage multiply
very rapidly (versus the replication time of bacteria) within
their target bacteria, producing tens to thousands of progeny
phage that are released partially due to pressure increases
from within the cell or due to a singular cellular burst event.
The increase in concentration of the bacteriophage due to the
presence of the target bacteria signals its presence.
In
antibiotic tests, the bacteria are exposed to the target antibiotic
in addition to the bacteriophage. Since bacteriophage amplification
requires a viable, replicating bacterial host, susceptible organisms
cannot support phage amplification and can be differentiated
from resistant bacteria that do support bacteriophage amplification.
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