| Pharmacology
Bactericidal and fungicidal activity (suspension
tests)
The antimicrobial activity of Microcyn has been demonstrated against a variety
of microorganisims in several in-vitro studies.
Microcyn has been tested against a variety of
organisms, including the five most common bacteria
found in hospitals (Mangram, 1999): Staphylococcus
aureus, Coagulase-negative Staphylococcus spp.
(such as Staphylococcus epidermidis), Enterococcus
spp. (such as Enterococcus hirae), Escherichia
coli, and Pseudomonas aeruginosa. Microcyn
demonstrated a 106 reduction after 15 seconds
of exposure against all five organisms.
An in vitro time
kill evaluation was performed using Microcyn
versus challenge suspensions of 50 different
microorganism strains (25 American Type Culture
Collection [ATCC] strains and 25 clinical isolates
of those same species) as described in the
Tentative Final Monograph .12. After exposure
for 30 seconds, there was a reduction of the
bacterial load >5 log10 in the following samples: Pseudomonas
aeruginosa, Escherichia coli, Enterococcus hirae,
Acinetobacter baumanni, Acinetobacter species,
Bacteroides fragilis, Enterobacter aerogenes,
Enterococcus faecalis, Vancomycin-resistant Enterococcus
(VRE), Haemophilus influenzae, Klebsiella oxytoca,
Klebsiella pneumoniae, Micrococcus luteus, Proteus
mirabilis, Serratia marcescens, Staphylococcus
aureus, Staphylococcus epidermidis, Staphylococcus
haemolyticus, Staphylococcus pyogenes, and Candida
albicans (BioScience Labs, Bozeman, Mont.).
(Gutiérrez 2006).
Bactericidal and fungicidal activity
(carrier tests)
In various tests, the bactericidal and fungicidal
properties of Microcyn have been tested in accordance
to EPA DIS/TSS guidelines. Under these conditions,
Microcyn Technology has totally inhibited the
growth of the following microorganisms: Mycobacterium
bovis (OT #105401) in 5 minutes; P.
aeruginosa (ATCC #15442), S. aureus (ATCC
#6538), Salmonella choleraesuis (ATCC
#10708), Methicillin-resistant S. aureus (MRSA,
ATCC #33592); and Trichophyton mentagrophytes (ATCC
#9533) in 10 minutes; and Vancomycin-resistant Enterococcus
faecalis (VRE, ATCC#51299) in 15 minutes
(ATS Labs, Eagan, MN).
Virucidal
Microcyn was tested to determine the virucidal
characteristics against the Human Immunodeficiency
Virus type 1 (HIV-1), Strain HTLV-IIIB, in
accordance with the U.S. EPA DIS/TSS-07 guidelines.
The virus was applied as a dried film on sterile,
glass Petri dishes, followed by exposure to
MCN for 10 minutes. Subsequently the virus
was separated from the test substance by gel
filtration and titrated by serial dilutions
for infectivity assay. Conclusion: per dilution
groups (7 groups: 101 through 107), 8 samples
were observed and in no sample infective activity
was detected. The reduction in viral titer
was ≥ 3.75 log10 for all samples. Under
the conditions of this investigation, Microcyn
demonstrated complete inactivation of HIV-1
following a 10-minute exposure time, in accordance
with virucidal requirements as defined by the
EPA. [ATS labs, U.S.]
Other viral inactivation
studies have shown that Microcyn reduces ≥ 3 log the load of
Influenza A virus (A/HK68), Rhinovirus type 37
(ATCC VR1147 ) and Human coronavirus (ATCC 740)
after 30 seconds of exposure (APPTEC –ATS
labs, U.S.).
Sporicidal
Microcyn was tested to determine sporicidal characteristics
against spores of Bacillus subtilis (ATCC
#6633). The test was conducted in accordance
with the BS EN 14347:2002 ‘draft’ standard.
A spore solution with a concentration of 108 – 109
spores/mL was prepared from a purchased spore
suspension. Test samples contained 1 mL of
the spore solution, 1 mL water and 8 mL Microcyn.
The spore solution was exposed for 15 minutes
to Microcyn, after exposure the samples were
plated and incubated for four days at 36 ± 1 °C.
Conclusion: Under the conditions
of this experiment Microcyn was sporicidal against Bacillus
subtilis spores. The reduction in spores
was 6.5 log on average, thus completing the requirements
of the applied test method. [Micromed Laboratories
Inc., U.S.]
Microcyn does not kill
spores by inactivation of some component of
the spore’s germination
apparatus, but by damaging the spore’s
inner membrane such that Microcyn treated spores
lyse rapidly upon spore germination. Microcyn
also appeared to inactivate at least one enzyme,
CwlJ, located in the spore’s outer layers.
Microcyn killing of spores was not accompanied
by the release of the spore’s large pool
of dipicolinic acid (DPA). (Rose et al, 2006;
Paul M et al, 2006)
|