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The
breakthrough technology behind STERRAD Sterilization Systems.
The limitations of traditional instrument sterilization methods, including
ethylene oxide gas (EtO) and steam led ASP researchers to develop an
alternative sterilization technology in the early 80s. The result? A
unique method based on a patented process implementing low-temperature
hydrogen peroxide gas plasma. This evolutionary technology formed the
basis for the revolutionary STERRAD Sterilization Systems.
The ASP technology uses a combination of hydrogen peroxide vapor and
low-temperature gas plasma to rapidly sterilize medical instruments
without leaving toxic residues. With this technology STERRAD Sterilization
Systems sterilize your instruments and medical devices safely and
effectively, without the limitations or risks associated with peracetic
acid, steam, and ethylene oxide gas (EtO) systems.
The ASP technology, which is particularly suited to heat-sensitive and
moisture-sensitive instruments, includes 5 phases:
1.
The Vacuum Phase
The chamber is evacuated, reducing internal pressure in preparation for
the subsequent reaction.
2.
The Injection Phase
A measured amount of liquid peroxide is injected into the chamber,
evaporating the aqueous hydrogen peroxide solution and dispersing it into
the chamber, where it kills bacteria on any surface it can reach.
3.
The Diffusion Phase
The hydrogen peroxide vapor permeates the chamber, exposing all load
surfaces to the sterilant and rapidly sterilizes devices and materials
without leaving any toxic residues. At the completion of this phase, the
chamber pressure is reduced and the plasma discharge is initiated.
4.
The Plasma Phase
An electromagnetic field is created in which the hydrogen peroxide vapor
breaks apart, producing a low-temperature plasma cloud that contains
ultraviolet light and free radicals. Following the reaction, the activated
components lose their high energy and recombine to form oxygen and water
Phases
1, 2, and 3 are then run a second time for added efficacy. This built-in
reprocessing assures optimal sterilization for even the most
difficult-to-sterilize devices.
5.
The Vent Phase
The chamber is vented to equalize the pressure enabling the chamber door
to be opened. There is no need for aeration or cool-down. Devices are
ready for immediate use.
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