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M³UVTM STEADY-STATE* IRRADIATION ©

WORLD MAXIMUM MICROBE KILL-POWER *Photon Capacitance

MolecuCare ®, Inc.

…Living better for less

Thank you

Disinfection R&D, Consultants and Equipment Builders

Consultant to: Government, Industry, Corporate America, Foreign Ministries and Military, Healthcare, etc.

All equipments manufactured in the U.S.A. in our facility

We Do Not Promote Client

ALL MolecuCare equipments are analog functional and self-correct to optimum specification performance

Engineering, Architectural, Environmental, Hydrological special interests note our equipment procedure; inquiries invited from your arena

Indoor air ‘cleaning’ is mismanaged by a mechanical misrepresentation named the “HEPA” (*) filter. The HEPA is unable to separate pathogens generated and cultured within the hospital business of treating pathogenic origin. Arguably, the HEPA filter is a left over claim of the mid Twentieth Century era of early refrigeration, “balloon” tires and the first airliners.

Failure of the HEPA of physical results of millions of infectious events is due to a failure to recognize that HEPA ‘efficacy’ ratings cannot be measured and/or verified in terms of living microorganisms, and methodology has no substantive place in molecular science, bio-physics or physiology. A specification for micron size is to the filter as mesh is to a fish net and has absolutely no indication of what percent of efficiency is afforded and relates to nothing whatsoever due to the nature of both the test itself and use as a living microbe management tool.

There is a litany of falsehood and erroneous if not misleading performance attached to the HEPA ‘efficacy’ rating itself: the HEPA is used in a bio-dynamic situation and the micron size rating is established by one shot resistance to passage whereas a filter capability has three probabilities: increased pressure on remaining content in the mesh due to the decreasing free space allowing flow through, and use of micro-pellets to indicate usage in a live pathogen theater - in the realm of microbe billions beginning with disregard for the fluidity of the microbe itself. There is no possibility of actual performance assessment in terms of seconds, minutes or hours of continued use as to microbe ratio of capture with respect to the surviving flow through and challenge ratio: by weight, count or culture. (*) Definition: “High Efficiency Particulate Air”.

Seven hundred thousand patients a year become infected and most expire, at a cost of $15,000 hospital expense each, annually in the U.S. The death toll is in the hundreds of thousands, and $Billions of insurance costs adding as “healthcare” cost into the system.

AT LAST

Changing Medical Building Indoor Air Disinfection Method

The world’s certifiable performance air hygiene

AIRcaire ™

CLINICAL

Hospital Safe Air Generator ©

“Whole-building” protection

As air is contaminated with airborne cellular life anywhere in the building, the bio-mass is a bio-report of all air breathed by all occupants. Man is the second occupant within the building bio-mass: the airborne cellular life is the first. Airborne pathogens are greatly concentrated in medical facilities.

It is very possible that intimately touching (gloved or otherwise), wound dressing, house-cleaning, transporting and servicing bodily functions and care needs, constitute stirring of pathogen resources and crossing of offensive/ defensive barriers of infection condition. Beyond the frequent coughing and sneezing within any hospital, with exudation of ill-body fluids, care-founded airborne cellular life is propelled airborne with the rustling of bed clothing and sundry mobile services incessantly provided from one case-type bedside to another. Basic needed maintenance such as floor ‘dry-mopping’, the rolling wheels of supply carts, the physical movement of medical equipment between routine and emergency care and from floor to floor, etc. each serve to distribute the vapor-contact airborne cellular life by-products of the ill and the infirm into a common mix with other elements of air spaces. We suggest this industrious phenomena reaches into all the individual and famous personal “bio-sphere’ of all occupants and is continually cultured onto all surfaces of a medical facility. It is also quite possible that some immune systems become more adaptable to this challenge.

Such airborne cellular life as an infectious constant, are circulated by the forceful central air system that prevails in most ‘modern’ medical facility. We further infer the airborne cellular life of the air is not removed by the HEPA filter. We declare that almost exclusive use of the HEPA failure is no more efficient than the airliner HEPA filter that is not preventing international event , e.g. ‘Airliner Effect”.

Mechanically, the ‘HIGH EFFICIENCY’ filter caches greater-sized particulate matter such as the mold spore, and the filter itself becomes a platform catch basin of living micro-organisms, feeding on each other and creating toxic by-products. Filters are installed in the “return” side of the central air system ductwork at a location where the air is warmed and moist while contaminated with fresh airborne cellular life in the building. Located , ‘before’ or in front of, the fan blower moving that air about a building, many duct passages may be directed as freshly ‘returned’ air to the filter at the heating/cooling process. An un-measurable portion of this life is killed by dehydration (evaporation caused by continued air contact.[iv]). However, ‘Snipet’ DNA becomes part of airborne cellular life contained in that filter habitat. Thus, infectious airborne microbe (suspension) is never removed from the building as it is never removed from the airliner.

AND

AIRcaire ™

Isolation

Hospital Safe Air Generator ©

In practiced difficulties of the Negative Isolation Room air treatment, hospital ‘air’ follows natural law, violating Isolation Room precepts of man, atmospherically seeps into the Isolation Room from the hospital by the very forces created with the negative pressure. In medical facilities around the world, the often hastily and economically retrofitted ‘isolation room’ consists of a fan power in the room that creates a high rate of contaminated air ‘pulled’ from the room to exhaust outdoors. We assume ‘positive’ flow of bio-mass airborne cellular life into the room of the infirm and possibly immune-compromised from the general hospital supply is the only source for air for that room. MolecuCare approach to Isolation Room care with much experience in this need, eliminates both contaminated air entry into the Isolated patient, as well as contaminated air delivery elsewhere – anywhere. We believe this to be better healthcare.

Multiple-Isolation Care Capacity

Special room protection / airborne cellular life environmental separation

Cost effective

Versatile

Assurance

Increased Isolation capacity

Low operating cost

- ISOLATION AIRcaire™ air quality separation assurance from common building air flow, fail-safe ‘common’ wall separation regardless of atmospheric change, room use and size. Economical operation, increased room-type capacity and care revenue. Also for emergency field service need. Power protection-loss stand-by override assures minimum ten day operation.

☻ Highest performance airborne cellular life disinfection first and foremost

☻ 100% constant Isolation assurance

☻ Intensive healthcare accent

☻ Cost effective reliability

☻ Occupant air health

☻ Unlimited IR facility

☻ Zero Failure

since 1989

Prototype MolecuCare Chamber:

Left: automatic hand cleaning (hand washing inadequacies considered the cause of infection in Healthcare) under the equipment title “Ultron Silkman”. This unit was linked with automatic control limiting the number of ‘personal’ times used in a 24 hour period by any one healthcare worker, to avoid over-exposure. Entered into trials after laboratory tests by American Sterilizer Corporation (Media, PA. & Apex, N.C., U.S.A. Joseph P Dalmasso, Ph.D., Director) and sixty-five participants concluding the chamber results exceeded quality of wash with anti-microbial soap and reported skin texture with use as “silky”. Non-Significant Risk FDA trials authorized by this body, halted by an FDA authority for reasons mot clearly defined by FDA wariness of ultraviolet at the time (circa 1994). Right: Prototype laboratory chamber for research studies, cellular response.

MolecuCare®, Inc. R&D, Genl Admn/ Sales P.O. Box 1748 New Milford, CT. 06776 1 800 966 9853, Facilities: Wallingford, CT

Below : First use of Ultra High strength Steady-State Ultraviolet Irradiation, [the console “H-10”] located in [left] Emergency Room South Bronx Hospital Special AIDS Patient care, [Right] AIDS Drug Resistance Tuberculosis Isolation Room (note reflection on wire-glass wall between camera and room, of exit sign and fluorescent light fixture exterior to the room, Circa 1996.

ICU AIDS DR Tuberculosis,

South Bronx, New York

(circa 1996)

Background, Indoor Air :Safe Air Generator floor Console

Made in the U.S.A.

Original Central Air (MRAD) Modular Return Air Disinfection

Will your air ‘cleaning’ provider attest by affidavit to kill-remove these microbes?

Off the shelf product and Licensors to the OEM, product engineering and production prototyping for your market in our facility under license agreement, equipment to all with Prototype Testing by International Laboratory

Steady-State Irradiation Disinfection POWER

U.S. and International Patents and Patents Pending