Integrated Cell Processing Work StationMHE-PF4025CW2-PA

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The Essential Work Station for Cell TherapeuticsIn designing the industry’s first viable alternative to a conventional Class 10,000 cleanroom for both Class 100 air quality and barrier isolation, Panasonic has introduced the Cell Processing Work Station (CPWS). It brings the potential of cell therapeutics to more facilities, while decreasing acquisition costs, operation costs and protracted time lines.

Global Cell Therapy and Tissue Engineering Market ( 2010 & 2015 )

Minimizes Cleanroom ExpenseSelf-ContainedSpace-SavingEasy to Install

Neurology

CardiologyCord Blood and Cell Banking

Cancer

General

Dental/Oral

SkinUrology

Ophthalmalogy and Organ Replacement/ Preservation

Orthopedics/Spine

Cell/Issue Banking

Cancer

General Sur GI,Gyn,Others

Ophthalmalo

Organ

Dental

Skin

Urology

Osthol

Neuro

Cardio

$25,000

Mill

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of D

olla

rs

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$20,000

$15,000

$10,000

$5,000

2010 2015

GMP Compliant for Aseptic ProcessesUser FriendlyEnergy Efficient, Green Design

Panasonic Integrated Cell Processing Work Station (CPWS)

Self-Contained System, Small Footprint

The Panasonic concept of a self-contained work station is enabled by the company’s demonstrated proficiency for in situ decontamination.This is necessary to separate the processes from one patient to the next, or one protocol to another. By using a highly effective hydrogen peroxide (H2O2) decontamination process, the CPWS can be completely decontaminated without heat and prepared for the next protocol within two hours. This is extremely time efficient as compared to a cleanroom decontamination function that can take up to days or weeks.By increasing throughput within the compliant parameters of GMP criteria, the CPWS is deployed for research, cellular manipulation, cell growth, cell product extraction, and emerging processes that fall within similar guidelines. Current and future applications of the CPWS include organ and tissue regeneration such as skin, cartilage, alveolar bone, cornea, cardiac muscle, nerve, liver, and pancreas regeneration. Immunotherapy applications may extend to dendritic cells, T-cells, and more.

Immediate beneficiaries of the CPWS include researchfocused institutions and scale-up development to treat a broad range of diseases. The focused research can be related to human cells, cellular therapies in clinical trials, and hospitals deploying FDA approved cellular therapeutics. As the science progresses, results are propagated throughout the medical and scientific community. This exponentially expands the need for bench-level research and production. In such situations, Panasonic's approach with free-standing and self contained work station is quite novel considering the conventional layered cleanroom approach of containment and protection.

The CPWS brings the capability for on-site cellular therapeutics to more number of facilities rather quickly, at a lower capital and reduced operational cost. All this is within the GMP (Good Manufacturing Practices) performance envelope required of the cell technology itself.

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Making it Work

Improving efficiency in human interaction is the primary goal of the CPWS. All work must be performed without human error, in an aseptic environment with detailed documentation to assure quality and compliance. Gown-up time, expense, and inconvenience is minimized or eliminated altogether. Integrated systems within the CPWS permit cellular extraction, preparation, culturing, and administration with aseptic assurance as well as economic practicality. Because conventional autoclaving is not possible, the Panasonic H2O2 decontamination process diminishes both time and labor associated with this critical step between patients. This positions the CPWS squarely in the equation for cost/benefit justification associated with investment decision-making. Allowances for integrated centrifuge, microscopy, data acquisition, and incubation functions are important considerations in the CPWS design. A unique docking station permits interface and exchange with an unlimited number of cell culture incubators dedicated to individual patients or cell lines.

On the Work SurfaceSince humans remain the single most common source of contamination, the CPWS provides both physical and work flow benefits to minimize contamination and cross contamination in the work area. Within the four-port glove box, the CPWS delivers more than a conventional Class II, Type A2 biological safety cabinet, typically installed within a cleanroom to achieve the same objective. Here, the manually initiated, automatically deployed H2O2 decontamination process supplements continuous HEPA filtration. As 0.3 micron particles are removed from the fresh air exchange, H2O2 decontamination neutralizes contaminants brought forth by instrumentation or equipment. A number of decontamination sequences are available to protect the aseptic environment.

The glove box design offers barrier isolation protection for the operator and the work inside. User comfort and ergonomics are inherent to the CPWS design, including a sloped front for ease of access and glare reduction.

The CPWS Advantage

The relatively small footprint permits installation into existing or new Class 100,000 lab space with conventional utilities and minimal site preparation. Multi-layered airlocks in multiple treated rooms are avoided. Capital intensive expenses are lowered, while the lead times from decision to operation are shortened. Once in place, operational costs are highly contained and predictable, with decontamination available more frequently and at a fraction of conventional cost.

The Panasonic Difference

For over forty years, Panasonic has established a reputation as a premier manufacturer of precision biomedical and laboratory equipment. Known throughout the world as a leading brand in consumer electronics and appliances, Panasonic addresses global needs such as energy, food, housing, healthcare, and information technology.

As a part of the Panasonic product line worldwide, the CPWS exemplifies our unique vertical component integration approach to product development. This combines ideas and innovations from our global industrial and consumer products network into an integrated product featuring advanced technology, controls, construction, and performance attributes.

The CPWS and subcomponent systems have been extensively tested to meet the toughest quality standards for performance, ergonomics, and cost of ownership. The CPWS is designed to minimize its carbon footprint through energy savings and environmental stewardship.

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The Panasonic CPWS is a component-based design that permits a long-term or quick turnover of self-contained protocols with efficiency and safety. As an integrated system, all functions associated with good laboratory technique, environmental control, and ergonomic comfort are selected for compatibility and complementary functional performance.

Technical Attributes

The Panasonic CPWS work station is designed to deliver efficient, cost effective, GMP compliant cell therapy, and manufacturing capability without the expense and inconvenience of a class 10,000 cleanroom. The CPWS offers significant advantages over conventional hard wall cleanroom construction.

Work is easily suspended and resumed without the need to de-gown and re-gown, improving user comfort.

Fast decontamination increase throughput and deliver quicker return on investment.

Record-keeping and process documentation are easier to manage.

Optional centrifuge integrated into the work surface

Optional CO2 incubator with docking collar

Components and operating systems are configured around a central work station with a HEPA filtration and air management system. This is designed to deliver Class 100 air to the work surface within the glove box.

The CPWS is less expensive than a cleanroom.

It is quicker to acquire and place into operation.

The small footprint increases options for location and orientation.

The user-friendly glove box design eliminates gowning, improves operator comfort, and convenience.

Operating costs are lower than cleanroom costs

Central barrier isolator

Pass box interchange

Integrated H2O2 decontamination system

Optional cell observation system with microscope and monitor

The optional incubator and optional centrifuge operate within a Class 100 environment.

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Interior fluorescent lamps

Centrifuge module accessible for the aseptic work area.

Glove port

Hinged front access assembly. Front lifts up when total interior access is required.

Electrical compartment

System controller

HEPA supply and exhaust filtration blower motor assembly

Interchange pass box with manually initiated, automatic sequence H2O2, decontamination system.

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3

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Centrifuge controller

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Adjustable leveling feet10

Modular CO2 incubator, shown on cart, docked to barrier isolator.

Optional cell monitor LCD

Incubator cart with locking casters; offset casters nest with frame assembly when docked.

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Applications

The Panasonic CPWS enables a broader access to cellular therapeutic research related to both, minimally manipulated and non-minimally manipulated cell products. It lowers the cost of entry, extends the process to the widest range of applications, and minimizes operating expenses, when compared to a conventional cleanroom environment.

• Minimally manipulated products are associated with cell washing, enrichment, selection, HSC (PB, BM, CB), cancer therapies, and other under GTP requirements.

• Non-minimally manipulated products are associated with expanded, differentiated or transformed cells (DC, MSC, ESC, TC) in cancer centers, biotech labs, stem cell institutes, and contract manufacturing facilities operating under GMP requirements.

• GMPs (Good Manufacturing Practices) are mandated by the United States Food and Drug Administration to ensure that drug development and manufacturing is safe, under controlled environment, reproducible, and thoroughly documented.

• GMPs typically require expensive hard wall laboratories with laboratory suites that use biological safety cabinets in Class 10,000 cleanrooms within a Class 100,000 room.

DISEASE STATES CELL THERAPIES

CANCER

HEMATOPOIETIC STEM CELL (HSC) TRANSPLANTATION

Autologous and allogeneic HSC; Ex vivo expansion of HSC; ‘Suicide’ T-cells – gene transfer; Stem cell transportation

IMMUNOTHERAPYDendritic cells; NK/T cells; Macrophage-activated killer cells;

T-cell expansion; NK cells; Co-stimulatory molecules (gene transfer)

ORTHOPEDIC Expanded chondrocytes; Mesenchymal stem cells

NEURODEGENERATIVE DISORDERS/TRAUMA

Adult stem cell-derived cells; Embryonic stem cell-derived neural cells

CARDIOVASCULAR DISEASE Infusion of marrow/blood-derived angio blasts; CD34 stem cells; cardiac cells*

ORGAN REPLACEMENT

PANCREAS (DIABETES) Pancreatic islet cells; Embryonic stem cell-derived islet cells; Adult stem cell-derived islet cells

LIVER (FAILURE, METABOLIC DISORDERS)

Bioartificial liver; Isolated hepatocytes; Hepatocyte stem cells

KIDNEY (FAILURE) Bioartificial kidney

WOUND HEALING Keratinocytes; Skin stem cells

INFECTIOUS DISEASESAntigen-loaded dendritic cells; Lymphocyte expansion;

Macrophages

GENETIC DEFICIENCIES

HEMOPHILIA Gene Therapy

SCID Gene Therapy

CYSTIC FIBROSIS Gene Therapy

AUTOIMMUNE DISEASES

IMMUNOTHERAPY Dendritic cells; T-cells, Mesenchymal stem cells*; Lymphocyte expansion; Natural Killer cells

ApplicationsClinical Applications of Cell Therapies

HSC, hematopoietic stem cells; NK, Natural Killer; SCID, severe combined immunodeficiency * Currently in clinical studies.

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MARKET FACILITY PROTOCOL CPWS BENEFIT

ACADEMIC Cancer centers Cancer treatment, translational medicine Easy segregation of patient-specific cells

ACADEMIC Medical research Regenerative medicine

CLINICAL Hospitals

PRIVATE INDUSTRY Biotechnology, Pharmaceutical

Easier transition from animal models to human clinical trials

PANASONIC CELL PROCESSING WORK STATION (CPWS) CONVENTIONAL GMP CLEANROOM

FUNCTION ANNUAL BUDGET (NOMINAL) FUNCTION

ANNUAL BUDGET (NOMINAL)

H2O2 Cartridge, 25g, Total System Decontamination $9,000 Disinfection, Cleaning $9,000

H2O2 Cartridge, 5g, Pass Box Only Decontamination $13,320 Routine Sanitation $12,000

Residual H2O2 Detector $2,664 Particle Sensors $3,000

Gloves, 3 gloves, 2× $1,140 Sterilized, Non-Shedding Gowns $18,000

Sleeves, 3 gloves, 1× $3,640 HEPA FILTERS

HEPA FILTERS Biosafety Cabinet, Supply Filter $343

Work Station $907 Biosafety Cabinet, Exhaust Filter $190

Interchange Pass Box $294 Certifier Labor, BSC Formalin Decontamination $956

Room $833 Cleanroom Air Supply $2,916

Labor $1,330 Cleanroom Air Exhaust $1,516

VALIDATION EXPENSES Certifier Labor, CR Formalin Decontamination $1,500

Cleanliness and Air Volume Report $1,440 VALIDATION EXPENSES

Decontamination Performance BI Inspection $3,230 Biosafety Cabinet and Report $1,050

H2O2 Mist Uniformity Inspection $720 Cleanroom and Report $10,000

Centrifuge Module and Report $1,350 Centrifuge and Report $1,350

CO2 Incubator Module and Report $1,250 CO2 Incubator Module and Report $850

POWER CONSUMPTION $18,057 POWER CONSUMPTION $28,972

NOMINAL ANNUAL BUDGET $60,000 NOMINAL ANNUAL BUDGET $91,600

1 Comparative operating costs listed herein are nominal and based on actual installations in Japan. Total cost of ownership and operation will vary according to type of installation, method of use, geographic location and other factors. Panasonic offers consultative assistance in developing a cost/benefit analysis specific to your facility and protocol. Contact Panasonic to arrange a report unique to your prospective application

Approximately 35% Less Expensive to Operate

The Panasonic CPWS offers significantly lower operating costs when compared to a conventional cleanroom (open system). Comparison methodology and assumptions are available from Panasonic. Soft-cost benefits related to user convenience, user comfort, flexibility, throughput, and other demonstrated advantages of the CPWS can be established through consultative review. Contact Panasonic for details.

Cost Benefit Analysis

Who Benefits from CPWS

35%

Les

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Comparative Operating Costs1 (Nominal), Panasonic CPWS vs. Conventional Cleanroom,

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COMPARISON PANASONIC CPWS BARRIER ISOLATOR

CLEANROOM WITH BIOLOGICAL SAFETY CABINETS

GENERAL Closed system, requires only Class 100,000 air

Open system, requires significant investment and maintenance of background environment,

Class 10,000 air

PLANNING AND LEAD TIME Minimal; Cost of Class 100,000 room plus CPWS High; Cost of Class 10,000 cleanroom plus Class 100 one or more Class 100 biological safety cabinets

SPACE/FOOTPRINT ALLOWANCE Minimal footprint in existing space Dedicated new/retrofit facility with significant requirement for HVAC, filtration, air showers

VALIDATION COSTS Minimal; Requires Class 100,000 only. High; Requires both Class 100 and Class 100,000.

OPERATION COST Low High; Repeated decontamination and maintenance costs. Higher consumables cost

IMPLEMENTATION Weeks Months or Years

ERGONOMICS AND USER COMFORTNo second gowning required. Central barrier isolator

with ergonomically angled front permits easy access through glove ports. Reduces stress on workforce.

Conventional first and second gowning, external air supply, interlock doors/air showers

FLEXIBILITY

Elimination of hazardous fumes for decontamination permits diverse applications. Elimination of depolymerizing formaldehyde, formalin and other toxic chemicals permits

transition between applications seamlessly.

Inflexible

THROUGHPUTExpanded. Quick changeover extends use,

optimizes return on investment. Component integration streamlines workflow while enhancing aseptic processing.

Limited due to product changeover criteria

DECONTAMINATION Two Hours Up to Two Weeks

EQUIPMENT AND INSTRUMENTATION

Microscopes and other instrumentation can be dedicated to the work station.

Shared instrumentation in an open system exposes processes to cross contamination.

ISO14644-1 FDA EU-GMP ANNEX 1 JP WHO-GMP TRS902 ANNEX 6

CLASS 5 Class 100 In Operation 3,520

Grade A In Operation 3,500

Grade A In Operation 3,520

Grade A In Operation 3,500

CLASS 7 Class 10,000 In Operation 35,200

Grade B In Operation 350,000

At rest 3,500

Grade B In Operation 352,000

At rest 3,520

Grade B In Operation 350,000

At rest 3,500

CLASS 8 Class 100,000 In Operation 3,520,000

Grade C In Operation 3,500,000

At rest 350,000

Grade C In Operation 3,520,000

At rest 352,000

Grade C In Operation 3,500,000

At rest 350,000

CLASS 9 — Grade D At rest 3,500,000

Grade D At rest 3,520,000

Grade D At rest 3,500,000

Feature Benefit Analysis

CPWS SOLUTION

More CostEfficient

35%

Pass Box

Glove BoxHEPA Filters

Class 100

DetachableIncubator

Centrifuge

TYPICAL CLEANROOM

* Drawing not to scale

Change Room

Class 100,000

Class 100,000

Class 10,000

Class 10,000

Class10,000

Class 100,000

Class 100-BSC

Aseptic Environment Required for Cell PreparationUsually, human derived cells must be guaranteed that they are prepared and cultured in an aseptic environment because they cannot be treated by heat or pressure.

ExtractionOrginal Cells

Prepared Cells

Preparation Culture Administration

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Cleanroom: The biological safety cabinets within the cleanroom are open systems, which require a stricter background environment. Access in and out of the cleanroom must comply with gown-up protocols consistent with GMP facilities. Class 100 air is ultimately delivered to the work product in one or more biological safety cabinet(s) operating independent of the cleanroom. Decontamination is costly and time-consuming; changeover from one protocol to another is difficult and expensive.

Conventional GMP Cleanroom Facility (Open System) with Biological Safety Cabinets

Panasonic CPWS, Barrier Isolator with Integrated Systems

The Panasonic CPWS offers significant throughput potential in a comparatively small footprint.

The CPWS can be installed in manageable Grade D (Class 100,000) environment, providing biological and physical protection between the work and the user.

Access through the glove ports improves user comfort.

The integral H2O2 decontamination system is completed in less than two hours, permitting frequent changeover and assuring separation integrity from one cell process to the next.

Aseptic Environment

4 m2

18 m2

18 m2

6 m2

16 m2

3 m2

10 m2

16 m27 m2

10 m211 m211 m2

PS

PS

PSPSPS

PS

Class B(10,000)

Class CIO(100,000)

Class DAR(100,000)

Class A(100)

PSPS

PS PS PS

-152ºC

-32ºC

4 m2

18 m2

18 m2

6 m2

16 m2

3 m2

10 m2

16 m27 m2

10 m211 m211 m2

PS

PS

PSPSPS

PS

Class B(10,000)

Class CIO(100,000)

Class DAR(100,000)

Class A(100)

PSPS

PS PS PS

-152ºC

-32ºC

Aseptic levellow (D)

Aseptic levelmid (C)

Aseptic levelhigh (B)

(A)Aseptic level raised gradually

Highest aspect level = Aseptic(safety cabinets, etc)

Air lock

General environment (not clean)

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Barrier IsolatorThe barrier isolator forms the central component to the work station and contains the primary operating systems required to establish and maintain aseptic conditions to meet GMP criteria.

• The barrier completely isolates the interior work product from the operator.

• The barrier isolator creates a closed Class 100 environment, eliminating the need for biological safety cabinets in a cleanroom.

• Isolator interior air is 100% Class 100 total exhaust. No recirculated air is used.

• The polished stainless steel glove box interior is designed for maximum exposure of all interior surfaces subject to H2O2 decontamination.

• Before commissioning and initial use, the isolator front can be opened on a

locking hinged frame for installation of instrumentation or other devices larger than the interchange pass box opening.

• The HEPA filter and airflow system is mounted on top of the isolator.

• The internal airflow system is designed to create a positive pressure to mitigate the possibility of inflow contamination.

• Viability of the containment area is not delegated to third-party cleanroom contractors who are hired to decontaminate.

Ergonomics and SafetyBecause second gowning is not required, user comfort and productivity is significantly improved. The workplace routine, including bathroom breaks, is unencumbered by the need to leave and re-enter a cleanroom, bleach, and/or shower.

H2O2 Decontamination System

• The manually initiated, automatically sequenced H2O2 decontamination system offers a fast, safe, and proven decontamination process. It enhances the performance of the CPWS by allowing more frequent turnover of segregated cell lines.

• The validated H2O2 system generates an H2O2 vapor that permeates all exposed surfaces from the central interchange pass box nebulizer, which contains a replaceable bottle of enriched hydrogen peroxide.

• When deployed, the H2O2 vaporization sequence decontaminates the pass box, work station interior, centrifuge, CO2 incubator exterior, and docking gaskets.

• Once the vaporization is complete, the H2O2 program implements a dwell period to ensure that proper exposure times are maintained for a wide range of pathogens.

• At the end of the pre-programmed dwell period a resolution process eliminates fumes and toxic residuals.

Isolator Interchange

• The interchange pass box allows safe access to the work area for supplies, instruments, devices, sterile media, and labware.

• When materials are brought into the work station they are first positioned inside the interchange for H2O2 decontamination.

• Decontamination is manually initiated and automatically sequenced once started.

• When the H2O2 decontamination process is complete, the inner door is opened and the transfer is completed.

• Door interlocks permit simultaneous opening to protect the barrier isolator.

Series Features• The inconvenience and expense of

cumbersome containments suits with air and vacuum hoses is eliminated. If working with BL3 agents, the buddy system is not required.

• The barrier eliminates the potential for room contamination from blood or other aerosols. Workflow is not impacted by routine colds.

• Staff confidence in total containment improves morale.

• Glove ports permit easier handling of red bag materials when required.

• A 6º angled front includes three glove ports to permit access to all interior surfaces.

• The interior cabinet includes independent interior fluorescent lamps to supplement ambient light.

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Decontaminated Contaminated Possible cell-derivedcontaminated

Pass Box OnlyInstruments or materials introduced into the glove box are decontaminated by a pass box cycle only, avoiding the need to decontaminate the entire glove box work area. Work can continue in the glove box while the cycle is in process.

Cell Culture IncubatorIncubator and Work Area. After aseptic protocols are completed, cultures are transferred to the (optional) CO2 incubator where growth can continue under aseptic conditions after the incubator is detached. Unwanted materials are removed through the pass box interchange.

ChangeoverWhen handling different cells from the previous protocol, the next (optional) cell culture incubator is docked to the work station glove box. The work station, interchange pass box (optional) centrifuge and incubator door are decontaminated prior to opening. The changeover process is completed in less than two hours.

Total DecontaminationA total H2O2 vapor decontamination creates aseptic conditions in the interchange pass box, the glove box and (optional) centrifuge module.

Decontamination Sequence

One CPWS can service multiple CO2 incubators to permit easier cell segregation. One incubator is attached to the work station at the docking collar and subjected to a quick, safe H2O2 decontamination process. When work is completed, the incubator is sealed and returned to the staging area and another incubator is attached and the process is repeated.

Series Features

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CO2 Incubator

The modular CO2 incubator is an adaptation of the full-performance Panasonic MCO-5AC(IS). This incubator is designed for precise temperature and CO2 control with elevated relative humidity to minimize cell desiccation.

• By using multiple, detachable CO2 incubators, the CPWS can manage multiple patient protocols through complete product segregation, thereby assuring aseptic conditions and eliminating any possibility of cross-contamination or mishandling of patient-specific cells.

• Segregation permits compliance with published criteria associated with regenerative medicine and in vivo cell therapies.

• The incubator attaches to a docking collar adjacent to the barrier isolator.

• Once attached, the barrier isolator undergoes a 2-hour H2O2 decontamination process before the incubator door is opened. This process decontaminates the work area, incubator face, centrifuge and pass-thru interchange.

• The H2O2 effectively decontaminates the CO2 connection.

• When work is complete, the incubator is sealed, detached and moved to a user-defined staging location on a wheeled cart.

• The next incubator can be moved into position to repeat the process for another patient.

• There is no limit to the number of Panasonic MCO-5AC(IS) incubators that can be used with the work station.

Incubator Features and Benefits

The incubator is a modification of Panasonic’s popular MCO-5AC. The compact 1.4 cu.ft. (49 liter) interior chamber is constructed of Panasonic’s exclusive inCu-saFe® copper-enriched stainless steel, creating a natural germicidal barrier against airborne contamination.

• An integrated microprocessor controller supervises all functions including temperature and CO2 setpoints, control, alarm and monitoring.

• The patented Direct Heat and Air Jacket control system assures temperature uniformity and stability essential to the most sensitive cell lines.

• The rounded-corner, electropolished interior is configured for use with a variety of standard cell culture vessels.

• All interior components are designed to withstand repeated H2O2 decontamination cycles expected in high turnover environments. Components are removable without tools.

Centrifuge

The centrifuge is installed beneath the interior work surface and accessible under aseptic conditions without removing cells from the protected environment.

• The position and orientation of the centrifuge assures thorough decontamination during the H2O2 decontamination cycle.

• The integrated design eliminates the requirement for additional floor space in a GMP environment.

• A variety of fixed and swinging rotors available.

• Centrifuge controls are located external to the work area at the front of the centrifuge module.

Series Features

Modular Incubator Model MCO-5AC(IS) docked to the CPWS

CPWS Centrifuge

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Cell Monitoring System (Optional)

An integrated cell monitoring system reduces additional footprint required in a GMP environment. Cell monitor components are located within the barrier isolator and designed to withstand repeated H2O2 decontamination sequences.

• The interior components include a LCD monitor and a separate collection module.

• The collection module includes a high-performance CCD camera (charge coupled device) with objective lens and phase difference filter.

• The monitor displays real time images with total magnification of 110×.

• Images can be captured via a non- contact photo sensor, 2.4 × 1.8 mm for monitor display and digital recording.

• A standard personal computer, external to the aseptic isolator work area, is used for data acquisition and image management.

Series Features

Work station Glove BoxThe work station creates Grade A Class 100 air quality within the glove box, and permits installation within a Grade D Class 100,000 room, eliminating the need for a typical cleanroom. The self-contained, closed system protects both the user and the work product without the need for a second gowning. An ergo-nomically shaped front access is angled 6° for user comfort, glare reduction, and reach throughout the work surface.

1. Pass Box DecontaminationMaterials are brought into the work chamber from the outside through the pass box interchange. The H2O2 decon-tamination is manually initiated and automatically sequenced, thoroughly decontaminating the pass thru material and protecting the integrity of the work surface. The interchange contamination process can function alone, independent of the glove box.

2. Decontamination SystemThe CPWS includes an H2O2 decontamina-tion system that generates H2O2 vapor to produce validated results. This system covers the pass box interchange, glove box work area, optional centrifuge, and optional CO2 incubator. The enriched H2O2 solution is contained in a replaceable bottle and inserted as a cartridge inside the decontamination module.

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PC for CapturingCamera IF

Various Signals IF

Control/Relay Box

Images from PC

AC Power

Power SW Signal Capture SW Signal

Observation Module

Lighting VCC,GNDLight Dimming Sygnal

Cameral IF (power, image signals)

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COMPONENT ORDER NUMBER

BASE WORK STATION, BARRIER ISOLATOR MHE-PF4025CW2-PA

INTERCHANGE Included

HEPA FILTRATION SYSTEM Included

CENTRIFUGE Included

CELL OBSERVATION MODULE Optional

CO2 INCUBATOR MCO-5ACIS

COMPONENT DESCRIPTION

BARRIER ISOLATOR Base Unit

INTERCHANGE PASS BOX Included

AIRFLOW AND HEPA FILTRATION SYSTEM Included

H2O2 SYSTEM Included

CENTRIFUGE Included

CO2 INCUBATOR Optional

CELL OBSERVATION SYSTEM Optional

Specifications

FEATURE SPECIFICATION

EXTERIOR DIMENSIONS (W X F-B X H) 21.25" × 22.9" × 30.3" / 540 x 582 x 771 mm

MAXIMUM SPEED 2100 RPM

MAXIMUM CENTRIFUGAL ACCELERATION 10 to 970G centrifugal acceleration settable range

CONTROLS, ALARMS Externally mounted, front, with foot switch for cut-off.Door lock status displayed.

PRE-SETS Up to 4 patterns in memory

TIME SETTABLE RANGE 10 to 50 seconds (10 second increments); 1 to 99 minutes (1 minute increments); and infinite

ACCELERATION/DECELERATION SETTINGS 3 stage

MOTOR SHAFT Stainless steel

CAPACITY 1000ml (50ml tubes, × 20)

Component Specifications

Centrifuge and Module

System Summary Specifications

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Specifications

DIMENSIONS

OVERALL EXTERIOR DIMENSIONS (W X F-B X H) 115" × 41" × 87.8" / 2920 × 1045 × 2230 mm net of attached optional incubator

INTERIOR DIMENSIONS (W X F-B X H) 70.7" × 28.5" × 34" / 1796 × 726 × 864 mm

INTERIOR WORK SURFACE ELEVATION 31.5" above floor / 800 mm

GLOVE ELEVATION 41.3" above floor / 1050 mm

PASS BOX INTERCHANGE (W X F-B X H) 19.6" × 16.7" × 15.8" / 500 × 425 × 400 mm

NET WEIGHT 2207 lbs / 1000 kg, nominal

CONTROLS, ALARMS

PRESSURE MONITOR Red LCD and audible alarm if pressure falls below alarm setpoint.

FAN MOTOR Audible alarm during motor shutdown

CONSTRUCTION

EXTERIOR FINISH Painted steel

INTERIOR FINISH Polished stainless steel

FRONT GLOVE PORT PANEL, ANGLE 6° Polycarbonate with painted steel frame. Hinged for opening to load equipment.

AIR SYSTEM

AIR QUALITY Grade A Class 100 over work surface; installation in a Grade D, Class 100,000 ambient room

AIRFLOW SYSTEM AND VELOCITY Vertical downflow over work surface, 0.2~0.3 m/s ± 20% @6" below supply filter screen (150 mm)

FILTRATION SYSTEM Independent HEPA supply and exhaust filters, efficiency 99.99% (0.3 µm PAO), scan tested and passed

FILTRATION SYSTEM, PASS BOX Independent HEPA supply and exhaust filters, efficiency 99.99% (0.3 µm PAO), scan tested and passed

INTAKE AND EXHAUST Electrically switched system. Room air intake thru HEPA supply filter; return exhaust to room thru HEPA exhaust filter

RELATIVE AIR PRESSURE

WORK STATION Positive pressure after decontamination of work station and pass box; audible notification when ready, 60Pa

PASS BOX INTERCHANGE Positive pressure after decontamination of pass box only; audible notification when ready, 220Pa

INTERIOR WORK AREA

LIGHTING Fluorescent lamps (3), 30w each, top of panel, top of right, left

ELECTRICAL OUTLET Duplex, drip-proof receptacle

PASS BOX INTERCHANGE

DOOR Front opening to outside; left side opening to interior work area

MATERIAL Polished stainless steel

DECONTAMINATION SYSTEM

FUNCTION H2O2 vaporization; simultaneous decontamination of interior barrier isolator work station, pass box interchange, optional centrifuge and optional CO2 incubator

H2O2 RESOLUTION AND AERATION Catalytic, external to the work area. Residual H2O2 density at catalytic outlet is at or below 1ppm (by TLV-TWA). Fresh, HEPA filtered air follows resolution

DECONTAMINATION CYCLE TIME Load dependent; typical cycle times range from 1.0 to 2.0 hours from manual initiation of automatic sequence.

UTILITIES

ELECTRICAL Main system, 4500w, 220V, AC, 60Hz. Electrical outlet 120V, AC, 60Hz.

Barrier Isolator

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Specifications

DIMENSIONS

EXTERIOR DIMENSIONS WITHOUT STAND (W X F-B X H) 23.5"W× 22.1" × 24.7" / 597 × 561 × 626 mm)

INTERIOR DIMENSIONS (W X F-B X H) 13.8" × 14.9" × 14.8" / 350 × 378 × 375 mm)

NET WEIGHT, NOMINAL 110 lbs / 50 kg

VOLUME 1.7 cu.ft. / 49 liters nominal

OPERATING SYSTEM

CO2 SENSOR Thermal

INCU-SAFE® COPPER ENRICHED STAINLESS STEEL INTERIOR Standard

MICROPROCESSOR CONTROLLER/DISPLAY, DOOR MOUNTED Standard

DIRECT HEAT, AIR (DHA) JACKET Standard

DECONTAMINATION

H2O2 DECONTAMINATION When docked to work station

STANDARD, COPPER ENRICHED STAINLESS STEEL INTERIOR Germicidal protection

ENVIRONMENTAL PERFORMANCE

TEMPERATURE CONTROL RANGE +7.0°C above ambient to 50°C in a 5°C to 35°C ambient

TEMPERATURE CONTROL UNIFORMITY AND DEVIATION ±0.25°C in 25°C ambient, setting 37°C, 5% CO2, no load

CO2 CONTROL RANGE AND DEVIATION 0% to 20%, ±0.15% in 25°C ambient, setting 37°C, 5% CO2, no load

AIRFLOW Continuous with inner door closed

INTERIOR HUMIDITY 95%RH @ 37°C through evaporation via DHA heating system; optional reflective/deflective optical low water sensor

CONTROL, MONITORING, ALARM

TEMPERATURE AND CO2 CONTROL Setpoint resolution 0.1°, 0.1%

DISPLAY LED, resolution 0.1°, 0.1%

COMMUNICATIONS Optional 4-20mA connection; Optional PC interface MTR-480

CABINET DESIGN AND CONSTRUCTION

SUPERSTRUCTURE, EXTERIOR CABINET AND DOOR Galvanized steel exterior, baked-on enamel finish

INTERIOR AND SHELVES Copper-enriched stainless steel

INNER DOOR Tempered glass

INSULATION Rigid foam polyurethane

OUTER DOOR Side oriented for docking with work station

ACCESS PORT Single, 1.18" / 30mm with silicone stopper

LEVELING FEET Adjustable

ENERGY, ELECTRICAL, UTILITIES

MAXIMUM POWER CONSUMPTION 205W

MAXIMUM HEAT DISCHARGE 740kJ/h

ELECTRICAL 115V,60Hz

CO2 GAS CONNECTION 4 to 6 mm barbed fitting

CO2 GAS INPUT PRESSURE Nominal 0.03 MPaG/0.3kg/cm2/5.0lbs/sq.in; from two-stage CO2 regulator

CO2 Incubator (Modular), Panasonic MCO-5ACIS

Professional Service and Support

Convenience of Panasonic Product Service

• Panasonic service specialists are trained to:

- perform remote and on-site diagnostics

- repair and replace worn components

- offer preventative maintenance programs as per your needs and budget

We provide full product service support to main-tain Panasonic standards of product safety, reli-ability and high performance. The combination of our multi-national network of factory-trained service professionals, detailed documentation of field performance, and high-value on the cus-tomer feedback helps us to deliver best-in-class, end-user support for our customers.

• Because our products are sold and serviced world-wide, products acquired in one country under grant or facility-sharing programs are easily supported if moved to facilities in the next city or around the world.

• We offer training to selected facility biomedical engineers and service staff for authorized in warranty and post-warranty repairs.

• Many Panasonic Healthcare products include self-di-agnostics that permit authorized service technicians to determine how and when service calls are required.

Validation Services Panasonic offers a wide range of high-quality ser-vices for all our equipment. These services include on-site validation, customer validation support packages, factory acceptance testing and NIST calibration.

Choosing Panasonic as an equipment supplier and validation consultant can greatly reduce the time and cost involved with getting new equipment com-pliant and ready for use.

Unique Services Panasonic Offers:• On-site consultation

• Unit specific authorized protocol documents

• Customizable testing procedures to meet customer specific requirements

• Free archiving of unexecuted testing protocols

• Unbiased testing of competitive equipment

Pre-delivery Services:• validation support,

• consultation,

• factory acceptance testing,

• calibration

• temperature mapping

On-site Services:• installation qualification,

• operational qualification,

• performance qualification,

• calibration and

• temperature mapping.

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Panasonic Healthcare Corporation of North America1300 Michael Drive, Suite A, Wood Dale, IL 60191Toll Free USA (800) 858-8442, Fax (630) 238-0074us.panasonic-healthcare.com

AW/08/2014

© Panasonic Printed in USA