AquaSense MB
AQUASense MB neu
Aqu@sense MB
AquaSense MB
AQUASense MB neu
Aqu@sense MB

AQU@Sense MB

Demander un devis
Référence: P06170006

  • Fully Automated In-Process Control: Seamlessly integrates into water purification systems for automated, real-time monitoring.
  • Trend Monitoring: Early detection of deviations or adverse trends in water purification systems allows for proactive intervention.
  • Rapid Pharmaceutical Water Release: Enables PW or WFI systems to be released within 2-3 hours post-sanitization.
  • Primary Validated Instrument: Thoroughly validated according to European Pharmacopeia, USP and PDA TR33
  • Proven Technology: Utilizes Flow Cytometry with integrated dyeing, to reliably detect intact microorganisms.
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The Future of Micro­bial Moni­toring: AQU@Sense MB

Fully automated In-Process Control for enumeration of microorganisms is available today.

Gain comprehensive insights into PW and WFI systems through regular measurements and trend monitoring. Results are delivered within 20 minutes, facilitating rapid decision-making and early trend detection. Enhance product quality and process efficiency with an fully automated instrument tool for microbiological monitoring.

AQUASense MB neu 1280x640
AQUASense MB neu 1280x640

ICC instead of CFU: A new measure­ment

Intact Cell count is signif­i­cantly higher than Colony forming Units

Comparison of different methods to detect microorganisms has shown that the number of individual cells is by far higher than the results of HPC. Scan RDI and fluorescence microscopy have shown, that one colony on the plate typically origins from many individual cells.

CFU, the «Gold Stan­dard» for micro­bial moni­toring has serious disad­van­tages.

 

  • Long time to result… minimum 3 to 5 days
  • Only considers growing organisms
  • Prone to human errors
  • Just an estimation, not a real count for microorganisms
  • VBNC organisms are invisible
  • Conglomerates of cells will only generate only one colony
Plate R2A Agar

Flow Cytometry: the perfect tool for real cell count

A new way to determine the microbial load in pharmaceutical water.

 

  • Proven tech­nology in many appli­ca­tions
  • Highly specific for intact microor­gan­isms thanks to the staining proce­dure
  • No inter­fer­ence with parti­cles or cell frag­ments
  • Fully auto­mated without any user inter­ven­tion
Flow Cytometry

Primary validation: The first step in the validation process

 

  • According to regulatory guidelines
  • Tested for preci­sion, accu­racy, speci­ficity, limit of quan­tifi­ca­tion, linearity, range, and robust­ness.
  • Executed by experts for micro­bi­o­log­ical studies
  • Statis­tical Analysis by experts
  • Result: AQU@Sense MB is not infe­rior to HPC
Validation

Measurement out of the Box

The AQU@Sense MB comes with a conve­nient cartridge that contains all the neces­sary solu­tions for staining, cleaning, and decon­t­a­m­i­nating its media-exposed compo­nents. Addi­tion­ally, a waste container is included.

 

  • The AQU@Sense MB can perform up to 1,000 measure­ments without any user inter­ven­tion.
  • Child Proof Cartridge Replace­ment: After 1,000 measure­ments, simply replace the empty cartridge with a new one, and your AQU@Sense MB will be ready to use within minutes.
  • Effi­cient Recy­cling: The empty cartridge can be sent back to BWT for revi­sion and refilling, ensuring sustain­ability and mini­mizing waste.
Aqu@sense MB

IPC based on Trend monitoring allows for implementing criteria to identify critical changes in the bioburden.

 

  • Continuous measurement allows for trend monitoring
  • Early signs of microbial contamination are visible
  • Early planning of Corrective and Preventive Actions (CAPA)
  • No investigation due to false positive
Monitoring


Fast Release after Sanitza­tion

  
  • Time to result: 20 minutes
  • Imme­diate moni­toring of the sani­ti­za­tion effect
  • Energy saving with opti­mized sani­ti­za­tion proce­dures
  • Faster release of the system after sani­ti­za­tion
Release

Stratégie de contrôle de la contamination - Guide pour les systèmes d'eau pharmaceutique

Apprenez à mettre en œuvre une stratégie de contrôle de la contamination pour votre système de purification de l'eau, conformément à l'annexe 1 des BPF de l'UE.

L'eau est un ingrédient essentiel pour l'industrie pharmaceutique, mais elle présente également un risque important de contamination microbienne. Pour garantir la qualité et la sécurité de l'eau, il convient de mettre en œuvre une stratégie de contrôle de la contamination (CCS) pour le système de purification de l'eau, conformément à l'annexe I des BPF de l'UE. Une stratégie de contrôle de la contamination est une approche globale qui couvre la conception, le fonctionnement, l'entretien, la surveillance et la documentation de votre système de purification de l'eau. Elle repose sur une gestion des risques de contamination (CRM) qui identifie et atténue toutes les sources potentielles de contamination.

Seam­less Inte­gra­tion

Mechanical Integration:

Single Sampling Point
Multi Point with up to 4 Sampling points

The AQU@Sense MB can be combined with a valve system that can connect up to four sampling points to one AQU@Sense MB. The control of the measurement sequence is done by the control unit of the water system.

Measurement Modes:

  • Manual: The measurement can be started manually with a minimum sampling interval of 30 minutes
  • Automatic: An automatic measurement interval between 30 minutes and 6 hours can be programmed in the AQU@Sense MB
  • Remote controlled: The measurement can be triggered via digital input signals with a minimum sampling interval of 30 minutes.

Data transfer:

  • 4 to 20 mA
  • Modbus

Tech­nical Details

Tech­nical Details
Product Id P06170006
Dimen­sions (W x D x H): 350x270x373mm
Weight: 14 kg
Degree of Protec­tion: IP65
Oper­ating Envi­ron­ment: Indoor, +5°C - +35°C, 10% - 90% RH
Measure­ment Prin­ciple: Flow Cytom­etry with DNA specific staining
Side Scatter and 2 Fluo­res­cence Signals
Sample Volume: 90 µl
Sampling: Online, offline single measure­ment or offline with sample manager for up to 30 samples
Analysis Time: 30 minutes (Time to result ~20 minutes)
Measuring interval:
min 30 minutes (manual, auto­matic or trig­gered with digital input)
Sani­ti­z­able:
Ozone up to 100 ppb / hot water up to 85 °C
Power Supply: 18 VDC, 1.4A, 20W
Commu­ni­ca­tion Output: 2x4 ... 20mA analog outputs (freely config­urable)
4 digital outputs
Modbus
TCP/IP
Commu­ni­ca­tion Input: 3 digital inputs (start-​, stop-, abort measure­ment)
Data storage: Memory card 32GB
Data Export: USB 2.0, Ethernet
Elec­tronic Docu­men­ta­tion: 21 CFR Part 11 compliant elec­tronic docu­men­ta­tion
Audit Trail
Logbook
User manage­ment with 4 user levels
Compli­ance and Certi­fi­ca­tion: CE Certi­fi­ca­tion, Factory Vali­da­tion Certifi­cate

Stan­dard scope of delivery Item  Article No. P06170006
  AQU@Sense MB
Cartridge
Online Sampling Device
Manual Sampling Device
Power Supply / Cable

What are the differences between Heterotrophic Plate Count (HPC) and AQU@Sense MB?

  Heterotrophic Plate Count AQU@Sense MB
Technology Growth based, dependent on culture medium Fluorescence analysis after DNA-specific staining
Sampling Manual Automatic
Measuring unit Colony Forming Unit (CFU) Intact Cell Count (ICC)
Time to result 3-7 Days 20 Minutes (30 Minutes measurement interval)
LOD 1 Colony 1 ICC
Range 1-300 colonies per sample

1-1 000 000 ICC per sample

Identification

Colonies
Limited morphological determination

Individual Cells
Dot-plot / fingerprint of a population
Interpretation of the results according to different events (trend monitoring)
Enumeration Visual counting by humans Automatic
Sample size 100 or 200ml 90µl

How can the AQU@Sense MB differentiate intact and damaged/dead cells in one sample?

The AQU@Sense MB employs two specific staining agents: SYBR Green I and Propidium Iodide. SYBR Green I penetrates intact cell membranes and selectively binds to the cell’s DNA. In contrast, Propidium Iodide cannot penetrate intact membranes and binds exclusively to the DNA of compromised cells.

To determine whether only SYBR Green I or both SYBR Green I and Propidium Iodide are bound to a cell, the cells are passed through a very thin capillary and illuminated with a laser, stray light and fluorescence light from is generated and analyzed with a specific detection system. As SYBR Green I and Propidium Iodide emit fluorescence at distinct wavelengths, the system can differentiate between intact or damaged cells.

Which advantages has AQU@Sense MB compared to other RMMs?

  • Primary-validated technology by independent scientists, ensuring high credibility and reliability
  • Clear and unambiguous results, with differentiation between intact and damaged cells/debris
  • Reproducible results
  • High autonomy with a user-friendly plug-and-play setup, minimizing manual intervention
  • Robust/industrial design
  • No direct user contact with chemicals or waste
  • Minimal maintenance requirements
  • Advanced detection capabilities, identifying individual cells, even within conglomerates or biofilm fragments, enabling comprehensive trend monitoring.

What is the correlation between the two measuring units CFU and ICC?

Intact Cell Counts (ICC) and Colony Forming Units (CFU) do not exhibit a direct correlation. Primarily due to the presence of Viable but Non-Culturable Cells (VBNC), which are not detected on HPC but easily detected in flow cytometer. Secondly, due to difference in time and environmental factors between two methods. Flow cytometry provides an instantaneous snapshot of cell presence. Therefore, cells that may not thrive under HPC conditions might still be detected by flow cytometry.

Consequently, when the AQU@Sense MB is employed as a tool in Quality Control (QC), a performance qualification (PQ) is necessary at the customer's site to establish parameters, including baseline, warning, and action levels.

What are Viable But Non-Culturable (VBNC) organisms? Are they of big importance for patients’ safety?

For microorganisms, entering the VBNC (viable but non-culturable) stage is a survival strategy in response to stress conditions like unfavorable environments, nutrient depletion, and temperature fluctuations, which are main features of PW/WFI water systems.
These VBNC bacteria remain alive and metabolically active but are unable to grow in standard laboratory conditions. Recent studies have shown that the VBNC state is reversible, meaning these microorganisms can return to a multiplying state, posing a potential bioburden, and in turn, health risk. Flow cytometry helps detect VBNC microorganisms in pharmaceutical water because it uses non-growth-based methods.

Is it possible to identify the strain with AQU@Sense MB?

No, the AQU@Sense MB does not identify the strain. However, since flow cytometry is applied, a fingerprint of the distribution of the cells is given which can give more information about the state of the microbial population.

How to use AQU@Sense MB in daily monitoring?

There are two possible fields of application for daily routine analysis. In-Process Control (IPC) and Quality Control (QC).
For IPC it can be can be integrated into the water system as an online control system for monitoring bioburden. When operating at its maximum capacity, the AQU@Sense MB can perform batchwise continuously up to 48 measurements per day (minimum measurement interval: 30 minutes). The measurement interval is adjustable according to the needs and standard operation of water system. The benefits of frequent measurements are noticeable - for rapid detection of even minor changes, in contrast to the conventional plate count method. This system can be utilized not only to continuously monitor bioburden levels in the plant but also e.g., to release the water system after sanitation or maintenance for technical water release.

Is it possible to make QC releases with the AQU@Sense MB?

Yes, it is possible to perform a QC release using the AQU@Sense MB. However, to incorporate it into current QC release process, customers must conduct a performance qualification (PQ) to confirm its suitability for the intended purpose. According to regulatory guidelines, the AQU@Sense MB or any other Rapid Microbiological Method (RMM) can be validated as a QC release method. Since the AQU@Sense MB is already primary validated the performance qualification procedure is much simpler.

An equivalence testing must be conducted using appropriate parameters, followed by statistical analysis, since it indicates a new measuring unit (Intact Cell Counts, ICC) instead of Colony Forming Units (CFU). The results of the testing must demonstrate that the results of the AQU@Sense MB allow for an unequivocal decision regarding compliance with the standards outlined in the monographs, even when compared to the conventional HPC.

Is AQU@Sense MB acknowledged by the authorities (EMA, USP, FDA etc.)?

The AQU@Sense MB, along with other RMM devices (Status November 2023), is not specifically authorized by name by any regulatory body. However, it can be validated and qualified as a QC release method, since the EU GMP Annex I strongly recommend to incorporate RMM’s.

At BWT, we are working on obtaining authorization for the applied method (flow cytometry).

Load more

Seam­less Inte­gra­tion

Mechanical Integration:

Single Sampling Point
Multi Point with up to 4 Sampling points

The AQU@Sense MB can be combined with a valve system that can connect up to four sampling points to one AQU@Sense MB. The control of the measurement sequence is done by the control unit of the water system.

Measurement Modes:

  • Manual: The measurement can be started manually with a minimum sampling interval of 30 minutes
  • Automatic: An automatic measurement interval between 30 minutes and 6 hours can be programmed in the AQU@Sense MB
  • Remote controlled: The measurement can be triggered via digital input signals with a minimum sampling interval of 30 minutes.

Data transfer:

  • 4 to 20 mA
  • Modbus

Tech­nical Details

Tech­nical Details
Product Id P06170006
Dimen­sions (W x D x H): 350x270x373mm
Weight: 14 kg
Degree of Protec­tion: IP65
Oper­ating Envi­ron­ment: Indoor, +5°C - +35°C, 10% - 90% RH
Measure­ment Prin­ciple: Flow Cytom­etry with DNA specific staining
Side Scatter and 2 Fluo­res­cence Signals
Sample Volume: 90 µl
Sampling: Online, offline single measure­ment or offline with sample manager for up to 30 samples
Analysis Time: 30 minutes (Time to result ~20 minutes)
Measuring interval:
min 30 minutes (manual, auto­matic or trig­gered with digital input)
Sani­ti­z­able:
Ozone up to 100 ppb / hot water up to 85 °C
Power Supply: 18 VDC, 1.4A, 20W
Commu­ni­ca­tion Output: 2x4 ... 20mA analog outputs (freely config­urable)
4 digital outputs
Modbus
TCP/IP
Commu­ni­ca­tion Input: 3 digital inputs (start-​, stop-, abort measure­ment)
Data storage: Memory card 32GB
Data Export: USB 2.0, Ethernet
Elec­tronic Docu­men­ta­tion: 21 CFR Part 11 compliant elec­tronic docu­men­ta­tion
Audit Trail
Logbook
User manage­ment with 4 user levels
Compli­ance and Certi­fi­ca­tion: CE Certi­fi­ca­tion, Factory Vali­da­tion Certifi­cate

Stan­dard scope of delivery Item  Article No. P06170006
  AQU@Sense MB
Cartridge
Online Sampling Device
Manual Sampling Device
Power Supply / Cable

What are the differences between Heterotrophic Plate Count (HPC) and AQU@Sense MB?

  Heterotrophic Plate Count AQU@Sense MB
Technology Growth based, dependent on culture medium Fluorescence analysis after DNA-specific staining
Sampling Manual Automatic
Measuring unit Colony Forming Unit (CFU) Intact Cell Count (ICC)
Time to result 3-7 Days 20 Minutes (30 Minutes measurement interval)
LOD 1 Colony 1 ICC
Range 1-300 colonies per sample

1-1 000 000 ICC per sample

Identification

Colonies
Limited morphological determination

Individual Cells
Dot-plot / fingerprint of a population
Interpretation of the results according to different events (trend monitoring)
Enumeration Visual counting by humans Automatic
Sample size 100 or 200ml 90µl

How can the AQU@Sense MB differentiate intact and damaged/dead cells in one sample?

The AQU@Sense MB employs two specific staining agents: SYBR Green I and Propidium Iodide. SYBR Green I penetrates intact cell membranes and selectively binds to the cell’s DNA. In contrast, Propidium Iodide cannot penetrate intact membranes and binds exclusively to the DNA of compromised cells.

To determine whether only SYBR Green I or both SYBR Green I and Propidium Iodide are bound to a cell, the cells are passed through a very thin capillary and illuminated with a laser, stray light and fluorescence light from is generated and analyzed with a specific detection system. As SYBR Green I and Propidium Iodide emit fluorescence at distinct wavelengths, the system can differentiate between intact or damaged cells.

Which advantages has AQU@Sense MB compared to other RMMs?

  • Primary-validated technology by independent scientists, ensuring high credibility and reliability
  • Clear and unambiguous results, with differentiation between intact and damaged cells/debris
  • Reproducible results
  • High autonomy with a user-friendly plug-and-play setup, minimizing manual intervention
  • Robust/industrial design
  • No direct user contact with chemicals or waste
  • Minimal maintenance requirements
  • Advanced detection capabilities, identifying individual cells, even within conglomerates or biofilm fragments, enabling comprehensive trend monitoring.

What is the correlation between the two measuring units CFU and ICC?

Intact Cell Counts (ICC) and Colony Forming Units (CFU) do not exhibit a direct correlation. Primarily due to the presence of Viable but Non-Culturable Cells (VBNC), which are not detected on HPC but easily detected in flow cytometer. Secondly, due to difference in time and environmental factors between two methods. Flow cytometry provides an instantaneous snapshot of cell presence. Therefore, cells that may not thrive under HPC conditions might still be detected by flow cytometry.

Consequently, when the AQU@Sense MB is employed as a tool in Quality Control (QC), a performance qualification (PQ) is necessary at the customer's site to establish parameters, including baseline, warning, and action levels.

What are Viable But Non-Culturable (VBNC) organisms? Are they of big importance for patients’ safety?

For microorganisms, entering the VBNC (viable but non-culturable) stage is a survival strategy in response to stress conditions like unfavorable environments, nutrient depletion, and temperature fluctuations, which are main features of PW/WFI water systems.
These VBNC bacteria remain alive and metabolically active but are unable to grow in standard laboratory conditions. Recent studies have shown that the VBNC state is reversible, meaning these microorganisms can return to a multiplying state, posing a potential bioburden, and in turn, health risk. Flow cytometry helps detect VBNC microorganisms in pharmaceutical water because it uses non-growth-based methods.

Is it possible to identify the strain with AQU@Sense MB?

No, the AQU@Sense MB does not identify the strain. However, since flow cytometry is applied, a fingerprint of the distribution of the cells is given which can give more information about the state of the microbial population.

How to use AQU@Sense MB in daily monitoring?

There are two possible fields of application for daily routine analysis. In-Process Control (IPC) and Quality Control (QC).
For IPC it can be can be integrated into the water system as an online control system for monitoring bioburden. When operating at its maximum capacity, the AQU@Sense MB can perform batchwise continuously up to 48 measurements per day (minimum measurement interval: 30 minutes). The measurement interval is adjustable according to the needs and standard operation of water system. The benefits of frequent measurements are noticeable - for rapid detection of even minor changes, in contrast to the conventional plate count method. This system can be utilized not only to continuously monitor bioburden levels in the plant but also e.g., to release the water system after sanitation or maintenance for technical water release.

Is it possible to make QC releases with the AQU@Sense MB?

Yes, it is possible to perform a QC release using the AQU@Sense MB. However, to incorporate it into current QC release process, customers must conduct a performance qualification (PQ) to confirm its suitability for the intended purpose. According to regulatory guidelines, the AQU@Sense MB or any other Rapid Microbiological Method (RMM) can be validated as a QC release method. Since the AQU@Sense MB is already primary validated the performance qualification procedure is much simpler.

An equivalence testing must be conducted using appropriate parameters, followed by statistical analysis, since it indicates a new measuring unit (Intact Cell Counts, ICC) instead of Colony Forming Units (CFU). The results of the testing must demonstrate that the results of the AQU@Sense MB allow for an unequivocal decision regarding compliance with the standards outlined in the monographs, even when compared to the conventional HPC.

Is AQU@Sense MB acknowledged by the authorities (EMA, USP, FDA etc.)?

The AQU@Sense MB, along with other RMM devices (Status November 2023), is not specifically authorized by name by any regulatory body. However, it can be validated and qualified as a QC release method, since the EU GMP Annex I strongly recommend to incorporate RMM’s.

At BWT, we are working on obtaining authorization for the applied method (flow cytometry).

Load more
AquaSense MB

AQU@Sense MB