Masterflex Quattroflow Peristaltic Pump System with 74000-35 Drive Unit
| Brand | Masterflex |
|---|---|
| Origin | USA |
| Model | 74000-35 |
| Drive Type | Brushless DC Motor Drive |
| Enclosure | ABS Plastic (IP33) |
| Max Speed | 3000 rpm |
| Speed Accuracy | ±0.1% |
| Max Pressure | 58 PSI (4 bar) |
| Flow Control Mode | Volume-based or Time-based Dispensing |
| Display | Graphical LCD showing RPM, Flow Rate, Dispensed Volume, Total Volume, Interval Time, Repeat Count |
| Input Voltage | 90–260 VAC |
| Pump Head Compatibility | QF150SU (disposable), QF1200SU (disposable), QF150 (reusable), QF1200 (reusable) |
| Fluid Path | Single-use, gamma-irradiated, double-bagged polypropylene wetted housing |
| Compliance | Designed for cGMP, GLP, and FDA 21 CFR Part 11–ready environments (when paired with audit-trail-enabled software) |
Overview
The Masterflex Quattroflow Peristaltic Pump System (Model 74000-35) is an engineered solution for precise, low-shear, sterile fluid transfer in biopharmaceutical manufacturing, clinical diagnostics, and advanced R&D laboratories. Unlike conventional peristaltic pumps that rely on rollers compressing tubing, the Quattroflow platform employs a patented four-chamber diaphragm displacement mechanism driven by an eccentric shaft. This design eliminates pulsation artifacts and minimizes shear stress—critical when handling shear-sensitive biologics such as monoclonal antibodies, viral vectors, vaccines, plasma-derived therapeutics, and cell culture media. The system operates without mechanical seals, rotating shafts, or dynamic gaskets in contact with the process fluid; only the disposable pump head’s polypropylene wetted path interfaces with the medium. This architecture ensures intrinsic sterility assurance, eliminates cleaning validation burdens, and supports rapid changeover between batches or product campaigns.
Key Features
- Four-chamber diaphragm pumping principle delivering <0.5% pulsation amplitude—significantly lower than roller-based peristaltic systems
- Brushless DC drive unit (74000-35) with ±0.1% speed accuracy across full 0–3000 rpm range, enabling reproducible volumetric delivery
- Graphical LCD interface displaying real-time operational parameters: motor RPM, calculated flow rate, dispense volume per cycle, cumulative total volume, programmable interval time, and repeat count
- Volume- or time-triggered dispensing modes with user-defined inter-cycle delay, supporting automated batch processing and multi-step protocols
- Two enclosure options: ABS plastic (IP33) for standard benchtop use; stainless steel (IP66/NEMA 4X) for washdown environments requiring frequent sanitization
- Pre-sterilized, double-bagged disposable pump heads (QF150SU, QF1200SU) constructed entirely from USP Class VI-certified polypropylene—no cleaning, no autoclaving, no extractables risk
- Dry-run tolerant operation with self-priming capability up to 5 m suction lift and sustained pressure output of 4 bar (58 PSI)
Sample Compatibility & Compliance
The Quattroflow system is validated for use with biological fluids exhibiting viscosities up to 5000 cP and particulate loads typical of clarified harvests or formulated drug products. Its single-use pump heads eliminate cross-contamination risks between batches and support closed-system processing under ISO 5 (Class 100) conditions. The polypropylene fluid path complies with USP and cytotoxicity and systemic injection testing requirements. When integrated into larger automation platforms, the drive unit supports digital I/O and analog 0–10 V control signals—enabling synchronization with SCADA, MES, or LIMS systems. While the drive itself does not embed electronic audit trails, its deterministic control logic and parameter logging capability align with FDA 21 CFR Part 11 expectations when deployed alongside compliant data acquisition software and procedural controls.
Software & Data Management
The 74000-35 drive operates as a standalone instrument with embedded firmware controlling all motion and timing functions. No proprietary PC software is required for basic operation; however, optional RS-232 or USB connectivity allows integration with third-party laboratory automation suites. All displayed parameters—including total dispensed volume and cycle timestamps—are retained in non-volatile memory during power loss. For regulated environments, users may configure external data loggers to capture serial output streams containing RPM, elapsed time, and volume counters at configurable intervals (e.g., every 100 ms). This facilitates retrospective analysis, deviation investigation, and electronic batch record generation consistent with ALCOA+ principles.
Applications
- Buffer and media preparation in upstream and downstream bioprocessing
- Fill-finish operations for clinical trial materials using disposable fluid paths
- Automated sampling in continuous bioreactors and perfusion systems
- Low-shear transfer of fragile cell suspensions during cryopreservation or formulation
- Calibration fluid delivery in analytical instrumentation requiring pulse-free flow
- QC/QA lab workflows involving precise reagent addition, dilution series generation, or fraction collection
FAQ
What distinguishes Quattroflow from traditional peristaltic pumps?
Quattroflow replaces roller compression with synchronized diaphragm displacement—eliminating tube fatigue, particle generation, and high-shear zones inherent in tubing-based designs.
Can the same drive unit operate both disposable and reusable pump heads?
Yes—the 74000-35 drive is mechanically and electrically compatible with all QF-series pump heads, including QF150SU (disposable), QF1200SU (disposable), QF150 (reusable), and QF1200 (reusable).
Is the pump suitable for sterile filtration integration?
Absolutely—the disposable pump heads maintain integrity up to 4 bar and are rated for inline sterilizing-grade filter compatibility (0.22 µm PES or PVDF membranes).
How is calibration performed and maintained?
Speed calibration is factory-set and traceable to NIST standards; volumetric calibration requires user-specific gravimetric or timed-collection verification using actual process fluid and tubing.
Does the system meet IP ratings for cleanroom or industrial washdown use?
The stainless steel variant (74000-37) carries IP66 and NEMA 4X certification, making it suitable for high-humidity or frequent-spray environments typical of CIP/SIP stations.





