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BIOCOOL FastDry-3 Vacuum Centrifugal Concentrator

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Brand BIOCOOL
Origin Tianjin, China
Model FastDry-3
Instrument Type Vacuum Centrifugal Concentrator
Temperature Range 4°C to 80°C
Temperature Control Gradient PID Control
Sample Capacity 132 × 1.5 mL tubes
Vacuum Pump Direct-coupled rotary vane pump
Display Touchscreen interface
Control Mode Multi-stage programmable (12 segments)
Rotor Recognition Auto-identification for up to 50 rotor types
Chamber & Rotor Coating PTFE (Teflon®)-coated
Cold Trap Compatibility Optional ultra-low temperature condenser (< −110°C)
Safety Features Vacuum interlock (vacuum applied only after target speed reached), automatic venting, overload/overheat protection
Compliance Designed for GLP/GMP environments

Overview

The BIOCOOL FastDry-3 Vacuum Centrifugal Concentrator is an engineered solution for high-efficiency, low-temperature sample concentration and solvent removal in molecular biology, proteomics, metabolomics, and pharmaceutical development laboratories. It integrates centrifugal force, controlled vacuum, and precise thermal management to accelerate solvent evaporation while preserving thermolabile analytes—including nucleic acids, proteins, antibodies, enzymes, and viral particles. Unlike conventional evaporators or simple vacuum desiccators, the FastDry-3 operates on the principle of simultaneous rotational acceleration (up to 1800 rpm), dynamic vacuum regulation (down to <10 Pa), and gradient temperature control (4–80°C), enabling reproducible mass transfer kinetics across diverse solvents—ranging from aqueous buffers to volatile organic compounds (e.g., ethanol, acetonitrile, chloroform). Its sealed, PTFE-coated rotor chamber minimizes surface adsorption and corrosion, ensuring compatibility with acidic, alkaline, and halogenated solvents. The system’s modular architecture—comprising independent concentrator, vacuum pump, and optional cryogenic cold trap—supports flexible configuration for both routine QC workflows and method-development studies.

Key Features

  • 12-segment touchscreen programming with independent setpoints for rotational speed (400–1800 rpm, infinitely variable), chamber temperature (4–80°C), vacuum level, and dwell time per stage
  • PTFE-coated centrifuge chamber and rotor—resistant to chemical degradation and validated for autoclave sterilization (121°C, 20 min) per ISO 17665-1
  • Magnetic drive coupling ensures hermetic vacuum integrity without mechanical shaft seals, eliminating lubricant contamination and enhancing long-term reliability
  • Intelligent vacuum sequencing: vacuum application is gated until target rotational speed is achieved—preventing ice crystal formation in frozen samples and reducing foaming in viscous lysates
  • Auto-identifying rotor system supporting over 50 distinct rotor geometries—including PCR strip rotors, microplate carriers, and deep-well formats—for seamless method transfer across sample types
  • Integrated active cooling protection mode (−4°C to +4°C) optimized for labile biomolecules, minimizing thermal denaturation during prolonged concentration cycles
  • Real-time remote monitoring via encrypted mobile application (iOS/Android), with push notifications for cycle completion, fault alerts, and parameter deviation

Sample Compatibility & Compliance

The FastDry-3 accommodates standard 1.5 mL microcentrifuge tubes (132 positions), with full compatibility for low-retention, DNase/RNase-free, and certified sterile consumables. Its PTFE-coated surfaces meet USP Class VI biocompatibility requirements and resist etching by TFA, formic acid, and DMSO. For regulated environments, the system supports audit-ready operation: all program executions are timestamped and logged with user ID, parameter history, and event flags (e.g., vacuum breach, temperature excursion). Data export complies with FDA 21 CFR Part 11 when paired with BIOCOOL’s optional LIMS-integrated software package. The unit’s construction adheres to IEC 61010-1 safety standards for laboratory electrical equipment, and its chamber design permits validation per ASTM E2500 for equipment qualification (DQ/IQ/OQ/PQ).

Software & Data Management

Control firmware is built on a deterministic PLC platform with industrial-grade touchscreen HMI (10.1″ capacitive display). All protocols—including multi-stage ramp-and-hold profiles—are stored locally with version control and user-access permissions (admin/operator/guest tiers). Raw operational logs (speed, temp, vacuum, time) are exportable as CSV or PDF reports. Optional BioLink™ Software enables centralized fleet management, electronic signature capture, and integration with ELN systems via RESTful API. Audit trails record all parameter modifications, login/logout events, and emergency stops—fully traceable for GLP audits. Firmware updates are delivered via secure HTTPS and require cryptographic signature verification prior to installation.

Applications

  • Concentration of dilute DNA/RNA extracts post-column purification or enzymatic digestion
  • Removal of volatile organic solvents (e.g., ethyl acetate, hexane) from lipidomics or small-molecule extractions
  • Lyophilization pre-concentration of monoclonal antibody formulations prior to freeze-drying
  • High-throughput sample preparation for LC-MS/MS—reducing matrix effects through solvent exchange and volume normalization
  • Stabilization of heat-sensitive vaccine antigens and viral vectors under controlled sub-zero thermal gradients
  • Preparative-scale peptide synthesis workup, including TFA cleavage mixture cleanup

FAQ

What vacuum level can the FastDry-3 achieve?
The system reaches a base pressure of ≤10 Pa when paired with the included direct-coupled rotary vane pump. With optional ultra-low temperature cold trap (<−110°C), residual solvent vapor pressure is further suppressed, improving capture efficiency for low-boiling-point organics.
Is the rotor chamber suitable for sterilization?
Yes—the PTFE-coated chamber and aluminum rotor are rated for steam sterilization at 121°C for 20 minutes, complying with ISO 17665-1 for reusable labware.
Can I run unattended overnight protocols?
Absolutely. The system includes hardware-based safety interlocks (overtemperature, overspeed, vacuum loss) and auto-venting upon cycle completion. Remote status monitoring and email/SMS alerts ensure operational awareness without physical presence.
Does it support compliance with FDA 21 CFR Part 11?
When configured with BioLink™ Software and enabled electronic signatures, full Part 11 compliance—including audit trail generation, role-based access, and data integrity controls—is achievable.
What cold trap options are available for aggressive solvents?
Two configurations are offered: a standard −50°C/−80°C dual-stage cold trap for general use, and an optional ultra-low temperature condenser (<−110°C) with stainless-steel coil and acid-resistant coating—validated for HCl, HF, and trifluoroacetic acid vapors.

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