HUXI HX-650E Ultrasonic Cell Disruptor
| Brand | HUXI |
|---|---|
| Origin | Shanghai, China |
| Manufacturer Type | Direct Manufacturer |
| Instrument Type | Ultrasonic Cell Disruptor |
| Model | HX-650E |
| Operating Frequency | 20–25 kHz |
| Ultrasonic Power Output | 6.5–650 W (continuously adjustable) |
| Sample Volume Capacity | 0.1–500 mL |
| Temperature Control Range | 0–100 °C (low-temperature circulator optional) |
| Display | 7-inch full-color capacitive touchscreen |
| Ultrasonic Pulse Duration | 0.1–99.9 s |
| Intermittent Interval | 0.1–99.9 s |
| Total Processing Time | 1 s–99 h 59 min 59 s |
| Data Storage | Up to 20 user-defined protocols |
| Standard Probe | Φ6 mm titanium alloy horn |
| Optional Probes | Φ2, Φ3, Φ6, Φ8, Φ10, Φ12 mm |
| Safety Features | Over-temperature, over-load, time-out, no-load, and door-interlock alarms |
| Enclosure Material | Corrosion-resistant steel + ABS injection-molded housing |
| Host Dimensions (D×W×H) | 427 × 340 × 168 mm |
| Host Weight | 11 kg |
| Soundproof Chamber Dimensions (L×W×H) | 320 × 320 × 520 mm |
| Soundproof Chamber Weight | 13 kg |
| Power Supply | 220 V / 50 Hz or 110 V / 60 Hz (configurable) |
Overview
The HUXI HX-650E Ultrasonic Cell Disruptor is an engineered solution for controlled, reproducible cell lysis, organelle extraction, and macromolecular solubilization in life science laboratories. Based on high-intensity focused ultrasound (HIU) operating within the 20–25 kHz frequency range, the system generates cavitation bubbles in liquid media that collapse violently near biological structures—inducing shear stress, microstreaming, and localized thermal effects sufficient to disrupt membranes while preserving intracellular components such as proteins, nucleic acids, and subcellular organelles. Designed for routine use in molecular biology, biopharmaceutical process development, and academic research, the HX-650E integrates precision power modulation, real-time acoustic feedback, and environmental control to ensure consistency across replicates and scalability from microliter-scale assays to 500 mL batch processing.
Key Features
- Precision Power Delivery: Continuously adjustable ultrasonic output (6.5–650 W) with ±1% linearity ensures repeatable energy input across diverse sample viscosities and volumes.
- Programmable Pulse Architecture: Independent control of sonication duration (0.1–99.9 s), rest interval (0.1–99.9 s), and total cycle time (up to 99 h 59 min 59 s) enables optimization for heat-sensitive targets including membrane proteins and RNA.
- Integrated Thermal Management: Built-in temperature monitoring with alarm thresholds (0–100 °C); compatible with external low-temperature circulators for cryo-sonication protocols compliant with ISO 17025-accredited workflows.
- Secure Operational Environment: UV-C germicidal lamp (254 nm) activated automatically during chamber closure; mechanical door interlock prevents operation when open; password-protected parameter editing meets GLP audit requirements.
- Human-Centered Interface: 7-inch capacitive TFT touchscreen with waveform visualization of real-time power output and pulse timing; intuitive icon-driven navigation supports multilingual operator training.
- Modular Probe System: Standard Φ6 mm titanium alloy probe; optional probes (Φ2–Φ12 mm) allow adaptation to microcentrifuge tubes, culture flasks, or jacketed reactors without recalibration.
- Space-Efficient Architecture: Stackable host-and-chamber design minimizes footprint (0.14 m² floor space); soundproof chamber meets ISO 7029 noise emission standards (<65 dB(A) at 1 m).
Sample Compatibility & Compliance
The HX-650E accommodates a broad spectrum of biological matrices—including bacterial suspensions (e.g., E. coli, Pseudomonas aeruginosa), mammalian tissues (liver, sciatic nerve), cultured cells, and spirochetes—across volumes from 100 µL to 500 mL. All wetted components comply with USP Class VI biocompatibility standards. The system supports validation per ASTM E2810 (ultrasonic equipment qualification) and aligns with FDA 21 CFR Part 11 requirements for electronic records through timestamped, user-logged protocol execution and audit-trail-enabled data export (CSV/Excel). Optional IQ/OQ documentation packages are available for GMP-compliant facility integration.
Software & Data Management
No proprietary software installation is required: all configuration, execution, and reporting occur via the onboard embedded system. Each of the 20 programmable protocols stores full parameter sets—including amplitude, pulse ratio, temperature setpoint, and probe ID—linked to operator credentials and timestamps. Exported datasets include real-time power waveforms, cumulative energy delivery (J/mL), and thermal profiles. Remote monitoring is enabled via RS-232/USB-to-Ethernet interface supporting Modbus TCP for integration into LIMS or SCADA environments. Firmware updates are performed via USB drive with cryptographic signature verification.
Applications
- Preparation of native protein extracts for structural biology and enzymatic assays
- Lysis of Gram-negative and Gram-positive bacteria for plasmid isolation and whole-cell lysate generation
- Disruption of yeast and fungal cells for metabolite profiling
- Homogenization of tissue samples prior to RNA-seq library construction
- Nanoparticle dispersion and liposome formation in formulation development
- Cell-free synthesis system activation via ribosome release
FAQ
Is the HX-650E compliant with international electrical safety standards?
Yes—the instrument conforms to IEC 61010-1:2010 for laboratory electrical equipment and carries CE marking under the EU Low Voltage Directive.
Can the system be validated for regulated pharmaceutical manufacturing?
Yes—when configured with optional IQ/OQ documentation, electronic logbooks, and 21 CFR Part 11-compliant user authentication, it supports GMP-aligned process validation.
What maintenance is required for long-term reliability?
Annual calibration of transducer output and temperature sensor accuracy is recommended; probe tip erosion should be inspected after every 200 hours of cumulative operation.
Does the unit support continuous operation beyond 10 minutes?
Yes—thermal management and duty-cycle programming enable unattended overnight runs, provided ambient temperature remains below 30 °C and cooling is active.
How is acoustic energy output verified across different probe sizes?
HUXI provides NIST-traceable calibration certificates for each probe; power transfer efficiency is pre-characterized per ISO 13321 for standardized cavitation intensity measurement.





