Fast MDx is the first fully automated, high-throughput, near-patient testing system. It can detect many pathogens with unrivalled speed without the need for expensive biosecure laboratories. Developed by London-based social enterprise company Fast MDx, the eponymous testing system cuts the typical 24 to 48 hour waiting time to just one to two hours.

"The Fast MDx test platform is mobile and can be used anywhere,” explains Richard Lewis, founder and CEO of Fast MDx. “Only one technician is required to operate it, rather than the five normally needed in a central laboratory to process up to 1,000 patient samples in an 8-hour shift."

Thanks mainly to economies of scale, Fast MDx is the first system in the world to make molecular testing and diagnostics accessible everywhere, not just in more affluent countries. It will be launched in June 2023 with a multiplexed, CE-IVDr-approved test for the most common respiratory pathogens: influenza A, influenza B, RSV A, RSV B and Covid-19. The company will be expanding the range of tests in 2023/24 to include tests for infections such as C-Diff and MRSA, as well as for sepsis, which kills about 11 million people worldwide every year. It is also the perfect system for conducting genomic testing, which informs doctors what screening tests to request based on their patients' own DNA, in order to detect hereditary diseases at an early stage.

Automation reduces errors

The Fast MDx platform relies on automation technology from Festo for pipetting and dispensing. Included in the system are Festo handling gantries with electric axes, heat sealing from Kbiosystems and Fast MDx’s patented, ultra-fast qPCR thermal cycler, the NGX2.

During sample preparation, Festo’s EXCM planar surface gantry operates in the X and Y planes. The 92 patient samples are scanned using Festo's optical sensors to track and confirm that all the samples are present. The automated pipetting system, consisting of the Festo DHOE pipetting head and the DHAO disposable syringe ejector, is mounted on the planar surface gantry in the Z direction. The pipetting head can accurately dispense volumes in the range of 10 µl and the pipetting speed can be adjusted to dispense up to 10 ml/s.

The master mix is prepared, placed in the microtiter plate and then the samples are added. The disposable tip pierces the Fast MDx’s Pathtube® cap, and aspirates and pipettes each patient sample into the master mix in one of the microtiter plate wells. Piercing the Pathtube® cap saves a lot of time and money, as no conventional opening and closing systems are needed, and eliminates the human handling errors that so often occur when manually pipetting hundreds of samples into tubes.

A separate Festo handling system uses an EHPS-16 electric gripper to pick up the filled microtiter plate and place it in the heat sealer. The sealed plate is then placed in the RT block, which triggers the conversion of the RNA, if present, into complementary DNA (cDNA). Finally, the plate is placed in the NGX2 qPCR thermal cycler, where the PCR reaction takes place and the cDNA is amplified. The NGX2 uses an ultrafast fluorescence detection system to determine whether the cDNA sequence of the pathogen of interest is present in any of the patient samples. The Biosero software used on the platform integrates and controls all the modules and makes operating it very easy.

To avoid having to use an external pneumatic supply, the Fast MDx test platform uses Festo's PGVA pressure and vacuum generator, which produces a pressure or vacuum of +/-0.5 bar using a 24-volt power supply. The PGVA integrates a mini compressor, air filter unit, reservoir and electronic pressure and vacuum control in a very small space, providing a totally self-contained solution for liquid handling in laboratory automation.

Special machine manufacturer, Applied Automation, is responsible for assembling the complete test system including safety, risk analysis and CE marking.

"Thanks to the close cooperation between Fast MDx and Festo, we were able to build the first prototypes quickly and efficiently, despite the extremely high degree of complexity," says Richard Lewis. "We were able to combine Fast MDx's extensive expertise in qPCR thermal cycling with Festo's proven 3D gantries, controllers and pipetting systems." Tamara Seivwright-Blake, Project Engineer at Festo GB says ‘I’ve enjoyed working on such a socially conscious project bringing together and coordinating the different parties involved and continuously developing and refining the platform”.

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Fast MDx’s flagship NGX 124 platform receives European Union CE-IVDr mark

Fast MDx, the developers of the world’s first low-cost, high-throughput molecular diagnostic test system, have announced CE-IVDr marking for its flagship NGX 124 platform, following the signing of a Declaration of Conformity to the IVD Regulation 2017/746.

CE-IVDr marking represents the latest milestone in the on-going development of NGX 124 and paves the way for an official launch.

Jointly designed and developed by Fast MDx and Festo, the Fast MDx platform is the first fully automated, high-throughput, mobile Molecular Diagnostic (MDx) test platform and incorporates Fast MDx’s latest, ultra-fast, “NGx2” 4-Channel qPCR thermal cycler and Reverse Transcription “RT” block technology.

Richard Lewis, Fast MDx Founder and CEO said: "Applying the CE-IVDr mark for the NGX 124 platform is a significant milestone in our work to develop the world’s first low cost, high throughput molecular diagnostic test system. As a social enterprise, we pride ourselves on our aim to bring sustainable, molecular diagnostic testing to billions worldwide, regardless of geographic location. Providing clinicians quickly with accurate test results will enable them to treat their patients faster and more appropriately than ever before, resulting in better patient outcomes and a large reduction in the use and expense of critical care facilities.”

Ana Fernandez, Fast MDx Chief Scientific Officer said: Fast MDx offers the opportunity for laboratories accredited to ISO 15189 to automate testing of their Laboratory Developed Tests (LDT), Research Use Only (RUO) assays and any existing CE-IVDd approved assays that they use. The European Commission’s CE-IVDr mark embodies Fast MDx’s commitment to technical excellence and demonstrates that the NGX 124 is performing as expected and will rapidly provide accurate diagnostic results, electronically to clinicians.”