PathogenDx Expands Reach of Its Patented Multiplexed Molecular Testing Technology, Bringing It to the Clinical, Food and Agriculture Sectors

PathogenDx (“PathogenDx” or “Company”), a leader in next-generation microarray technology for better health and safety, announced it has expanded the reach of its patented multiplexed molecular testing technology – Dynamic Dimensional Detection (“D3 Array™”) – beyond the cannabis and hemp sectors. The Company is bringing its D3 Array™, which addresses the challenges microarray technology has suffered in prior generations as well as the gap that qPCR and next-generation sequencing (“NGS”) has created in multiplexing, performance, throughput and cost, to the clinical, food and agriculture sectors.

The Company’s proprietary D3 Array™ features a flexible, open, lattice-like architecture that is rich with highly accessible target-probe binding sites. The benefit of this is the ability of amplicon targets to: move easily through the 3D structure; locate target:probe binding sites; and bind more easily with significantly reduced steric hindrance. Consequently, the duplex pairing hybridization reaction is rapid at room temperature and delivers high sensitivity and specificity results to labs and their clients.

“Today, even with two well-established diagnostic technologies, there are instances where sensitivity and multiplexing limitations of the well-adopted qPCR are insufficient and the costs, turn-around time and heavy lifting needed for bioinformatics of NGS are problematic in the clinical, food and agricultural sectors,” said PathogenDx Co-founder and CEO Milan Patel. “For example, in the traditional array, a probe monolayer is printed directly onto a surface, and typically the probe is much smaller than the amplicon itself, which provides limited binding access to the much longer amplicon target. This essentially reduces target binding affinity due to surface crowding. In contrast, our D3 Array™ features a 3D cross-linked lattice structure with surface-bound oligonucleotide probes accessible throughout the 3D structure, thus increasing access and allowing for a faster, higher affinity target amplicon binding reaction.”

Patel added, “The D3 Array™ has emerged as our core of the technology platform, and the tests built upon it are in commercial deployment in more than 100 regulated laboratories. Additionally, our D3 Array™ is a more flexible, higher throughput and cost-effective approach than a series of multiplex qPRC/PCR assays. It also delivers a much faster and more affordable alternative to NGS, delivering high specificity, but without the complex sample prep, data analysis and reporting encumbered with NGS.”

Lux Diagnostics CEO and Founder Dr. Jonathan Goss said, “PathogenDx D3 Array™ provides the best-of-both-worlds alternative. It holds promise in clinical diagnostics, where accelerating medical diagnosis and saving money are high priorities. We have been able to run PathogenDx’s Detectx-Cv kit for COVID variant testing for more than a year, and at some points the platform was able to process 1,200 samples a day in variant identification. The D3 Array™ allowed us to get single gene mutation level identification on positive COVID samples in a single day, whereas NGS would have taken weeks. This is the promise that PathogenDx technology holds in terms of addressing other clinical diagnostics areas where there is a large unmet need in throughput, cost, accuracy and time to yield results.”

PathogenDx’s D3 Array™ is readily adaptable to high throughput 96-well plate processing from sample to answer. Using standard lab equipment and basic PCR lab-tech proficiency, the D3 Array™ features include:

  • 3D cross-linked, flexible architecture

  • Increased access to target: probe binding sites

  • Solution-like target:probe binding interaction

  • Room temperature hybridization

  • High affinity

  • Minimized non-specific surface crowding

  • Increases fidelity to enable SNP level detection

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version