CN Bio introduces PhysioMimix NASH ‘in-a-box’ reagent kit

First product within new ‘in-a-box’ range, which harnesses next-generation, human-relevant Liver-on-a-Chip technology to improve the accuracy and efficiency of NASH drug discovery

25 Apr 2022
Rory Shadbolt
Publishing / Media

Product news

CN Bio, a leading Organ-on-a-chip Company (OOC) that designs and manufactures single- and multi-organ microphysiological systems (MPS), today introduced its PhysioMimix™ ‘in-a-box’ reagent kit for Non-alcoholic steatohepatitis (NASH), the most severe form of non-alcoholic fatty liver disease (NAFLD). Previously only accessible via its contract research services, CN Bio’s best-in-class NASH in vitro model supports the urgent development of therapeutics to treat this emerging global healthcare priority.

Despite research efforts to combat the growing prevalence of NASH, to date, there are no regulatory approved therapeutics due to the inability of traditional in vivo animal experiment approaches to predict the human response to this complex disease. In conjunction with CN Bio’s PhysioMimix MPS, the NASH-in-a-box (NIAB) kit provides researchers with in-house capabilities to gain physiologically relevant insights into the mechanism of disease, human drug efficacy, and safety toxicology. The assay addresses the human-relevance limitations of existing approaches, bridging the gap between human 2D cell culture and expensive animal models, which are ineffective in mimicking the full disease spectrum. This enables NIAB kit users to generate clinically translatable and predictive data that facilitate more insightful, accurate, and cost-effective drug development.

Through its ‘in-a-box’ range, CN Bio aims to fast-track the incorporation of MPS into drug discovery workflows by providing a straightforward and quick route to recreating its industry-proven OOC assays. Within the NIAB kit, new users are guided through a simple-to-follow, software-based protocol for successfully co-culturing internally-validated primary human hepatocytes, stellate, and Kupffer cells. The protocol enables the formation of 3D microtissue structures that accurately emulate the microarchitecture of the human liver. By introducing fatty acids, researchers can recapitulate key NAFLD/NASH disease states: intracellular fat accumulation, inflammation, and fibrosis1. Once created, the model enables the precise mechanistic effects of drugs (of any modality) and disease to be investigated via high content, clinically translatable end-point measurements.

Dr. David Hughes, CEO, CN Bio, said: “NASH-in-a-box enables CN Bio to expand our market reach from those who prefer to outsource their testing to our laboratories, to those who would rather develop in-house capabilities. As the first in our ‘in-a-box’ range, the launch of the NASH kit represents a significant step toward the widespread adoption of Organ-on-a-chip technology within the drug discovery industry. Consequently, we believe this product will enable discovery programs targeting this disease which is a large and growing burden on healthcare systems, yet lacks any approved therapies.”

Dr. Ovidiu Novac, Senior Scientist for CN Bio, commented: “This new product demonstrates the full advantages of our microphysiological systems, providing scientists with access to easy-to-use, yet best-in-class liver models in their own labs, streamlining the process and making it far quicker and more cost-effective. We believe this will allow for more thorough and accurate testing during the drug development process, which will increase the likelihood of much-needed new NASH drugs to make it to market.”

Want the latest science news straight to your inbox? Become a SelectScience member for free today>>

In vitro NASH Contract Research Services by CN Bio

CN Bio

CN Bio supports non-alcoholic steatohepatitis (NASH) therapeutic development via fast-track NASH Contract Research Services. NASH Services enable you to gain instant access to CN Bio’s expertise and one of the most advanced human in vitro models available. Submit lead candidates for screening and receive human translatable data for insightful preclinical candidate prioritization, clinical trial design and optimization.

(0)

Links

Tags

ADME-ToxicologyADME-toxicology (ADME-Tox) studies are used in pharmacology and pharmacokinetics to assess the activity/toxicity of drugs <i>in vivo</i> or <i>in vitro</i>. Find bioassays for absorption, distribution, metabolism, and excretion of drug molecules including cytotoxicity, transporter/permeability, metabolism and activity assays as well as hepatocytes and cell lines for ADME. Find the best ADME-toxicology products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Biopharmaceutical AdvancesBiopharmaceutical advances follow the development of pharmaceuticals derived from biotechnology, also known as biotechnology medicines. Biopharmaceuticals may be produced from cell lines, plants, or microbial cells. Important considerations of biopharmaceutical use include application, cost, production process and purification.Toxicology / Drugs of Abuse TestingToxicology and Drugs of Abuse Testing is the investigation into toxic and illegal substances found at the scene of a crime or from a suspect and / or victim associated with a scene of a crime. Analyzers, immunoassays and drugs of abuse test kits and presumptive test kits are an essential aspect of toxicology investigation.ToxicityToxicity is defined as the degree to which a substance can harm humans or animals. It is essential to study the toxicity of pharmaceutical products during the development process so that optimum dosage can be established for the administration of the drug.Forensic ToxicologyForensic toxicology is used to determine cause of death, drug use and contaminations. Toxicological evaluations are commonly used in analytical chemistry, clinical, life sciences and forensics.Drug DevelopmentDrug development refers to the process of bringing a new drug to market.