Replicating the Heart, Revolutionising Discovery
A biomimetic culture device for drug discovery and disease modelling
ADVANCING CARDIAC RESEARCH WITH PRECISION
MyoLoop is a cardiovascular research team from Imperial College London’s National Heart and Lung Institute, exploring the market potential of our cardiac culture device through the BBSRC-NC3Rs-ICURe programme
We want to provide a biologically relevant, in vitro platform for the drug discovery pipeline, resulting in a more predictable and cost-effective process for the pharmaceutical industry, CROs and academic researchers
By replicating the heart’s natural environment, we enable more precise drug testing and accelerate the discovery of new therapeutic targets for cardiac disease


HELP SHAPE THE FUTURE OF CARDIAC RESEARCH
The Challenge:
A Bottleneck in Drug Discovery
Cost and Delays
Therapeutic development is frequently plagued by failure, costing an estimated $28 billion per year, mostly due to efficacy (60%) and toxicity (30%). Absence of obvious cardiac toxicity (hERG binding) is a regulatory requirement for drug candidates. However, cardiotoxicity of marketed drugs still occurs, particularly within anti-cancer therapies, reducing quality of life and lifespan
Inaccurate Mechanical Environments
Mechanical load influences the cardiomyocyte phenotype and its drug response. 2D cell models lack mechanical stimuli and 3D models lack a physiological method of modelling circulatory pressure. Drugs are screened in these non-physiological systems, with poor predictions of cardiotoxicity or efficacy during in vivoanimal studies, where large biological and haemodynamic differences exist. Integrating physiologically relevant mechanical load at the preclinical stage is a critical gap in the drug development pipeline
The Solution: MyoLoop
Advancing Cardiac Research Using Realistic Mechanical Load
MyoLoop is a benchtop bioreactor recording functional output from human and animal cardiac muscle preparations such as Living Myocardial Slices (LMS), Engineered Heart Tissues (EHT) and cell-laden biomaterials
Interactive software uses customisable parameters to apply both healthy and diseased mechanical loading conditions, leveraged through real-time functional behaviour of cardiac tissue and a continuous feedback system
By introducing the effect of pressure of our valves and the circulation, cardiac tissue is exposed to a realistic model of the circulatory environment, maintaining the physiological cardiac response, and will accelerate the discovery of new therapeutic targets
PRECISE MECHANICAL LOADING
Mimic diastole and systole across various animal models by applying programmed preload and afterload parameters
DISEASE MODELLING
Vary mechanical parameters to match known disease conditions such those seen in hypertension, aortic stenosis and heart failure
ACCELERATED DRUG DISCOVERY
Determine effeciency and safety profile of pharmaceutical drugs and biologics on cardiac function and arrhythmia
LONG-TERM CULTURE
Undertake prolonged experiments to determine time-dependant reactions and monitoring of drug interaction

REDUCE ANIMAL USE
Leverage multicellular preparations to decrease costs associated with animal models and improve ethical research
IMAGING
Integrate microscopy and fluorescence imaging techniques to record visible data from tissue samples
Boosting Cardiac Research Across Sectors
MyoLoop has been designed for pioneering research in academia, the pharmaceutical industry and contract research organisations (CROs) by offering a physiologically-relevant, medium-throughput device for cardiac research, superseding outmoded in vitro systems

Pharmaceutical Manufacturers

Academic Researchers
