Our Platform

Our proprietary mini-Life Platform includes the award-winning mini-Heart Technology which offers a range of bioengineered human heart constructs, including the world’s first human heart-in-a-jar, as healthy and diseased human hearts for testing toxicity and efficacy.

Our Revolutionary Approach

This platform substantially increases the chances of saving and addressing maladies for millions with new discoveries

and far greater affordability for the patients.

Heart Disease Modeling and Drug Screening
mini-heart Platform

Single Cell

Novoheart's human ventricular Cardiomyocytes (hvCMs) are terminally differentiated cardiomyocytes derived from human pluripotent stem cells (hPSCs) using Novoheart’s proprietary differentiation method. These cells have been extensively characterized for their electrophysiology, calcium homeostasis, transcriptome, microRNAome, and proteome.


They exhibit ventricular-like action potentials and express ventricular-specific myosin light chain MLC2v. With virtually homogeneous ventricular properties, these cells provide the consistency necessary to achieve reliable and reproducible results in downstream applications.


                        hvCM

Biologics Ventricular Specific CM differentiation kit

                        hESC-vCM

                        hESC-vCM 

                        hiPSC-vCM

                        hiPSC-vCM

Media         hvCM maintenance medium


VIEW THE PLATFORM SHEET


Contractility

Contractile performance is an essential function of the human heart, yet conventional 2-D cardiomyocyte cultures are inadequate for assessing contractility as they cannot perform physiological contractions on rigid plasticware. Tissue engineering offers a superior contractile assay in the form of Novoheart’s human ventricular Cardiac Tissue Strip (hvCTS), which is structurally and functionally similar to native trabecular muscle. This assay consists of aligned hvCMs in 3-D hydrogel mixture that is constructed using Medera’s custom-designed bioreactor with integrated force-sensing posts at the ends. This model has been validated as a sensitive and reliable predictor of clinical effects of drugs or pathologies on cardiac contractility.


                 hvCTS

Biologics CTS Fabrication Kit

                 µCTS Fabrication Kit

                 µCTS Fabrication Kit

Media Maintenance medium 

Instruments CTScreen System

Software  mini-Heart T-Monitor

                   mini-Heart T-Processor 

                   mini-Heart T-Analyzer

Consumables    1-CTS Cartridge

    3-CTS Cartridge

    6-µCTS Cartridge

    96-well µCTS Plate


VIEW THE PLATFORM SHEET


EP and Arrhythmias

Effective modeling of arrhythmias in vitro is challenging: by definition, they are multicellular events that can only be recorded by monitoring conduction patterns in electrically coupled cardiomyocytes. Conventional assays can only use surrogate markers for arrhythmia: the hERG assay, standard in the industry, for example, uses inhibition of a single potassium channel exogenously expressed in non-cardiac cell lines as an indicator for proarrhythmic risk. Although these remain the standard tests for arrhythmogenicity, global drug regulators recognize their pitfalls and are actively seeking better alternatives, notably in the Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative of the FDA. Human pluripotent stem cell-derived cardiomyocytes are inherently prone to arrhythmic events when cultured as randomly oriented monolayers. Novoheart’s human ventricular Cardiac Anisotropic Sheet (hvCAS) assay utilizes specially designed microgrooved substrates that physically guide hvCMs to align in a similar manner to that in the native human ventricle. The aligned cells show anisotropic electrical conduction which has been validated to reduce the baseline arrhythmogenicity compared to monolayers without a cardiomimetic preferential conduction axis.


                                    hvCAS

Biologics            CAS Fabrication Kit

Media                Maintenance medium 

Instruments      CAScreen System

Software           mini-Heart A-Analyzer

Consumables    µPatterned PS Substrate 

                               4-CAS Module


VIEW THE PLATFORM SHEET


EP and Pressure

Novoheart’s fluid-ejecting 3-D human ventricular Cardiac Organoid Chamber (hvCOC), a.k.a. “human heart-in-a-jar” is the only technology available to date that enables the clinically informative assessment of human cardiac pump performance which no other human engineered heart tissues on the market are capable of. Combined with complementary custom-designed hardware and software, the best-in-class “human 

heart-in-a-jar” allows drug screening and disease modeling with unprecedented biofidelity.


                          hvCOC

Biologics  -  COC Fabrication Kit

                          µCOC Fabrication Kit

Media -  Maintenance medium 

Instruments - COScreen System

Software -   mini-Heart O-Monitor

                           mini-Heart O-Processor

                          mini-Heart O-Analyzer

Consumables -   1-COC Mold

                            24-μCOC Plate


VIEW THE PLATFORM SHEET


Human Ventricular Cardiomyocytes (hvCMs)

Single Cell

Novoheart's human ventricular Cardiomyocytes (hvCMs) are terminally differentiated cardiomyocytes derived from human pluripotent stem cells (hPSCs) using Novoheart’s proprietary differentiation method. These cells have been extensively characterized for their electrophysiology, calcium homeostasis, transcriptome, microRNAome, and proteome. They exhibit ventricular-like action potentials and express ventricular-specific myosin light chain MLC2v. The hvCMs are  the building blocks for the other mini-Heart assays.  With virtually homogeneous ventricular properties, these cells  provide the consistency necessary to achieve reliable and reproducible results in downstream applications.


Biologics            

Ventricular Specific CM differentiation kit

hESC-vCM 

hiPSC-vCM

Media

Maintenance Medium


VIEW THE PLATFORM SHEET


Human Ventricular Cardiac Anisotropic Sheet (hvCAS)

Electrophysiology and Arrhythmias

Effective modeling of arrhythmias in vitro is challenging: by definition, they are multicellular events that can only be recorded by monitoring conduction patterns in electrically coupled cardiomyocytes. Conventional assays can only use surrogate markers for arrhythmia: the hERG assay, standard in the industry, for example, uses inhibition of a single potassium channel exogenously expressed in non-cardiac cell lines as an indicator for proarrhythmic risk. Although these remain the standard tests for arrhythmogenicity, global drug regulators recognize their pitfalls and are actively seeking better alternatives, notably in the Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative of the FDA. Human pluripotent stem cell-derived cardiomyocytes are inherently prone to arrhythmic events when cultured as randomly oriented monolayers. Novoheart’s human ventricular Cardiac Anisotropic Sheet (hvCAS) assay utilizes specially designed microgrooved substrates that physically guide hvCMs to align in a similar manner to that in the native human ventricle. The aligned cells show anisotropic electrical conduction which has been validated to reduce the baseline arrhythmogenicity compared to monolayers without a cardiomimetic preferential conduction axis.


Biologics

CAS Fabrication Kit

Media                   

Maintenance medium 

Instruments     

CAScreen System

Software        

mini-Heart A-Analyzer

Consumables 

µPatterned PS Substrate 

4-CAS Module


VIEW THE PLATFORM SHEET


Human Ventricular Cardiac Tissue Strip (hvCTS)

Contractility

Contractile performance is an essential function of the human heart, yet conventional 2-D cardiomyocyte cultures are inadequate for assessing contractility as they cannot perform physiological contractions on rigid plasticware, and cell shortening is not an accurate surrogate for force generation. Tissue engineering offers a superior contractile assay in the form of Novoheart’s human ventricular Cardiac Tissue Strip (hvCTS), which is structurally and functionally similar to native trabecular muscle. This assay consists of aligned hvCMs in 3-D collagen hydrogel mixture that is constructed using Medera’s custom-designed bioreactor with integrated force-sensing posts at the ends. This model has been validated as a sensitive and reliable predictor of clinical effects of drugs or pathologies on cardiac contractility.


Biologics        

CTS Fabrication Kit

µCTS Fabrication Kit

µCTS Fabrication Kit

Media                

Maintenance medium 

Instruments     

CTScreen System

Software        

mini-Heart T-Monitor

mini-Heart T-Processor 

mini-Heart T-Analyzer

Consumables 

1-CTS Cartridge

3-CTS Cartridge

6-µCTS Cartridge

96-well µCTS Plate


VIEW THE PLATFORM SHEET


Human Ventricular Cardiac Organoid Chamber (hvCOC)

Electrophysiology and Pump Function

Novoheart’s fluid-ejecting 3-D human ventricular Cardiac Organoid Chamber (hvCOC), a.k.a. “human heart-in-a-jar” is the only commercially available technology to date that enables the clinically informative assessment of human cardiac pump performance, which is not possible with other human engineered heart tissues on the market. Combined with complementary custom-designed hardware and software, the best-in-class “human heart-in-a-jar” allows drug screening and disease modeling with unprecedented biofidelity.


Biologics

COC Fabrication Kit

µCOC Fabrication Kit

Media

Maintenance medium 

Instruments     

COScreen System

Software      

mini-Heart O-Monitor

mini-Heart O-Processor

mini-Heart O-Analyzer

Consumables  

1-COC Mold

24-μCOC Plate


VIEW THE PLATFORM SHEET


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