ReviewMicrosystems & nanoengineering2026
Advanced in vitro cardiac models for drug evaluation: integration of organoids, engineered tissues, and microphysiological systems.
Review in Microsystems & nanoengineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Induced Pluripotent Stem Cell-Based Platforms for Cardiac-Related Pain Research: Molecular Mechanisms, Experimental Models, and Therapeutic Applications.International journal of molecular sciences · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
In vitro cardiac model systems have rapidly advanced as complementary platforms to conventional two-dimensional (2D) cultures and animal models, which, despite their long-standing contributions, exhibit inherent limitations in predicting human cardiac responses. This review highlights recent progress in biomimetic platforms that more faithfully recapitulate the structure and function of the human myocardium, including engineered three-dimensional (3D) tissues, chambered ventricular constructs, self-organizing cardiac organoids, and microphysiological systems. These models are increasingly being applied as Drug Development Tools (DDTs) for safety pharmacology, efficacy testing, and cardiotoxicity assessment, offering improved predictive performance compared to traditional assays. By incorporating key features, such as three-dimensional tissue architecture, multicellular composition, electromechanical coupling, and physiological loading, these platforms enhance the translational relevance of preclinical studies. Recent innovations include maturation-enhanced organoids, vascularized engineered heart tissues, chamber models with physiological pressure-volume dynamics, and chip-based platforms that enable the real-time assessment of contractility and electrophysiology. Importantly, the integration of immune and vascular components, as well as multi-organ connectivity, further extends their applicability to systemic drug evaluations and disease modeling. Collectively, these advances bridge the gap between reductionist in vitro assays and clinical studies and align with emerging regulatory paradigms that emphasize human-relevant and non-animal testing methods. By enabling mechanistic insights into human cardiogenesis, cardiomyocyte maturation, and patient-specific disease modeling, advanced in vitro cardiac platforms hold great promise for precision pharmacology and regenerative medicine. Overall, in vitro cardiac models represent a transformative paradigm for advancing drug discovery, improving safety predictions, and reducing the reliance on animal testing in cardiovascular research.
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.