The estimated average industry cost per new prescription drug approval currently now exceeds $2.5 billion. One of the critical factors contributing to the rising costs of drug development is a non-optimal focus of pre- clinical studies for detecting potential cardiac liabilities of novel drug candidates. Recognizing this fact, the biomedical community has recently proposed a new paradigm for cardiac safety studies: the Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative. It includes a shift from over-simplified hERG-focused cardiotoxicity screening to evaluation of drug effects on multiple ion channels contributing to action potential in human stem cell-derived cardiomyocytes (CMs). Optical cell-based drug screening assays that monitor the dynamics of intracellular calcium concentrations and the cell membrane potential in stem cell-derived CMs are well-suited for detecting drug candidates with cardiac liabilities. Since drug-induced effects are often dependent on the activation state of cells, it is crucial to be able to stimulate CMs during drug screening. We propose to address this need by offering a revolutionary nanotechnology-based platform for non-invasive optical stimulation of CMs. We designed this optoelectronic platform by taking advantage of the unique properties of graphene, a ?wonder material of the 21th century?. These properties ensure excellent biocompatibility of graphene-coated substrates, the ability to efficiently convert light into electricity, and compatibility with optical detection methods. Our preliminary results demonstrate that light can induce fast and reversible changes in contractile and electrical activity of stem cell-derived CMs cultured on graphene-coated substrates. Furthermore, we confirmed that optical stimulation via G-coated substrates can enable all-optical evaluation of use-dependent drug effects on the CM activity. To streamline the customer adoption of our graphene-based optical stimulation platform and incorporation it in into optical drug-screening assays, we are proposing to perform the following activities: a) developing a procedure for graphene deposition into cell culture multi-well plates, following by manufacturing of high-quality graphene-coated plates; b) optimizing the various parameters of voltage and calcium all-optical assays (including a dual-light stimulation protocol) on a customized microscopy system; c) transferring optimized all-optical assays to well-regarded high-through and high-content imaging instruments and performing screening of multiple benchmark compounds on optically stimulated CMs. We expect that optical stimulation of CMs via graphene- based substrates will dramatically increase the predictive value of cardiotoxicity screening assays. The proposed all-optical assays will be instrumental in correctly detecting genuine pro-arrhythmia risks early in the drug discovery process, thus reducing the spending and drug development time.
A major public health concern is how to correctly identify potentially pro-arrhythmic drug candidates at the earlier stages of drug discovery, which would allow to increase the efficiency and reduce the costs of this process. Pre- clinical cardiotoxicity assessment is more physiologically relevant when performed on human stem cell-derived cardiomyocytes. The cardiomyocyte activity is electrically controlled, and therefore technological tools that can dynamically manipulate the cardiomyocyte membrane potential during drug screening assays will produce the results with the high predictive value. We propose to develop and manufacture a novel nanotechnology-based optical stimulation platform that will provide fast, reversible, non-invasive modulation of functional activity of cardiomyocytes. Combined with optical monitoring, our platform will enable all-optical cell-based assays that are expected to deliver a predictive mechanism-based assessment of potential pro-arrhythmic effects of novel drug candidates.
| Savchenko, Alex; Cherkas, Volodymyr; Liu, Chao et al. (2018) Graphene biointerfaces for optical stimulation of cells. Sci Adv 4:eaat0351 |
