Electroporation of in-vitro cultured cells is widely used in biological and medical areas to deliver molecules of interest inside cells. Since very high electric fields are required to electroporate the plasma membrane, depending on the geometry of the electrodes the required voltages can be very high and often critical to cell viability. Furthermore, in traditional electroporation configuration based on planar electrodes there is no a priori certain feedback about which cell has been targeted and delivered and the addition of fluorophores may be needed to gain this information. In this study we present a nanofabricated platform able to perform intracellular delivery of membrane-impermeable molecules by opening transient nanopores into the lipid membrane of adherent cells with high spatial precision and with the application of low voltages (1.5–2 V). This result is obtained by exploiting the tight seal that the cells present with 3D fluidic hollow gold-coated nanostructures that act as nanochannels and nanoelectrodes at the same time. The final soft-electroporation platform provides an accessible approach for controlled and selective drug delivery on ordered arrangements of cells.

Biological studies on in vitro cell cultures are of fundamental importance to investigate cells response to external stimuli, such as new drugs for treatment of specific pathologies, or to study communication between electrogenic cells. Although three-dimensional (3D) nanostructures brought tremendous improvements on biosensors used for various biological in vitro studies, including drug delivery and electrical recording, there is still a lack of multifunctional capabilities that could help gaining deeper insights in several bio-related research fields. In this work, the electrical recording of large cell ensembles and the intracellular delivery of few selected cells are combined on the same device by integrating microfluidics channels on the bottom of a multi-electrode array decorated with 3D hollow nanostructures. The novel platform allows to record intracellular-like action potentials from large ensembles of cardiomyocytes derived from human Induced Pluripotent Stem Cells (hiPSC) and from the HL-1 line, while different molecules are selectively delivered into single/few targeted cells. The proposed approach shows high potential for enabling new comprehensive studies that can relate drug effects to network level cell communication processes.

Since the birth of quantum mechanics the construction and control of novel hybrid quantum states are among the dream targets of scientists. In this regard, due to recent technological advances, hybrid states based on strong coupling occurring between light and matter have become a laboratory reality. For example, it is demonstrated that strong coupling involving microcavities or surface plasmon polaritons shows great potential for novel nanoplasmonic devices such as lasers, all-optical switching, field-effect transistors, and for the evergreen field of quantum computation. Further developments in this field require, however, a better understanding of the underlying mechanisms governing strong coupling, especially from a time-dependent point of view, time-resolved spectroscopy being one of the leading experimental approaches to address this aspect. In this perspective, after a brief introduction of the strong coupling concept, the recent research progress on the dynamics of strongly coupled systems involving J-aggregates, broadly absorptive dyes, semiconductor quantum dots, and perovskite films with either microcavities or surface plasmons polaritons is summarized and discussed. Finally, challenges and perspectives for developing strong coupling concept are further illustrated, with special attention to phonon-photon interaction, as one of the most intriguing topics in condensed matter physics.