Triboelectric nanogenerator (TENG) is a promising technology because it can harvest energy from the environment to enable self-sustainable mobile and wearable electronic devices. In this work, we present a flexible touch pad capable of detecting the contact location of an object and generating substantial energy simultaneously based on the coupling of triboelectric effects and electrostatic induction. The touch pad consists of Polytetrafluoroethylene (PTFE) thin film, multiple Aluminum (Al) electrodes and Polyethylene terephthalate (PET) layers, which can be achieved through low cost, simplified and scalable fabrication process. Different from the conventional multi-pixel-based positioning sensor (i.e., large array of sensing elements and electrodes), the analogue method proposed here is used to implement the positioning function with only four electrodes. Position location can achieve a detecting resolution of as small as 1.3 mm (the size of locating layer is 7.5 cm × 7.5 cm). For the energy harvesting part, a multilayer structure is designed to provide higher current output. The open circuit voltage of the device is around 420 V and the short circuit current can reach up to 6.26 µA with current density of 0.25 µA/cm². The maximum output power obtained is approximately 10 mW, which is 0.4 mW/cm². The flexibility and significantly reduced number of electrodes enable the proposed touch pad to be readily integrated into portable electronic devices, such as intelligent robots, laptops, healthcare devices, and environmental surveys, etc.

This paper presents a full-featured microfluidic platform ensuring long-term culturing and behavioral analysis of the radically different biological micro-objects. The platform uses all-glass lab-chips and MEMS-based components providing dedicated micro-aquatic habitats for the cells, as well as their intentional disturbances on-chip. Specially developed software was implemented to characterize the micro-objects metrologically in terms of population growth and cells’ size, shape, or migration activity. To date, the platform has been successfully applied for the culturing of freshwater microorganisms, fungi, cancer cells, and animal oocytes, showing their notable population growth, high mobility, and taxis mechanisms. For instance, circa 100% expansion of porcine oocytes cells, as well as nearly five-fold increase in E. gracilis population, has been achieved. These results are a good base to conduct further research on the platform versatile applications.

In the paper, the lab-on-chip platform applicable for the long-term cultivation of human cancer cells, as a solution meeting the demands of the CubeSat biological missions, is presented. For the first time, the selected cancer cell lines—UM-UC-3 and RT 112 were cultured on-chip for up to 50 days. The investigation was carried out in stationary conditions (without medium microflow) in ambient temperature and utilizing the microflow perfusion system in the incubation chamber assuring typical cultivation atmosphere (37 °C). All the experiments were performed to imitate the conditions that are provided before the biological mission starts (waiting for the rocket launch) and when the actual experiment is initialized on a CubeSat board in space microgravity. The results of the tests showed appropriate performance of the lab-on-chip platform, especially in the context of material and technological biocompatibility. Cultured cells were characterized by adequate morphology—high attachment rate and visible signs of proliferation in each of the experimental stage. These results are a good basis for further tests of the lab-on-chip platform in both terrestrial and space conditions. At the end of the manuscript, the authors provide some considerations regarding a potential 3-Unit CubeSat biological mission launched with Virgin Orbit company. The lab-on-chip platform was modelled to fit a 2-Unit autonomous laboratory payload.

In this paper, an autonomous payload proposal for a nanosatellite mission allowing for the cultivation of grains in space was presented. For the first time, a micropot made with 3D printing technology, enabling the parametric determination of plant growth, both on Earth and in the simulated microgravity condition, was presented. A completed system for dosing the nutrient solution and observing the growth of a single grain, where the whole size did not exceed 70 × 50 × 40 mm³, was shown. The cultivation of Lepidium sativum seeds was carried out in the developed system, in terrestrial conditions and simulated microgravity conditions, using the RPM (Random Position Machine) device. The differences in plant growth depending on the environment were observed. It could be seen that the grains grown in simulated microgravity took longer to reach the full development stage of the plant. At the same time, fewer grains reached this stage and only remained at the earlier stages of growth. The conducted research allowed for the presentation of the payload concept for a 3U CubeSat satellite for research into the development of plants in space.

In this paper, a lab-on-chip system dedicated to fungi cultivation in Earth’s gravity and simulated microgravity, being a solution that could be used in future nanosatellite missions, is shown. For the first time, a fully glass lab-on-chip structure enabling the proper environment for cultivation of fungi species—Fusarium culmorum—is presented. Apart from the biological validation of the fungi cultures with the use of the lab-on-chip system, tests were carried out under induced microgravity utilising a Rotary Wall Vessel. Correct functioning of the lab-on-chip system was obtained, enabling the growth of fungi spores both in ground and in simulated microgravity conditions. Interestingly, culturing tests have shown that microgravity stimulates the growth of fungi notably, compared to the ground-based experimentation performed simultaneously. The findings of this study can provide substantial new knowledge on microscopic fungi cultivation in lab-on-chip devices, other soil organisms, as well as a potential behavior of these species in microgravity conditions. Culturing system shown in this work can help mycologists to provide better understanding of microscopic fungi nature and their development mechanisms at a single spore level. This opens the way towards regular usage of microfluidic tools in agriculture and horticulture fields and more importantly, in future research on microscopic fungi in space, e.g., as a part of nanosatellite missions.

A miniature 3D printed membrane-based gas microflow regulator which delivers gaseous media to on-chip cell cultures is presented in this paper. The device uses a polydimethylosiloxane (PDMS) membrane to act as a diffusion barrier and maintain gas flow at the desired rate. The regulator was characterized, and repeatable flow values for different membrane thicknesses and gas types in the function of pressure were obtained. As a result, a long-term on-chip culture of Euglena gracilis was achieved, this was due to constant and stable carbon dioxide release from the regulator (flow rate: 0.3 μL/min).