48 research outputs found
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3D Bioelectronic Model of the Human Intestine
Organ on chip (OoC) technologies have the potential to improve the translation
of promising therapies currently failing in clinical trials at great expense and
time due to dissimilarities between animal and human biology. Successful OoC
models integrate human cells within 3D tissues with surrounding biomolecular
components, and have benefited from the use of inert 3D gels and scaffolds
used as templates, prompting tissue formation. However, monitoring technologies used to assess tissue integrity and drug effects are ill adapted to 3D
biology. Here, a tubular electroactive scaffold serves as a template for a 3D
human intestine, and enables dynamic electrical monitoring of tissue formation
over 1 month. Cell- and extracellular matrix component-invoked changes in the
properties of the scaffold alleviate the need for posthoc placement of invasive
metallic electrodes or downstream analyses. Formation of in vivo-like stratified
and polarized intestinal tissue compete with lumen contrasts with other quasi3D models of the intestine using rigid porous membrane to separate cell types.
These results provide unprecedented real-time information on tissue formation with highly sensitive multimodal operation, thanks to dual electrode and
transistor operation. This device and the methodology for tissue growth within
it represents a paradigm shift for disease modeling and drug discover
Small molecule additive for low-power accumulation mode organic electrochemical transistors
A small molecule additive, dodecylbenzenesulfonate (DBSA), is added to the electrolyte in OECTs to improve the device performance.ERC IMBIBE
EPSRC CDT Plastic Electronic
High mobility transistors based on electrospray-printed small-molecule/polymer semiconducting blends
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Biomimetic and electroactive 3D scaffolds for human neural crest-derived stem cell expansion and osteogenic differentiation
AbstractOsteoporosis is a skeletal disease characterized by bone loss and bone microarchitectural deterioration. The combination of smart materials and stem cells represents a new therapeutic approach. In the present study, highly porous scaffolds are prepared by combining the conducting polymer PEDOT:PSS with collagen type I, the most abundant protein in bone. The inclusion of collagen proves to be an effective way to modulate their mechanical properties and it induces an increase in scaffolds’ electrochemical impedance. The biomimetic scaffolds support neural crest-derived stem cell osteogenic differentiation, with no need for scaffold pre-conditioning contrarily to other reports.</jats:p
Performance of hybrid buffer Poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) layers doped with plasmonic silver nanoparticles
We compare the performance of a typical hole transport layer for organic photovoltaics (OPVs), Poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) thin film with a series of PEDOT:PSS layers doped with silver (Ag) nanoparticles (NPs) of various size distributions. These hybrid layers have attracted great attention as buffer layers in plasmonic OPVs, although there is no report up to date on their isolated performance. In the present study we prepared a series of PEDOT:PSS layers sandwiched between indium tin oxide (ITO) and gold (Au) electrodes. Ag NPs were deposited on top of the ITO by electron beam evaporation followed by spin coating of PEDOT:PSS. Electrical characterization performed in the dark showed linear resistive behavior for all the samples; lower resistance was observed for the hybrid ones. It was found that the resistivity of the samples decreases with increasing the particle's size. A substantial increase of the electric field between the ITO and the Au electrodes was seen through the formation of current paths through the Ag NPs. A striking observation is the slight increase in the slope of the current density versus voltage curves when measured under illumination for the case of the plasmonic layers, indicating that changes in the electric field in the vicinity of the NP due to plasmonic excitation is a non-vanishing factor