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Bisker, G.

Publications and source records attributed to Bisker, G..

3 recordsLinked to original sources

Quantifying Population Reversibility of Sensor Performance inMulti-Cycle Single-Sensor Recovery Assay

Quantitative chemical imaging requires sensors that reliably recover across repeated exposures. While solution-phase bulk measurements provide an averaged response of the sensor population, imaging at the single-sensor level enables mapping of biological processes with spatiotemporal resolution, revealing localized events and interaction sites. To translate such imaging into calibrated measurements, sensor variability under repeated analyte exposures must be analyzed. This work introduces a generic workflow that combines an automated microfluidic flow imaging platform with systematic characterization of the response, recovery, and reversibility of individual nanosensors across multi-cycle challenges. For representative implementation, three near-infrared fluorescent single-walled carbon nanotube (SWCNT) sensor models are tested, each with a distinct functionalization rendering it optically responsive to a corresponding exemplar target: dopamine, thiocholine, or serotonin. While first-cycle responses averaged over the entire field of view recapitulate ensemble calibration, single-sensor analysis uncovers broad heterogeneity in response magnitude, signal recovery, and reversibility across hundreds of individual SWCNTs under repeated exposure and wash cycles. To compare performance across cycles, a standardized Population Reversibility Score based on Kullback-Leibler Divergence is introduced, condensing response distributions into a single cycle- and concentration-dependent, quantitative metric. This framework is generally applicable to other sensor-analyte systems with transient readouts, guiding optimization for spatiotemporal analyte mapping.

bioengineering↗

Minimally invasive delivery of optical nanosensors using injectable hydrogels

Optimizing treatment plans based on an individuals drug concentration can significantly improve therapeutic outcomes, as drug efficacy is closely linked to its plasma levels. This motivates the development of precise tools for measuring drug concentration in situ. To address this, a minimally invasive optical sensing platform based on preformed, injectable hydrogels that encapsulate near-infrared fluorescent single-walled carbon nanotube (SWCNT) sensors is introduced. DNA-suspended SWCNTs are integrated into self-assembling peptide hydrogels reinforced with natural polysaccharide additives, yielding self-healing, shear-thinning gels that can be injected through a fine needle while maintaining both structural integrity and optical functionality. Using levodopa, the primary treatment for Parkinsons disease, as a model target analyte, the encapsulated SWCNTs exhibit a dose-dependent fluorescence response across physiologically relevant concentrations. Importantly, the SWCNTs within the hydrogel retain their fluorescence response to levodopa following injection, as well as in the presence of serum, and in a subcutaneous tissue phantom that mimics the mechanical and optical scattering properties of soft tissue. These results establish preformed injectable peptide-based hydrogels as a new class of function-preserving materials for the localized deployment of SWCNT optical nanosensors, enabling minimally invasive in situ monitoring of drug levels and offering a potential route toward personalized therapeutic drug monitoring.

bioengineering↗

Optical Nanosensors for Real-time Feedback on Insulin Secretion by β-Cells

Quantification of insulin is essential for diabetes research in general, and for the study of pancreatic {beta}-cell function in particular. Herein, fluorescent single-walled carbon nanotubes (SWCNT) are used for the recognition and real-time quantification of insulin. Two approaches for rendering the SWCNT sensors for insulin are compared, using surface functionalization with either a natural insulin aptamer with known affinity to insulin, or a synthetic PEGylated-lipid (C16-PEG(2000Da)-Ceramide), both of which show a modulation of the emitted fluorescence in response to insulin. Although the PEGylated-lipid has no prior affinity to insulin, the response of C16-PEG(2000Da)-Ceramide-SWCNTs to insulin is more stable and reproducible compared to the insulin aptamer-SWCNTs. The C16-PEG(2000Da)-Ceramide-SWCNTs optical response is excitation-wavelength dependent, where resonant excitation leads to a larger fluorescence decrease in response to insulin. The SWCNT sensors successfully detect insulin secreted by {beta}-cells within the complex environment of the conditioned media. The insulin is quantified by comparing the SWCNTs fluorescence response to a standard calibration curve, and the results are found to be in agreement with an enzyme-linked immunosorbent assay (ELISA). This novel analytical tool for real time quantification of insulin secreted by {beta}-cells provides new opportunities for rapid assessment of {beta}-cell function, with the ability to push forward many aspects of diabetes research.

bioengineering↗