A Metric for Quantifying the Resolution of Molecular Assays

Many assay developers focus on limit of detection (LOD) as a primary performance metric, and LOD is indeed useful for assays designed to determine the presence or absence of an analyte. However, LOD is less useful for continuous assays designed to discriminate between concentrations of an analyte-e.g., glucose monitoring in diabetes, where clinical care is guided by particular concentration ranges and thresholds. In such scenarios, it would be valuable to quantify discriminatory resolution-i.e., whether an assay can differentiate 1 pM from 10 pM-but no such standardized metric currently exists. Here, we propose a useful solution, termed "resolution of molecular concentration" (RMC). RMC offers a simple means for characterizing quantitative resolution and quickly comparing the quantitative performance of assays. By raising awareness of the limitations of current metrics for evaluating assay performance, we hope to empower the molecular diagnostics community to evaluate their methods in a more application-appropriate manner.

Photochemical Dissipative Structuring of the Fundamental Molecules of Life

It has been conjectured that the origin of the fundamental molecules of life, their proliferation over the surface of Earth, and their complexation through time, are examples of photochemical dissipative structuring, dissipative proliferation, and dissipative selection, respectively, arising out of the nonequilibrium conditions created on Earth’s surface by the solar photon spectrum. Here I describe the nonequilibrium thermodynamics and the photochemical mechanisms involved in the synthesis and evolution of the fundamental molecules of life from simpler more common precursor molecules under the long wavelength UVC and UVB solar photons prevailing at Earth’s surface during the Archean. Dissipative structuring through photochemical mechanisms leads to carbon based UVC pigments with peaked conical intersections which endow them with a large photon disipative capacity (broad wavelength absorption and rapid radiationless dexcitation). Dissipative proliferation occurs when the photochemical dissipative structuring becomes autocatalytic. Dissipative selection arises when fluctuations lead the system to new stationary states (corresponding to different molecular concentration profiles) of greater dissipative capacity as predicted by the universal evolution criterion of Classical Irreversible Thermodynamic theory established by Onsager, Glansdorff, and Prigogine. An example of the UV photochemical dissipative structuring, proliferation, and selection of the nucleobase adenine from an aqueous solution of HCN under UVC light is given.

Manipulating optical nonlinearities of molecular polaritons by delocalization

Optical nonlinearities are key resources in the contemporary photonics toolbox, relevant to quantum gate operations and all-optical switches. Chemical modification is often used to control the nonlinear response of materials at the microscopic level, but on-the-fly manipulation of such response is challenging. Tunability of optical nonlinearities in the mid-infrared (IR) is even less developed, hindering its applications in chemical sensing or IR photonic circuitry. Here, we report control of vibrational polariton coherent nonlinearities by manipulation of macroscopic parameters such as cavity longitudinal length or molecular concentration. Further two-dimensional IR investigations reveal that nonlinear dephasing provides the dominant source of the observed ultrafast polariton nonlinearities. The reported phenomena originate from the nonlinear macroscopic polarization stemming from strong coupling between microscopic molecular excitations and a macroscopic photonic cavity mode.

Deciphering ion concentration polarization-based electrokinetic molecular concentration at the micro-nanofluidic interface: theoretical limits and scaling laws

Elucidating the mechanism of electrokinetic molecular concentration in terms of theoretical limits for the concentration factor and their scaling laws.