Paper-based Diagnostic Devices

This chapter will provide an overview of existing diagnostic devices made primarily out of paper and then focus on paper-based microfluidic devices, the next generation of paper-based diagnostic devices that promises to extend the use of paper as a material for fabricating diagnostic devices well into the future. Chapter Contents: 2.1 Introduction 2.2 Current paper-based diagnostic devices 2.2.1 Dipstick devices 2.2.2 Lateral-flow devices 2.2.2.1 Vertical-flow devices 2.2.3 Paper-based arrays 2.3 Paper-based microfluidic devices 2.3.1 Fabrication of paper-based microfluidic devices 2.3.2 Applications of paper-based microfluidic devices 2.4 Conclusions Reference

Characterization of reagent pencils for deposition of reagents onto paper-based microfluidic devices

Reagent pencils allow for solvent-free deposition of reagents onto paper-based microfluidic devices. The pencils are portable, easy to use, extend the shelf-life of reagents, and offer a platform for customizing diagnostic devices at the point of care. In this work, reagent pencils were characterized by measuring the wear resistance of pencil cores made from polyethylene glycols (PEGs) with different molecular weights and incorporating various concentrations of three different reagents using a standard pin abrasion test, as well as by measuring the efficiency of reagent delivery from the pencils to the test zones of paper-based microfluidic devices using absorption spectroscopy and digital image colorimetry. The molecular weight of the PEG, concentration of the reagent, and the molecular weight of the reagent were all found to have an inverse correlation with the wear of the pencil cores, but the amount of reagent delivered to the test zone of a device correlated most strongly with the concentration of the reagent in the pencil core. Up to 49% of the total reagent deposited on a device with a pencil was released into the test zone, compared to 58% for reagents deposited from a solution. The results suggest that reagent pencils can be prepared for a variety of reagents using PEGs with molecular weights in the range of 2000 to 6000 g/mol

Reagent pencils: A new technique for solvent-free deposition of reagents onto paper-based microfluidic devices

Custom-made pencils containing reagents dispersed in a solid matrix were developed to enable rapid and solvent-free deposition of reagents onto membrane-based fluidic devices. The technique is as simple as drawing with the reagent pencils on a device. When aqueous samples are added to the device, the reagents dissolve from the pencil matrix and become available to react with analytes in the sample. Colorimetric glucose assays conducted on devices prepared using reagent pencils had comparable accuracy and precision to assays conducted on conventional devices prepared with reagents deposited from solution. Most importantly, sensitive reagents, such as enzymes, are stable in the pencils under ambient conditions, and no significant decrease in the activity of the enzyme horseradish peroxidase stored in a pencil was observed after 63 days. Reagent pencils offer a new option for preparing and customizing diagnostic tests at the point of care without the need for specialized equipment

Trace constituents in the middle atmosphere by high resolution UV spectroscopy

An array of 5 autonomous spectrometers, the imaging spectrometric observatory covers a broad wavelength range (approximately 200 to 12,000 A), has a resolution selectable down to approximately 0.5 A, and a dynamic range of approximately 10 to the 7th power and is designed to select experiment measurement sequences by software control. Because current models of thermospheric ionic processes produce too much N2(+) ionization, the N2(+) reaction with O and the chemistry of metastable (N(+) ions and of O2(+) ions are objects of study on Spacelab 1

Photoelectron Flux Build-Up in the Plasmasphere

Processes which confine photoelectrons to the plasmasphere (e.g., collisional backscattering from the thermosphere and magnetic trapping due to pitch angle redistribution through Coulomb collisions in the plasmasphere) tend to increase the steady state photoelectron flux in the plasmasphere above the amplitude level that would otherwise have been attained. Theoretical calculations are presented of steady state photoelectron fluxes in the plasmasphere, for specified atmospheric and ionospheric conditions. (Observational plasma line intensity data for these conditions exist and will be compared elsewhere.) General features of the angular distribution are presented and compared with observations. The transparency of the plasmasphere and the backscattering properties of the thermosphere are investigated. The buildup effect due to collisional backscatter alone is calculated, and the combined buildup effect of pitch angle diffusion and backscatter is estimated. It is found that the inclusion of these effects increases the steady state photoelectron flux amplitude in the plasmasphere by about 50% over the value obtained when the buildup effects are neglected. The calculated steady state photoelectron fluxes in the plasmasphere are in good agreement with the available observations

Rates of fixation by lightning of carbon and nitrogen in possible primitive atmospheres

A thermochemical-hydrodynamic model of the production of trace species by electrical discharges has been used to estimate the rates of fixation of C and N by lightning in the primitive atmosphere. Calculations for various possible mixtures of CH 4 , CO 2 , N 2 , H 2 , and H 2 O reveal that the prime species produced were probably HCN and NO and that the key parameter determining the rates of fixation was the ratio of C atoms to O atoms in the atmosphere. Atmospheres with C more abundant than O have large HCN fixation rates, in excess of 10 17 molecules J −1 , but small NO yields. However, when O is more abundant than C, the NO fixation rate approaches 10 17 molecules J −1 while the HCN yield is small. The implications for the evolution of life are discussed.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43346/1/11084_2004_Article_BF00931483.pd

Stratospheric chemistry: Multiple solutions

It is shown that the equations describing chemical partitioning among Clx (HCl, Cl, ClO, ClNO3), NOt (NO, NO2, NO3, N2O5, HNO2, ClNO3) and HOx (OH, HO2) may admit multiple solutions. These solutions apply to the high latitude winter stratosphere where abrupt spatial variations may be expected for NO2, ClO and ClNO3