8 research outputs found

    Microfluidic device for robust generation of two-component liquid-in-air slugs with individually controlled composition

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    Using liquid slugs as microreactors and microvessels enable precise control over the conditions of their contents on short-time scales for a wide variety of applications. Particularly for screening applications, there is a need for control of slug parameters such as size and composition. We describe a new microfluidic approach for creating slugs in air, each comprising a size and composition that can be selected individually for each slug. Two-component slugs are formed by first metering the desired volume of each reagent, merging the two volumes into an end-to-end slug, and propelling the slug to induce mixing. Volume control is achieved by a novel mechanism: two closed chambers on the chip are initially filled with air, and a valve in each is briefly opened to admit one of the reagents. The pressure of each reagent can be individually selected and determines the amount of air compression, and thus the amount of liquid that is admitted into each chamber. We describe the theory of operation, characterize the slug generation chip, and demonstrate the creation of slugs of different compositions. The use of microvalves in this approach enables robust operation with different liquids, and also enables one to work with extremely small samples, even down to a few slug volumes. The latter is important for applications involving precious reagents such as optimizing the reaction conditions for radiolabeling biological molecules as tracers for positron emission tomography

    Microfluidics for Positron Emission Tomography Probe Development

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    Owing to increased needs for positron emission tomography (PET), high demands for a wide variety of radiolabeled compounds will have to be met by exploiting novel radiochemistry and engineering technologies to improve the production and development of PET probes. The application of microfluidic reactors to perform radiosyntheses is currently attracting a great deal of interest because of their potential to deliver many advantages over conventional labeling systems. Microfluidics-based radiochemistry can lead to the use of smaller quantities of precursors, accelerated reaction rates, and easier purification processes with greater yield and higher specific activity of desired probes. Several proof-of-principle examples along with the basics of device architecture and operation and the potential limitations of each design are discussed. Along with the concept of radioisotope distribution from centralized cyclotron facilities to individual imaging centers and laboratories (“decentralized model”), an easy-to-use, stand-alone, flexible, fully automated, radiochemical microfluidic platform can provide simpler and more cost-effective procedures for molecular imaging using PET

    Ionic Strength and Solvent Control over the Physical Structure, Electronic Properties and Superquenching of Conjugated Polyelectrolytes Electronic Properties of Conjugated Polyelectrolytes

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    Abstract: In this paper, we investigate the photophysical properties of the conjugated polyelectrolyte poly(2-methoxy-5-propyloxy sulfonate phenylene vinylene), MPS-PPV, dissolved in both water and DMSO as a function of the solution ionic strength. Dynamic light scattering indicates that MPS-PPV chains exist in a highly agglomerated conformation in both solvents, and that the size of the agglomerates depends on both the ionic strength and the charge of the counterion. Even though the degree of agglomeration is similar in the two solvents, we find that the fluorescence quantum yield of MPS-PPV in DMSO is nearly 100 times greater than that in water. Moreover, intensity-dependent femtosecond pump-probe experiments show that there is a significant degree of exciton-exciton annihilation in water but not in DMSO, suggesting that the MPS-PPV chromophores interact to form interchain electronic species that quench the emission in water. Given that the emission quenching properties depend sensitively on the chain conformation and degree of chromophore contact, we also explore the superquenching properties of MPS-PPV in the two solvents as a function of ionic strength. We find that superquenching may be either enhanced or diminished in either of the solvents via addition of simple salts, and we present a molecular picture to rationalize how the conformational properties of conjugated polyelectrolytes can be tuned to enhance their emissive behavior for sensing applications
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