| Partner: Paweł Jankowski |
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Ostatnie publikacje
| 1. | Korczyk P.M., Dolega M.E.♦, Jakieła S.♦, Jankowski P.♦, Makulska S.♦, Garstecki P.♦, Scaling up the throughput of synthesis and extraction in droplet microfluidic reactors, Journal of Flow Chemistry, ISSN: 2062-249X, DOI: 10.1556/JFC-D-14-00038, Vol.5, No.2, pp.110-118, 2015 Streszczenie: Conducting reactions in droplets in microfluidic chips offers several highly attractive characteristics, among others, increased yield and selectivity of chemical syntheses. The use of droplet microfluidic systems in synthetic chemistry is, however, hampered by the intrinsically small throughput of micrometric channels. Here, we verify experimentally the potential to increase throughput via an increase of the scale of the channels.We use the results of these experiments characterizing the processes of (1) generation of droplets, (2) mixing in droplets, (3) inter-phase extraction, and (4) the yield of synthesis of pyrrole, to postulate a number of guidelines for scaling up the throughput of microfluidic droplet systems. In particular, we suggest the rules for maximizing the throughput via an increase of the size of the channels and via parallelization to optimize the throughput of synthesis against the cost of fabrication of the chips and against the kinetic requirements of specific reactions. Słowa kluczowe: flow chemistry, microfluidics, synthesis, emulsions, droplets Afiliacje autorów:
|  | 30p. | |||||||||||||||||||||
| 2. | Samborski A.♦, Jankowski P.♦, Węgrzyn J.♦, Michalski J.A.♦, Pawłowska S., Jakieła S.♦, Garstecki P.♦, Blood diagnostics using sedimentation to extract plasma on a fully integrated point-of-care microfluidic system, Engineering in Life Sciences, ISSN: 1618-0240, DOI: 10.1002/elsc.201400077, Vol.15, No.3, pp.333-339, 2015 Streszczenie: Blood is the richest source of diagnostic information. The growing interest in point-of-care analytics prompted several attempts to extract plasma from whole blood in simple diagnostic devices. The simplest method of separation is sedimentation. Here we show the first microfluidic system that uses sedimentation to extract plasma from undiluted blood and integrates execution of liquid assays on the extracted material. We present a microfluidic chip that accepts a small sample (27 μL) of whole blood, separates up to 6 μL of plasma, and uses metered volumes of plasma and of reagent (2-chloro-4-nitrophenyl-α-maltotrioside, CNP-G3) for a liquid enzymatic assay. With a custom designed channel, the system separates blood by sedimentation within few minutes of accepting the sample, mixes it with the reagent, and quantifies spectrophotometrically the product of the enzymatic reaction. As a model demonstration, we show a quantitative enzymatic α-amylase assay that is routinely used in diagnosis of pancreas diseases. The paper reports the design and characterization of the microfluidic device and the results of tests on clinically collected blood samples. The results obtained with the microfluidic system compare well to a reference bench-top analyzer. Afiliacje autorów:
| | 25p. |