Micro sequential injection: fermentation monitoring of ammonia, glycerol, glucose, and free iron using the novel lab-on-valve system.

Using an integrated lab-on-valve manifold in a microfluidic sequential injection format (microSI), automated sample processing has been developed for off-line and on-line monitoring of small-scale fermentations. Spectrophotometric assays of ammonia, glucose, glycerol, and free iron were downscaled to use micro-quantities of commercial reagents. By monitoring the reaction rate, the response curves in a stopped-flow mode generate linear calibration curves for ammonia [r2 = 1.000 (0.9% SE)], glycerol [r2 = 0.999 (1.1% SE)], glucose [r2 = 0.999 (1.1% SE)], and free iron [r2 = 0.999 (1.5% SE)]. Since sample dilution and reagent quantities are easily adjusted within the programmable SI format, the lab-on-valve system can accommodate samples over a wide concentration range (ammonia: 3-1200 ppm; glycerol: 20-120 ppm; glucose: 35-1000 ppm; and free iron: 80-400 ppm). This work demonstrates the key advantages of miniaturization through the reduction of sample and reagent use, minimizing waste and providing a compact yet reliable instrument. The lab-on-valve manifold uses a universal hardware configuration for all analyses, only requiring changes in software protocol and choice of reagents. All of these features are of particular importance to small-scale experimental fermentation where multiple analyte analyses are needed in real-time using small sample volumes. It is hoped that this first real-life application of the lab-on-valve manifold will serve not only as a model system to downscale assays in a practical fashion, but will also inspire and promote the use of the integrated microSI manifold approach for a wider range of biotechnological applications.

Detection of oxygen consumption of cultured adherent cells by bead injection spectroscopy.

This paper describes a method for detecting oxygen consumption of adherent cell cultures. The sensing is based on oxygen-dependent quenching of the phosphorescence of a Pt-porphyrin complex immobilized on microcarrier beads, which are used as the cell culture substrate. Bead injection, a recent variant of the flow injection technique, is used to pack an aliquot of the beads into a small sensing layer that can be easily and rapidly renewed. The technique is tested on a model system of Chinese Hamster Ovary M1 cells grown on Cytodex-3 microcarrier beads. Cellular respiration is monitored through O2 consumption measured across a period of 3 min. The method is validated by detecting the impairment of aerobic metabolism caused by 1.5 mM amobarbital. Further, it is shown to have enough precision to distinguish even more subtle changes, such as the increase in oxygen consumption caused by stimulation of the muscarinic m1 receptor with 100 microM carbachol.

Automation of functional assays by flow injection fluorescence microscopy.

Bead-injection spectroscopy is a novel technique that uses immobilized eukaryotic cells on microbeads as a renewable biosensor for fluorescence microscopy. The use of a flow injection instrument allows fast functional assays that generate full kinetic characterization of a drug. Because the cell population is automatically replaced for each assay, variability is minimized, thus allowing greater accuracy.

Experimental study of kinematic focusing. Comparison of electroinjection and sequential injection determination of copper.

The recently predicted phenomenon of kinematic focusing was studied experimentally using copper ions and EDTA as reactants. Kinematic focusing occurs, in electroinjection analysis, when the detected reaction product moves at the same rate as the reagent present in excess. Thus, reaction product accumulates without dispersion at the front of the excess reagent. Cu-EDTA(2-) complex was observed at 254 nm to form an exceptionally sharp peak as the front of the EDTA zone passed by the detector. The concentrating effect of kinematic focusing was quantified by electroinjection of premixed Cu-EDTA(2-). Sensitivity was compared to that of sequential injection analysis using a 1 cm optical pathlength. Sensitivity was highest in the electroinjection mode, in spite of its 120 mum capillary pathlength, due to kinematic focusing.

Hydrodynamics and mass transfer of the coaxial jet mixer in flow injection analysis.

A coaxial jet mixer that was previously proposed for rapid and efficient mixing under laminar flow conditions has been studied both theoretically and experimentally. A mathematical model that consists of a set of Navie-Stokes equations that determine the flow velocities and three diffusion-convection reaction equations that determine the reactant and product concentrations has been developed. Equations are solved with the help of finite difference techniques for different flow conditions. The quality of sample and reagent mixing is characterized by the mean product concentration and the amount of product produced. Theoretical results are compared with experimental ones for the mixing of bromothymol blue (a pH indicator) in the outer capillary with NaOH in the inner capillary of the jet mixer.

Coaxial flow mixer for real-time monitoring of cellular responses in flow injection cytometry.

Improved time resolution of kinetic cellular events in flow cytometry is demonstrated by using a coaxial flow-mixing device integrated within a flow-injection (FI) system. The instrument is used in combination with a Becton Dickinson FACS Analyzer for on-line reagent addition, rapid sample mixing, and temperature control of cell suspensions. The coaxial flow device can instantaneously (< 60 ms) mix reagent and sample streams, allowing cytometric analysis of subsecond events to be performed. Kinetic measurements can be performed on the FACS analyzer in a variable time range of from 100 ms to 3 min. The system also allows the collection of unlimited cellular events at a specific incubation time point. Because the system operates continuously and no boost in core flow is required, disturbances of flow conditions are avoided. The capabilities of the flow injection cytometer have been demonstrated by the determination of internal [Ca2+]i mobilization in Jurkat T lymphocytes perfused internally with INDO-1 and stimulated by ionomycin.

A coaxial jet mixer for rapid kinetic analysis in flow injection and flow injection cytometry.

A simple coaxial jet mixer for rapid and efficient confluent mixing under laminar flow conditions (Re < 5) is described. This device demonstrates exceptional control of mixing between two laminar streams by creating shear forces due to variable flow velocities at the point of confluence. It is suitable for flow injection and cytometric analyses of rapid kinetic events which require contact mixing of two solutions and subsecond measurements of the evolving reaction. This apparatus was devised for flow injection cytometry as performed on a Becton Dickinson FACS Analyzer. Under normal cytometric conditions and at a sample introduction rate of 60 microL/min, the laminar jet mixer is capable of complete mixing of two solutions within 55 ms. Kinetic measurements can be performed on the FACS Analyzer in a variable time range of 100 ms to 3 min with 14-30 ms temporal resolution of the studied event. Since no boost in core flow is required, potential spectral distortions due to core flow variations are eliminated. This coaxial jet mixer can be easily constructed and employed on a variety of cytometers as well as conventional flow injection analysis systems, since it is an effective mixer under most flow conditions.

Fast kinetic measurements and on-line dilution by flow injection cytometry.

An improved flow injection cytometry (FIC) system suitable for fast cellular kinetic measurements and on-line dilution is described. The instrument allows for measurements from 1.2 s (+/- 0.05 s) after the initiation of mixing, up to any time thereafter. Crucial factors in determining fast kinetic measurements, such as the displacement volume for sample introduction, rate of transport to cytometric interrogation point, and the mixing speed are evaluated and discussed. By varying the volume aspirated, this instrument can facilitate the dilution of cells and/or reagent over a range of one order of magnitude. The fast kinetic and on-line dilution capabilities were demonstrated by on-line staining of DNA in trout erythrocytes with 4',6-diamidino-2-phenylindole (DAPI). The utility of the instrument for measurement of enzyme kinetics was illustrated using human lymphocytes, measuring the glutathione S-transferase (GST) catalyzed reaction between monochlorobimane (MCB) and glutathione (GSH).