Also Flow injection analysis

See also Flow Injection Analysis Principles. Sensors Overview Amperometric Oxygen Sensors Calorimetric/ Enthalpimetric Chemically Modified Electrodes Microorganism-Based Photometric. 

Flow injection analysis has also found numerous applications in the analysis of clinical samples, using both enzymatic and nonenzymatic methods. A list of selected examples is given in Table 13.3. 

Immunosensors promise to become principal players ia chemical, diagnostic, and environmental analyses by the latter 1990s. Given the practical limits of immunosensors (low ppb or ng/mL to mid-pptr or pg/mL) and their portabiUty, the primary appHcation is expected to be as rapid screening devices ia noncentralized clinical laboratories, ia iatensive care faciUties, and as bedside monitors, ia physicians offices, and ia environmental and iadustrial settings (49—52). Industrial appHcations for immunosensors will also include use as the basis for automated on-line or flow-injection analysis systems to analyze and control pharmaceutical, food, and chemical processing lines (53). Immunosensors are not expected to replace laboratory-based immunoassays, but to open up new appHcations for immunoassay-based technology. 

Since 1970, new analytical techniques, eg, ion chromatography, have been developed, and others, eg, atomic absorption and emission, have been improved (1—5). Detection limits for many chemicals have been dramatically lowered. Many wet chemical methods have been automated and are controlled by microprocessors which allow greater data output in a shorter time. Perhaps the best known continuous-flow analy2er for water analysis is the Autoanaly2er system manufactured by Technicon Instmments Corp. (Tarrytown, N.Y.) (6). Isolation of samples is maintained by pumping air bubbles into the flow line. Recently, flow-injection analysis has also become popular, and a theoretical comparison of it with the segmented flow analy2er has been made (7—9). 

Another interesting, but rather complex system, which couples flow injection analysis, EC and GC has been recently reported (47). This system allows the determination of the total amount of potentially carcinogenic polycyclic aromatic compounds (PACs) in bitumen and bitumen fumes. This system could also be used for the analysis of specific PACs in other residual products. 

Enzyme linked electrochemical techniques can be carried out in two basic manners. In the first approach the enzyme is immobilized at the electrode. A second approach is to use a hydrodynamic technique, such as flow injection analysis (FIAEC) or liquid chromatography (LCEC), with the enzyme reaction being either off-line or on-line in a reactor prior to the amperometric detector. Hydrodynamic techniques provide a convenient and efficient method for transporting and mixing the substrate and enzyme, subsequent transport of product to the electrode, and rapid sample turnaround. The kinetics of the enzyme system can also be readily studied using hydrodynamic techniques. Immobilizing the enzyme at the electrode provides a simple system which is amenable to in vivo analysis. 

The determination of lead in blood is the most widespread clinical use of ASV The technique is attractive because it is rapid, simple and reproducible A recent advance is to couple ASV to flow injection analysis in order to automate the process so that smaller samples and shorter analysis time can be achieved Lead is also routinely determined in bonemeal meant for human consumption by ASV Both lead and cadmium are determined in agricultural crops by ASV... 

Sample preparation, injection, calibration, and data collection, must be automated for process analysis. Methods used for flow injection analysis (FLA) are also useful for reliable sampling for process LC systems.1 Dynamic dilution is a technique that is used extensively in FIA.13 In this technique, sample from a loop or slot of a valve is diluted as it is transferred to a HPLC injection valve for analysis. As the diluted sample plug passes through the HPLC valve it is switched and the sample is injected onto the HPLC column for separation. The sample transfer time typically is determined with a refractive index detector and valve switching, which can be controlled by an integrator or computer. The transfer time is very reproducible. Calibration is typically done by external standardization using normalization by response factor. Internal standardization has also been used. To detect upsets or for process optimization, absolute numbers are not always needed. An alternative to... 

The 1/16" x 0.02" i.d. transfer line also functioned as a sample dilution device in other applications, a stainless steel column packed with glass beads has been found to be useful for dilution. This simple dynamic dilution technique has been used extensively in flow injection analysis.3 A refractive index detector is typically used to measure the sample transfer time. As shown in Figure 4, approximately 5 minutes is required to transfer the sample plug to the Rheodyne valve. As the apex of the sample band passes though the Rheodyne valve, the valve is activated and 1 pi injected onto the liquid chromatographic column. The sample transfer time was checked periodically over 1 year of operation and found to be stable. 

Progress has been made in developing electrochemical methods for detection of amino acids without derivatization.74 75 Evaporative light scattering (ELSD) is also a promising detection method.76 Flow-injection analysis... 

Vinas et al. [46] also determined penicillamine by chemiluminescence - flow injection analysis. The sample was dissolved in water, and a portion of resulting solution was introduced into an FIA system consisting of 5 mM luminol in 0.1 M KOH-boric acid buffer (pH 10.4), 50 pM Cu(II), and 10 mM H202 eluted at 7.2 mL/min. Chemiluminescent detection was used, the calibration graphs were linear from 0.1 to 10 mM of penicillamine, and the coefficients of variation were from 1.2% and 2.1%i. 

Most of the reported methods of analysis of valproic acid and its sodium salt in biological fluids rely on the use of chromatography, especially gas chromatography, although high performance liquid chromatography (HPLC) is also reported. Other methods, such as flow injection analysis, enzyme-immunoassay, fluorescence-polarization capillary electrophoresis, and potentiometry are sometimes used. The reported methods can be classified as follows. 

A new cholesterol flow injection analysis biosensor has also been described as an application of the H2O2 ECL sensor56. In that work, the luminol electrochemiluminescence, previously studied in aqueous media, was implemented in Veronal buffer added of 0.3% triton X-100 (v/v), 0.3% PEG and 0.4% cholate to enable the solubilisation of the cholesterol and then its efficient oxidation catalyzed by the immobilized cholesterol oxidase. The ECL reaction occurred thus in a micellar medium and the performances of the H2O2 ECL sensor were investigated. 

As shown, the system incorporates an integrated plate changer that accommodates plates for analysis as well as plates for collecting fractions of interest. Plates can be of different formats for sampling and collection, for example, a 384-well plate could be used for samples and a 96-well plate for collection (of course, the same plate type may be used for both sampling and collection). The system also incorporates a dedicated rinse station at the fraction collection end. The number of fractions and the time intervals for collection are defined by the user and automatically controlled by the software. In this way, analytes can be isolated and collected using /.tPLC. Collected fractions can, for example, be injected onto MS instrumentation with minimal cycle time by employing a flow injection analysis approach. 

The analytical techniques used for additives analysis are reviewed below. They are mainly chromatographic but enzymatic, flow injection analysis, inductively coupled plasma-atomic emission spectrometry and atomic absorption methods are also used. 

There is increasing interest in the use of specific sensor or biosensor detection systems with the FIA technique (Galensa, 1998). Tsafack et al. (2000) described an electrochemiluminescence-based fibre optic biosensor for choline with flow-injection analysis and Su et al. (1998) reported a flow-injection determination of sulphite in wines and fruit juices using a bulk acoustic wave impedance sensor coupled to a membrane separation technique. Prodromidis et al. (1997) also coupled a biosensor with an FIA system for analysis of citric acid in juices, fruits and sports beverages and Okawa et al. (1998) reported a procedure for the simultaneous determination of ascorbic acid and glucose in soft drinks with an electrochemical filter/biosensor FIA system. 

There has been significant advancement in the applications of NMR to the development of small-molecule pharmaceutical products. For example, advances in NMR automation (e.g., flow-injection analysis) and directly coupled methods (e.g., LC-MS-NMR analysis) have made analysis and characterization of small-molecule drugs much easier.23 25 These improvements have helped chemists to develop and characterize small-molecule combinatorial libraries and to screen for active compounds.4 6 It is likely some of these techniques can also be used in biopharmaceutical product development. 

These miniaturized sensors are suitable for flow-injection analysis [130]. Similar systems have also been used in portable instruments [56]. A micro-ISFET was constructed for intracellular determination of K [53]. 

As already discnssed, intrinsic LIF bioreactor monitoring is the most common application within biopharmaceutical manufacturing. Other extrinsic PAT LIF methods are also possible for biopharmacenticals snch as varions flnorescence immunoassays facilitated by flow injection analysis " or other real-time approaches. As PAT begins to emerge within biopharmaceuticals the wider used of sensitive and precise in-line intrinsic and extrinsic approaches such as optodes and at-line extrinsic methods is likely to occnr. ... 

Future developments that may facilitate ocean measurements from vessels or buoys include miniaturization of chromatographic equipment (so less solvent is needed per analysis), new solvent transport systems, such as electrokinetic transport, to reduce power requirements on the pumps, and more sensitive detectors for liquid chromatography. Certain combinations of very short columns and flow injection analysis are also promising for real-time studies. 

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