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On-line Determination (on-line + determination)
Selected AbstractsOn-line Determination of Aggregate Size and Morphology in SuspensionsPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 3 2004Frédéric Gruy Abstract Information concerning the aggregation state of fine solid particles is an important element for process control and monitoring of product quality in many applications of industrial slurries. This work deals with the application of different in-line methods to the characterization of silica aggregate size and morphology. All of these methods exploit turbidity signals, obtained by various means including: from analysis of turbidity fluctuations in homogeneous suspension and from overall turbidity decrease during particle settling. This work also presents the opportunity to report progress in morphological and optical models of small aggregates. As a result of these models, the morphological characteristics of the aggregates along with the number of their constituting particles are derived from experimental results. Similarities between the different methods are examined and discussed. [source] Applications of PAT-Process Analytical Technology in Recombinant Protein Processes with Escherichia coliENGINEERING IN LIFE SCIENCES (ELECTRONIC), Issue 2 2008C. Kaiser Abstract Monitoring of bioprocesses and thus observation and identification of such processes is one of the main aims of bioprocess engineering. It is of vital importance in bioprocess development to improve the overall productivity by avoiding unintentional limitations to ensure not only optimal process conditions but also the observation of established production processes. Furthermore, reproducibility needs to be improved and final product quality and quantity be guaranteed. Therefore, an advanced monitoring and control system has been developed, which is based on different in-line, on-line and at-line measurements for substrates and products. Observation of cell viability applying in-line radio frequency impedance measurement and on-line determination of intracellular recombinant target protein using the reporter protein T-Sapphire GFP based on in-line fluorescence measurement show the ability for the detection of critical process states. In this way, the possibility for the on-line recognition of optimal harvest times arises and disturbances in the scheduled process route can be perceived. [source] Nondestructive Assessment of Lipid Oxidation in Minced Poultry Meat by Autofluorescence SpectroscopyJOURNAL OF FOOD SCIENCE, Issue 1 2000J.P. Wold ABSTRACT: To develop a rapid method to assess lipid oxidation, autofluorescence spectra (excitation wavelengths 365, 380, and 400 nm) from large samples (17 cm2) of minced poultry meat were collected by an optical system to determine directly lipid oxidation level. The same samples were also measured by 2-thiobarbituric acid method (TBARS). High correlations could be made between the TBARS method and autofluorescence spectra, especially those from 380 nm excitation. Partial least squares regression resulted in a root mean square error of 0.15 (R = 0.87) for chicken meat and 0.24 (R = 0.80) for mechanically recovered turkey meat. Classification analysis between fresh (TBARS < 0.25) and rancid (TBARS > 0.25) samples was done with high success rates. Autofluorescence spectroscopy might be well suited for rapid on-line determination of lipid oxidation level in minced poultry meat. [source] Direct analysis of 15N-label in amino and amide groups of glutamine and asparagineJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 2 2007Anne Marie Scharff-Poulsen Abstract A novel method for on-line determination of the amount and position of 15N-labeling in complex mixtures of amino acids is presented. Underivatized amino acids were analyzed by ion-pair chromatography in combination with mass spectrometry. This enables the direct determination of the 15N label distribution. The fragmentation pathways of the nitrogen moieties of glutamine (Gln) and asparagine (Asn) were studied in detail using all mono 15N isotopomers, which led to a method for differentiating between 15N-amide and 15N-amino labeling. The fragmentation involving the amino and amide groups of Gln led to distinct ion structures. The equivalent fragmentation pattern was not observed for Asn. Instead, the amide group of Asn was eliminated as HNCO in a secondary process. The developed analytical method was evaluated by analysis of a range of standard mixtures taking into account different levels of 15N abundance and distribution between the amino and amide groups. The detection limit (3 SD) for the presence of a 15N label was 0.7 and 1.0% for Gln and Asn, respectively. The determination of the positional labeling follows a nonlinear function. A representative example at 30% 15N was used as a benchmark resulting in average relative standard deviations of 2.7 and 15% for Gln and Asn, respectively. The corresponding expectation windows for the positional labeling were found to be 2 and 12%, respectively. Copyright © 2006 John Wiley & Sons, Ltd. [source] Evaluation of Process-Induced Dimensional Changes in the Membrane Structure of Biological Cells Using Impedance MeasurementBIOTECHNOLOGY PROGRESS, Issue 3 2002Alexander Angersbach The impact of high intensity electric field pulses, high hydrostatic pressure, and freezing-thawing on local structural changes of the membrane was determined for potato, sugar beet tissue, and yeast suspensions. On the basis of the electrophysical model of cell systems in biological tissues and suspensions, a method was derived for determining the extent of local damage of cell membranes. The method was characterized by an accurate and rapid on-line determination of frequency-dependent electrical conductivity properties from which information on microscopic events on cellular level may be deduced. Evaluation was based on the measurement of the relative change in the sampleapos;s impedance at characteristically low ( fl) and high ( fh) frequencies within the ,-dispersion range. For plant and animal cells the characteristic frequencies were fl , 5 kHz and fh > 5 MHz and for yeast cells in the range fl , 50 kHz and fh > 25 MHz. The observed phenomena were complex. The identification of the underlying mechanisms required consideration of the time-dependent nature of the processing effects and stress reactions of the biological systems, which ranged from seconds to several hours. A very low but significantly detectable membrane damage (0.004% of the total area) was found after high hydrostatic pressure treatment of potato tissue at 200 MPa. The membrane rupture in plant tissue cells was higher after freezing and subsequent thawing (0.9% of total area for potato cells and 0.05,0.07% for sugar beet cells determined immediately after thawing), which increased substantially during the next 2 h. [source] Determination of the enantiomeric excess of an M3 antagonist drug substance by chemometric analysis of the IR spectra of different guest-host complexesCHIRALITY, Issue 5 2006Lili Zhou Abstract A novel approach for the potential on-line determination of the enantiomeric excess (ee) of an M3 antagonist drug substance combining attenuated total reflectance infrared (ATR-IR) spectroscopy, guest-host complexes, and chemometric data analysis is described. Chiral recognition through a formation of diastereomeric complexes was measured by ATR-IR. Small changes on the IR spectra reflect the interaction between the guest (M3) and host (chiral selector). These changes are measured as a function of M3 enantiomer excess. The standard error of prediction is 1.3 ee%. The prediction results based on the IR method were in good agreement with the gravimetric method. The robustness of the calibration model was evaluated by varying the concentration of the chiral selector, the pH of the solution, and the organic solvents. The stability of the calibration model was also demonstrated through measuring different sets of samples on different days. Chirality, 2006. © 2006 Wiley-Liss, Inc. [source] | |||||||||||||