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Dilution system, serial

The chip micro reactor ([R 6]) was only one part of a complex serial-screening apparatus [20]. This automated system consists of an autosampler (CTC-HTS Pal system) which introduces the reactant solutions in the chip via capillaries. A pumping system (p-HPLC-CEC System) serves for fluid motion by hydro dynamic-driven flow. A dilution system [Jasco PU-15(5)] is used for slug dilution on-chip. The detection system was a Jasco UV-1575 and analysis was carried out by LC/MS (Agilent 1100 series capLC-Waters Micromass ZQ). All components were on-line and self-configured. [Pg.525]

The in vitro most antimicrobially active essential oils regularly (or normally) contain substances as main components, which are themselves known to exhibit pronounced antimicrobial properties. These are cinnamic aldehyde (cinnamon bark and cassia oil) and the phenolic compounds eugenol (clove and cinnamon leaf oil) and thymol (thyme oil) (Pauli, 2001). All these essential oils reveal a broadband spectrum of activity in various in vitro test systems (agar diffusion, dilution, and VP) due to their considerable water solubility and volatility. The evaluated antimicrobial inhibitory data of the essential oils obtained in agar dilution tests, serial DIL, and VP tests are summarized in Table 14.81. [Pg.608]

This is merely the ratio of final volume to original volume. If a serial dilution system has been used, / = the product of the individual dilution factors. [Pg.286]

Figure 4. Calibration curve for serial dilution of phenol in pH=7 buffered water at an instrument-to-analyte distance of 10 m, using the portable field system. Figure 4. Calibration curve for serial dilution of phenol in pH=7 buffered water at an instrument-to-analyte distance of 10 m, using the portable field system.
In the early stages of method development, when a suitable mobile phase has not yet been identified, the analyst will literally prepare nearly a 100 different mobile phases and plates to obtain the necessary separation. The HPTLC Vario Chamber system allows the user to take one HPTLC plate and cut it into six mini plates and expose them to six mini wells of mobile phase simultaneously. The analyst simply prepares a mixture of the components to be resolved and applies this solution to the six mini plates as a spot. This is a huge time saver since six mobile phases can be evaluated at a time and necessary dilutions can be serially prepared, (see Fig. 13.12). [Pg.428]

Finally, when the full set of chromatographic parameters are determined to be most suited for the proposed analysis, then the standards can be serially diluted to provide for a final estimation of the lower limit of detection with the system used. [Pg.410]

Figure 8.2. Comparison between actual and measured values for analyses results obtained by computer and manually. (Solutions prepared by serial dilution fixed amount of internal standard added. (7)) o. From minicomputer system, x. Triangulation procedure (manual). +, Peak height procedure (manual). Size of symbol indicates standard deviation. Figure 8.2. Comparison between actual and measured values for analyses results obtained by computer and manually. (Solutions prepared by serial dilution fixed amount of internal standard added. (7)) o. From minicomputer system, x. Triangulation procedure (manual). +, Peak height procedure (manual). Size of symbol indicates standard deviation.
The potential of the compound precipitating upon injection needs to be evaluated. This is particularly important for formulations containing cosolvent systems or formulations where the compound is solubilized via pH adjustment. In these cases, the solubility of the compound changes nonlinearly upon dilution and the compound may precipitate at the injection site (Yalkowsky and Rose man, 1981). Severalin vitro methods including static serial dilution, dynamic injection, and dropwise dilution have been successfully applied as a screening tool to detect the precipitation problem (Yalkowsky etal., 1983 V ferd and Yalkowsky, 1993 Ping etal., 1998). Details ofthese methods will be discussed in subsequent chapters. [Pg.87]

Deionised water from a Modulab system (Continental Water Systems, San Antonio, TX, USA) was used for all solutions. The S-captopril solutions were prepared from standard S-captopril solution (1(V2 mol/L) prepared in citrate buffer, pH 4.00, respectively, by serial dilutions. [Pg.990]

The dilution and mechanical agitation can be done by hand or by a machine. Manual preparation cannot be uniform in strength every time a vial is shaken. Machine is needed for the preparation of higher potencies like CM (diluted one hundred thousand times) and MM (diluted one million times). Hahnemann followed the duodecimal system, which was in vogue in his time, in choosing the potency numbers as 6, 12, 24 etc. Higher potencies like 200, 1M, CM, introduced later are based on the metric or decimal system in units. Besides decimal and centesimal series, based on serial dilution of 1 10 and 1 100, respectively, there exists the millesimal series which is based on the serial dilution of 1 1000 and is denoted with the suffix m (Cook, 1988). [Pg.6]

Cheng, S.B., Skinner, C.D., Harrison, D.J., Integrated serial dilution on a microchip for immunoassay sample treatment and flow injection analysis. Micro Total Analysis Systems 98, Proceedings pTAS 98 Workshop, Banff, Canada, 13-16 Oct. 1998, 157-160. [Pg.429]

In 1970, Eckman et al. devised the automation of a quantitative immunochemical analysis of transferrin (El). In this automated flow system, diluted samples were allowed to react with antitransferrin antiserum serially and the degree of light scattering of the resulting turbidity was measured in the fluorometer, used as a nephelometer. The optimal conditions for nephelometry were extensively studied. Subsequently, Buffone reported... [Pg.88]

Toxicant delivery systems are used to deliver, on a once-through basis, the various test concentrations to the test chambers in continuous-flow toxicity tests. The serial proportional diluter is the most common design used to mix the dilution water with the test substance to produce the desired test concentrations. The construction materials in toxicant delivery systems, like those for the test chambers, should not be rubber, certain plastics, or metallic materials. [Pg.2626]

The three ISE setups each required their own system solutions and calibrators which were purchased from the respective manufacturers. A stock solution of 50 mM LiCl in deionized water was serially diluted in lithium-free fresh human serum to test the linearity of the Cobas Integra 700 ISE method. The tested concentration range was from 0.06 mmol/l to 4.01 mmol/l of lithium. LiCl, p.a. 99% purity, was purchased from Merck (Germany). [Pg.103]

The Hewlett-Packard (HP) 7686 PrepStation System workstation allows you to write a program that will condition, load, rinse, and elute your SPE columns (Fig. 10.4, Table 10.4). A dedicated DOS-based ChemStation computer system by HP is required to run the instrument. The software uses a Menu Selectable Approach. The instrument operates in a serial mode and works with HP s disposable SPE cartridges. Individual flow rates for condition, load, rinse, and elute are selected. The workstation may be used to perform volumetric dilutions, sample mixing, bar-code reading, evaporation, and derivatization. When used with an HP 1050 HPLC or HP 5890 GC direct injections are possible. The instrument is also available in a stand-alone... [Pg.251]

Results from serial dilutions of E. herbicola assayed by AK in the integrated fluidic device in comparison with the manual luminometer are shown in Fig. 2. Results from dilution buffer blanks plus 2 standard deviations are shown to allow comparison of the backgrounds in the two systems. [Pg.225]

The standards and samples (n = 6) were analysed by using a Perkin Elmer 100 FAAS system with an air-acetylene flame. The metals were determined at the following wavelengths Cu, 324.8 nm Fe, 248.3 nm Pb, 217.0 nm Mn, 279.5 nm Ni, 232.0 nm Zn, 213.9 nm. Calibrations were produced by serial dilution of 1000 igml-1 stock solutions in the range 0-10 xgml-1. All calibration graphs exhibited linear relationships for each metal, except zinc, i.e. y = mx + c. For zinc, a curved relationship was obtained, i.e. y = ax2 +bx + c. All correlation coefficients were >0.96. [Pg.92]

Sample dilution is one of the most labor-intensive tasks in running an LBA. Add standard curve and quality control dilution (which these systems can easily do) [8], and it becomes over half the effort to run an assay. Depending on the specific practices of a laboratory, samples can be diluted in duplicate, triplicate, at four serial dilutions, at eight serial dilutions, with one or more sample diluents, at different dilutions for each sample, and from different size tubes (e.g., clinical versus nonclinical). Similarly, standard curve and control dilutions can be performed in a variety of ways. For these reasons, it can be challenging to implement an automated dilutor to meet all of these requirements. [Pg.307]

The issue is then to devise a system that will allow lipophilic materials to disperse in an aqueous environment using a solvent that does not interfere with antimicrobial activity. Dimethylformamide (DMF) and dimethylsulfoxide (DMSO) are two solvents that appear to be able to achieve this. Some authors have incorporated essential oils into DMSO, adding an aliquot into growth medium followed by serial dilutions in growth medium. This method causes both the active material and the solvent to be serially reduced. A better approach might be to dissolve the essential oils in solvent first, make serial dilutions in the same solvent, and then add aliquots to the growth medium. In this way, all the tubes contain the same amount of solvent. Our proposed protocol is the following ... [Pg.597]


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