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DR-CALUX

Site no. MSP Mutatox DR-CALUX (with clean-up dry sediment) Pore water ER-CALUX on polar fraction sediment YES on 10 X diluted sediment... [Pg.25]

Intra- and interlaboratory calibration of the DR CALUX bioassay for the analysis of dioxins and dioxin-like chemicals in sediments... [Pg.37]

The infralaboratory calibration study was performed by the Institute for Environmental Studies. Sediment was extracted and cleaned up as indicated here. The determination of dioxin and/or dioxin-like content was according to the method indicated under the section DR CALUX analysis. For the intralaboratory study, the following parameters were investigated limit of detection (LOD), limit of quantitation (LOQ), and reproducibility and repeatability of the bioassay. [Pg.40]

Phase 2. In the seeond phase of the study, the partieipants were asked to analyze three extraeted and cleaned sediment samples using the DR CALUX bioassay. Sediments used for extraetion and cleanup were freshwater sediments from the Western Seheldt, The Netherlands. The sediment extracts were prepared by the Royal Institute for Fishery Research (RIVODLO), IJmuiden, The Netherlands, aeeording to the protoeol given here. Dilutions of the supplied sediment extracts were prepared by the partieipants in DMSO and tested for dioxin and/or dioxinlike content. On each 96-well mierotiter plate, a 2,3,7,8-TCDD standard ealibration curve was analyzed. Raw data as well as eonverted data were used for statistieal evaluation. [Pg.41]

Defined standard solutions. The two defined standard solutions were prepared by dissolving either 2,3,7,8-TCDD or 2,3,7,8-TCDD, PCB 126, and PCB 169 in DMSO. The 2,3,7,8TCDD standard solution contained 2,3,7,8-TCDD in DMSO at a concentration of 7.5 nM. Sample 2 contained a mixture of 2,3,7,8 TCDD, PCB 126, and PCB 169 at concentrations of 5.0, 25, and 250 nM, respectively. The total 2,3,7,8-TCDD TEQ content of this mixture was calculated using both World Health Organization (Paris, France) WHO-TEF values and DR CALUX-relative potency (REP) values (Hosoe et al, 2002) and found to be 10 and 7.5 nM 2,3,7,8-TCDD TEQ, respectively. Overall, 27 individual measurements per sample and per participant were available for data analysis. [Pg.41]

On each 96-well microtiter plate, a eomplete 2,3,7,8-TCDD standard concentration range was incubated and analyzed in triplieate. A eurve fit of the 2,3,7,8-TCDD standard range was produced for the calculation of DR CALUX TEQ content in the samples tested. The analyzed relative light units (RLU) from the samples were interpolated on the 2,3,7,8-TCDD standard curve, and the DR CALUX TEQ content was quantified between the limit of quantitation (LOQ) and the concentration of 2,3,7,8-TCDD at whieh 50% of the maximum response is observed (EC50). [Pg.42]

For the determination of the limit of detection (LOD) and LOQ, 10 standard 2,3,7,8-TCDD calibration series were analyzed in triplicate using the DR CALUX bioassay. In Figure 1, a typical example of a standard 2,3,7,8-TCDD calibration curve is given. For each individual calibra-... [Pg.43]

For the determination of the repeatability, two sediments originating from coastal areas along the Duteh eoastline were extracted and cleaned up. One ofthe sediments had a low 2,3,7,8-TCDD TEQ eontent, whereas the second sediment had a relatively high 2,3,7,8-TCDD TEQ eontent (4.8 and 26 pg 2,3,7,8-TCDD TEQ/g sediment, respectively). The 2,3,7,8-TCDD TEQ eontent in both extracts was determined by DR CALUX analysis 10 times on the same day. The reprodueibility was determined by analyzing a 3-pM 2,3,7,8-TCDD standard and a cleaned sediment extraet. Both samples were analyzed on 10 different days and by various persons. The results are summarized in Table 1. [Pg.44]

Both the EC50 values and the 3-pM point of the 2,3,7,8TCDD ealibration curve serve as quality criteria. For each participant, the results for both data points from all 96-well plates analyzed during the presented study were collected and reeorded in Shewhart control charts. The Shewhart control chart is used to identify variations on performanee of the DR CALUX bioassay brought about by unexpected or unassigned causes. The Shewhart eontrol chart shows the mean of the EC50 and 3-pM control point and the upper and lower eontrol limits. In Figure 2, a typical Shewhart control chart is shown. Over the analysis period, none of the participants exceeded the aetion levels (AVG 3 S). [Pg.44]

Phase 1 Defined standard solutions. Partieipants were asked to measure the response of the two standard samples in the DR CALUX bioassay three times in triplicate. The total DR CALUX 2,3,7,8-TCDD TEQ content of both the 2,3,7,8TCDD sample as well as the mixed sample was calculated to be 7.5 uM TEQ. Since the DMSO eontent during exposure was 0.4% and the samples were diluted seven times by all partieipants, the expected DR CALUX TEQ... [Pg.44]

Table 1 Intralaboratory repeatability and reproducibility of the dioxin response-chemically activated lucerferase (DR CALUX ) bioassay for sediment extracts 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) TEQ = toxic equivalent. Table 1 Intralaboratory repeatability and reproducibility of the dioxin response-chemically activated lucerferase (DR CALUX ) bioassay for sediment extracts 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) TEQ = toxic equivalent.
In addition to the sediment extraets, all participants received a procedure blank. The procedure blank is analyzed to eheek for possible eontamination from chemicals and materials used during extraction and/or cleanup. DR CALUX analysis results from this procedure blank for all participants were below the limit of quantitation (1 pM 2,3,7,8-TCDD TEQ/well) and therefore eomply with the DR CALUX performanee eriteria (data not shown). [Pg.46]

Calibration curves were made with a dioxin standard and were used to eonvert DR CALUX response levels to concentrations expressed as 2,3,7,8-TCDD TEQs. The seetion of the 2,3,7,8-TCDD calibration curve between the LOQ (1 pM) and the EC50 is used to quantify DR CALUX analysis results. This section is not linear (see Fig. 1). However, when the ealibration eurve is plotted on a linear-linear scale, the indicated region can be regarded as linear. In addition, the region between the LOQ and EC50 is chosen for quantifieation of analysis results sinee this region of the 2,3,7,8-TCDD calibration curve is least sensitive to variations in observed DR CALUX activity. [Pg.47]

Table 4 Dioxin responsive-chemically activated lucerferase (DR CALUX ) repeatability and reproducibility for the bioanalysis of the defined standard solutions and sediment samples of the various phases of the present interlaboratory validation study. [Pg.48]

The aim of the present study was to identify the DR CALUX bioassay performance criteria for the analysis of PHAHs in sediment samples in order to implement the bioassay in the assessment of dredged materials for systematic monitoring in the eoming years. Therefore, both an intra-and interlaboratory validation study was performed. [Pg.49]

Beeause the 2,3,7,8-TCDD calibration curve is used for quantification of analysis results, the stability and quality of the calibration curves is important. Furthermore, the calibration curves themselves are used as a DR CALUX bioassay quality eriterion. Aecording to the performanee eriteria set for the DR CALUX bioassay, the fitted EC50 should be within the range of 6 to 18 pM... [Pg.49]


See other pages where DR-CALUX is mentioned: [Pg.6]    [Pg.10]    [Pg.11]    [Pg.15]    [Pg.24]    [Pg.25]    [Pg.32]    [Pg.32]    [Pg.32]    [Pg.33]    [Pg.38]    [Pg.38]    [Pg.39]    [Pg.39]    [Pg.39]    [Pg.39]    [Pg.40]    [Pg.40]    [Pg.40]    [Pg.41]    [Pg.42]    [Pg.45]    [Pg.45]    [Pg.46]    [Pg.46]    [Pg.46]    [Pg.49]    [Pg.49]    [Pg.49]    [Pg.49]    [Pg.50]    [Pg.50]   


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CALUX

DR CALUX bioassay for the analysis of dioxins and dioxin-like chemicals in sediments

DR-CALUX bioassay

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