Step Four Scenario Development

The complexity of the method in terms of number of steps and solvents needed depends on the sorbent chemistry. The development in a simplified scenario involves running an analyte in several concentrations in multiple replicates and assaying for recovery and performance. This procedure is described in detail for several silica and polymeric sorbents by Wells.42 However, if a number of sorbents are to be evaluated, the process becomes time-consuming if multiple 96-well plates (each with one sorbent packed in all the wells) must be screened separately. This process may take a week or more and consume an analyst s precious time as well. The most plausible solution is to pack different sorbents in the same well plate and use a universal procedure that applies to all of them. An example of such a multisorbent method development plate is the four-sorbent plate recently introduced by Phenomenex demonstrated124 to require only 1 to 2 hr to determine optimal sorbent and SPE conditions. 

Next, we will outline our formal development of such a mission-oriented SoS in Event-B. We will start with a very abstract description of a SoS (consisting of a single event) and then unfold the system complexity by four refinement steps, gradually introducing the notions of missions and their scenarios, the system environment and communication, the cyclic behaviour pattern, and finaiiy decomposing the SoS into its constituent systems. 

The four steps of the risk-assessment process are hazard identification, analysis of exposure, analysis of effect, and risk characterization. In the hazard identification step, the risk assessor identifies chemicals of concern, environmental pathways of exposure, and populations and subpopulations at risk. The exposure analysis develops exposure scenarios and estimates the chronic daily intake of each chemical of concern. In the analysis of effect, the risk assessor combines the chronic daily intake calculated in the exposure analysis with toxicity data from animal studies (and/or human epidemiological studies, if available) to estimate the risk of toxic effects in exposed populations, whereby risks to public health are divided into two broad categories noncancer health effects and cancer. The final step of the risk-assessment process, risk characterization, is a narrative that marshals all the evidence of risk to public health, including quantitative risk assessments and qualitative evidence of risk. The risk assessor weighs all the evidence and uses professional judgment to draw conclusions about risks. 

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