Selectivity profiles

We now wish to edit the simulation profile. Since we are using a previously created profile, we need to open the profile rather than create a new profile. Select PSpice and then Edit Simulation Profile from the Capture menus to edit the existing profile ... 

Since we are working with the previous example, a simulation profile has already been created and we just need to modify it. To edit the existing profile, select PSpice and then Edit Simulation Profile ... 

We must now set up the Parametric Sweep. If you are continuing from the previous example, you will already have created a simulation profile for the DC Sweep. To open the profile, select PSpice and then Edit Simulation Profile from the menus. If you started this example as a new circuit, select PSpice and then New Simulation Profile, specify a name for the new profile, and then click the Create button. Set up a DC Sweep as shown below. Using either procedure, you should have the screen below ... 

Since we have already created a simulation profile from the previous example, we do not need to create a new profile. To open the previous profile, select PSpice and then Edit Simulation PlOfllB from the Capture menus ... 

We must now create a new simulation profile. Select PSpice and then New Simulation Profile from the menus ... 

This file contains all of the models we created for the current schematic. Close the Notepad and return to the schematic. We will now look at the current library path. To view the libraries, we must set up a simulation profile. Select PSpice and then New Simulation Profile from the Capture menus ... 

Selection is the second decision point in the pharmaceutical system and is primarily a prioritization process (Cohen, Cercone, and Macaya 2002). Government selects drugs to meet the most important health needs of the population and cover the country s disease profile. Selection is critical in an NDP as it largely determines the goals for the health system (WHO 2002). Appropriate selection can lead to improved healthcare, management of medicines, and cost-effectiveness, all of which can result in improved access (Quick 2003). 

It is a straightforward matter to fit various model profiles to realistic, exact computed profiles, selecting a greater or lesser portion near the line center of the exact profile for a least mean squares fit. In this way, the parameters and the root mean square errors of the fit may be obtained as functions of the peak-to-wing intensity ratio, x = G(0)/G(comax)- As an example, Fig. 5.8 presents the root mean square deviations thus obtained, in units of relative difference in percent, for two standard models, the desymmetrized Lorentzian and the BC shape, Eqs. 3.15 and 5.105, respectively. 

Standard Atmosphere Profile Selection (1 = use default atmosphere) IATM1... 

Adequate Protein and Balanced AA Profile—Selection Within Normal Limits.251... 

Additional improvements in DIPE productivity may be anticipated through furlher optimization of die hydrogenation/dehydration activities of the three catalyst compositions, as well as the tenperature profiles selected for DIPE generation. 

Fig. 31.3 lontrap LC-MS profile (selected pseudo-molecular ions) of an alkaloid extract from Schizanthus grahamii (stem bark). Separation of isomcaic series is achieved on a porous graphitic... 

J. K. Whear, Separator Profile Selection for Optimal Battery Performance, LPow Soun-.es. Yll (2008), 226-230. 

Another popular technique to obtain the firee energies profiles is based on the calculation of the Potential of Mean Force, PMF, associated to a particular distinguished reaction coordinate [70]. A proper selection of this coordinate is critical to obtain meaningful free energy profiles. Selection of this reaction coordinate should be based on the exploration of the PES including the environment, or even better, on IRCs traced down to the corresponding products and reactants valleys from transition stmctures located and characterized in the enzyme active site. 

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