Aim To develop a method to estimate population pharmacokinetic parameters with the limited sampling time points provided clinically during therapeutic drug monitoring. Methods Various simulations were attempted using ...Aim To develop a method to estimate population pharmacokinetic parameters with the limited sampling time points provided clinically during therapeutic drug monitoring. Methods Various simulations were attempted using a one-compartment open model with the first order absorption to determine PK parameter estimates with different sampling strategies as a validation of the method. The estimated parameters were further verified by comparing to the observed values. Results The samples collected at the single time point close to the non-informative sampling time point designed by this method led to bias and inaccurate parameter estimations. Furthermore, the relationship between the estimated non-informative sampling time points and the values of the parameter was examined. The non-informative sampling time points have been developed under some typical occasions and the results were plotted to show the tendency. As a result, one non-informative time point was demonstrated to be appropriate for clearance and two for both volume of distribution and constant of absorption in the present study. It was found that the estimates of the non-informative sampling time points developed in the method increase with increases of volume of distribution and the decrease of clearance and constant of absorption. Conclusion A rational sampling strategy during therapeutic drug monitoring can be established using the method present in the study.展开更多
Segmenting a complex 3D surface model into some visually meaningful sub-parts is one of the fundamental problems in digital geometry processing. In this paper, a novel segmentation approach of point-sampled surfaces i...Segmenting a complex 3D surface model into some visually meaningful sub-parts is one of the fundamental problems in digital geometry processing. In this paper, a novel segmentation approach of point-sampled surfaces is proposed, which is based on the level set evolution scheme. To segment the model so as to align the patch boundaries with high curvature zones, the driven speed function for the zero level set inside narrow band is defined by the extended curvature field, which approaches zero speed as the propagating front approaches high curvature zone. The effectiveness of the proposed approach is demonstrated by our ex- perimental results. Furthermore, two applications of model segmentation are illustrated, such as piecewise parameterization and local editing for point-sampled geometry.展开更多
基金National Natural Science Foundation of China(Grant No. 30472165) the 985 Projects of the State KeyLaboratory of Natural and Biomimetic Drugs (Grant No.268705077280).
文摘Aim To develop a method to estimate population pharmacokinetic parameters with the limited sampling time points provided clinically during therapeutic drug monitoring. Methods Various simulations were attempted using a one-compartment open model with the first order absorption to determine PK parameter estimates with different sampling strategies as a validation of the method. The estimated parameters were further verified by comparing to the observed values. Results The samples collected at the single time point close to the non-informative sampling time point designed by this method led to bias and inaccurate parameter estimations. Furthermore, the relationship between the estimated non-informative sampling time points and the values of the parameter was examined. The non-informative sampling time points have been developed under some typical occasions and the results were plotted to show the tendency. As a result, one non-informative time point was demonstrated to be appropriate for clearance and two for both volume of distribution and constant of absorption in the present study. It was found that the estimates of the non-informative sampling time points developed in the method increase with increases of volume of distribution and the decrease of clearance and constant of absorption. Conclusion A rational sampling strategy during therapeutic drug monitoring can be established using the method present in the study.
基金Project supported by the National Basic Research Program (973) of China (No. 2002CB312101)the National Natural Science Foundation of China (Nos. 60503056, 60373036, 60333010)the Education Department of Zhejiang Province, China (No. 20060797)
文摘Segmenting a complex 3D surface model into some visually meaningful sub-parts is one of the fundamental problems in digital geometry processing. In this paper, a novel segmentation approach of point-sampled surfaces is proposed, which is based on the level set evolution scheme. To segment the model so as to align the patch boundaries with high curvature zones, the driven speed function for the zero level set inside narrow band is defined by the extended curvature field, which approaches zero speed as the propagating front approaches high curvature zone. The effectiveness of the proposed approach is demonstrated by our ex- perimental results. Furthermore, two applications of model segmentation are illustrated, such as piecewise parameterization and local editing for point-sampled geometry.
