東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

Mathematical modeling of pharmacokin...

Lee, Yung-Jin.

Linked to FindBook

Google Book

Amazon

博客來

Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model./
Author:	Lee, Yung-Jin.
Published:	Ann Arbor : ProQuest Dissertations & Theses, : 1994,
Description:	260 p.
Notes:	Source: Dissertation Abstracts International, Volume: 55-02, Section: B, page: 3790.
Contained By:	Dissertation Abstracts International55-02B.
Subject:	Pharmacology. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=9418926

Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model.
Lee, Yung-Jin.

Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model. - Ann Arbor : ProQuest Dissertations & Theses, 1994 - 260 p.

Source: Dissertation Abstracts International, Volume: 55-02, Section: B, page: 3790.

Thesis (Ph.D.)--The University of Oklahoma Health Sciences Center, 1994.

The present study attempted to propose a PK-PD model, including a drug-plasma protein binding model, for a highly protein bound drug.Subjects--Topical Terms:

634543
Pharmacology.

Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model.
LDR:03013nmm a2200337 4500 001 2116956
005 20170508094400.5
008 180830s1994 ||||||||||||||||| ||eng d
035 $a (MiAaPQ)AAI9418926
035 $a AAI9418926
040 $a MiAaPQ $c MiAaPQ
100 1 $a Lee, Yung-Jin. $3 3278706
245 1 0 $a Mathematical modeling of pharmacokinetics and pharmacodynamics with a nonlinear drug-plasma protein binding model.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 1994
300 $a 260 p.
500 $a Source: Dissertation Abstracts International, Volume: 55-02, Section: B, page: 3790.
500 $a Chair: David W. A. Bourne.
502 $a Thesis (Ph.D.)--The University of Oklahoma Health Sciences Center, 1994.
520 $a The present study attempted to propose a PK-PD model, including a drug-plasma protein binding model, for a highly protein bound drug.
520 $a A drug-plasma protein binding model was proposed and tested with ceftriaxone-cefotaxime in vitro and in vivo drug-plasma binding data in rats. The results were comparable to previous reports. Therefore, the in vivo drug-plasma protein competitive binding model was validated. The model was applied further to the tolbutamide (TBM)-sulfadimethoxine (SDM) in vivo drug-plasma protein interaction to evaluate the change in pharmacological effects of TBM caused by coadministration of different SDM doses.
520 $a The experimental assay methods used in this study including the in vitro and the in vivo study were developed. These included TBM and SDM HPLC assays, insulin RIA method and blood glucose assay. The results suggested that these assay methods be reliable and accurate enough to be used for this study.
520 $a The in vitro and in vivo TBM and SDM drug-plasma protein binding data in rabbits were analyzed to determine PK and PD parameters to validate the proposed model. The results obtained from the in vitro data suggests that, although SDM has a lower association constant than TBM, SDM still can compete with TBM for plasma protein binding. The parameters from the in vitro study were used as initial values for the in vivo data fitting. The results obtained from the in vivo study provided pharmacokinetic parameters for both model drugs that were comparable to those found in the in vitro study, as well as those previously reported. Some of TBM pharmacodynamic parameters for both insulin release and blood glucose concentration lowering are reported for first time in the present study. The observed data were well described by the proposed model.
520 $a In conclusion, a mathematical PK-PD model including drug-protein plasma binding has been successfully proposed and proved to be useful in the analysis of the results obtained in the present study.
590 $a School code: 0361.
650 4 $a Pharmacology. $3 634543
650 4 $a Pharmaceutical sciences. $3 3173021
650 4 $a Pharmacy sciences. $3 3174369
690 $a 0419
690 $a 0572
690 $a 0491
710 2 $a The University of Oklahoma Health Sciences Center. $3 1023966
773 0 $t Dissertation Abstracts International $g 55-02B.
790 $a 0361
791 $a Ph.D.
792 $a 1994
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=9418926