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Cycle-time and residence-time density approximations in a stochastic model for circulatory transport
Charles E. Smith, Petr Lánský, Te-Hsin Lung
Language English Country United States
Document type Research Support, Non-U.S. Gov't
Grant support
IZ4034
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
ProQuest Central
from 1997-01-01 to 2019-01-31
Health & Medicine (ProQuest)
from 1997-01-01 to 2019-01-31
PubMed
8980303
Knihovny.cz E-resources
- MeSH
- Models, Biological * MeSH
- Pharmacokinetics * MeSH
- Humans MeSH
- Mathematics MeSH
- Metabolic Clearance Rate MeSH
- Stochastic Processes MeSH
- Check Tag
- Humans MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
The concentration of a drug in the circulatory system is studied under two different elimination strategies. The first strategy--geometric elimination--is the classical one which assumes a constant elimination rate per cycle. The second strategy--Poisson elimination--assumes that the elimination rate changes during the process of elimination. The problem studied here is to find a relationship between the residence-time distribution and the cycle-time distribution for a given rule of elimination. While the presented model gives this relationship in terms of Laplace-Stieltjes transform., the aim here is to determine the shapes of the corresponding probability density functions. From experimental data, we expect positively skewed, gamma-like distributions for the residence time of the drug in the body. Also, as some elimination parameter in the model approaches a limit, the exponential distribution often arises. Therefore, we use Laguerre series expansions, which yield a parsimonious approximation of positively skewed probability densities that are close to a gamma distribution. The coefficients in the expansion are determined by the central moments, which can be obtained from experimental data or as a consequence of theoretical assumptions. The examples presented show that gamma-like densities arise for a diverse set of cycle-time distribution and under both elimination rules.
Department of Statistics North Carolina State University Raleigh 27695 8203 USA
Department of Statistics North Carolina State University Raleigh USA
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- $a Smith, Charles E., $d 1956- $7 xx0203897 $u Department of Statistics, North Carolina State University, Raleigh 27695-8203, USA. cesmith@stat.ncsu.edu
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- $a The concentration of a drug in the circulatory system is studied under two different elimination strategies. The first strategy--geometric elimination--is the classical one which assumes a constant elimination rate per cycle. The second strategy--Poisson elimination--assumes that the elimination rate changes during the process of elimination. The problem studied here is to find a relationship between the residence-time distribution and the cycle-time distribution for a given rule of elimination. While the presented model gives this relationship in terms of Laplace-Stieltjes transform., the aim here is to determine the shapes of the corresponding probability density functions. From experimental data, we expect positively skewed, gamma-like distributions for the residence time of the drug in the body. Also, as some elimination parameter in the model approaches a limit, the exponential distribution often arises. Therefore, we use Laguerre series expansions, which yield a parsimonious approximation of positively skewed probability densities that are close to a gamma distribution. The coefficients in the expansion are determined by the central moments, which can be obtained from experimental data or as a consequence of theoretical assumptions. The examples presented show that gamma-like densities arise for a diverse set of cycle-time distribution and under both elimination rules.
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