saam ii software applications for kinetic analysis data (SAAM Institute Inc)
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SAAM Institute Inc
saam ii software applications for kinetic analysis data
Saam Ii Software Applications For Kinetic Analysis Data, supplied by SAAM Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/saam+ii+kinetics+analysis+software/saam+ii+pharmacokinetic+program/pm25283970-113-15-18
Average 90 stars, based on 1 article reviews
Saam Ii Software Applications For Kinetic Analysis Data, supplied by SAAM Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/saam+ii+kinetics+analysis+software/saam+ii+pharmacokinetic+program/pm25283970-113-15-18
Average 90 stars, based on 1 article reviews
saam ii software applications for kinetic analysis data - by Bioz Stars,
2026-09
90/100 stars
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Software:Article Title: Ketamine distribution described by a recirculatory pharmacokinetic model is not stereoselective. Article Snippet: Background: Differences in the pharmacokinetics of the enantiomers of ketamine have been reported.. The authors sought to determine whether these differences extend to pulmonary uptake and peripheral tissue distribution and to test the hypothesis that tissue distribution of the stereoisomers differs because of carrier-mediated drug transport.. Methods: The dispositions of markers of intravascular space and blood flow (indocyanine green, ICG) and total body water and tissue perfusion (antipyrine) were determined along with S-(1)and R-(2)-ketamine in five mongrel dogs. Article Title: Indocyanine green kinetics characterize blood volume and flow distribution and their alteration by propranolol. Article Snippet: We have developed a recirculatory pharmacokinetic model to describe the disposition of markers with welldefined distribution from the moment of right atrial injection based on frequent early arterial blood sampling.1,2 Indocyanine green is an intravascular marker because it binds to plasma proteins rapidly and completely, impeding its extravascular distribution.. Therefore it can be used to estimate blood volume based on back extrapolation of the post-mixing monoexponential blood indocyanine green concentration versus time relationship.3,4 Indicator (dye) dilution cardiac output can be estimated from the first-pass arterial blood indocyanine green concentration history.5 Combined description of both the monoexponential blood indocyanine green concentration history and its first-pass and subsequent recirculation peaks (the mixing phase) with use of a recirculatory pharmacokinetic model allows characterization of intravascular events, such as mixing, by deriving estimates of not only blood volume and cardiac output but also their systemic distribution (Fig 1).1,2 Because indocyanine green is irreversibly removed from the blood in a flow-dependent manner, its elimination clearance (CLE) can be used to estimate hepatic blood flow in humans.6,7 Indocyanine green kinetics characterize blood volume and flow distribution and their alteration by propranolol MTT Assay:Article Title: Ketamine distribution described by a recirculatory pharmacokinetic model is not stereoselective. Article Snippet: Background: Differences in the pharmacokinetics of the enantiomers of ketamine have been reported.. The authors sought to determine whether these differences extend to pulmonary uptake and peripheral tissue distribution and to test the hypothesis that tissue distribution of the stereoisomers differs because of carrier-mediated drug transport.. Methods: The dispositions of markers of intravascular space and blood flow (indocyanine green, ICG) and total body water and tissue perfusion (antipyrine) were determined along with S-(1)and R-(2)-ketamine in five mongrel dogs. |