Predicting Volume of Distribution in Neonates: Performance of Physiologically Based Pharmacokinetic Modelling [PDF]
The volume of distribution at steady state (Vss) in neonates is still often estimated through isometric scaling from adult values, disregarding developmental changes beyond body weight.
Pieter-Jan De Sutter+4 more
doaj +2 more sources
Interdisciplinary Collaboration on Real World Data to Close the Knowledge Gap: A Reflection on “De Sutter et al. Predicting Volume of Distribution in Neonates: Performance of Physiologically Based Pharmacokinetic Modelling” [PDF]
This commentary further reflects on the paper of De Sutter et al. on predicting volume of distribution in neonates, and the performance of physiologically based pharmacokinetic models We hereby stressed the add on value to collaborate on real world data ...
Karel Allegaert+2 more
doaj +2 more sources
Methods to Predict Volume of Distribution. [PDF]
Prior to human studies, knowledge of drug disposition in the body is useful to inform decisions on drug safety and efficacy, first in human dosing, and dosing regimen design. It is therefore of interest to develop predictive models for primary pharmacokinetic parameters, clearance, and volume of distribution.
Holt K, Nagar S, Korzekwa K.
europepmc +4 more sources
Distribution of Citations in one Volume of a Journal [PDF]
Citations to published scientific articles are regularly collected and processed, bringing about the impact factor and a large number of other bibliometric indicators.
Antonio Protić+2 more
doaj +3 more sources
Applying linear and non-linear methods for parallel prediction of volume of distribution and fraction of unbound drug. [PDF]
Volume of distribution and fraction unbound are two key parameters in pharmacokinetics. The fraction unbound describes the portion of free drug in plasma that may extravasate, while volume of distribution describes the tissue access and binding of a drug.
Eva M del Amo+5 more
doaj +2 more sources
Effects of drug transporters on volume of distribution. [PDF]
Recently, drug transporters have emerged as significant modifiers of a patient's pharmacokinetics. In cases where the functioning of drug transporters is altered, such as by drug-drug interactions, by genetic polymorphisms, or as evidenced in knockout animals, the resulting change in volume of distribution can lead to a significant change in drug ...
Grover A, Benet LZ.
europepmc +5 more sources
Conceptos y aplicaciones de los parámetros farmacocinéticos: Una guía para el salón de clases. | [Concepts and applications of pharmacokinetic parameters: A guide for the classroom] [PDF]
Context: Pharmacokinetic studies play a fundamental role in making informed decisions during the drug development stage and fulfilling regulatory agencies’ requirements for drug approval.
Jorge Duconge-Soler+2 more
doaj +1 more source
Comparison of pharmacokinetic parameters of ranolazine between diabetic and non-diabetic rats [PDF]
Objective(s): Diabetes mellitus (DM) affects the pharmacokinetics of drugs. Ranolazine is an antianginal drug that is prescribed in DM patients with angina.
Habibeh Mashayekhi-sardoo+5 more
doaj +1 more source
Infection and sepsis are a main cause of acute-on-chronic liver failure (ACLF). Besides bacteria, molds play a role. Voriconazole (VRC) is recommended but its pharmacokinetics (PK) may be altered by ACLF.
Jörn Grensemann+9 more
doaj +1 more source
Probability distributions of landslide volumes [PDF]
Abstract. We examine 19 datasets with measurements of landslide volume, VL, for sub-aerial, submarine, and extraterrestrial mass movements. Individual datasets include from 17 to 1019 landslides of different types, including rock fall, rock slide, rock avalanche, soil slide, slide, and debris flow, with individual landslide volumes ranging over 10−4 m3≤
Brunetti MT, Guzzetti F, Rossi M
openaire +6 more sources