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Data-driven modeling of the cellular pharmacokinetics of degradable chitosan-based nanoparticles

Bibliographic Details
Summary:Nanoparticle drug delivery vehicles introduce multiple pharmacokinetic processes, with the delivery, accumulation, and stability of the therapeutic molecule influenced by nanoscale pro-cesses. Therefore, considering the complexity of the multiple interactions, the use of data-driven models has critical importance in understanding the interplay between controlling processes. We demonstrate data simulation techniques to reproduce the time-dependent dose of trimethyl chi-tosan nanoparticles in an ND7/23 neuronal cell line, used as an in vitro model of native peripheral sensory neurons. Derived analytical expressions of the mean dose per cell accurately capture the pharmacokinetics by including a declining delivery rate and an intracellular particle degradation process. Comparison with experiment indicates a supply time constant, t = 2 h. and a degradation rate constant, b = 0.71 h-1. Modeling the dose heterogeneity uses simulated data distributions, with time dependence incorporated by transforming data-bin values. The simulations mimic the dynamic nature of cell-to-cell dose variation and explain the observed trend of increasing numbers of high-dose cells at early time points, followed by a shift in distribution peak to lower dose between 4 to 8 h and a static dose profile beyond 8 h.
Subject:Drug delivery Imaging flow cytometry Nanoparticle dosimetry Data-driven models Pharmacokinetics Nanomedicine
Country:Portugal
Document type:journal article
Access type:Open
Associated institution:Repositório Aberto da Universidade do Porto
Language:English
Origin:Repositório Aberto da Universidade do Porto
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conditionsOfAccess_str open access
country_str PT
description Nanoparticle drug delivery vehicles introduce multiple pharmacokinetic processes, with the delivery, accumulation, and stability of the therapeutic molecule influenced by nanoscale pro-cesses. Therefore, considering the complexity of the multiple interactions, the use of data-driven models has critical importance in understanding the interplay between controlling processes. We demonstrate data simulation techniques to reproduce the time-dependent dose of trimethyl chi-tosan nanoparticles in an ND7/23 neuronal cell line, used as an in vitro model of native peripheral sensory neurons. Derived analytical expressions of the mean dose per cell accurately capture the pharmacokinetics by including a declining delivery rate and an intracellular particle degradation process. Comparison with experiment indicates a supply time constant, t = 2 h. and a degradation rate constant, b = 0.71 h-1. Modeling the dose heterogeneity uses simulated data distributions, with time dependence incorporated by transforming data-bin values. The simulations mimic the dynamic nature of cell-to-cell dose variation and explain the observed trend of increasing numbers of high-dose cells at early time points, followed by a shift in distribution peak to lower dose between 4 to 8 h and a static dose profile beyond 8 h.
documentTypeURL_str http://purl.org/coar/resource_type/c_6501
documentType_str journal article
id e1346bc0-9d76-4eee-87db-7d31f6c900cb
identifierHandle_str https://hdl.handle.net/10216/153796
language eng
relatedInstitutions_str_mv Repositório Aberto da Universidade do Porto
resourceName_str Repositório Aberto da Universidade do Porto
spellingShingle Data-driven modeling of the cellular pharmacokinetics of degradable chitosan-based nanoparticles
Drug delivery
Imaging flow cytometry
Nanoparticle dosimetry
Data-driven models
Pharmacokinetics
Nanomedicine
title Data-driven modeling of the cellular pharmacokinetics of degradable chitosan-based nanoparticles
topic Drug delivery
Imaging flow cytometry
Nanoparticle dosimetry
Data-driven models
Pharmacokinetics
Nanomedicine