Evaluation of drug carrier hepatotoxicity using primary cell culture models
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Tarih
2023
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
This study aims to establish a primary rat hepatocyte culture model to evaluate dose-dependent hepatotoxic effects of drug carriers (lipopolymer nanoparticles; LPNs) temporal. Primary rat hepatocyte cell cultures were used to determine half-maximal Inhibition Concen-trations (IC50) of the drug-carrier library. Drug-carrier library, at concentrations <50 mu g/mL, is benign to primary rat hepatocytes as determined using albumin and urea secretions. Albumin, as a hepatic biomarker, exhibited a more sensitive and faster outcome, compared to urea, for the determination of the IC50 value of LPNs. Temporal measurements of hepatic biomarkers including urea and albumin, and rigorous physi-cochemical (hydrodynamic diameter, surface charge, etc.) characterization, should be combined to evaluate the hepatotoxicity of drug carrier libraries in screens.(c) 2023 Published by Elsevier Inc.
Açıklama
Anahtar Kelimeler
Lipopolymer nanoparticle (LPN), Nanotoxicity, Primary rat hepatocyte, In vitro culture, Hepatotoxicity
Kaynak
Nanomedicine-Nanotechnology Biology and Medicine
WoS Q Değeri
Q2
Scopus Q Değeri
Q1
Cilt
48
