Impact of the functional coating of silver nanoparticles on their in vivo performance and biosafety

体内 肾毒性 体内分布 银纳米粒子 化学 药理学 药物输送 肾功能 生物相容性 肌酐 毒性 纳米技术 纳米颗粒 体外 医学 内科学 生物化学 材料科学 生物 生物技术 有机化学
作者
Hesham M. Tawfeek,Mahmoud A. Younis,Basmah N. Aldosari,Alanood S. Almurshedi,Ahmed Abdelfattah,Jelan A. Abdel-Aleem
出处
期刊:Drug Development and Industrial Pharmacy [Taylor & Francis]
卷期号:49 (5): 349-356 被引量:7
标识
DOI:10.1080/03639045.2023.2214207
摘要

Silver nanoparticles (AgNPs) have become an interesting therapeutic modality and drug delivery platform. Herein, we aimed to investigate the impact of functional coating on the in vivo performance of AgNPs as an economic and scalable method to modulate their behavior.AgNPs were coated with chitosan (CHI) as a model biopolymer using a one-pot reduction-based method, where CHI of two molecular weight ranges were investigated. The resultant CHI-coated AgNPs (AgNPs-CHI) were characterized using UV-VIS spectroscopy, DLS, and TEM. AgNPs were administered intravenously to rats and their biodistribution and serum levels of hepato-renal function markers were monitored 24 h later compared to plain AgNO3 as a positive control.UV-VIS spectroscopy confirmed the successful coating of AgNPs with CHI. DLS revealed the superiority of medium molecular weight CHI over its low molecular weight counterpart. AgNPs-CHI demonstrated a semi-complete clearance from the systemic circulation, a liver-dominated tissue tropism, and limited renal exposure. On the other hand, AgNO3 was poorly cleared from the circulation, with relatively high renal exposure and a non-specific tissue tropism. AgNPs-CHI were well-tolerated by the liver and kidney without signs of toxicity or inflammation, in contrary with AgNO3 which resulted in a significant elevation of Creatinine (CRE), Urea, and Total Protein (TP), suggesting a significant nephrotoxicity and inflammation.Functional coating of AgNPs with CHI substantially modulated their in vivo behavior, promoting their hepatic selectivity and biotolerability, which can be invested in the development of drug delivery systems for the treatment of liver diseases.

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