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纳米颗粒制剂安全性评估的新方法和途径:聚焦于模型和不良结局途径

Novel Methods and Approaches for Safety Evaluation of Nanoparticle Formulations: A Focus Towards Models and Adverse Outcome Pathways.

作者信息

Tirumala Mounika Gayathri, Anchi Pratibha, Raja Susmitha, Rachamalla Mahesh, Godugu Chandraiah

机构信息

Department of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.

Department of Biology, University of Saskatchewan, Saskatoon, SK, Canada.

出版信息

Front Pharmacol. 2021 Sep 9;12:612659. doi: 10.3389/fphar.2021.612659. eCollection 2021.

Abstract

Nanotoxicology is an emerging field employed in the assessment of unintentional hazardous effects produced by nanoparticles (NPs) impacting human health and the environment. The nanotoxicity affects the range between induction of cellular stress and cytotoxicity. The reasons so far reported for these toxicological effects are due to their variable sizes with high surface areas, shape, charge, and physicochemical properties, which upon interaction with the biological components may influence their functioning and result in adverse outcomes (AO). Thus, understanding the risk produced by these materials now is an important safety concern for the development of nanotechnology and nanomedicine. Since the time nanotoxicology has evolved, the methods employed have been majorly relied on cell-based evaluations, while these simple methods may not predict the complexity involved in preclinical and clinical conditions concerning pharmacokinetics, organ toxicity, and toxicities evidenced through multiple cellular levels. The safety profiles of nanoscale nanomaterials and nanoformulations in the delivery of drugs and therapeutic applications are of considerable concern. In addition, the safety assessment for new nanomedicine formulas lacks regulatory standards. Though the studies are greatly needed, the end parameters used for risk assessment are not predicting the possible toxic effects produced by various nanoformulations. On the other side, due to increased restrictions on animal usage and demand for the need for high-throughput assays, there is a need for developing and exploring novel methods to evaluate NPs safety concerns. The progress made in molecular biology and the availability of several modern techniques may offer novel and innovative methods to evaluate the toxicological behavior of different NPs by using single cells, cell population, and whole organisms. This review highlights the recent novel methods developed for the evaluation of the safety impacts of NPs and attempts to solve the problems that come with risk assessment. The relevance of investigating adverse outcome pathways (AOPs) in nanotoxicology has been stressed in particular.

摘要

纳米毒理学是一个新兴领域,用于评估纳米颗粒(NPs)对人类健康和环境产生的意外有害影响。纳米毒性影响细胞应激诱导和细胞毒性之间的范围。迄今为止报道的这些毒理学效应的原因是它们具有高表面积、形状、电荷和物理化学性质的可变尺寸,与生物成分相互作用时可能会影响其功能并导致不良后果(AO)。因此,了解这些材料产生的风险现在是纳米技术和纳米医学发展的重要安全问题。自从纳米毒理学发展以来,所采用的方法主要依赖于基于细胞的评估,而这些简单方法可能无法预测临床前和临床条件下涉及药代动力学、器官毒性以及通过多个细胞水平证实的毒性的复杂性。纳米级纳米材料和纳米制剂在药物递送和治疗应用中的安全性备受关注。此外,新纳米药物配方的安全性评估缺乏监管标准。尽管迫切需要进行研究,但用于风险评估的最终参数无法预测各种纳米制剂可能产生的毒性作用。另一方面,由于对动物使用的限制增加以及对高通量检测的需求,需要开发和探索新的方法来评估纳米颗粒的安全问题。分子生物学取得的进展以及几种现代技术的可用性可能提供新颖的创新方法,通过使用单细胞、细胞群体和整个生物体来评估不同纳米颗粒的毒理学行为。本综述重点介绍了最近开发的用于评估纳米颗粒安全影响的新方法,并试图解决风险评估中出现的问题。特别强调了在纳米毒理学中研究不良结局途径(AOPs)的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf3/8458898/0da85a399c9a/fphar-12-612659-g001.jpg

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