纳米载体系统毒性研究进展

R. Bhatia
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引用次数: 0

摘要

各种纳米载体体系的实用性和多样化应用导致了各种具有智能性能的配方的发展。尽管这些制剂比传统的给药系统提供了一些优势,如特定部位、时间依赖性和药物的控制给药,但不幸的是,这些药物的毒理学行为仍未被探索。文献中有几篇报道描述了对动物主要器官的显著毒性。这种毒性主要与活性氧(ROS)的形成、生物标志物水平的升高/降低、细胞凋亡的诱导和其他一些分子变化有关。在这篇简短的汇编中,我们总结了一些基于临床前证据和归因于动物多器官的毒性报道。这些器官包括肾、心、肺、肝和胃肠道。此外,我们还试图强调所报道的毒性机制以及毒性剂量。这种汇编可能有助于药物开发人员和研究人员了解这些问题,并在制定过程中设计新的策略来绕过这些并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perspectives of Toxicity Associated with Nanocarrier Systems
The utility and diversified applications of various nanocarrier systems have led to the development of a wide variety of formulations with smart properties. Although these formulations offer several advantages over traditional delivery systems such as site-specific, time-dependent and controlled delivery of the medicaments but unfortunately the toxicological behavior of these has remained unexplored. There are several reports in the literature that have described the significant toxicity in major organs of animals. This toxicity has majorly associated with the formation of reactive oxygen species (ROS), elevation/ reduction in biomarker levels, induction of apoptosis and several other molecular changes. In this short compilation, we have summarized some toxicity reports which have been based on pre-clinical evidences and attributed to multiple organs of animals. These include the kidney, heart, lungs, liver and GIT prominently. Also, we have made an attempt to highlight the mechanism of the reported toxicity along with the toxic dose. This compilation may be helpful to drug developers and researchers to understand these issues and to design newer strategies during formulation to bypass these complications.
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