Translational Health Science and Technology Institute (THSTI), Faridabad, Haryana 121001, India.
School of Pharmacy, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Selangor 47500, Malaysia; Centre for Drug Delivery and Molecular Pharmacology, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Selangor, Malaysia.
Eur J Pharm Biopharm. 2021 Apr;161:100-119. doi: 10.1016/j.ejpb.2021.02.010. Epub 2021 Feb 25.
Potential research outcomes on nanotechnology-based novel drug delivery systems since the past few decades attracted the attention of the researchers to overcome the limitations of conventional deliveries. Apart from possessing enhanced solubility of poorly water-soluble drugs, the targeting potential of the carriers facilitates longer circulation and site-specific delivery of the entrapped therapeutics. The practice of these delivery systems, therefore, helps in maximizing bioavailability, improving pharmacokinetics profile, pharmacodynamics activity and biodistribution of the entrapped drug(s). In addition to focusing on the positive side, evaluation of nanoparticulate systems for toxicity is a crucial parameter for its biomedical applications. Due to the size of nanoparticles, they easily traverse through biological barriers and may be accumulated in the body, where the ingredients incorporated in the formulation development might accumulate and/or produce toxic manifestation, leading to cause severe health hazards. Therefore, the toxic profile of these delivery systems needs to be evaluated at the molecular, cellular, tissue and organ level. This review offers a comprehensive presentation of toxicity aspects of the constituents of nanoparticular based drug delivery systems, which would be beneficial for future researchers to develop nanoparticulate delivery vehicles for the improvement of delivery approaches in a safer way.
在过去几十年中,基于纳米技术的新型药物传递系统的潜在研究成果引起了研究人员的关注,以克服传统传递方法的局限性。除了提高疏水性药物的溶解度外,载体的靶向潜力还促进了包封治疗剂的更长循环和靶向传递。因此,这些传递系统的应用有助于最大限度地提高生物利用度、改善药代动力学特征、药效学活性和包封药物的生物分布。除了关注积极方面外,纳米颗粒系统的毒性评估是其生物医学应用的关键参数。由于纳米颗粒的大小,它们很容易穿透生物屏障并可能在体内积累,其中制剂开发中包含的成分可能会积累和/或产生毒性表现,导致严重的健康危害。因此,需要在分子、细胞、组织和器官水平上评估这些传递系统的毒性特征。这篇综述全面介绍了基于纳米颗粒的药物传递系统成分的毒性方面,这将有助于未来的研究人员开发纳米颗粒传递载体,以更安全的方式改进传递方法。