Metrology Research Centre, National Research Council of Canada, 100 Sussex Drive, Ottawa, ON K1A 0R6, Canada.
Ottawa-Carleton Institute for Biomedical Engineering, University of Ottawa, 800 King Edward Avenue, Ottawa, ON K1N 6N5, Canada.
Int J Mol Sci. 2022 Jun 18;23(12):6802. doi: 10.3390/ijms23126802.
Functionalized graphene oxide (GO) nanoparticles are being increasingly employed for designing modern drug delivery systems because of their high degree of functionalization, high surface area with exceptional loading capacity, and tunable dimensions. With intelligent controlled release and gene silencing capability, GO is an effective nanocarrier that permits the targeted delivery of small drug molecules, antibodies, nucleic acids, and peptides to the liquid or solid tumor sites. However, the toxicity and biocompatibility of GO-based formulations should be evaluated, as these nanomaterials may introduce aggregations or may accumulate in normal tissues while targeting tumors or malignant cells. These side effects may potentially be impacted by the dosage, exposure time, flake size, shape, functional groups, and surface charges. In this review, the strategies to deliver the nucleic acid via the functionalization of GO flakes are summarized to describe the specific targeting of liquid and solid breast tumors. In addition, we describe the current approaches aimed at optimizing the controlled release towards a reduction in GO accumulation in non-specific tissues in terms of the cytotoxicity while maximizing the drug efficacy. Finally, the challenges and future research perspectives are briefly discussed.
功能化氧化石墨烯(GO)纳米粒子由于其高度功能化、高比表面积和特殊的负载能力以及可调尺寸,正被越来越多地用于设计现代药物传递系统。GO 具有智能控制释放和基因沉默能力,是一种有效的纳米载体,可将小分子药物、抗体、核酸和肽等靶向递送到液体或实体瘤部位。然而,基于 GO 的制剂的毒性和生物相容性应该进行评估,因为这些纳米材料在靶向肿瘤或恶性细胞时可能会引起聚集或在正常组织中积累。这些副作用可能会受到剂量、暴露时间、薄片尺寸、形状、官能团和表面电荷的影响。在这篇综述中,总结了通过 GO 薄片功能化来传递核酸的策略,以描述对液体和固体乳腺癌的特异性靶向。此外,我们还描述了目前旨在优化控制释放的方法,以减少 GO 在非特异性组织中的积累,同时最大限度地提高药物疗效,从而降低细胞毒性。最后,简要讨论了挑战和未来的研究前景。