Shinde Swapnil, Shah Saurabh, Famta Paras, Wagh Suraj, Pandey Giriraj, Sharma Abhishek, Vambhurkar Ganesh, Jain Akshita, Srivastava Saurabh
Pharmaceutical Innovation and Translational Research Lab (PITRL), Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad 500037, India.
Mol Pharm. 2025 Jun 2;22(6):2783-2806. doi: 10.1021/acs.molpharmaceut.4c01495. Epub 2025 May 3.
Nanomedicine has significantly advanced the treatment of various cancer phenotypes, addressing numerous challenges associated with conventional therapies. Researchers have extensively investigated the physicochemical properties of nanocarriers, such as charge, morphology, and surface chemistry, to optimize drug delivery systems. In the context of transformable nanomedicine, these properties are particularly critical for overcoming existing limitations, including suboptimal blood circulation times, sequestration by the reticuloendothelial system and mononuclear phagocyte system, and inefficient targeting of the tumor microenvironment (TME). Alterations in nanocarrier geometry, surface charge, and hydrophilicity have shown potential in mitigating these barriers, offering improved therapeutic outcomes and enhanced biomedical applications. This review explores controlled modulation of these properties in the context of anticancer therapy, offering an in-depth exploration of transformable strategies activated by both internal and external stimuli. We analyze the implications of these tunable characteristics on pharmacokinetics, biodistribution, and targeted delivery to the TME. Additionally, we address the current challenges in the clinical translation of these advanced nanocarriers and propose strategies to overcome these obstacles to enhance the clinical feasibility of nanomedicine-based cancer therapies.
纳米医学显著推动了各种癌症表型的治疗,解决了与传统疗法相关的众多挑战。研究人员广泛研究了纳米载体的物理化学性质,如电荷、形态和表面化学,以优化药物递送系统。在可转化纳米医学的背景下,这些性质对于克服现有局限性尤为关键,这些局限性包括血液循环时间不理想、被网状内皮系统和单核吞噬细胞系统截留以及对肿瘤微环境(TME)的靶向效率低下。纳米载体几何形状、表面电荷和亲水性的改变已显示出减轻这些障碍的潜力,带来了改善的治疗效果和增强的生物医学应用。本综述探讨了在抗癌治疗背景下对这些性质的可控调节,深入探讨了由内部和外部刺激激活的可转化策略。我们分析了这些可调特性对药代动力学、生物分布以及向肿瘤微环境靶向递送的影响。此外,我们阐述了这些先进纳米载体临床转化中的当前挑战,并提出克服这些障碍的策略,以提高基于纳米医学的癌症治疗的临床可行性。