Department of Pharmacy, Birla Institute of Technology & Science, Pilani, Vidya Vihar, Pilani, Rajasthan, 333031, India.
Drug Deliv Transl Res. 2018 Oct;8(5):1508-1526. doi: 10.1007/s13346-018-0578-5.
After the discovery of the enhanced permeability and retention effect in 1986, it was envisioned that nanoparticle-mediated tumor-targeted delivery of chemotherapeutics would make a radical change in cancer therapy. However, after three decades of extensive research, only a few nanotherapeutics have been approved for clinical use. Although significant advantages of nanomedicines have been demonstrated in pre-clinical studies, clinical outcome was found to be variable. Advanced research has revealed that significant biochemical and structural variations exist between (and among) different tumors. These variations can considerably affect the tumor delivery and efficacy of nanomedicines. Tumor penetration is an important determining factor for positive therapeutic outcome and same nanomedicine can show diverse efficacy against different tumors depending on the extent of tumor accumulation and penetration. Recent research has started shading light on how the tumor variations can influence nanoparticle tumor delivery. These findings indicate that there is no "ideal" design of nanoparticles for exhibiting equally high efficacy against a broad spectrum of tumors. For achieving maximum benefit of the nanotherapeutics, it is necessary to analyze the tumor microenvironment for understanding the biological and structural characteristics of the tumor. Designing of the nanomedicine should be done according to the tumor characteristics. In this comprehensive review, we have first given a brief overview of the design characteristics of nanomedicine which impact their tumor delivery. Then we discussed about the variability in the tumor architecture and how it influences nanomedicine delivery. Finally, we have discussed the possibility of delivery system personalization based on the tumor characteristics.
自 1986 年发现增强的通透性和保留效应后,人们设想通过纳米颗粒介导的化疗药物靶向递送来彻底改变癌症治疗方法。然而,经过三十年的广泛研究,只有少数几种纳米药物被批准用于临床应用。尽管纳米医学在临床前研究中显示出了显著的优势,但临床结果却存在差异。深入的研究揭示了不同肿瘤之间(和肿瘤内部)存在显著的生化和结构差异。这些差异会极大地影响纳米药物的肿瘤递释和疗效。肿瘤穿透性是治疗效果积极的重要决定因素,同一种纳米药物针对不同的肿瘤可能表现出不同的疗效,这取决于肿瘤的积累和穿透程度。最近的研究开始揭示肿瘤的这些变化如何影响纳米颗粒的肿瘤递释。这些发现表明,不存在针对广谱肿瘤具有同等高效性的“理想”纳米颗粒设计。为了从纳米治疗中获得最大益处,有必要分析肿瘤微环境,以了解肿瘤的生物学和结构特征。纳米药物的设计应根据肿瘤特征进行。在这篇综述中,我们首先简要概述了影响其肿瘤递释的纳米药物设计特征。然后我们讨论了肿瘤结构的可变性及其如何影响纳米药物的递释。最后,我们讨论了根据肿瘤特征进行递释系统个性化的可能性。