Haider Tanweer, Sandha Kamalpreet Kaur, Soni Vandana, Gupta Prem N
Department of Pharmaceutical Sciences, Dr. Harisingh Gour University, Sagar, Madhya Pradesh 470003, India.
Formulation & Drug Delivery Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu, J&K 180001, India.
Mater Sci Eng C Mater Biol Appl. 2020 Nov;116:111229. doi: 10.1016/j.msec.2020.111229. Epub 2020 Jun 23.
As per a report of the world health organization, an estimated 9.6 million people died due to cancer in 2018, globally. Most of the cancer death attributed to the lack of early detection and effective treatment. In the case of solid tumors, various factors such as leaky vasculature, angiogenesis, interstitial fluid pressure and lymphatic drainage are important in cancer chemotherapy. The poor penetration and retention of the drug/drug delivery system in tumor tissue are most critical issues in the way of effective treatment. In this scenario, the challenges are to design the specific nano-therapeutics with the potential to penetrate inside the adverse condition of tumor microenvironment (TME) including high interstitial pressure region and abnormal vasculature. The modification of nanocarriers surfaces with enzymes, peptides, pH-responsive moieties, antibodies etc. could be a promising strategy to improve the nanocarriers penetration inside the solid tumor. The priming with the drug before the administration of nanotherapeutics may also represents an efficient approach for solid tumor treatment. Further, the growth factors including fibroblast growth factor (FGF), platelet-derived growth factor (PDGF), vascular endothelial growth factor (VEGF) and their pathways could offer potential targeting opportunities for anticancer treatment. Recently, there is a surge in various approaches and formulation design directed towards abnormal TME for more effective cancer therapy. In this review, various factors related to the poor penetration, retention and specific delivery of chemotherapeutics inside tumor cells/tissues are discussed. The emerging formulations strategies directed to the TME and various methodologies for evaluation of their efficacy are also included in this review.
根据世界卫生组织的一份报告,2018年全球估计有960万人死于癌症。大多数癌症死亡归因于缺乏早期检测和有效治疗。对于实体瘤,诸如血管渗漏、血管生成、间质液压力和淋巴引流等各种因素在癌症化疗中很重要。药物/药物递送系统在肿瘤组织中的渗透性差和滞留性差是有效治疗的最大关键问题。在这种情况下,挑战在于设计具有穿透肿瘤微环境(TME)不利条件(包括高间质压力区域和异常血管)潜力的特定纳米疗法。用酶、肽、pH响应部分、抗体等修饰纳米载体表面可能是提高纳米载体在实体瘤内渗透性的一种有前途的策略。在施用纳米疗法之前用药物进行预处理也可能是实体瘤治疗的一种有效方法。此外,包括成纤维细胞生长因子(FGF)、血小板衍生生长因子(PDGF)、血管内皮生长因子(VEGF)及其信号通路在内的生长因子可为抗癌治疗提供潜在的靶向机会。最近,针对异常TME的各种方法和制剂设计激增,以实现更有效的癌症治疗。在这篇综述中,讨论了与化疗药物在肿瘤细胞/组织内渗透性差、滞留性差和特异性递送相关的各种因素。本综述还包括针对TME的新兴制剂策略及其疗效评估的各种方法。