Center for Nanomedicine and Department of Anesthesiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Adv Mater. 2017 Sep;29(33). doi: 10.1002/adma.201700141. Epub 2017 Jul 6.
The application of nanoparticles (NPs) to drug delivery has led to the development of novel nanotherapeutics for the treatment of various diseases including cancer. However, clinical use of NP-mediated drug delivery has not always translated into improved survival of cancer patients, in part due to the suboptimal properties of NP platforms, such as premature drug leakage during preparation, storage, or blood circulation, lack of active targeting to tumor tissue and cells, and poor tissue penetration. Herein, an innovative reactive oxygen species (ROS)-responsive polyprodrug is reported that can self-assemble into stable NPs with high drug loading. This new NP platform is composed of the following key components: (i) polyprodrug inner core that can respond to ROS for triggered release of intact therapeutic molecules, (ii) polyethylene glycol (PEG) outer shell to prolong blood circulation; and (iii) surface-encoded internalizing RGD (iRGD) to enhance tumor targeting and tissue penetration. These targeted ROS-responsive polyprodrug NPs show significant inhibition of tumor cell growth both in vitro and in vivo.
纳米颗粒(NPs)在药物传递中的应用导致了新型纳米治疗药物的发展,可用于治疗包括癌症在内的各种疾病。然而,由于 NP 平台的性能不理想,如在制备、储存或血液循环过程中药物过早泄漏、缺乏对肿瘤组织和细胞的主动靶向以及组织穿透性差,NP 介导的药物传递的临床应用并未总是转化为癌症患者生存的改善。在此,报道了一种创新的活性氧(ROS)响应性多前药,可自组装成具有高载药量的稳定 NPs。该新型 NP 平台由以下关键组件组成:(i)多前药内核,可响应 ROS 触发完整治疗分子的释放,(ii)聚乙二醇(PEG)外壳以延长血液循环;和(iii)表面编码的内化 RGD(iRGD)以增强肿瘤靶向和组织穿透性。这些靶向 ROS 响应性多前药 NPs 在体外和体内均显示出对肿瘤细胞生长的显著抑制作用。