College of Life Science, Zhuhai College of Science and Technology, Zhuhai, 519041, People's Republic of China.
College of Life Science, Jilin University, Changchun, 130012, People's Republic of China.
Int J Nanomedicine. 2024 Nov 7;19:11445-11462. doi: 10.2147/IJN.S479125. eCollection 2024.
The poor delivery and limited penetration of nanoparticles into breast cancer tumors remain essential challenges for effective anticancer therapy. This study aimed to design a promising nanoplatform with efficient tumor targeting and penetration capability for effective breast cancer therapy.
A pH-sensitive mitoxantrone (MTO) and copper ion-loaded nanosystem functionalized with cyclic CRGDfK and r9 peptide (TPRN-CM) was rationally designed for chemo-chemodynamic combination therapy. TPRN-CM would be quiescent in blood circulation with the CRGDfK peptide on the surface of the nanoparticle to improve its targeting to the tumor. Then, the structure of TPRN-CM changes in the acidic tumor microenvironment, and the r9 peptide can be exposed to make a surface charge reversal to promote deep penetration in the tumor and facilitate their internalization by cancer cells, which was characterized using transmission electron microscopy, dynamic light scattering, flame atomic absorption, etc. The drug release behavior, anti-tumor effects in vivo and in vitro, and the biosafety of the nanoplatform were evaluated.
TPRN-CM exhibited remarkable capability to load MTO and Cu with good stability in serum. It can achieve pH-responsive charge reversal, MTO, and Cu release, and can further generate toxic hydroxyl radicals in the presence of glutathione (GSH) and HO. In vitro experiments demonstrated that this nanoplatform significantly inhibited proliferation, migration, invasion activities and 3D-tumorsphere growth. In vivo experiments suggested that rationally designed TPRN-CM can be effectively delivered to breast cancer tumors with deep tumor penetration, thereby resulting in a notable reduction in tumor growth and suppression of lung metastasis without causing any apparent side effects.
The constructed TPRN-CM nanoplatform integrated tumor targeting, tumor penetration, drug-responsive release, and chemo-chemodynamic combination therapy, thereby providing an intelligent drug delivery strategy to improve the efficacy of breast cancer treatment.
纳米颗粒在乳腺癌肿瘤中的递药效果差且穿透深度有限,这仍然是实现有效抗癌治疗的重大挑战。本研究旨在设计一种具有高效肿瘤靶向和穿透能力的有前途的纳米平台,用于有效治疗乳腺癌。
合理设计了一种 pH 敏感的米托蒽醌(MTO)和负载铜离子的纳米系统,该纳米系统通过环状 CRGDfK 和 r9 肽(TPRN-CM)进行功能化,用于化学-化学动力学联合治疗。TPRN-CM 在血液循环中处于静止状态,纳米颗粒表面的 CRGDfK 肽可提高其对肿瘤的靶向性。然后,TPRN-CM 的结构在酸性肿瘤微环境中发生变化,并且 r9 肽可以暴露出来,使表面电荷反转,以促进在肿瘤中的深层穿透,并促进癌细胞的内化,这是通过透射电子显微镜、动态光散射、火焰原子吸收等进行表征的。评价了该纳米平台的药物释放行为、体内和体外抗肿瘤效果以及生物安全性。
TPRN-CM 表现出显著的载药 MTO 和 Cu 的能力,在血清中具有良好的稳定性。它可以实现 pH 响应性电荷反转、MTO 和 Cu 释放,并且在存在谷胱甘肽(GSH)和 HO 的情况下可以进一步产生有毒的羟基自由基。体外实验表明,该纳米平台可显著抑制增殖、迁移、侵袭活性和 3D 肿瘤球生长。体内实验表明,合理设计的 TPRN-CM 可以有效地递送到乳腺癌肿瘤中,具有深层肿瘤穿透性,从而导致肿瘤生长显著减少和肺转移抑制,而没有引起任何明显的副作用。
构建的 TPRN-CM 纳米平台集成了肿瘤靶向、肿瘤穿透、药物响应性释放以及化学-化学动力学联合治疗,从而提供了一种智能药物输送策略,以提高乳腺癌治疗的疗效。