Mo Zhimin, Luo Yuxuan, Xu Qi, Liang Jiexi, Wang Zimeng, He Qianyuan, Xu Zushun
Guangxi Colleges and Universities Key Laboratory of Natural and Biomedical Polymer Materials, and College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, PR China; Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science and Engineering, Hubei University, Wuhan 430062, PR China.
Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science and Engineering, Hubei University, Wuhan 430062, PR China.
Colloids Surf B Biointerfaces. 2025 Jan;245:114287. doi: 10.1016/j.colsurfb.2024.114287. Epub 2024 Oct 2.
The acidic nature of malignant tumors leads to increased drug sequestration and the evasion of apoptotic damage, which is further exacerbated by abnormal lysosomes in tumor cells. In this study, a "lysosomal bomb" will be constructed using a type of acid-neutralized amorphous calcium carbonate (ACC) to encapsulate the sonosensitizer protoporphyrin IX (PpIX), and then coated with homologous tumor cell membranes to increase water solubility and homologous targeting. The PpIX-ACC@CMs designed in this paper are popcorn-like structures, which can not only neutralize the tumor's acidic microenvironment to balance the pH value and release excess Ca, but also cause lysosomal dysfunction and achieve drug lysosomal escape to increase drug accumulation. Additionally, the CO gas nucleus produced by the acid reaction of ACC can increase the ultrasonic cavitation effect to amplify the sonodynamic therapy (SDT) effect. In vitro and in vivo experiments demonstrated that PpIX-ACC@CMs, serving as a "lysosomal bomb," successfully localized to lysosomes of tumor cells and exhibited lysosomal escape ability through its acid reaction ability, achieving excellent SDT efficacy under ultrasound stimulation. Furthermore, exogenous Ca overload also increased the likelihood of tumor calcification, which could contribute to in vivo tumor inhibition and facilitate CT medical imaging to monitor treatment efficacy.
恶性肿瘤的酸性性质导致药物隔离增加和凋亡损伤的逃避,肿瘤细胞中异常的溶酶体进一步加剧了这种情况。在本研究中,将使用一种酸中和的无定形碳酸钙(ACC)构建“溶酶体炸弹”,以包裹声敏剂原卟啉IX(PpIX),然后用同源肿瘤细胞膜包被以增加水溶性和同源靶向性。本文设计的PpIX-ACC@CMs是爆米花状结构,它不仅可以中和肿瘤的酸性微环境以平衡pH值并释放过量的Ca,还会导致溶酶体功能障碍并实现药物溶酶体逃逸以增加药物积累。此外,ACC酸反应产生的CO气体核可以增加超声空化效应以放大声动力疗法(SDT)效果。体外和体内实验表明,PpIX-ACC@CMs作为“溶酶体炸弹”,成功定位于肿瘤细胞的溶酶体,并通过其酸反应能力表现出溶酶体逃逸能力,在超声刺激下实现了优异的SDT疗效。此外,外源性Ca过载也增加了肿瘤钙化的可能性,这可能有助于体内肿瘤抑制并促进CT医学成像以监测治疗效果。