Institute of Ultrasound Imaging, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, P. R. China.
Department of Ultrasound, Zhongda Hospital, Southeast University, Nanjing 210009, P. R. China.
Theranostics. 2018 Nov 29;8(22):6178-6194. doi: 10.7150/thno.29569. eCollection 2018.
Multifunctional nanoplatforms with diagnostic-imaging and targeted therapeutic functionality (theranostics) are of great interest in the field of precision nanomedicine. The emerging sonodynamic therapy (SDT) combined with sonosensitizers under the guidance of photoacoustic (PA) imaging is highly expected to accurately eliminate cancer cells/tissue. Unique core/shell-structured theranostic FA-HMME-MNPs-PLGA nanoparticles (FHMP NPs, FA: folate, HMME: hematoporphyrin monomethyl ether, MNPs: melanin nanoparticles, PLGA: poly (lactic-co-glycolic) acid) were constructed by the integration of MNPs (for PA imaging) in the core and HMME in the shell for enhanced PA imaging-guided SDT, which were further functionalized with a tumor-targeting ligand, FA. The PA imaging-guided SDT was systematically and successfully demonstrated both and . The high biosafety of FHMP NPs was also systematically evaluated. The synthesized FHMP NPs with a broad optical absorption not only possess high PA-imaging contrast enhancement capability but also exhibit significant SDT efficiency. Importantly, such a PLGA based nanoplatform improved light stability of HMME, enhancing sonodynamic performance and facilitated delivery of MNPs to the tumor region. Meanwhile, a combined effect between HMME and MNPs was discovered and verified. Furthermore, a sonosensitizer assisted by ultrasound irradiation engenders reactive oxygen species (ROS)-mediated cytotoxicity toward tumor cells/tissue. Both cell-level and systematic xenograft evaluations on tumor-bearing mice demonstrated that the selective killing effect of ROS on tumor cells was assisted by FHMP NPs, which played an active role in the suppression of tumor growth with high biosafety. A theranostic nanoplatform was successfully constructed, achieving PA imaging-guided SDT against breast cancer cells/tissue. More importantly, MNPs and HMME in one platform with combined effect for enhancing PA imaging was demonstrated. This unique theranostic nanoplatform with multiple capabilities paves a new way toward personalized medicine by rational utilization.
多功能纳米平台具有诊断成像和靶向治疗功能(治疗学),在精准纳米医学领域引起了极大的关注。新兴的声动力学治疗(SDT)结合声敏剂在光声(PA)成像的指导下,有望准确消除癌细胞/组织。独特的核/壳结构的治疗 FA-HMME-MNPs-PLGA 纳米粒子(FHMP NPs,FA:叶酸,HMME:血卟啉单甲醚,MNPs:黑色素纳米粒子,PLGA:聚(乳酸-共-乙醇酸))是通过 MNPs(用于 PA 成像)在核中和 HMME 在壳中构建的,用于增强 PA 成像引导的 SDT,并进一步功能化肿瘤靶向配体 FA。PA 成像引导的 SDT 被系统地和成功地证明了。FHMP NPs 的高生物安全性也得到了系统的评估。合成的 FHMP NPs 具有宽的光吸收,不仅具有高的 PA 成像对比度增强能力,而且具有显著的 SDT 效率。重要的是,这种基于 PLGA 的纳米平台提高了 HMME 的光稳定性,增强了声动力学性能,并促进了 MNPs 向肿瘤区域的递送。同时,发现并验证了 HMME 和 MNPs 之间的协同作用。此外,超声辐照辅助声敏剂产生活性氧(ROS)介导的肿瘤细胞/组织细胞毒性。在荷瘤小鼠的细胞水平和系统水平的异种移植评价中,ROS 对肿瘤细胞的选择性杀伤作用是由 FHMP NPs 辅助的,FHMP NPs 在抑制肿瘤生长方面发挥了积极作用,具有很高的生物安全性。成功构建了一种治疗学纳米平台,实现了 PA 成像引导的乳腺癌细胞/组织的 SDT。更重要的是,展示了具有增强 PA 成像的协同作用的单一平台中的 MNPs 和 HMME。这种具有多种功能的独特治疗学纳米平台为个性化医学的发展开辟了新途径。