State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD), College of Pharmacy, Harbin Medical University, Harbin, China.
State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD), College of Pharmacy, Harbin Medical University, Harbin, China.
Acta Biomater. 2024 Oct 1;187:328-339. doi: 10.1016/j.actbio.2024.08.020. Epub 2024 Aug 22.
Balancing biocompatibility and drug-loading efficiency in nanoparticles presents a significant challenge. In this study, we describe the facile fabrication of poly (acrylic acid)-mesoporous zinc phosphate/polydopamine (PAA-mZnP/PDA) Janus nanoparticles (JNPs). The PDA half-shell itself can serve as a photothermal agent for photothermal therapy (PTT), as well as to offers sites for polyethylene glycol (PEG) to enhance biocompatibility. Concurrently, the mesoporous ZnP core allows high loading of doxorubicin (DOX) for chemotherapy and the Cy5.5 dye for fluorescence imaging. The resultant PAA-mZnP/PDA-PEG JNPs exhibit exceptional biocompatibility, efficient drug loading (0.5 mg DOX/1 mg JNPs), and dual pH/NIR-responsive drug release properties. We demonstrate the JNPs' satisfactory anti-cancer efficacy, highlighting the synergistic effects of chemotherapy and PTT. Furthermore, the potential for synergistic fluorescence imaging-guided chemo-phototherapy in cancer treatment is illustrated. Thus, this work exemplifies the development of biosafe, multifunctional JNPs for advanced applications in cancer theranostics. STATEMENT OF SIGNIFICANCE: Facile fabrication of monodispersed nanomedicine with multi-cancer killing modalities organically integrated is nontrivial and becomes more challenging under the biocompatibility requirement that is necessary for the practical applications of nanomedicines. In this study, we creatively designed PAA-mZnP/PDA JNPs and fabricated them under mild conditions. Our method reliably yields uniform JNPs with excellent monodispersity. To maximize functionalities, we achieve fourfold advantages including efficient drug/fluorescent dye loading, PTT, pH/NIR dual-responsive properties, and optimal biocompatibility. The as-fabricated JNPs exhibit satisfactory anti-cancer performance both in vitro and in vivo, and demonstrate the potential of JNPs in fluorescence imaging-guided synergistic cancer chemo-phototherapy. Overall, our research establishes a pathway in versatile inorganic/polymer JNPs for enhanced cancer diagnosis and therapy.
平衡纳米粒子的生物相容性和药物载药量是一个重大挑战。在本研究中,我们描述了聚(丙烯酸)-介孔磷酸锌/聚多巴胺(PAA-mZnP/PDA) 双节 Janus 纳米粒子(JNPs)的简便制备方法。PDA 半壳本身可用作光热治疗(PTT)的光热剂,并提供聚乙二醇(PEG)的附着点以增强生物相容性。同时,介孔 ZnP 核允许高载药量的阿霉素(DOX)用于化学疗法和 Cy5.5 染料用于荧光成像。所得的 PAA-mZnP/PDA-PEG JNPs 表现出优异的生物相容性、高效的药物负载(0.5mg DOX/1mg JNPs)和双 pH/NIR 响应性药物释放特性。我们证明了 JNPs 令人满意的抗癌功效,突出了化学疗法和 PTT 的协同作用。此外,还说明了在癌症治疗中协同荧光成像引导的化学-光疗的潜力。因此,这项工作展示了生物安全、多功能 JNPs 的开发,可用于癌症治疗的先进应用。
在生物相容性要求下,将具有多种抗癌杀伤模式的纳米药物有机整合在一起,制备出单分散的纳米药物并非易事,而对于纳米药物的实际应用而言,这一要求变得更加具有挑战性。在本研究中,我们创造性地设计了 PAA-mZnP/PDA JNPs,并在温和的条件下制备了它们。我们的方法可靠地生成具有优异单分散性的均匀 JNPs。为了最大化功能,我们实现了四重优势,包括高效的药物/荧光染料负载、PTT、pH/NIR 双重响应性和最佳的生物相容性。所制备的 JNPs 在体外和体内均表现出令人满意的抗癌性能,并展示了 JNPs 在荧光成像引导协同癌症化学-光疗中的潜力。总体而言,我们的研究为多功能无机/聚合物 JNPs 用于增强癌症诊断和治疗建立了一条途径。