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槲皮素@掺钆普鲁士蓝纳米立方体制剂诱导 MDA-MB-231 细胞发生细胞焦亡:联合靶向多模态治疗、双模态 MRI、弛豫率直观模拟。

Quercetin@Gd doped Prussian blue nanocubes induce the pyroptotic death of MDA-MB-231 cells: combinational targeted multimodal therapy, dual modal MRI, intuitive modelling of - relaxivities.

机构信息

School of Materials Science and Nanotechnology, Jadavpur University, Kolkata-700032, India.

Agricultural and Ecological Research Unit, Biological Science Division, Indian Statistical Institute, Giridih, Jharkhand, India.

出版信息

J Mater Chem B. 2023 Jul 19;11(28):6646-6663. doi: 10.1039/d3tb00316g.

Abstract

Quercetin (Qu), a potential bioflavonoid has gained considerable interest as a promising chemotherapeutic drug which can inhibit the proliferation of triple-negative breast cancer (TNBC) cells due to its regulation of the expression of tumor-suppressor gene metastasis and antioxidant property. Notably, Qu exhibits a very negligible cytotoxic effect on normal cells, even with high-dose treatment, while it is shows high affinity to TNBC. However, the efficiency of Qu is limited clinically due to its poor bioavailability, caused by its low aqueous solubility (2.15 μg mL at 25 °C), rapid gastrointestinal digestion and chemical instability in alkaline and neutral media. Herein, polydopamine (PDA)-coated, NH-PEG-NH and hyaluronic acid (HA)-functionalized Gd-doped Prussian blue nanocubes (GPBNC) are reported as a multifunctional platform for the codelivery of Qu as a chemotherapeutic agent and GPBNC as a photodynamic (PDT) and photothermal (PTT) agent with improved therapeutic efficiency to overcome theses barriers. PDA, NH-PEG-NH and HA stabilize GPBNC@Qu and facilitate bioavailability and active-targeting, while absorption of near infrared (NIR) (808 nm; 1 W cm) induces PDT and PTT activities and dual --weighted magnetic resonance imaging (MRI) with high relaxometric parameters ( 10.06 mM s and 24.96 mM s at a magnetic field of 3 T). The designed platform shows a pH-responsive Qu release profile and NIR-induced therapeutic efficiency of ∼79% in 20 minutes of irradiation, wherein N-terminal gardermin D (N-GSDMD) and a P2X7-receptor-mediated pyroptosis pathway induces cell death, corroborating the up-regulation of NLRP3, caspase-1, caspase-5, N-GSDMD, IL-1β, cleaved Pannexin-1 and P2X7 proteins. More interestingly, the increasing relaxivity values of Prussian blue nanocubes with Gd doping have been explained on the basis of Solomon-Bloembergen-Morgan theory, considering inner- and outer-sphere relaxivity, wherein crystal defects, coordinated water molecules, tumbling rate, metal to water proton distance, correlation time, magnetisation value play a significant role. In summary, our study suggests that GPBNC could be a beneficial nanocarrier for theranostic purposes against TNBC, while our conceptual study clearly demonstrates the role of various factors in increasing relaxometric parameters.

摘要

槲皮素 (Qu) 是一种有潜力的生物类黄酮,由于其调节肿瘤抑制基因转移和抗氧化特性,已成为一种有前途的化疗药物,可抑制三阴性乳腺癌 (TNBC) 细胞的增殖,因此备受关注。值得注意的是,Qu 对正常细胞的细胞毒性作用非常小,即使高剂量治疗也是如此,而它对 TNBC 具有高亲和力。然而,由于其低水溶解度 (25°C 时为 2.15μg mL)、快速胃肠道消化和在碱性和中性介质中的化学不稳定性,Qu 的临床效率受到限制。在此,报道了聚多巴胺 (PDA) 涂层、NH-PEG-NH 和透明质酸 (HA) 功能化的 Gd 掺杂普鲁士蓝纳米立方 (GPBNC) 作为一种多功能平台,用于共递送 Qu 作为化疗药物和 GPBNC 作为光动力 (PDT) 和光热 (PTT) 剂,以提高治疗效率,克服这些障碍。PDA、NH-PEG-NH 和 HA 稳定 GPBNC@Qu 并促进生物利用度和主动靶向,而吸收近红外 (NIR) (808nm; 1W cm) 诱导 PDT 和 PTT 活性以及具有高弛豫率参数的双重量磁共振成像 (MRI)(在 3T 磁场下为 10.06mM s 和 24.96mM s)。设计的平台显示出 pH 响应的 Qu 释放曲线和 NIR 诱导的治疗效率,在 20 分钟的照射下约为 79%,其中 N 端 Gardemin D (N-GSDMD) 和 P2X7 受体介导的细胞焦亡途径诱导细胞死亡,证实 NLRP3、半胱天冬酶-1、半胱天冬酶-5、N-GSDMD、IL-1β、cleaved Pannexin-1 和 P2X7 蛋白的上调。更有趣的是,基于 Solomon-Bloembergen-Morgan 理论,考虑到内球和外球弛豫率,解释了具有 Gd 掺杂的普鲁士蓝纳米立方的弛豫率值的增加,其中晶体缺陷、配位水分子、翻转率、金属与水质子的距离、相关时间、磁化值 起着重要的作用。总之,我们的研究表明,GPBNC 可能是治疗 TNBC 的治疗性纳米载体,而我们的概念性研究清楚地表明了各种因素在增加弛豫率参数方面的作用。

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