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Multifunctional theranostic agents based on prussian blue nanoparticles for tumor targeted and MRI-guided photodynamic/photothermal combined treatment

机译:基于普鲁士蓝纳米粒子的多功能治疗剂肿瘤靶向和MRI引导光动力/光热组合治疗

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The independence of photodynamic or photothermal modality create difficulties in the success of tumor therapy. In this current study, a multifunctional nanotheranostic agent of PDE-Ce6-HA was developed for tumor targeted and MRI-guided photodynamic/photothermal combined therapy (PDT/PTT). For this purpose, the near-infrared-absorbing nanoparticles of prussian blue were coated with polydopamine and successively conjugated with chlorin e6 (Ce6) for reactive oxygen species (ROS) generation. The resultant nanoparticles, denoted as PDE-Ce6, were then modified with hyaluronic acid (HA) through electrostatic interaction to yield the final therapeutic agent of PDE-Ce6-HA NPs. PDE-Ce6-HA NPs not only exhibited high colloid stability, good biocompatibility and suitable transverse relaxation rate (0.54 mM(-1 )s(-1)), but also high photothermal conversion efficiency (40.4%) and excellent ROS generation efficiency under NIR light irradiation. The confocal microscopy images demonstrated a selective uptake of PDE-Ce6-HA by CD44 overexpressed HeLa cells via HA-mediated endocytosis. Meanwhile, in vitro anti-cancer evaluation verified the significant photodynamic and photothermal combined effects of PDE-Ce6-HA on cancer cells. Moreover, PDE-Ce6-HA led to an increase of T-1-MRI contrast in tumor site. Furthermore, in vivo anti-tumor evaluation proved that the PDE-Ce6-HA under both 808 and 670 nm laser showed significantly high tumor growth inhibition effects compared with individual PTT or PDT. Hence, PDE-Ce6-HA is applicable in tumor targeted and MRI-guided photodynamic/photothermal combined treatment.
机译:光动力学或光热模态的独立性在肿瘤治疗的成功方面产生了困难。在本前研究中,为肿瘤靶向和MRI引导的光动力/光热组合治疗(PDT / PTT)开发了PDE-CE6-HA的多功能纳米移植剂。为此目的,普鲁士蓝的近红外吸收纳米颗粒涂覆有多碳双胺并连续与氯庚烷E6(CE6)缀合,用于反应性氧(ROS)产生。然后通过透明化相互作用将所得纳米颗粒用透明质酸(HA)改性,得到PDE-CE6-HA NP的最终治疗剂。 PDE-CE6-HA NPS不仅表现出高胶体稳定性,良好的生物相容性和合适的横向弛豫率(0.54mm(-1)(-1)),而且高热的转换效率(40.4%)和优异的ROS生成效率尼尔光线照射。共聚焦显微镜图像通过HA介导的内吞作用,通过CD44过表达HELA细胞进行了选择性摄取PDE-CE6-HA。同时,体外抗癌评估验证了PDE-CE6-HA对癌细胞的显着光动力和光热组合效应。此外,PDE-CE6-HA导致肿瘤部位的T-1-MRI对比度增加。此外,在体内抗肿瘤评价中证明,与单独的PTT或PDT相比,在808和670nm激光下的PDE-CE6-HA显示出明显高的肿瘤生长抑制作用。因此,PDE-CE6-HA适用于肿瘤靶向和MRI引导的光动力/光热组合治疗。

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