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首页> 外文期刊>Materials Chemistry Frontiers >Aza-BODIPY encapsulated polymeric nanoparticles as an effective nanodelivery system for photodynamic cancer treatment
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Aza-BODIPY encapsulated polymeric nanoparticles as an effective nanodelivery system for photodynamic cancer treatment

机译:Aza-BODIPY封装聚合物纳米颗粒一个有效的nanodelivery光动力系统癌症治疗

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摘要

Polymeric nanoparticles represent an emerging technology in the field of theranostic nanomedicine that combines diagnostic and therapeutic applications in a single agent. In this work, iodo-substituted aza- BODIPY (AZB-I) encapsulated nanoparticles were prepared via the nanoprecipitation method using the amphiphilic poly(ethylene glycol)-block-poly(e-caprolactone) polymer (PEG-b-PCL) for a targeted nanodelivery system. The resulting nanoparticles (AZB-I@PEG-b-PCL) exhibited a monodisperse spherical morphology with hydrodynamic average sizes ranging from 44.6 to 48.2 nm. Apart from cellular imaging through near-infrared (NIR) light, the AZB-I@PEG-b-PCL NPs can be efficiently applied for 4T1 breast cancer cell treatment upon 660 nm red LED lamp irradiation for 30 min with up to 40 mM of AZB-I content. Detection of intracellular reactive oxygen species (ROS) in cells as well as the live/ dead viability/cytotoxicity assay after NIR light exposure confirmed the PDT efficacy of the NPs. Finally, the in vivo PDT capability of the obtained NPs was systematically investigated in 4T1 tumor-bearing mice. The results indicated that mice treated with AZB-I@PEG-b-PCL NPs at 32 mg kg1 (equivalent to 2mgkg1 AZB-I) showed 49.8% tumor growth inhibition at day-3 post PDT and tumor growth suppression for up to 14 days post PDT.
机译:聚合物纳米粒子表示一个新兴theranostic领域的技术诊断和纳米相结合单药治疗应用。这项工作,iodo-substituted阿扎- BODIPY (AZB-I)封装的纳米粒子通过就做好了准备nanoprecipitation使用两亲性方法聚(乙二醇)-block-poly (e-caprolactone)有针对性的nanodelivery聚合物(PEG-b-PCL)系统。(AZB-I@PEG-b-PCL)表现出一种单分散的球形形态与水动力的平均水平尺寸从44.6到48.2纳米。细胞成像通过近红外(NIR)光,AZB-I@PEG-b-PCL NPs可以有效申请4 t1乳腺癌细胞治疗660纳米红色LED灯照射30分钟40毫米的AZB-I内容。细胞内活性氧(ROS)细胞以及生活/死了近红外光谱光后生存能力/细胞毒性试验曝光证实了PDT NPs的功效。最后,体内PDT的能力获得NPs是系统地研究4 t1带有肿瘤的老鼠。老鼠接受AZB-I@PEG-b-PCL NPs在32mg kg1(相当于2 mgkg1 AZB-I)显示,49.8%在第三天发布PDT和肿瘤生长抑制肿瘤生长抑制长达14天牧师逃离。

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