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基于近红外光激活上转换纳米粒子(UCNP)的光动力学疗法治疗前列腺癌:一项体外研究。

Near infrared light activated upconversion nanoparticles (UCNP) based photodynamic therapy of prostate cancers: An in vitro study.

机构信息

Bogazici Universitesi Biyomedikal Muhendisligi Enstitusu, Institute of Biomedical Engineering, Kandilli Kampüs Çengelköy, Uskudar, Istanbul 34684, Turkey; Halic University, Beyoglu, Istanbul 34445, Turkey.

Department of Chemistry, Koc University Beyoglu, Sariyer, Istanbul 34450, Turkey.

出版信息

Photodiagnosis Photodyn Ther. 2021 Dec;36:102616. doi: 10.1016/j.pdpdt.2021.102616. Epub 2021 Nov 2.

Abstract

Photodynamic therapy (PDT), has a potential to cure cancerous prostate tissue with minimal side effects. Traditional PDT, however, mostly utilized visible (VIS) light range with direct application of hydrophobic photosensitizers which may not be adequate in clinical practice for especially deep-seated cancer cells because of poor penetration of VIS wavelengths. Here, we report near infrared light (NIR) induced and dual photosensitizers (PS) encapsulated PDT strategy to reduce prostate cancer cells - PC3. The designed nanoplatform (MC540/ZnPc-UCNP@Au), in this study, include upconversion nanoparticles (UCNP) synthesis to convert NIR light into multiple VIS wavelengths, porous silica coating to upload dual photosensitizers (MC540/ZnPc), and gold (Au) functionalization to enhance PDT treatment. High chemical stabilization provided MC540/ZnPc-UCNP@Au show excellent biocompatibility, and efficient PDT treatment for prostate cancer cells. In fact, the fluorescence of the synthesized nanoplatforms, upon NIR light excitation, can produce considerable amount of ROS in 5 min, as it is well matched with the absorption of MC540, ZnPc and Au nanoparticles (np). In addition, the easy visualization of cellular internalized/adsorbed nanoplatforms reveal the in situ cell imaging possibility for diagnosis. Based on the evidence of the results, NIR light activated MC540/ZnPc-UCNP@Au may offer a PDT technique for the treatment of prostate cancer.

摘要

光动力疗法(PDT)具有最小副作用治愈癌性前列腺组织的潜力。然而,传统的 PDT 主要利用可见光(VIS)范围,直接应用疏水性光敏剂,由于 VIS 波长的穿透性差,在临床实践中可能不足以治疗特别是深层癌细胞。在这里,我们报告了近红外光(NIR)诱导和双光敏剂(PS)封装 PDT 策略,以减少前列腺癌细胞 - PC3。在这项研究中,所设计的纳米平台(MC540/ZnPc-UCNP@Au)包括上转换纳米粒子(UCNP)的合成,以将 NIR 光转换为多个 VIS 波长,多孔硅涂层以上传双光敏剂(MC540/ZnPc),和金(Au)功能化以增强 PDT 治疗。MC540/ZnPc-UCNP@Au 提供了高化学稳定性,表现出优异的生物相容性和对前列腺癌细胞的高效 PDT 治疗。实际上,合成的纳米平台在 NIR 光激发下的荧光,可以在 5 分钟内产生相当数量的 ROS,因为它与 MC540、ZnPc 和 Au 纳米粒子(np)的吸收很好地匹配。此外,细胞内吞/吸附纳米平台的易可视化揭示了用于诊断的原位细胞成像的可能性。基于结果的证据,NIR 光激活的 MC540/ZnPc-UCNP@Au 可能为治疗前列腺癌提供 PDT 技术。

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