光动力疗法
乙二醇
材料科学
纳米颗粒
光敏剂
赫拉
PEG比率
复合数
纳米技术
光化学
体外
化学
有机化学
经济
复合材料
生物化学
财务
作者
Jingning Shan,Stephanie J. Budijono,Guohong Hu,Nan Yao,Yibin Kang,Yiguang Ju,Robert K. Prud’homme
标识
DOI:10.1002/adfm.201002516
摘要
Abstract The utilization of upconverting nanophosphors (UCNP) for photodynamic therapy (PDT) has gained significant interests due to its ability to convert deep‐penetrating near‐infra red (NIR) light (i.e., 978 nm) to visible light. Previous attempts to co‐localize UCNPs with photosensitizers suffer from low photosensitizer loading and problems with nanoparticle aggregation. Here, the preparation of a novel composite nanoparticle formulation comprising 100 nm β −NaYF 4 :Yb 3+ ,Er 3+ UCNPs, and meso ‐tetraphenyl porphine (TPP) photosensitizer, stabilized by biocompatible poly(ethylene glycol‐ block ‐( dl )lactic acid) block copolymers (PEG‐ b ‐PLA) is presented. A photosensitizer loading of 10 wt% with respect to UCNP crystal was achieved via the Flash NanoPrecipitation (FNP) process. A sterically stabilizing PEG layer on the composite nanoparticle surface prevents nanoparticle aggregation and ensures nanoparticle stability in water, PBS buffer, and culture medium containing serum proteins, resulting in nanoparticle suitable for in vivo applications. Based on in vitro studies utilizing HeLa cervical cancer cell lines, the composite nanoparticles are shown to exhibit low dark toxicity and efficient cancer cell‐killing activity upon NIR excitation. Exposure with 134 W cm −2 of 978 nm light for 45 min resulted in 75% HeLa cell death. This is the first quantification of the cell‐killing capabilities of the UCNP/TPP composite nanoparticles formulated for photodynamic therapy.
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