光动力疗法
间充质干细胞
材料科学
光敏剂
纳米技术
光毒性
归巢(生物学)
纳米颗粒
癌症治疗
癌症研究
癌症
医学
化学
病理
生物
内科学
有机化学
体外
生物化学
生态学
作者
Greta Butkiene,Aleja Marija Daugelaite,Vilius Poderys,Riccardo Marin,Simona Steponkienė,Evelina Kazlauskė,Ilona Uzielienè,Dainius Daunoravičius,Daniel Jaque,Ričardas Rotomskis,Artiom Skripka,Fiorenzo Vetrone,Vitalijus Karabanovas
标识
DOI:10.1021/acsami.4c10098
摘要
Nanoparticles engineered to combat cancer and other life-threatening diseases may significantly improve patient outcomes. However, inefficient nanoparticle delivery to tumors limits their use and necessitates the development of complex delivery approaches. Here, we examine this issue by harnessing the tumor-homing abilities of human mesenchymal stem cells (MSCs) to deliver a decoupled theranostic complex of rare earth-doped nanoparticles (dNPs) and photosensitizer chlorin e6 (Ce6) to tumors. We show that both bone-marrow- and skin-derived MSCs can transport the dNP-Ce6 complex inside tumor spheroids, which is challenging to accomplish by passive delivery alone. MSCs deliver the dNP-Ce6 complex across the tumor spheroid, facilitating more effective photodynamic damage and tumor destruction than passively accumulated dNP-Ce6. The dNP-Ce6 complex also provides the built-in ability to monitor the MSC migration without causing undesired phototoxicity, which is essential for maximal and side-effect-free delivery of nanoparticles. Our results demonstrate how MSCs can be used as delivery vehicles for the transportation of the dNP-Ce6 complex, addressing the limitations of passive nanoparticle delivery and providing light-based theranostics.
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