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Indocyanine green loaded APTMS coated SPIONs for dual phototherapy of cancer

  • Kubra Bilici
  • , Abdullah Muti
  • , Alphan Sennaroğlu
  • , Havva Yagci Acar*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • Koc University

Araştırma sonucu: Dergiye katkıMakalebilirkişi

27 Atıf (Scopus)

Özet

Superparamagnetic iron oxide nanoparticles (SPIONs) have been recently recognized as highly efficient photothermal therapy (PTT) agents. Here, we demonstrate, for the first time to our knowledge, dose and laser intensity dependent PTT potential of small, spherical, 3-aminopropyltrimethoxysilane coated cationic superparamagnetic iron oxide nanoparticles (APTMS@SPIONs) in aqueous solutions upon irradiation at 795 nm. Indocyanine green (ICG) which has been recently used for photodynamic therapy (PDT), was loaded to APTMS@SPIONs to improve the stability of ICG and to achieve an effective mild PTT and PDT (dual therapy) combination for synergistic therapeutic effect on cancer cells via a single laser treatment in the near infrared (NIR). Neither APTMS@SPIONs nor ICG-APTMS@SPIONs showed dark toxicity on MCF7 breast and HT29 colon cancer cell lines. A safe laser procedure was determined as 10 min irradiation at 795 nm with 1.8 W/cm2 of laser intensity, at which APTMS@SPION did not cause a significant cell death. However, free ICG reduced cell viability at and above 10 μg/ml under these conditions along with generation of reactive oxygen species (ROS), more effectively in MCF7. ICG-APTMS@SPION treated cells showed 2-fold increase in ROS generation and near complete cell death at and below 5 μg/ml ICG dose, even in less sensitive HT29 cells after a single laser treatment at NIR, which would be safe for the healthy tissue and provide a longer penetration depth. Besides, both components can be utilized for diagnosis and the overall composition may be used for optical-image guided phototherapy in the NIR region.

Orijinal dilİngilizce
Makale numarası111648
DergiJournal of Photochemistry and Photobiology B: Biology
Hacim201
DOI'lar
Yayın durumuYayınlandı - Ara 2019
Harici olarak yayınlandıEvet

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Publisher Copyright:
© 2019 Elsevier B.V.

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