4.8 Article

Size-Tunable Gd2O3@Albumin Nanoparticles Conjugating Chlorin e6 for Magnetic Resonance Imaging-Guided Photo-Induced Therapy

期刊

THERANOSTICS
卷 7, 期 3, 页码 764-774

出版社

IVYSPRING INT PUBL
DOI: 10.7150/thno.15757

关键词

albumin nanoreactor; gadolinium oxide; photosensitizer; magnetic resonance imaging; photodynamic therapy

资金

  1. National Basic Research Program [2014CB931900]
  2. National Natural Science Foundation of China [31671016, 31422021, 51473109, 21505096]
  3. Postdoctoral Science Foundation of China [2015T80575, 2014M560442]
  4. Jiangsu Provincial Special Program of Clinical Medical Science [BL2014040]
  5. Suzhou Scientific and Technological Development Project [SYSD2013094]
  6. Priority academic program development of Jiangsu higher education institutions (PAPD)
  7. Jiangsu Provincial Key Laboratory of Radiation Medicine and Protection
  8. Jiangsu Key Laboratory of Translational Research and Therapy for Neuro-Psycho-Diseases [BM2013003]

向作者/读者索取更多资源

Protein nanoparticles as nanocarriers are of particular interest in the field of cancer therapy. Nevertheless, so far a facile fabrication of theranostic protein nanoparticles have been explored with limited success for cancer imaging and therapy. In this work, we demonstrate the controllable synthesis of size-tunable Gd2O3@albumin conjugating photosensitizer (PS) (GA-NPs) using hollow albumin as the nanoreactor for magnetic resonance imaging (MRI)-guided photo-induced therapy. The growth of Gd2O3 nanocrystals within the hollow nanoreactors is well regulated through reaction time, and a typical PS (e.g. chlorin e6) is further conjugated with the protein corona of the nanoreactor through facile chemical coupling, followed by the formation of theranostic GA-NPs. GA-NPs exhibit good longitudinal relaxivity, ideal photostability, enhanced cellular uptakes, and preferable size-dependent tumor accumulation. Moreover, GA-NPs effectively generate remarkable photothermal effect, intracellular reactive oxygen species from Ce6, and subsequent cytoplasmic drug translocation, thereby leading to severe synergistic photothermal and photodynamic cell damages. Consequently, GA-NPs exhibit an in vivo size-dependent MRI capacity with enhanced imaging contrast for effective tumor localization, and also generate a potent synergistic photodynamic therapy/photothermal therapy efficacy under irradiation owing to their enhanced tumor accumulation and strong photo-induced cytotoxicity. These results suggest that GA-NPs can act as a promising theranostic protein nanoplatform for cancer imaging and photo-induced therapy.

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