4.7 Article

Biocompatible Mesoporous Silica-Polydopamine Nanocomplexes as MR/Fluorescence Imaging Agent for Light-Activated Photothermal-Photodynamic Cancer Therapy In Vivo

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2021.752982

关键词

chlorin e6; magnetic resonance imaging; fluorescence imaging (FI); photothermal therapy; photodynamic theraphy; core shell nanoparticles

资金

  1. National Natural Science Foundation of China [81602533, 81901798]
  2. China Postdoctoral Science Foundation [2021M692710]
  3. Jiangsu Qinglan Project
  4. Postdoctoral Research Funding Program of Jiangsu Province [2021K190B]
  5. Promotion Fund for Youth Talent of Jiangsu Association for Science and Technology [TJ-2021-069]
  6. Postgraduate Research and Practice Innovation Program of Jiangsu Province [KYCX21_2644, KYCX21_2645]

向作者/读者索取更多资源

This study successfully designed a novel multifunctional nanocomplex with superior properties in MR imaging, photothermal conversion, and generation of reactive oxygen species. The nanocomplexes exhibited strong inhibition to the growth of MDA-MB-231 tumor in vitro and in vivo under the guidance of MR and fluorescence imaging.
Conventional cancer phototherapy with single modality suffers from low therapeutic efficacy and undesired posttreatment damage for adjacent normal tissues. Therefore, the lower NIR laser irradiation power is vital to the reduction or preclusion of risk of scalds and burns in normal tissues. Herein, we rationally proposed a novel multifunctional nanocomplex, which enabled good magnetic resonance (MR) imaging contrast effect and promising photothermal conversion efficacy. The prepared core/shell nanocomplexes [MSN-Ce6@PDA (Mn)] were composed of chlorin e6-embedded mesoporous silica/nanoparticle composites as the cores, and then polydopamine and manganese ions were conjugated on the cores to form protective shells. The MSN-Ce6@PDA (Mn) nanocomplexes revealed superior properties in colloidal stability, photothermal conversion, reaction oxygen species generation, magnetic resonance imaging, etc. Under the guidance of MR and fluorescence imaging, these MSN-Ce6@PDA (Mn) nanocomplexes were found to be primarily accumulated in the MDA-MB-231 tumor area. Furthermore, the combined photodynamic and photothermal therapy exhibited strong inhibition to the growth of MDA-MB-231 tumor in vitro and in vivo. Besides, the MSN-Ce6@PDA (Mn) nanocomplexes also exhibited excellent biocompatibility and low damage to the healthy animals. Hence, the results demonstrated that the prepared MSN-Ce6@PDA (Mn) nanocomplex would be a promising potential for multimodal imaging-guided phototherapy.

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