4.8 Article

Tumor-Selective Immune-Active Mild Hyperthermia Associated with Chemotherapy in Colon Peritoneal Metastasis by Photoactivation of Fluorouracil-Gold Nanoparticle Complexes

Journal

ACS NANO
Volume 15, Issue 2, Pages 3330-3348

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c10276

Keywords

peritoneal metastasis; photothermal therapy; gold nanoparticles; 5-fluorouracil; carcinomatosis

Funding

  1. Paris-IdF region SESAME [12015908]
  2. ITMO-Inserm Plan Cancer 2014-2019 [PC201620]
  3. ANR [CarGold-16-CE09026, Coligomere-18-CE06-0006]
  4. Fondation ARC Association pour la Recherche sur le Cancer (ARC) [20150603405, 20190508933]
  5. Institut thematique mutli-organsismes (ITMO) Cancer
  6. doctorale school Frontieres du Vivant (FdV)-Programme Bettencourt
  7. doctoral school Physique en Ile de France (EDPIF)
  8. medical school of Toulouse
  9. European Union's Horizon 2020 research and innovation program [685795, 801305]

Ask authors/readers for more resources

A strategy using near-infrared photoactivated gold nanoparticles coupled with chemotherapy drug was proposed to achieve precise treatment of tumor nodules within the peritoneal cavity, providing potential to overcome the off-target toxicity and high morbidity of traditional HIPEC. The combined photothermal and chemotherapy mediated by the AuNP-drug complex showed efficient antitumor effects and activation of immune response while leaving healthy tissues undamaged.
Peritoneal metastasis (PM) is considered as the terminal stage of metastatic colon cancer, with still poor median survival rate even with the best recent chemotherapy treatment. The current PM treatment combines cytoreductive surgery, which consists of resecting all macroscopic tumors, with hyperthermic intraperitoneal chemotherapy (HIPEC), which uses mild hyperthermia to boost the diffusion and cytotoxic effect of chemotherapeutic drugs. As HIPEC is performed via a closed circulation of a hot liquid containing chemotherapy, it induces uncontrolled heating and drug distribution in the whole peritoneal cavity with important off-site toxicity and a high level of morbidity. Here, we propose a safer precision strategy using near-infrared (NIR) photoactivated gold nanoparticles (AuNPs) coupled to the chemotherapeutic drug 5-fluorouracil (5-FU) to enable a spatial and temporal control of mild chemo-hyperthermia targeted to the tumor nodules within the peritoneal cavity. Both the 16 nm AuNPs and the corresponding complex with 5-FU (AuNP-5-FU) were shown as efficient NIR photothermal agents in the microenvironment of subcutaneous colon tumors as well as PM in syngeneic mice. Noteworthy, NIR photothermia provided additional antitumor effects to 5-FU treatment. A single intraperitoneal administration of AuNP-5-FU resulted in their preferential accumulation in tumor nodules and peritoneal macrophages, allowing light-induced selective hyperthermia, extended tumor necrosis, and activation of a pro-inflammatory immune response while leaving healthy tissues without any damage. From a translational standpoint, the combined and tumor-targeted photothermal and chemotherapy mediated by the AuNP-drug complex has the potential to overcome the current off-target toxicity of HIPEC in clinical practice.

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