Dual-Modal Near-Infrared Organic Nanoparticles: Integrating Mild Hyperthermia Phototherapy with Fluorescence Imaging

Int J Nanomedicine. 2024 Sep 5:19:9071-9090. doi: 10.2147/IJN.S472882. eCollection 2024.

Abstract

Purpose: Our study seeks to develop dual-modal organic-nanoagents for cancer therapy and real-time fluorescence imaging, followed by their pre-clinical evaluation on a murine model. Integrating NIR molecular imaging with nanotechnology, our aim is to improve outcomes for early-stage cutaneous melanoma by offering more effective and less invasive methods. This approach has the potential to enhance both photothermal therapy (PTT) and Sentinel Lymph Node Biopsy (SLNB) procedures for melanoma patients.

Methods: NIR-797-isothiocyanate was encapsulated in poly(D,L-lactide-co-glycolide) acid (PLGA) nanoparticles (NPs) using a two-step protocol, followed by thorough characterization, including assessing loading efficiency, fluorescence stability, and photothermal conversion. Biocompatibility and cellular uptake were tested in vitro on melanoma cells, while PTT assay, with real-time thermal monitoring, was performed in vivo on tumor-bearing mice under irradiation with an 808 nm laser. Finally, ex vivo fluorescence microscopy, histopathological assay, and TEM imaging were performed.

Results: Our PLGA NPs, with a diameter of 270 nm, negative charge, and 60% NIR-797 loading efficiency, demonstrated excellent stability and fluorescence properties, as well as efficient light-to-heat conversion. In vitro studies confirmed their biocompatibility and cellular internalization. In vivo experiments demonstrated their efficacy as photothermal agents, inducing mild hyperthermia with temperatures reaching up to 43.8 °C. Ex vivo microscopy of tumor tissue confirmed persistent NIR fluorescence and uniform distribution of the NPs. Histopathological and TEM assays revealed early apoptosis, immune cell response, ultrastructural damage, and intracellular material debris resulting from combined NP treatment and irradiation. Additionally, TEM analyses of irradiated zone margins showed attenuated cellular damage, highlighting the precision and effectiveness of our targeted treatment approach.

Conclusion: Specifically tailored for dual-modal NIR functionality, our NPs offer a novel approach in cancer PTT and real-time fluorescence monitoring, signaling a promising avenue toward clinical translation.

Keywords: NIR fluorescence imaging; NIR phototherapeutic agents; dual-modal agents; melanoma; mild hyperthermia; organic nanoparticles.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Humans
  • Hyperthermia, Induced* / methods
  • Melanoma / diagnostic imaging
  • Melanoma / therapy
  • Mice
  • Nanoparticles* / chemistry
  • Optical Imaging*
  • Phototherapy / methods
  • Photothermal Therapy / methods
  • Polylactic Acid-Polyglycolic Acid Copolymer* / chemistry
  • Skin Neoplasms / diagnostic imaging
  • Skin Neoplasms / pathology
  • Skin Neoplasms / therapy

Substances

  • Polylactic Acid-Polyglycolic Acid Copolymer

Grants and funding

This work was supported by a grant from the Ministry of Research and Innovation, CNCS-UEFISCDI, project number PN-III-P4-ID-PCCF-2016-0142, within PNCDI III and by the project Plasmon mediated biology: Exploitation of plasmonics to investigate and enhance biological processes and application to biomedical issues (acronym: BioPlasmonics) funded by European Union – NextgenerationEU and Romanian Government, under National Recovery and Resilience Plan for Romania, contract no760037/23.05.2023, cod PNRR-C9-I8-CF-199/28.11.2023, through the Romanian Ministry of Research, Innovation and Digitalization, within Component 9, Investment I8. Madalina Tudor is thankful for the Special Scholarship for Scientific Activity, grant awarded by STAR-UBB (Babes-Bolyai University), contract number 36617/25.11.2022.