Porphyrin-Based Self-Assembled Nanoparticles for PET/MR Imaging of Sentinel Lymph Node Metastasis

ACS Appl Mater Interfaces. 2024 May 29;16(21):27139-27150. doi: 10.1021/acsami.4c03611. Epub 2024 May 16.

Abstract

Diagnosing of lymph node metastasis is challenging sometimes, and multimodal imaging offers a promising method to improve the accuracy. This work developed porphyrin-based nanoparticles (68Ga-F127-TAPP/TCPP(Mn) NPs) as PET/MR dual-modal probes for lymph node metastasis imaging by a simple self-assembly method. Compared with F127-TCPP(Mn) NPs, F127-TAPP/TCPP(Mn) NPs synthesized by amino-porphyrins (TAPP) doping can not only construct PET/MR bimodal probes but also improve the T1 relaxivity (up to 456%). Moreover, T1 relaxivity can be adjusted by altering the molar ratio of TAPP/TCPP(Mn) and the concentration of F127. However, a similar increase in T1 relaxivity was not observed in the F127-TCPP/TCPP(Mn) NPs, which were synthesized using carboxy-porphyrins (TCPP) doping. In a breast cancer lymph node metastasis mice model, subcutaneous injection of 68Ga-F127-TAPP/TCPP(Mn) NPs through the hind foot pad, the normal lymph nodes and metastatic lymph nodes were successfully distinguished based on the difference of PET standard uptake values and MR signal intensities. Furthermore, the dark brown F127-TAPP/TCPP(Mn) NPs demonstrated the potential for staining and mapping lymph nodes. This study provides valuable insights into developing and applying PET/MR probes for lymph node metastasis imaging.

Keywords: PET/MR; dual-modal imaging; porphyrin; self-assembly; sentinel lymph node metastasis.

MeSH terms

  • Animals
  • Breast Neoplasms / diagnostic imaging
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Female
  • Humans
  • Lymphatic Metastasis* / diagnostic imaging
  • Magnetic Resonance Imaging* / methods
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles* / chemistry
  • Porphyrins* / chemistry
  • Positron-Emission Tomography*
  • Sentinel Lymph Node* / diagnostic imaging
  • Sentinel Lymph Node* / pathology

Substances

  • Porphyrins