Gold Nanobipyramids for Near-Infrared Fluorescence-Enhanced Imaging and Treatment of Triple-Negative Breast Cancer.
Ioannis G TheodorouFotios MpekrisParis PapagiorgisMyrofora PanagiMaria KalliLouiza PotamitiKyriacos KyriacouGrigorios ItskosTriantafyllos StylianopoulosPublished in: Cancers (2023)
There is an imminent need for novel strategies for the diagnosis and treatment of aggressive triple-negative breast cancer (TNBC). Cell-targeted multifunctional nanomaterials hold great potential, as they can combine precise early-stage diagnosis with local therapeutic delivery to specific cell types. In this study, we used mesoporous silica (MS)-coated gold nanobipyramids (MS-AuNBPs) for fluorescence imaging in the near-infrared (NIR) biological window, along with targeted TNBC treatment. Our MS-AuNBPs, acting partly as light amplification components, allow considerable metal-enhanced fluorescence for a NIR dye conjugated to their surfaces compared to the free dye. Fluorescence analysis confirms a significant increase in the dye's modified quantum yield, indicating that MS-AuNBPs can considerably increase the brightness of low-quantum-yield NIR dyes. Meanwhile, we tested the chemotherapeutic efficacy of MS-AuNBPs in TNBC following the loading of doxorubicin within the MS pores and functionalization to target folate receptor alpha (FRα)-positive cells. We show that functionalized particles target FRα-positive cells with significant specificity and have a higher potency than free doxorubicin. Finally, we demonstrate that FRα-targeted particles induce stronger antitumor effects and prolong overall survival compared to the clinically applied non-targeted nanotherapy, Doxil. Together with their excellent biocompatibility measured in vitro, this study shows that MS-AuNBPs are promising tools to detect and treat TNBCs.
Keyphrases
- mass spectrometry
- fluorescence imaging
- multiple sclerosis
- ms ms
- cancer therapy
- photodynamic therapy
- early stage
- drug delivery
- induced apoptosis
- energy transfer
- single cell
- single molecule
- cell cycle arrest
- molecular dynamics
- squamous cell carcinoma
- escherichia coli
- fluorescent probe
- bone marrow
- lymph node
- staphylococcus aureus
- combination therapy
- signaling pathway
- replacement therapy
- simultaneous determination