In a new cutting-edge study, Associate Professor Eijiro Miyako and his colleagues from Japan Advanced Institute of Science and Technology (JAIST) synthesized multifunctional Ga-based nanoparticles that combine cancer phototherapy with immunotherapy. The synthesized novel LM nanoparticle (PEG-IMIQ-LM) contains a eutectic gallium-indium (EGaIn) LM alloy and an immunological modulator imiquimod (IMIQ), both embedded inside a biocompatible surfactant DSPE-PEG2000-NH2. The detailed findings of their study were published in Advanced Functional Materials.
“We believe that the convergence of nano-immuno engineering and LM technology could provide a promising modality to trigger ideal immune responses for advancing cancer immunotherapy. In this study, we report light-activatable multifunctional LM nanoparticles with immunostimulants to combine photothermal therapy with immunotherapy,” says Dr. Miyako, while discussing the team’s motivation to conduct this study.
First, the research team prepared water-dispersible LM nanoparticles through a simple one-step sonication process using DSPE-PEG2000-NH2 to introduce IMIQ. This is considered a huge breakthrough, as EGaIn LM is inherently a water-immiscible material. Further investigations confirmed that LM disintegrates to ensure IMIQ delivery to the target. Moreover, the prepared nanoparticle displayed a linear increase in absorbance in the near-infrared (NIR) region at 808 nm, confirming its optically activatable nature.
When the aqueous solution of the LM nanoparticle was irradiated by the NIR laser (808 nm), the team observed a notable increase in the temperature of the solution, which was proportional to the increase in the nanoparticle concentration. These findings confirmed that PEG-IMIQ-LM nanoparticle was a robust and stable photothermal drug carrier, suitable for immunotherapy.
Further experiments revealed that LM nanoparticles were extremely safe and did not cause cytotoxicity in human fibroblast (MRC5) and mouse colon cancer (Colon26) cells. To assess the degree of internalization and distribution of the particles, a fluorescent dye known as indocyanine green (ICG) was introduced into the particle through sonication resulting in PEG–ICG–IMIQ–LM particle. Fluorescent (FL) microscopy equipped with a laser beam demonstrated that the LM particle displayed strong fluorescence at various NIR wavelengths and immediately destroyed the Colon26 cells. Thus, LM particles could not only efficiently deliver the immunomodulant, but could also enable their real time tracking and eliminate specific cancer cells.
Finally, the team developed a multifaceted LM immune nanostimulator for cancer theranostics. To do so, they added anti-programmed death ligand-1 antibody (Anti-PD-L1), one of the most promising immune checkpoint inhibitors, to the existing fluorescent LM nanoparticle. The modified particle, Anti-PD-L1‒PEG–ICG–IMIQ–LM, was dispersed efficiently with significant fluorescence. With increasing time post irradiation, the tumor surface temperature increased linearly, indicative of the antitumor effect of the nanoparticle.
Addition of Anti-PD-L1 onto the nanoparticle enabled binding of the LM particle to PD-L1 on the cancer cells, marking them for phagocytosis by macrophages and dendritic cells (DC). Laser-induced Anti-PD-L1–PEG–IMIQ–LM particles exhibited the highest and complete cancer removal, along with faster healing and recovery.
Moreover, when the tumor recurred, mice treated with laser-induced Anti-PD-L1–PEG–IMIQ–LM particles displayed sustained antitumor effectiveness and prolonged survival.
MEDICA-tradefair.com; Source: ETH Zurich
