153 Sm-labeled Fe 3 O 4 @lapatinib nanoparticles as a potential therapeutic agent for breast cancer: synthesis, quality control, and in vivo evaluation

The present study introduces Fe O -coated lapatinib-labeled Sm nanoparticles (denoted as Fe O @lapatinib- Sm) as a promising avenue for advancing breast cancer treatment. The radiolabeled nanoparticles combine various attributes, offering enhanced therapeutic precision. The integration of lapatinib confers therapeutic effects and targeted delivery. The inherent magnetic characteristics of Fe O nanoparticles contribute to improved imaging contrast and targeted localization. Incorporating the gamma-emitting Sm isotope permits single-photon emission computed tomography imaging and radiation dose evaluation, while its beta-emitting nature ensures targeted cancer cell eradication. The synthesis of Fe O @lapatinib- Sm was meticulously optimized by investigating the effects of parameters on radiolabeling efficiency. Physicochemical attributes were scrutinized using several analytical techniques. In-depth assessment evaluated the biocompatibility, toxicity, and biodistribution in a murine model, illuminating clinical utility. Optimal conditions ( SmCl concentration of 10 mCi mL , pH 7.4, a reaction time of 30 min, and a temperature of 25 °C) achieved >99% labeling efficiency and radiochemical purity. The TEM analysis indicated that the diameter of Fe O @lapatinib- Sm nanoparticles ranged from 10 to 40 nm. Vibrating-sample magnetometry verified their superparamagnetic behaviour with a saturation magnetization of 41.4 emu g . The synthesized radiopharmaceutical exhibited high sterility and stability. Acute toxicity studies showed the mild effects of Fe O @lapatinib- Sm at a dose of 20 mCi kg , with no observed mortality. Notably, lesions from Fe O @lapatinib- Sm use recovered naturally over time. Radiation doses below 20 mCi kg were recommended for clinical trials. The biodistribution study in BT474 xenograft mice revealed rapid clearance of Fe O @lapatinib- Sm within 48 h. Significant accumulation occurred in the liver, spleen, and tumor tissue, while minimal accumulation was found in other tissues. Future steps involve studying biocorona formation and therapeutic efficacy on tumour models, refining its clinical potential.