Radiolabeled Trastuzumab Solid Lipid Nanoparticles for Breast Cancer Cell: in Vitro and in Vivo Studies.
Emre OzgencMerve KarpuzEge ArzukMarta González-ÁlvarezMarival Bermejo SanzEvren GundogduIsabel González-ÁlvarezPublished in: ACS omega (2022)
Radiolabeled trastuzumab (TRZ) loaded solid lipid nanoparticles (SLNs) were prepared by high shear homogenization and sonication techniques. The apoptosis mechanism of TRZ-SLNs was studied only with the MCF-7 cell line, while the cytotoxicity and cell binding capacity were investigated using breast cancer cells (MCF-7 and MDA-MB-231) and the human keratinocyte cell line (HaCaT). The particle sizes of TRZ-SLNs were found to be below 100 nm, and they possessed a negative charge. The high radiolabeling efficiency and good radiolabeling stability in saline and a cell culture medium were obtained in the results of radiolabeling studies. According to the in vitro studies, TRZ-SLNs were found to be biocompatible, and they effectively induced apoptosis in MCF-7 cells. After the parenteral injection of TRZ-SLNs into rats, a sustained release profile in blood circulation was achieved compared with free drug solution by the evaluation of pharmacokinetic parameters. As a conclusion, the study reveals that Technetium-99m ( 99m Tc radiolabeled) TRZ loaded SLN formulations could be promising theranostic agents based on their characterization profiles, in vitro cellular uptake and apoptosis induction capacity, and in vivo pharmacokinetic profiles.
Keyphrases
- breast cancer cells
- induced apoptosis
- endoplasmic reticulum stress
- oxidative stress
- cell cycle arrest
- signaling pathway
- drug delivery
- cell death
- case control
- photodynamic therapy
- epidermal growth factor receptor
- endothelial cells
- pi k akt
- single cell
- wound healing
- radiation therapy
- squamous cell carcinoma
- fatty acid
- cancer therapy
- ultrasound guided
- metastatic breast cancer
- drug release
- adverse drug
- solid state
- single molecule
- dna binding
- neoadjuvant chemotherapy