Targeted Delivery of Nanoparticle-Conveyed Neutrophils to the Glioblastoma Site for Efficient Therapy.
Chunxian PiaoJaeho LeeGi Eun KimYoung Ho ChoeHaerang LeeYoung-Min HyunPublished in: ACS applied materials & interfaces (2024)
Glioblastoma is a common brain tumor that poses considerable challenges in drug delivery. In this study, we investigated the potential of cell-based nanoparticles for targeted drug delivery to the glioblastoma sites. The anticancer drug of temozolomide (TMZ)-loaded T7-cholesterol nanoparticle micelles efficiently delivered nanoparticles to neutrophils and, subsequently, to the tumors. T7 is a cell-penetrating peptide that enhances the delivery of T7/TMZ to the target cells. T7 also serves as a transferrin target peptide, enabling targeted delivery to tumors. T7-conjugated cholesterol can self-assemble into micelles in aqueous solution and attach to the membrane of neutrophils. We confirmed that T7/TMZ nanoparticle micelles were efficiently located inside the neutrophils. Thereafter, T7/TMZ-conveyed neutrophils were administered to a glioblastoma mouse model, enabling neutrophils to penetrate the blood-brain barrier and deliver drugs directly to the tumor site. We evaluated the drug delivery efficiency and therapeutic effects of intravenous injection of T7/TMZ-conveyed neutrophils to a glioblastoma mouse model. These results demonstrate the promising role of neutrophil-based nanoparticle delivery systems in the targeted therapy of glioblastoma.
Keyphrases
- drug delivery
- cancer therapy
- mouse model
- drug release
- single cell
- cell therapy
- induced apoptosis
- emergency department
- iron oxide
- stem cells
- photodynamic therapy
- mass spectrometry
- low density lipoprotein
- mesenchymal stem cells
- climate change
- high resolution
- replacement therapy
- adverse drug
- hyaluronic acid
- smoking cessation
- human health
- single molecule