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J Mater Chem B ; 12(24): 5884-5897, 2024 Jun 19.
Artículo en Inglés | MEDLINE | ID: mdl-38775254

RESUMEN

Pancreatic cancer is an aggressive and highly fatal malignant tumor. Recent studies have shown that cancer stem cells (CSCs) play an important role in resisting current therapeutic modalities. Furthermore, CD133 is highly expressed in CSCs. High-intensity focused ultrasound (HIFU) is a promising non-invasive therapeutic strategy for unresectable pancreatic cancers. In our study, we synthesized targeted CD133 organosilane nanomicelles by encapsulating perfluorohexane (PFH). The CD133 antibody on the surface could specifically bind to CD133-positive pancreatic cancer cells and selectively concentrate in pancreatic cancer tumor tissues. PFH was introduced to improve the ablation effect of HIFU due to its liquid-gas phase transition properties. By combining with the dorsal skinfold window chamber model (DSWC) of pancreatic cancer in nude mice, multiphoton fluorescence microscopy was used to evaluate the targeting effect of nanomicelles on pancreatic cancer tumor tissue. These multifunctional nanomicelles synergistically affected HIFU treatment of pancreatic cancer, providing an integrated research platform for diagnosing and treating pancreatic cancer with HIFU.


Asunto(s)
Antígeno AC133 , Ultrasonido Enfocado de Alta Intensidad de Ablación , Ratones Desnudos , Micelas , Neoplasias Pancreáticas , Animales , Neoplasias Pancreáticas/diagnóstico por imagen , Neoplasias Pancreáticas/patología , Neoplasias Pancreáticas/terapia , Antígeno AC133/metabolismo , Ratones , Humanos , Línea Celular Tumoral , Fluorocarburos/química , Fluorocarburos/farmacología , Ratones Endogámicos BALB C , Nanopartículas/química
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