Near Infrared Biomimetic Hybrid Magnetic Nanocarrier for MRI-Guided Thermal Therapy.
João Victor Ribeiro RochaRafael Freire KrauseCarlos Eduardo RibeiroNathália Corrêa de Almeida OliveiraLucas Ribeiro de SousaJuracy Leandro SantosSamuel de Melo CastroMarize Campos ValadaresMauro Cunha Xavier PintoMarcilia Viana PavamEliana Martins LimaSebastião Antônio MendanhaAndris Figueiroa BakuzisPublished in: ACS applied materials & interfaces (2024)
Cell-membrane hybrid nanoparticles (NPs) are designed to improve drug delivery, thermal therapy, and immunotherapy for several diseases. Here, we report the development of distinct biomimetic magnetic nanocarriers containing magnetic nanoparticles encapsulated in vesicles and IR780 near-infrared dyes incorporated in the membranes. Distinct cell membranes are investigated, red blood cell (RBC), melanoma (B16F10), and glioblastoma (GL261). Hybrid nanocarriers containing synthetic lipids and a cell membrane are designed. The biomedical applications of several systems are compared. The inorganic nanoparticle consisted of Mn-ferrite nanoparticles with a core diameter of 15 ± 4 nm. TEM images show many multicore nanostructures (∼40 nm), which correlate with the hydrodynamic size. Ultrahigh transverse relaxivity values are reported for the magnetic NPs, 746 mM -1 s -1 , decreasing respectively to 445 mM -1 s -1 and 278 mM -1 s -1 for the B16F10 and GL261 hybrid vesicles. The ratio of relaxivities r 2 / r 1 decreased with the higher encapsulation of NPs and increased for the biomimetic liposomes. Therapeutic temperatures are achieved by both, magnetic nanoparticle hyperthermia and photothermal therapy. Photothermal conversion efficiency ∼25-30% are reported. Cell culture revealed lower wrapping times for the biomimetic vesicles. In vivo experiments with distinct routes of nanoparticle administration were investigated. Intratumoral injection proved the nanoparticle-mediated PTT efficiency. MRI and near-infrared images showed that the nanoparticles accumulate in the tumor after intravenous or intraperitoneal administration. Both routes benefit from MRI-guided PTT and demonstrate the multimodal theranostic applications for cancer therapy.
Keyphrases
- drug delivery
- cancer therapy
- red blood cell
- molecularly imprinted
- iron oxide
- drug release
- contrast enhanced
- photodynamic therapy
- magnetic resonance imaging
- magnetic nanoparticles
- diffusion weighted imaging
- single cell
- deep learning
- tissue engineering
- convolutional neural network
- optical coherence tomography
- cell therapy
- atomic force microscopy
- oxide nanoparticles
- magnetic resonance
- fatty acid
- machine learning
- solid phase extraction
- mass spectrometry
- pain management