Biomimetic Magnetite Nanoparticles as Targeted Drug Nanocarriers and Mediators of Hyperthermia in an Experimental Cancer Model.
Francesca OltolinaAna PeigneuxDonato ColangeloNausicaa ClementeAnnarita D'UrsoGuido ValenteGuillermo R IglesiasConcepción Jiménez LópezMaria PratPublished in: Cancers (2020)
Biomimetic magnetic nanoparticles mediated by magnetosome proteins (BMNPs) are potential innovative tools for cancer therapy since, besides being multifunctional platforms, they can be manipulated by an external gradient magnetic field (GMF) and/or an alternating magnetic field (AMF), mediating targeting and hyperthermia, respectively. We evaluated the cytocompatibility/cytotoxicity of BMNPs and Doxorubicin (DOXO)-BMNPs in the presence/absence of GMF in 4T1 and MCF-7 cells as well as their cellular uptake. We analyzed the biocompatibility and in vivo distribution of BMNPs as well as the effect of DOXO-BMNPs in BALB/c mice bearing 4T1 induced mammary carcinomas after applying GMF and AMF. Results: GMF enhanced the cell uptake of both BMNPs and DOXO-BMNPs and the cytotoxicity of DOXO-BMNPs. BMNPs were biocompatible when injected intravenously in BALB/c mice. The application of GMF on 4T1 tumors after each of the repeated (6×) iv administrations of DOXO-BMNPs enhanced tumor growth inhibition when compared to any other treatment, including that with soluble DOXO. Moreover, injection of DOXO-BMNPs in the tumor combined with application of an AMF resulted in a significant tumor weight reduction. These promising results show the suitability of BMNPs as magnetic nanocarriers for local targeted chemotherapy and as local agents for hyperthermia.
Keyphrases
- cancer therapy
- drug delivery
- magnetic nanoparticles
- drug release
- high fat diet induced
- induced apoptosis
- papillary thyroid
- cell cycle arrest
- tissue engineering
- single cell
- diabetic rats
- high grade
- stem cells
- locally advanced
- squamous cell carcinoma
- weight loss
- metabolic syndrome
- cell therapy
- type diabetes
- weight gain
- insulin resistance
- signaling pathway
- risk assessment
- oxidative stress
- cell proliferation
- molecularly imprinted
- emergency department
- mass spectrometry
- electronic health record
- ultrasound guided
- human health
- high resolution
- adverse drug
- endoplasmic reticulum stress
- tandem mass spectrometry
- lymph node metastasis