2022
DOI: 10.1016/j.ijbiomac.2022.08.063
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Bevacizumab encapsulation into PLGA nanoparticles functionalized with immunouteroglobin-1 as an innovative delivery system for atherosclerosis

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Cited by 13 publications
(10 citation statements)
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“…Nanocarriers can be used in targeted delivery of anti-inflammatory agents such as interleukins, especially IL-10. While IL-10 systemic administration has appeared to not be linked to significant reduction in serum levels of cytokines, its targeted release when linked to PLGA appears to induce cap fibrosis and thickness and to reduce the necrosis percentage in the plaque core, inducing plaque stability [ 74 , 75 ]. Preliminary studies showed encouraging results in inflammation reduction when using statins as targeted therapy.…”
Section: Biological and Clinical Effectsmentioning
confidence: 99%
“…Nanocarriers can be used in targeted delivery of anti-inflammatory agents such as interleukins, especially IL-10. While IL-10 systemic administration has appeared to not be linked to significant reduction in serum levels of cytokines, its targeted release when linked to PLGA appears to induce cap fibrosis and thickness and to reduce the necrosis percentage in the plaque core, inducing plaque stability [ 74 , 75 ]. Preliminary studies showed encouraging results in inflammation reduction when using statins as targeted therapy.…”
Section: Biological and Clinical Effectsmentioning
confidence: 99%
“…However, the lack of selectivity/specificity of antineoplastic agents and their distribution to healthy tissues/organs requires the administration in high doses, resulting in significant toxicity and undesirable side effects. [1,2] Bevacizumab (BVZ) is an antiangiogenic monoclonal antibody used in clinic to treat diseases such as corneal neovascularization, [3] atheroma, [4] melanoma, [5] atherosclerosis, [6] macular degeneration, [7] and different types of cancer. [8][9][10][11] It inhibits the vascular endothelial growth factor (VEGF) binding to its tyrosine kinase receptors on the surface of endothelial cells (VEGFR-1 and VEGFR-2).…”
Section: Introductionmentioning
confidence: 99%
“…[12] Similarly, to other anticancer chemotherapeutics, BVZ can trigger several adverse effects, that can be surpassed using targeted delivery systems. [6,[13][14][15] Although the combination of nanotechnology with several chemotherapeutic agents has been largely explored as a promising treatment approach in cancer, nanomedicines translation to the clinic has often been hampered by the absence of reliable and representative cellular models that can provide predictive outcomes on the in vivo efficiency of the formulation. As a result, a high percentage of drugs and nanomedicines fail at later stages of drug development pipeline.…”
Section: Introductionmentioning
confidence: 99%
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