2023
DOI: 10.1039/d2bm02072f
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Mannose-mediated nanodelivery of methotrexate to macrophages augments rheumatoid arthritis therapy

Abstract: Inflammation targeted delivery of methotrexate using mannose-installed polymersomes (Man-PMTX) can repolarize macrophages from M1 type to M2 type and mitigate proinflammatory cytokines, leading to effectively augmented rheumatoid arthritis therapy.

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Cited by 5 publications
(3 citation statements)
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“…high macrophage uptake confirmed the role of ligand active targeting in enabling augmented macrophage uptake, corroborated other reports on carbohydrate enabled mannose receptor mediated uptake. [40][41][42] Nevertheless, we confirmed the same by performing the mannose receptor blocking assay, aided by confocal microscopy. A significant reduction in uptake of the FITC-ACEM LIPOMER in mannose treated macrophages validated the mannose receptor mediated uptake facilitated by ACEM.…”
Section: Rsc Pharmaceutics Papersupporting
confidence: 67%
“…high macrophage uptake confirmed the role of ligand active targeting in enabling augmented macrophage uptake, corroborated other reports on carbohydrate enabled mannose receptor mediated uptake. [40][41][42] Nevertheless, we confirmed the same by performing the mannose receptor blocking assay, aided by confocal microscopy. A significant reduction in uptake of the FITC-ACEM LIPOMER in mannose treated macrophages validated the mannose receptor mediated uptake facilitated by ACEM.…”
Section: Rsc Pharmaceutics Papersupporting
confidence: 67%
“…In recent years, many efforts have been made to develop sustained-release delivery routes, including microneedles [ 27 ], liposomes [ 28 ], nanoparticles [ 29 ] and hydrogels [ 30 ]. Yang et al [ 31 ] showed that mannose-modified polymer vesicles can be targeted and absorbed at RA lesion sites. Methotrexate was then slowly released to induce macrophage repolarization to M2 phenotype, thereby alleviating inflammation and preventing synovium damage.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, glucocorticoids may suppress the regenerative capacity of bone and cartilage tissue [ 6 ]. Recent approaches for RA treatment using anti-inflammatory nanoparticles [ 7 , 8 ] have been reported. However, their application is also limited because they were unable to stimulate the repair process in the joints.…”
Section: Introductionmentioning
confidence: 99%