S
Seyed Moghimi
Researcher at University of Nottingham
Publications - 25
Citations - 1965
Seyed Moghimi is an academic researcher from University of Nottingham. The author has contributed to research in topics: Mononuclear phagocyte system & Poloxamer. The author has an hindex of 17, co-authored 23 publications receiving 1857 citations. Previous affiliations of Seyed Moghimi include University of Brighton.
Papers
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Journal ArticleDOI
Non-phagocytic uptake of intravenously injected microspheres in rat spleen: Influence of particle size and hydrophilic coating
TL;DR: It is demonstrated that this strategy to minimize the removal by macrophages of the reticuloendothelial system by covering their surface with hydrophilic polymers may not necessarily prolong the circulatory half-life of drug carriers in all animal models.
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Coating particles with a block co-polymer (poloxamine-908) suppresses opsonization but permits the activity of dysopsonins in the serum
TL;DR: It is demonstrated that organ-specific receptors, opsonin activities and plasma dysopsonins regulate the in vivo clearance of particulate materials from the circulation by modulating particle clearance by effectively blocking opsonization but still allowing for Dysopsonization.
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Serum-mediated recognition of liposomes by phagocytic cells of the reticuloendothelial system - The concept of tissue specificity.
TL;DR: A multiplicity of physicochemical and physiopathological factors which influence the clearance kinetics and tissue distribution of liposomes administered into the circulation are addressed.
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An investigation of the filtration capacity and the fate of large filtered sterically-stabilized microspheres in rat spleen
TL;DR: It is demonstrated that the macrophages of the red-pulp can effectively phagocytose the filtered poloxamine-coated microspheres 24 h post-administration, which could be the result of either the loss of the surface absorbed polxamine, and hence the steric barrier, or 'neutralization' of the effect of the anti-phagocytic material poloxamines-908 within the spleen.
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Surface engineered nanospheres with enhanced drainage into lymphatics and uptake by macrophages of the regional lymph nodes
TL;DR: Observations suggest that a lymphatic delivery composition based on polymer‐coated particles will be advantageous for many applications in clinical and experimental medicine.