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See detailHemocompatibility of liposomes loaded with lipophilic prodrugs of methotrexate and melphalan in the lipid bilayer
Kuznetsova, Natalia R.; Sevrin, Chantal ULg; Lespineux, David et al

in Journal of Controlled Release (2012)

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See detailPoly(2-dimethylamino ethylmethacrylate)-based polymers to camouflage red blood cell antigens.
Cerda-Cristerna, Bernardino Issac; Cottin, Sophie; Flebus, Luca et al

in Biomacromolecules (2012), 13(4), 1172-80

Poly(2-dimethylamino-ethylmethacrylate) (PDMAEMA) is a cationic polymer when dissolved in a 7.4 pH fluid. Owing to its ionic nature, this polycation interacts with the negatively charged cell membrane ... [more ▼]

Poly(2-dimethylamino-ethylmethacrylate) (PDMAEMA) is a cationic polymer when dissolved in a 7.4 pH fluid. Owing to its ionic nature, this polycation interacts with the negatively charged cell membrane surface of red blood cells (RBCs). The electrostatic self-assembly of PDMAEMA on RBCs membrane can be employed for inducing the formation of a polymeric shield camouflaging blood group antigens on RBCs as a valuable strategy for developing "universal RBCs" for blood transfusion. The purpose of this research was to evaluate the camouflaging ability of PDMAEMA homopolymers and PDMAEMA-co-poly(ethylene glycol) copolymers differing in molecular weight and architecture. Surprisingly, the PDMAEMAs caused a partially masking, no masking, and sensitization of the same RBCs population. The MW and architecture of the polymers as well as temperature of PDMAEMA-RBCs treatment influenced the results observed. Herein, the very particular reactivity of PDMAEMAs and RBCs is analyzed and discussed. [less ▲]

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See detailEffect of drug candidates for the treatment of Alzheimer's disorber on hippocampus-dependent learning, glutamate receptors and mitochondria
Vignisse, Julie ULg; Steinbusch, H.W.M; Bolkunov, A. et al

Conference (2011, November 12)

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See detailCharacterization of the interaction between nanoformulated drugs and model lipid membranes towards improved drug delivery systems
De Battice, Laura; Frost, Rickard; Sevrin, Chantal ULg et al

Poster (2011, October 25)

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See detailCharacterization of the interaction between nanoformulated drugs and model lipid membranes towards improved drug delivery systems
De Battice, Laura; Frost, Rickard; Sevrin, Chantal ULg et al

Poster (2011, October)

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See detailCharacteristics of antitumor liposomess loaded with lipophilic prodrugs of methotrexate and mephalan in relation to their hemocompatibility
Kuznetsova, N.; Sevrin, Chantal ULg; Lespineux, David et al

Conference (2011, September 19)

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See detailInspired bio- nanobiomaterials for tissue engineering
Grandfils, Christian ULg

Conference (2011, September 19)

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See detailProduction of biodegradable polyesters from industrial and agricultural by-products
de Almeida, C.; Calvaheiro, J.; Raposo, R. et al

Conference (2011, September)

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See detailNanoparticles tailored for the delivery of biopharmaceutic drugs
Grandfils, Christian ULg; Sevrin, Chantal ULg; Kuznetsova et al

Conference (2011, May 20)

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See detailChitosan/polyester copolymers prepared by solid-phase synthesis as promising biomaterials
Demina, T; Akopova, T; Tsoy, A et al

Conference (2011, May 05)

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See detailStructural Rearrangements of Polymeric Insulin-loaded Nanoparticles Interacting with Surface-Supported Model Lipid Membranes
Frost, Rickard; Grandfils, Christian ULg; Cerda, Bernardino et al

in Journal of Biomaterials and Nanobiotechnology (2011)

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See detailDimebon Enhances Hippocampus-Dependent Learning in Mouse Models of Appetitive Y-Maze and Inhibitory Step-Down Memory Tasks in Mice
Vignisse, Julie ULg; Steinbusch, Harry W.M.; Bolkunov, Alexei et al

Poster (2011, February 23)

Dimebon, a compound recently proposed for a treatment of Alzheimer’s disorder, was suggested to have memory enhancing properties in pre-clinical and clinical studies. We investigated whether dimebon at ... [more ▼]

Dimebon, a compound recently proposed for a treatment of Alzheimer’s disorder, was suggested to have memory enhancing properties in pre-clinical and clinical studies. We investigated whether dimebon at doses acutely (0.1 mg/kg and 0.5 mg/kg) or repeatedly (0.1 mg/kg) administered to mice via i.p. injections, increases memory scores respectively in an appetitive and an inhibitory learning task. Acute treatment with dimebon at the dose 0.1 mg/kg did not affect learning scores in 3-month-old C57BL/6N. Acute treatment with higher dose of dimebon (0.5mg/kg) was found to enhance inhibitory learning in 3-month-old mice as shown in the step-down avoidance paradigm in C57BL/6N mice. In a model of appetitive learning, a spatial version of the Y-maze, repeated treatment with dimebon increased the rate of correct choices and decreased the latency of accessing a water reward after water deprivation. Repeated administration of dimebon also increased the duration of drinking behaviour during training/testing procedures although water consumption behaviour was not altered. Additional behavioural tests were carried out to investigate possible non-specific effects of dimebon on parameters of drinking, anxiety and exploration/locomotion. Our data suggest that dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory tasks in mice. [less ▲]

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See detailDimebon enhances hippocampus-dependent learning in both appetitive and inhibitory memory tasks in mice
Vignisse, Julie ULg; Steinbusch, Harry W.M.; Bolkunov, Alexei et al

Poster (2011, January 31)

Dimebon, a compound recently proposed for a treatment of Alzheimer’s disorder was suggested to have memory enhancing properties in pre-clinical and clinical studies. We investigated whether dimebon at ... [more ▼]

Dimebon, a compound recently proposed for a treatment of Alzheimer’s disorder was suggested to have memory enhancing properties in pre-clinical and clinical studies. We investigated whether dimebon at doses acutely (0.1 mg/kg and 0.5 mg/kg) or repeatedly (0.1 mg/kg) administered to mice via i.p. injections, increases memory scores respectively in an appetitive and an inhibitory learning task. Acute treatment with dimebon at the dose 0.1 mg/kg did not affect learning scores in either 3-month-old C57BL/6N or CD1 mice. Acute treatment with higher dose of dimebon (0.5mg/kg) was found to enhance inhibitory learning in 3- and 7-month-old mice as shown in the step-down avoidance paradigm in C57BL/6N mice. No effects on learning were seen in CD1 mice. In a model of appetitive learning, a spatial version of the Y-maze, repeated treatment with dimebon increased the rate of correct choices and decreased the latency of accessing a water reward after water deprivation. Repeated administration of dimebon also increased the duration of drinking behaviour during training/testing procedures although behaviours in others tests or water consumption were not altered. Acute treatment of water-deprived and non-water-deprived mice with dimebon also did not affect their water intake. Our data suggest that dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory tasks in mice. [less ▲]

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See detailHemocompatibility and biofunctionality of two poly(2- (dimethylamino)ethyl methacrylate-co-poly(ethyleneglycol) copolymers
Riquelme, Bibiana D.; Dumas, Dominique; Fontana, Alicia et al

in Journal of Biomedical Materials Research (2011), 99A (3)