Authors:
Trapani, G
Franco, M
Latrofa, A
Reho, A
Liso, G
Citation: G. Trapani et al., Synthesis, in vitro and in vivo cytotoxicity, and prediction of the intestinal absorption of substituted 2-ethoxycarbonyl-imidazo[2,1-b]benzothiazoles, EUR J PH SC, 14(3), 2001, pp. 209-216
Authors:
Franco, M
Trapani, G
Latrofa, A
Tullio, C
Provenzano, MR
Serra, M
Muggironi, M
Biggio, G
Liso, G
Citation: M. Franco et al., Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and -polyvinylpyrrolidone K-30 solid dispersions, INT J PHARM, 225(1-2), 2001, pp. 63-73
Authors:
Latrofa, A
Trapani, G
Franco, M
Harris, MJ
Serra, M
Biggio, G
Liso, G
Citation: A. Latrofa et al., Synthesis of the [H-3] labelled potent and selective peripheral benzodiazepine receptor ligand CB 34, J LABEL C R, 44(7), 2001, pp. 521-528
Authors:
Trapani, G
Latrofa, A
Franco, M
Pantaleo, MR
Sanna, E
Massa, F
Tuveri, F
Liso, G
Citation: G. Trapani et al., Complexation of zolpidem with 2-hydroxypropyl-beta-, methyl-beta-, and 2-hydroxypuopyl-gamma-cyclodextrin: Effect on aqueous solubility, dissolution rate, and ataxic activity in rat, J PHARM SCI, 89(11), 2000, pp. 1443-1451
Authors:
Trapani, G
Franco, M
Latrofa, A
Pantaleo, MR
Provenzano, MR
Sanna, E
Maciocco, E
Liso, G
Citation: G. Trapani et al., Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000, INT J PHARM, 184(1), 1999, pp. 121-130
Authors:
Trapani, G
Franco, M
Latrofa, A
Ricciardi, L
Carotti, A
Serra, M
Sanna, E
Biggio, G
Liso, G
Citation: G. Trapani et al., Novel 2-phenylimidazo[1,2-a]pyridine derivatives as potent and selective ligands for peripheral benzodiazepine receptors: Synthesis, binding affinity, and in vivo studies, J MED CHEM, 42(19), 1999, pp. 3934-3941
Authors:
Sanna, E
Motzo, C
Usala, M
Serra, M
Dazzi, L
Maciocco, E
Trapani, G
Latrofa, A
Liso, G
Biggio, G
Citation: E. Sanna et al., Characterization of the electrophysiological and pharmacological effects of 4-iodo-2,6-diisopropylphenol, a propofol analogue devoid of sedative-anaesthetic properties, BR J PHARM, 126(6), 1999, pp. 1444-1454