Cationic solid lipid nanoparticles enhance ocular hypotensive effect of melatonin in rabbit
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作者:
Leonardi, Antonio
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Univ Catania, Res Ctr Ocular Nanotechnol, Dept Drug Sci, NANO i, Catania, ItalyUniv Catania, Res Ctr Ocular Nanotechnol, Dept Drug Sci, NANO i, Catania, Italy
Leonardi, Antonio
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Bucolo, Claudio
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Univ Catania, Sch Med, Dept Clin & Mol Biomed, Sect Pharmacol & Biochem, I-95125 Catania, ItalyUniv Catania, Res Ctr Ocular Nanotechnol, Dept Drug Sci, NANO i, Catania, Italy
Bucolo, Claudio
[2
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Drago, Filippo
[2
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Salomone, Salvatore
[2
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Pignatello, Rosario
[1
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机构:
[1] Univ Catania, Res Ctr Ocular Nanotechnol, Dept Drug Sci, NANO i, Catania, Italy
[2] Univ Catania, Sch Med, Dept Clin & Mol Biomed, Sect Pharmacol & Biochem, I-95125 Catania, Italy
The study was aimed at evaluating whether the ocular hypotensive effect of melatonin (MEL) was enhanced by its encapsulation in cationic solid lipid nanoparticles (cSLN), as well as at determining the tolerability of these formulations on the ocular surface. MEL was loaded in cSLN that had already been shown to be suitable for ophthalmic use. The formulations were prepared using Softisan (R) 100 as the main lipid matrix, with the presence of either stearic (SA) or palmitic acid (PA) as lipid modifiers. A fixed positive charge was provided by the addition of a cationic lipid (didecyldimethylammonium bromide). The ocular hypotensive effect was evaluated by measuring the intraocular pressure (TOP) during 24h in albino rabbits. MEL elicited a significant (p < 0.01) IOP reduction in rabbit eye. All the formulations tested in vivo demonstrated a good tolerability. The nanocarrier containing SA was the most effective in terms of IOP reduction (maximum IOP reduction: -7 mmHg), and its effect lasted approximately 24 h. The experimental data indicate that the new formulations based on cSLN loaded with MEL represent a potent anti-glaucoma treatment with a safe profile, warranting further clinical evaluation of the proposed nanotechnological strategy. (C) 2014 Elsevier B.V. All rights reserved.
机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
De Campos, AM
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Sánchez, A
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机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Sánchez, A
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Gref, R
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机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Gref, R
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Calvo, P
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机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Calvo, P
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Alonso, MJ
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Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, SpainUniv Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
De Campos, AM
;
Sánchez, A
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h-index: 0
机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Sánchez, A
;
Gref, R
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机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Gref, R
;
Calvo, P
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机构:Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
Calvo, P
;
Alonso, MJ
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Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, SpainUniv Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain