Assessment of drug entrapment within liposomes using photophysical probes

The photophysical and photochemical behavior of (R)-cinacalcet (CIN) and (S)-naproxen (NPX) entrapped within liposomes has been studied. For this purpose, liposome encapsulated drugs have been prepared through thin layer evaporation and characterized by transmission electron microscopy, cryoscopy sc...

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Detalles Bibliográficos
Autores: Oliverio, Filomena, Nuin Plá, Neus Edurne, Ragno, Gaetano, Miranda Alonso, Miguel Ángel, Andreu, Inmaculada|||0000-0003-3409-9443
Tipo de recurso: artículo
Fecha de publicación:2014
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/60873
Acceso en línea:https://riunet.upv.es/handle/10251/60873
Access Level:acceso abierto
Palabra clave:Cinacalcet
Drug carrier
Drug delivery
Fluorescence
Laser flash photolysis
Liposome
Naphthalene chromophore
Naproxen
Singlet excited states
Triplet excited states
QUIMICA ORGANICA
Descripción
Sumario:The photophysical and photochemical behavior of (R)-cinacalcet (CIN) and (S)-naproxen (NPX) entrapped within liposomes has been studied. For this purpose, liposome encapsulated drugs have been prepared through thin layer evaporation and characterized by transmission electron microscopy, cryoscopy scanning electron microscopy and dynamic light scattering. Steady state and time-resolved fluorescence experiments showed similar spectra, emission quantum yields, singlet energies and lifetimes for the selected drugs, outside and inside liposomes. By contrast, laser flash photolysis experiments revealed an important enhancement of the triplet lifetimes for entrapped drugs inside liposomes, indicating the spatial confinement existing in the microenvironment prevailing in these biomimetic entities. Thus, this photophysical property shows potential as a non-invasive, direct and valuable tool to monitor encapsulation of photoactive drugs and to probe the intraliposome environment. In addition, it provides a new quantitative indicator of the capability of liposomes to act as drug carriers.