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1.
Curr Pharm Des ; 27(42): 4300-4314, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34042031

RESUMEN

Surfactants are amphiphilic molecules of great interest in the pharmaceutical field which are used in combination with other adjuvants to solubilize poorly soluble drugs, improve their dissolution profile, promote permeation, improve drug delivery, enhance stabilization, among other characteristics. Literature shows that surfactants are included in several pharmaceutical compositions: tablets, solid dispersions, emulsions, microemulsions, nanoemulsions, liposomes and niosomes. This review aims to elucidate the different classes of surfactants based on their charges (cationic, anionic, nonionic, zwitterionic, and dimeric), the micelles formation process, and how surfactant molecules geometry can affect this phenomenon. Moreover, current studies regarding the benefits of surfactants in the development of formulations are presented. Finally, a discussion on how charges and chain length of surfactants can affect the stratum corneum epithelial cells leading to increased permeation or skin irritability is reported.


Asunto(s)
Micelas , Tensoactivos , Sistemas de Liberación de Medicamentos , Emulsiones , Humanos , Absorción Cutánea
2.
Int J Pharm ; 506(1-2): 351-60, 2016 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-27130362

RESUMEN

Microemulsion containing pentoxifylline was developed and characterized for use as a topical alternative to treat skin disorders. The transparent formulation was developed and optimized based on a pseudoternary phase diagram. Pentoxifylline-loaded microemulsion (PTX-ME) was composed of 44% Tween 80™/Brij 52™ mix as surfactants (S), 51% of caprylic/capric triglycerides as the oil phase (O) and 5% of water as aqueous phase (A). It was classified as an isotropic water-in-oil (W/O) system with droplets that had a heterogeneous spherical shape within the nanosized range (67.36±8.90nm) confirmed by polarized light microscopy, differential scanning calorimetry (DSC), transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis. In vitro studies using static diffusion Franz cells revealed that the release of PTX from ME followed the Higuchi kinetic model. Topical PTX-ME application developed superior anti-inflammatory activity when compared to the PTX solution, reducing the paw edema up to 88.83%. Our results suggested that this colloidal nanosystem is a promising agent for the delivery of pentoxifylline, increasing its ability to modulate the inflammatory aspects of skin disorders.


Asunto(s)
Excipientes/química , Pentoxifilina/administración & dosificación , Inhibidores de Fosfodiesterasa/administración & dosificación , Administración Cutánea , Animales , Química Farmacéutica/métodos , Modelos Animales de Enfermedad , Liberación de Fármacos , Edema/tratamiento farmacológico , Emulsiones , Inflamación/tratamiento farmacológico , Masculino , Nanopartículas , Tamaño de la Partícula , Pentoxifilina/química , Pentoxifilina/farmacocinética , Transición de Fase , Inhibidores de Fosfodiesterasa/química , Inhibidores de Fosfodiesterasa/farmacocinética , Ratas , Ratas Wistar , Absorción Cutánea , Tensoactivos/química
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