2004
DOI: 10.1016/j.biomaterials.2003.12.013
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Fabrication and characterizations of a novel drug delivery device liposomes-in-microsphere (LIM)

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Cited by 75 publications
(44 citation statements)
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“…While burst releases are useful in dermal and systemic delivery, they may lead to a significant and unpredictable toxicity especially for potent drugs and treatments of chronic diseases. Several strategies have been proposed and controlled release can be achieved by bi-association of liposomes encapsulated inside a polymeric particle [92] as well as chitosan associated with alginate which demonstrate a controlled release and prevention of burst release [93]. Similar strategies can be achieved by using microparticles containing nanoparticles [91].…”
Section: Surface Functionalization Controlledmentioning
confidence: 99%
“…While burst releases are useful in dermal and systemic delivery, they may lead to a significant and unpredictable toxicity especially for potent drugs and treatments of chronic diseases. Several strategies have been proposed and controlled release can be achieved by bi-association of liposomes encapsulated inside a polymeric particle [92] as well as chitosan associated with alginate which demonstrate a controlled release and prevention of burst release [93]. Similar strategies can be achieved by using microparticles containing nanoparticles [91].…”
Section: Surface Functionalization Controlledmentioning
confidence: 99%
“…Diversos trabalhos comprovaram o aumento da efi cácia e a redução da toxicidade de substâncias bioativas de origem natural ou sintética, administrados em lipossomas (Ratner, 2002), sistemas nanoparticulados (Feng et al, 2004;Berkland et al, 2002) ou micropartículas (Gupte;Ciftci, 2004;Ribeiro-Costa et al, 2004). Relatos recentes demonstram a atividade antitumoral do taxol (Gupte;Ciftci, 2004) e do ácido úsnico (Cladonia substellata) em microesferas (Ribeiro-Costa et al, 2004), da lectina de Cratylia mollis encapsulada em lipossomas (Andrade et al, 2004), de xantonas (Teixeira et al, 2005), da doxorrubicina em nanopartículas (Barraud et al, 2005) e 5-fl uorouracil em lipossomas (Jin et al, 2005), atividade antiparasitária do praziquantel em lipossomas (Mourão et al, 2005), atividade antibiótica da vancomicina em micropartículas (Le Ray et al, 2005) e anfotericina B em lipossomas (Bellocchio et al, 2005), atividade hipoglicemiante da insulina em micropartículas (Kim et al, 2005) e anti-estrógenos em lipossomas e nanopartículas para tratamento do câncer de mama (Maillard et al, 2005;Memisoglu-Bilensoy et al, 2005).…”
Section: Toxicidade E Viabilização Da Biodisponibilização Da Dctnunclassified
“…Active and passive targeting of liposomes are extensively utilized for the enhanced permeability and retention (EPR) effect and ligand conjugation. [3][4][5] Thermosensitive liposomes are commonly used as drug carriers, and function through externally thermo-stimulated content release. Photosensitive liposomes are commonly triggered to release loaded drugs after reaching a lower critical solution temperature.…”
Section: Introductionmentioning
confidence: 99%