作者: Joseph D'Arrigo
DOI: 10.1016/B978-0-444-53798-0.00024-9
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摘要: Abstract Lipid polymorphism is complex, but important and useful for intravenous drug delivery. Various structural/physicochemical considerations lead to the resultant judgment that dispersed (inverse) cubic phase probably represents preferred (lipid polymorph or liquid-crystalline nanoparticle) structure of “dispersed lipid-mesophase nanoparticle (LMN)” in “lipid-coated microbubble/nanoparticle-derived” nanoemulsions. This conclusion helps explain observed efficacy such nanoemulsion formulations solubilizing, encapsulating, delivering selected lipophilic drugs, by receptor-mediated endocytosis, certain disease sites animals. As concerns polymorphic mechanism, expected physicochemical tendency LMN adopt nonlamellar mesostructural topology a function head-group hydration, acyl chain length, cholesterol content.