Spontaneous In Situ Formation of Liposomes from Inert Porous Microparticles for Oral Drug Delivery

Spontaneous In Situ Formation of Liposomes from Inert Porous Microparticles for Oral Drug Delivery

Despite the wide-spread use of liposomal drug delivery systems, application of these systems for oral purposes is limited due to their large-scale formulation and storage issues. Proliposomes are one of the formulation approaches for achieving solid powders that readily form liposomes upon hydration...

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Bibliographic Details
Main Authors: Maryam Farzan, Gabriela Québatte, Katrin Strittmatter, Florentine Marianne Hilty, Joachim Schoelkopf, Jörg Huwyler, Maxim Puchkov
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Pharmaceutics
Subjects:
oral drug delivery
dissolution enhancement
phospholipids
liposomes
solid dosage forms
porous microparticles
Online Access:https://www.mdpi.com/1999-4923/12/8/777

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https://www.mdpi.com/1999-4923/12/8/777

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