| Literature DB >> 27639683 |
Doris Gabriel1, Thibault Mugnier2, Herve Courthion2, Ksanthi Kranidioti3, Niki Karagianni3, Maria C Denis3, Maria Lapteva4, Yogeshvar Kalia4, Michael Möller2, Robert Gurny2.
Abstract
We have developed a composite hydrogel for improved topical delivery of the poorly soluble drug Tacrolimus (TAC) to psoriasis lesions. TAC is efficiently solubilized in methoxy poly- (ethylene glycol) hexyl substituted poly-(lactic acid) (mPEGhexPLA) based nanocarriers. For convenient and patient-friendly topical administration, TAC loaded polymeric nanocarriers were incorporated in a Carbopol® based hydrogel, to yield a composite hydrogel formulation (TAC composite hydrogel). TAC composite hydrogel was designed to have superior pharmaceutical formulation properties, delivery efficiency and local bioavailability, compared to currently available paraffin-based TAC ointments. Composite hydrogel formulations had good local tolerance and showed no signs of immediate toxicity after repeated topical administration in healthy mice. Skin delivery of TAC composite hydrogel in an imiquimod-induced psoriasis mouse model was found to be twice as high as for the commercial formulation Protopic™, used as benchmark. TAC composite hydrogel showed significant improvement in the in vivo and histopathological features of the imiquimod-induced psoriasis model.Entities:
Keywords: Dermatology; Hydrogel; Immune-mediated skin disease; Methoxy poly (ethylen glycol) hexyl-substituted poly (lactic acid); Polymeric nanocarriers; Skin topical drug delivery; Tacrolimus
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Year: 2016 PMID: 27639683 DOI: 10.1016/j.jconrel.2016.09.007
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776