Tailored dendritic core-multishell nanocarriers for efficient dermal drug delivery: A systematic top-down approach from synthesis to preclinical testing

被引:31
作者
Hoenzke, Stefan [1 ]
Gerecke, Christian [2 ]
Elpelt, Anja [1 ]
Zhang, Nan [1 ]
Unbehauen, Michael [3 ]
Kral, Vivian [1 ]
Fleige, Emanuel [4 ]
Paulus, Florian [3 ]
Haag, Rainer [3 ]
Schaefer-Korting, Monika [1 ]
Kleuser, Burkhard [2 ]
Hedtrich, Sarah [1 ]
机构
[1] Free Univ Berlin, Inst Pharm Pharmacol & Toxicol, Berlin, Germany
[2] Univ Potsdam, Dept Toxicol, Inst Nutr Sci, Potsdam, Germany
[3] Free Univ Berlin, Inst Chem & Biochem, Berlin, Germany
[4] DendroPharm GmbH, Berlin, Germany
关键词
Dendritic core-multishell nanocarriers; Biocompatibility; Dexamethasone; Inflammatory skin disease; Dermal drug delivery; Skin model; RECONSTRUCTED HUMAN SKIN; SOLID LIPID NANOPARTICLES; POLYMERIC NANOPARTICLES; STRATUM-CORNEUM; IN-VITRO; PENETRATION ENHANCEMENT; TH2; CYTOKINES; GLUCOCORTICOIDS; MODELS; BIOTRANSFORMATION;
D O I
10.1016/j.jconrel.2016.06.030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Drug loaded dendritic core-multishell (CMS) nanocarriers are of especial interest for the treatment of skin diseases, owing to their striking dermal delivery efficiencies following topical applications. CMS nanocarriers are composed of a polyglycerol core, connected by amide-bonds to an inner alkyl shell and an outer methoxy poly(ethylene glycol) shell. Since topically applied nanocarriers are subjected to biodegradation, the application of conventional amide-based CMS nanocarriers (10-A-18-350) has been limited by the potential production of toxic polyglycerol amines. To circumvent this issue, three tailored ester-based CMS nanocarriers (10-E-12-350, 10-E-15-350, 10-E-18-350) of varying inner alkyl chain length were synthesized and comprehensively characterized in terms of particle size, drug loading, biodegradation and dermal drug delivery efficiency. Dexamethasone (DXM), a potent drug widely used for the treatment of inflammatory skin diseases, was chosen as a therapeutically relevant test compound for the present study. Ester-and amide-based CMS nanocarriers delivered DXM more efficiently into human skin than a commercially available DXM cream. Subsequent in vitro and in vivo toxicity studies identified CMS (10-E-15-350) as the most biocompatible carrier system. The anti-inflammatory potency of DXM-loaded CMS (10-E-15-350) nanocarriers was assessed in TNF alpha supplemented skin models, where a significant reduction of the pro-inflammatory cytokine IL-8 was seen, with markedly greater efficacy than commercial DXM cream. In summary, we report the rational design and characterization of tailored, biodegradable, ester-based CMS nanocarriers, and their subsequent stepwise screening for biocompatibility, dermal delivery efficiency and therapeutic efficacy in a top-down approach yielding the best carrier system for topical applications. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 63
页数:14
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