Development of biodegradable hyperbranched core-multishell nanocarriers for efficient topical drug delivery

被引:31
|
作者
Du, Fang [1 ]
Hoenzke, Stefan [2 ]
Neumann, Falko [1 ,3 ]
Keilitz, Juliane [1 ]
Chen, Wei [1 ]
Ma, Nan [1 ,3 ]
Hedtrich, Sarah [2 ]
Haag, Rainer [1 ]
机构
[1] Free Univ Berlin, Inst Organ Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
[2] Free Univ Berlin, Inst Pharm Pharmacol & Toxicol, D-14195 Berlin, Germany
[3] Helmholtz Zentrum Geesthacht, Inst Biomat Sci, D-14513 Teltow, Germany
关键词
Topical application; Dexamethasone; Core-multishell (CMS) nanocarriers; Drug delivery systems; SOLID LIPID NANOPARTICLES; SKIN PENETRATION; TRANSDERMAL DELIVERY; ABSORPTION; ENHANCERS; COPOLYMER; PH;
D O I
10.1016/j.jconrel.2016.06.048
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The topical application of drugs allows for a local application in skin disease and can reduce side effects. Here we present biodegradable core-multishell (CMS) nanocarriers which are composed of a hyperbranched polyglycerol core functionalized with diblock copolymers consisting of polycaprolactone (PCL) and poly(ethylene glycol) (mPEG) as the outer shell. The anti-inflammatory drug Dexamethasone (Dexa) was loaded into these CMS nanocarriers. DLS results suggested that Dexa loaded nanoparticles mostly act as a unimolecular carrier system. With longer PCL segments, a better transport capacity is observed. In vitro skin permeation studies showed that CMS nanocarriers could improve the Nile red penetration through the skin by up to 7 times, compared to a conventional cream formulation. Interestingly, covalently FITC-labeled CMS nanocarriers remain in the stratum corneum layer. This suggests the enhancement is due to the release of cargo after being transported into the stratum corneum by the CMS nanocarriers. In addition, the hPG-PCL-mPEG CMS nanocarriers exhibited good stability, low cytotoxicity, and their production can easily be scaled up, which makes them promising nanocarriers for topical drug delivery. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 49
页数:8
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