Gefitinib/gefitinib microspheres loaded polyurethane constructs as drug-eluting stent coating

被引:14
作者
Chen, Weiluan [1 ]
Clauser, Johanna [2 ]
Thiebes, Anja Lena [3 ]
McGrath, Donnacha J. [4 ]
Kelly, Nicola [4 ]
van Steenbergen, Mies J. [1 ]
Jockenhoevel, Stefan [3 ]
Steinseifer, Ulrich [2 ]
McHugh, Peter E. [4 ]
Hennink, Wim E. [1 ]
Kok, Robbert J. [1 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, Univ Sweg 99, NL-3584 CG Utrecht, Netherlands
[2] RVVTH Aachen Univ, Helmholtz Inst, Inst Appl Med Engn, Dept Cardiovasc Engn, Pauwelsstr 20, D-52074 Aachen, Germany
[3] Rhein Westfal TH Aachen, ITA Inst Text Tech, AME Helmholtz Inst Biomed Engn, Dept Biohybrid & Med Text BioTex, Aachen, Germany
[4] Natl Univ Ireland, Coll Engn & Informat, Biomed Engn, Biomech Res Ctr, Univ Rd, Galway, Ireland
关键词
Polyurethane; Polymeric microspheres; Drug-eluting stents; Bronchotracheal stent; Controlled release; RELEASE; RESTENOSIS; PREVENTION; INHIBITOR; SYSTEM;
D O I
10.1016/j.ejps.2017.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the complications of bronchotracheal cancer is obstruction of the upper airways. Local tumor resection in combination with an airway stent can suppress intraluminal tumor (re)growth. We have investigated a novel drug-eluting stent coating for local release of the anticancer drug gefitinib. A polyurethane (PU) sandwich construct was prepared by a spray coating method in which gefitinib was embedded between a PU support layer of 200 pm and a PU top layer of 50-200 pm. Gefitinib was either embedded in the construct as small crystals or as gefitinib-loaded poly(lactic-co-glycolic acid) (PLGA) microspheres (MSP). The drug was incorporated in the PU constructs with high recovery (83-93%), and the spray coating procedure did not affect the morphologies of the embedded microspheres as demonstrated by scanning electron microscopy (SEM), confocal laser scanning microscopy and fluorescence microscopy analysis. PU constructs loaded with gefitinib crystals released the drug for 7-21 days and showed diffusion based release kinetics. Importantly, directional release of the drug towards the top layer, which is supposed to face the tumor mass, was controlled by the thicknesses of the PU top layer. PU constructs loaded with gefitinib microspheres released the drug in a sustained manner for >6 months indicating that drug release from the microspheres became the rate limiting step. In conclusion, the sandwich structure of drug-loaded PLGA microspheres in PU coating is a promising coating for airway stents that release anticancer drugs locally for a prolonged time. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 103
页数:10
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