Electrospun Fibrous Architectures for Drug Delivery, Tissue Engineering and Cancer Therapy

被引:211
|
作者
Ding, Yaping [1 ]
Li, Wei [1 ]
Zhang, Feng [1 ]
Liu, Zehua [1 ]
Ezazi, Nazanin Zanjanizadeh [1 ]
Liu, Dongfei [1 ,2 ]
Santos, Helder A. [1 ,2 ]
机构
[1] Univ Helsinki, Drug Res Program, Div Pharmaceut Chem & Technol, Fac Pharm, FI-00014 Helsinki, Finland
[2] Univ Helsinki, Helsinki Inst Life Sci, FI-00014 Helsinki, Finland
基金
欧洲研究理事会;
关键词
cancer therapy; drug delivery; electrospinning; tissue engineering; DIAMETER VASCULAR GRAFTS; CORE-SHEATH NANOFIBER; VIRAL GENE DELIVERY; COMPOSITE NANOFIBERS; STEM-CELLS; GROWTH-FACTOR; IN-VITRO; EXTRACELLULAR-MATRIX; CONTROLLED-RELEASE; CARDIAC TISSUE;
D O I
10.1002/adfm.201802852
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The versatile electrospinning technique is recognized as an efficient strategy to deliver active pharmaceutical ingredients and has gained tremendous progress in drug delivery, tissue engineering, cancer therapy, and disease diagnosis. Numerous drug delivery systems fabricated through electrospinning regarding the carrier compositions, drug incorporation techniques, release kinetics, and the subsequent therapeutic efficacy are presented herein. Targeting for distinct applications, the composition of drug carriers vary from natural/synthetic polymers/blends, inorganic materials, and even hybrids. Various drug incorporation approaches through electrospinning are thoroughly discussed with respect to the principles, benefits, and limitations. To meet the various requirements in actual sophisticated in vivo environments and to overcome the limitations of a single carrier system, feasible combinations of multiple drug-inclusion processes via electrospinning could be employed to achieve programmed, multi-staged, or stimuli-triggered release of multiple drugs. The therapeutic efficacy of the designed electrospun drug-eluting systems is further verified in multiple biomedical applications and is comprehensively overviewed, demonstrating promising potential to address a variety of clinical challenges.
引用
收藏
页数:35
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