3D-printed polycaprolactone-chitosan based drug delivery implants for personalized administration

被引:62
|
作者
Yang, Yutong [1 ]
Wu, Haichao [1 ]
Fu, Qiliang [2 ]
Xie, Xinfeng [3 ]
Song, Yongming [1 ]
Xu, Min [1 ]
Li, Jian [1 ]
机构
[1] Northeast Forestry Univ, Key Lab Biobased Mat Sci & Technol, Minist Educ, Harbin 150040, Peoples R China
[2] Scion, 49 Sala St, Rotorua 3020, New Zealand
[3] Michigan Technol Univ, Coll Forest Resources & Environm Sci, Houghton, MI 49931 USA
基金
中国国家自然科学基金;
关键词
Personalized administration; Drug delivery implant; 3D printing; Polycaprolactone; Chitosan; FORMULATION; SCAFFOLD; RELEASE; PRODUCTS; TABLETS;
D O I
10.1016/j.matdes.2022.110394
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Fused deposition molding (FDM) can complete most complex preparation of drug delivery implants to meet the personalized needs of patients. However, the drug activity has strict requirements on processing temperature and preparation method of filaments, the implant also has strict biocompatibility requirements for the materials. In this study, a drug delivery implant was prepared with good biocompatibility, controlled and efficient drug release using FDM printing for personalized administration. Drug-loaded filaments were developed for FDM process by hot-melt extrusion (HME). Polycaprolactone was used as a drug delivery carrier, and ibuprofen as the model drug. Notably, chitosan was dissolved to form controlled and efficient release channels. The printability, changes in physical and chemical properties during HME and FDM processes of the filament, and drug release behavior, mechanism and biocompatibility of the implants were investigated. The results showed that the filament tensile strength decreased with the increase of drug and chitosan content. No obvious degradation and chemical change occurred during the whole process. The drug release efficiency could reach>99% and lasted for 120 h mainly via the diffusion - erosion mechanism. The viability of cells cultured for 24 h in 72 h, 100% implant extract was 75.3%. (C) 2022 The Authors. Published by Elsevier Ltd.
引用
收藏
页数:10
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