A 3D printed chitosan-pectin hydrogel wound dressing for lidocaine hydrochloride delivery

被引:218
|
作者
Long, Jingjunjiao [1 ]
Etxeberria, Alaitz Etxabide [1 ,3 ]
Nand, Ashveen, V [4 ]
Bunt, Craig R. [5 ]
Ray, Sudip [6 ]
Seyfoddin, Ali [1 ,2 ]
机构
[1] Auckland Univ Technol, Fac Hlth & Environm Sci, Sch Sci, Drug Delivery Res Grp, Level 5,WS Bldg,34 St Paul St, Auckland 1010, New Zealand
[2] Auckland Univ Technol, Fac Hlth & Environm Sci, Sch Interprofess Hlth Studies, Auckland, New Zealand
[3] Univ Basque Country, BIOMAT Res Grp, Dept Chem & Environm Engn, Engn Coll Gipuzkoa,UPV EHU, Donostia San Sebastian, Spain
[4] Unitec Inst Technol, Hlth & Community & Environm & Anim Sci Network, 139 Carrington Rd, Auckland 1025, New Zealand
[5] Lincoln Univ, Fac Agr & Life Sci, Dept Agr Sci, Canterbury, New Zealand
[6] Univ Auckland, Sch Chem Sci, MBIE Biocide Toolbox & NZ Prod Accelerator Progra, Auckland, New Zealand
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2019年 / 104卷
关键词
3D printing; Hydrogel; Chitosan; Pectin; Lidocaine hydrochloride; Wound dressing; DRUG-RELEASE; IN-VITRO; THERMOSENSITIVE HYDROGELS; MUCOADHESIVE; COMPOSITES; COMPLEXES; SYSTEMS; TISSUE;
D O I
10.1016/j.msec.2019.109873
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A chitosan-pectin (CS-PEC) biopolymeric hydrogel wound dressing was investigated for lidocaine delivery. Here we demonstrate for the first time the feasibility of three-dimensional (3D) printed CS-PEC hydrogel incorporating the local anaesthetic drug lidocaine hydrochloride (LDC) as a potential wound dressing candidate. The hydrogels were prepared by physical crosslinking of CS and PEC polysaccharides. The scaffolds were printed using an extrusion-based 3D printer using a mechanical positive displacement dispensing system followed by lyophilisation. The 3D printed hydrogels showed good printability, dimensional integrity and self-adhesion to skin. The high swelling ratio and water absorption of 3D printed hydrogels indicated suitability for absorbing exudates and maintaining a moist wound healing environment. Fourier transform infrared (FTIR) spectroscopy results indicated that the CS-PEC hydrogel was formed by hydrogen bonds. Incorporation of LDC in the hydrogel did not interfere with its functional stability. In vitro drug release studies of LDC over 6 h fitted the Korsmeyer-Peppas model. This work demonstrates the possibility of a 3D printed hydrogel as a suitable candidate for wound dressings.
引用
收藏
页数:9
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