Three-Dimensional Printing of Drug-Eluting Implantable PLGA Scaffolds for Bone Regeneration

被引:5
|
作者
Annaji, Manjusha [1 ]
Mita, Nur [1 ,2 ]
Poudel, Ishwor [1 ]
Boddu, Sai H. S. [3 ,4 ]
Fasina, Oladiran [5 ]
Babu, R. Jayachandra [1 ]
机构
[1] Auburn Univ, Harrison Coll Pharm, Dept Drug Discovery & Dev, Auburn, AL 36849 USA
[2] Mulawarman Univ, Fac Pharm, Samarinda 75119, Kalimantan Timu, Indonesia
[3] Ajman Univ, Coll Pharm & Hlth Sci, Dept Pharmaceut Sci, POB 346, Ajman, U Arab Emirates
[4] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, POB 346, Ajman, U Arab Emirates
[5] Auburn Univ, Samuel Ginn Coll Engn, Dept Biosyst Engn, Auburn, AL 36849 USA
来源
BIOENGINEERING-BASEL | 2024年 / 11卷 / 03期
关键词
3D printing; ketoprofen; PLGA scaffolds; sustained release; thermoplastic extrusion;
D O I
10.3390/bioengineering11030259
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Despite rapid progress in tissue engineering, the repair and regeneration of bone defects remains challenging, especially for non-homogenous and complicated defects. We have developed and characterized biodegradable drug-eluting scaffolds for bone regeneration utilizing direct powder extrusion-based three-dimensional (3D) printing techniques. The PLGA scaffolds were fabricated using poly (lactic-co-glycolic acid) (PLGA) with inherent viscosities of 0.2 dl/g and 0.4 dl/g and ketoprofen. The effect of parameters such as the infill, geometry, and wall thickness of the drug carrier on the release kinetics of ketoprofen was studied. The release studies revealed that infill density significantly impacts the release performance, where 10% infill showed faster and almost complete release of the drug, whereas 50% infill demonstrated a sustained release. The Korsmeyer-Peppas model showed the best fit for release data irrespective of the PLGA molecular weight and infill density. It was demonstrated that printing parameters such as infill density, scaffold wall thickness, and geometry played an important role in controlling the release and, therefore, in designing customized drug-eluting scaffolds for bone regeneration.
引用
收藏
页数:18
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