Material extrusion 3D-printing technology: A new strategy for constructing water-soluble, high-dose, sustained-release drug formulations

被引:1
|
作者
Liu, Zhiting [1 ,4 ]
Huang, Jiaying [3 ,6 ]
Fang, Danqiao [3 ]
Feng, Bohua [5 ]
Luo, Jianxu [5 ]
Lei, Peixuan [3 ]
Chen, Xiaoling [3 ]
Xie, Qingchun [3 ]
Chen, Meiwan [1 ]
Chen, Peihong [2 ,3 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Peoples R China
[3] Guangdong Pharmaceut Univ, Ctr New Drug Res & Dev, Guangzhou 510006, Peoples R China
[4] Guangdong Pharmaceut Univ, Sch Tradit Chinese Med, Guangzhou 510006, Peoples R China
[5] Guangdong Prov Engn &Technol Res Ctr Med 3D Printe, Guangzhou 510006, Peoples R China
[6] YUEBEI Peoples Hosp, Shaoguan 512026, Peoples R China
关键词
Material extrusion; Direct ink writing; Metformin hydrochloride; Core-shell system; High drug loading; Sustained release; DELIVERY;
D O I
10.1016/j.mtbio.2024.101153
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The advantage of low-temperature forming through direct ink writing (DIW) 3D printing is becoming a strategy for the construction of innovative drug delivery systems (DDSs). Optimization of the complex formulation, including factors such as the printing ink, presence of solvents, and potential low mechanical strength, are challenges during process development. This study presents an application of DIW to fabricate water-soluble, high-dose, and sustained-release DDSs. Utilizing poorly compressible metformin hydrochloride as a model drug, a core-shell delivery system was developed, featuring a core composed of 96 % drug powder and 4 % binder, with a shell structure serving as a drug-release barrier. This design aligns with the sustained-release profile of traditional processes, achieving a 25.8 % reduction in volume and enhanced mechanical strength. The strategy facilitates sustained release of high-dose water-soluble formulations for over 12 h, potentially improving patient compliance by reducing formulation size. Process optimization and multi-batch flexibility were also explored in this study. Our findings provide a valuable reference for the development of innovative DDSs and 3D-printed drugs.
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页数:12
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