Hydroxypropyl methylcellulose-based controlled release dosage by melt extrusion and 3D printing: Structure and drug release correlation

被引:156
作者
Zhang, Jiaxiang [1 ]
Yang, Weiwei [2 ]
Vo, Anh Q. [1 ]
Feng, Xin [1 ]
Ye, Xingyou [1 ]
Kim, Dong Wuk [1 ]
Repka, Michael A. [1 ,3 ]
机构
[1] Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Univ Mississippi, Dept Chem & Biochem, University, MS 38677 USA
[3] Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USA
关键词
Hydroxypropyl methylcellulose; Acetaminophen; Hot-melt extrusion; Fused deposition modeling 3D printing; Controlled release; Dissolution kinetics; AMORPHOUS SOLID DISPERSIONS; DELIVERY-SYSTEMS; EXTENDED-RELEASE; SOLUTE RELEASE; POLYMER; FORMULATIONS; HYDROGEL; HPMC; STABILITY; MECHANISM;
D O I
10.1016/j.carbpol.2017.08.058
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The objective of this study was to develop a new approach for fabrication of zero order release of active pharmaceutical ingredients (APIs) using hot-melt extrusion (HME) and 3D printing technology to generate tablets with specific 3D structures. By correlating the geometry of the 3D printed tablets with their dissolution and drug release rates, mathematical models that have been developed to describe drug release mechanisms were also studied. Acetaminophen was used as a model drug, and Benecel (TM) hydroxypropyl methylcellulose (HPMC) E5 and Soluplus (R) were used to formulate nine fuse depositional 3D-printed tablets with different inner core fill densities and outside shell thicknesses. This work reports the successful fabrication of solid-dispersion filaments with an API dispersed in HPMC based matrix via HME technology, and the production of zero order controlled release tablets with different 3D structures (tablets #3, 5, 6, and 9) using a 3D printer.
引用
收藏
页码:49 / 57
页数:9
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