共 38 条
Hot melt extrusion paired fused deposition modeling 3D printing to develop hydroxypropyl cellulose based floating tablets of cinnarizine
被引:83
作者:

Vo, Anh Q.
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h-index: 0
机构:
Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Hanoi Univ Pharm, Dept Phys Chem & Phys, Hanoi, Vietnam Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA

Zhang, Jiaxiang
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h-index: 0
机构:
Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA

Nyavanandi, Dinesh
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h-index: 0
机构:
Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA

Bandari, Suresh
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h-index: 0
机构:
Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA

Repka, Michael A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USA Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
机构:
[1] Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USA
[3] Hanoi Univ Pharm, Dept Phys Chem & Phys, Hanoi, Vietnam
基金:
美国国家卫生研究院;
关键词:
3D printing;
Printlet;
Individualized medicine;
Floating drug delivery system;
Hot melt extrusion;
CONTROLLED DRUG-DELIVERY;
DOSAGE FORMS;
RELEASE;
FABRICATION;
D O I:
10.1016/j.carbpol.2020.116519
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Three-dimensional printing could serve as a platform to fabricate individualized medicines and complex-structured solid dosage forms. Herein, hot melt extrusion was coupled with 3D printing to develop a unique gastro retentive dosage form to personalize treatment of cinnarizine or other narrow absorption window drugs. The mechanical strength of the extruded strands was optimized for printing by combining two polymers, hydroxypropyl cellulose and vinylpyrrolidone vinyl acetate copolymer. The unit dose, floating force, and release profile were controlled by the printing parameters and object design. The tablets floated immediately within the FaSSGF, and floating force was relatively constant up to 12 h. Drug release followed zero-order kinetics and could be controlled from 6 h to >= 12 h. Input variables had a good correlation (R > 0.95) with unit dose, floating force, and dissolution profile (p < 0.05). Authors successfully proposed and tested a new paradigm of individualized medicine fabrication to meet individual patient needs.
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