Hydroxypropyl methylcellulose-based controlled release dosage by melt extrusion and 3D printing: Structure and drug release correlation
被引:156
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作者:
Zhang, Jiaxiang
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Zhang, Jiaxiang
[1
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Yang, Weiwei
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Univ Mississippi, Dept Chem & Biochem, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Yang, Weiwei
[2
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Vo, Anh Q.
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Vo, Anh Q.
[1
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Feng, Xin
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Feng, Xin
[1
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Ye, Xingyou
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Ye, Xingyou
[1
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Kim, Dong Wuk
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Kim, Dong Wuk
[1
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Repka, Michael A.
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Repka, Michael A.
[1
,3
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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
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.
机构:
Kyungpook Natl Univ, Res Inst Pharmaceut Sci, Coll Pharm, Vessel Organ Interact Res Ctr VOICE,MRC,BK21 FOUR, Daegu 41566, South KoreaKyungpook Natl Univ, Res Inst Pharmaceut Sci, Coll Pharm, Vessel Organ Interact Res Ctr VOICE,MRC,BK21 FOUR, Daegu 41566, South Korea
机构:
Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Zhang, Jiaxiang
Feng, Xin
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Feng, Xin
Patil, Hemlata
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Patil, Hemlata
Tiwari, Roshan V.
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Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Tiwari, Roshan V.
Repka, Michael A.
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h-index: 0
机构:
Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USAUniv Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA