Manufacture of tablets with structurally-controlled drug release using rapid tooling injection moulding

被引:7
作者
Walsh, Erin [1 ,2 ]
Maclean, Natalie [1 ,2 ]
Turner, Alice [1 ,2 ]
Alsuleman, Moulham [1 ,2 ]
Prasad, Elke [1 ,2 ]
Halbert, Gavin [1 ,2 ]
ter Horst, Joop H. [1 ,3 ]
Markl, Daniel [1 ,2 ]
机构
[1] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow, Scotland
[2] Univ Strathclyde, Ctr Continuous Mfg & Adv Crystallisat CMAC, Glasgow, Scotland
[3] Univ Rouen Normandie, Lab Sci & Methodes Separat, Mont St Aignan, France
基金
英国工程与自然科学研究理事会;
关键词
Injection moulding; Rapid tooling; Specific surface area; Additive manufacture; Dissolution; SHRINKAGE; POLYMER;
D O I
10.1016/j.ijpharm.2022.121956
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
With advancements in the pharmaceutical industry pushing more towards tailored medicines, novel approaches to tablet manufacture are in high demand. One of the main drivers towards micro-scale batch production is the ability to fine-tune drug release. This study demonstrates the use of rapid tooling injection moulding (RTIM) for tablet manufacture. Tablets were manufactured with varying structural features to alter the surface area whilst maintaining the same volume, resulting in differing specific surface area (SSA). The precision of this technique is evaluated based on eleven polymer formulations, with the tablets displaying <2% variability in mass. Further tablets were produced containing paracetamol in three different polymer-based formulations to investigate the impact of SSA on the drug release. Significant differences were observed between the formulations based on the polymers polyvinyl alcohol (PVA) and Klucel ELF. The polymer base of the formulation was found to be critical to the sensitivity of the drug release profile to SSA modification. The drug release profile within each formulation was modified by the addition of structural features to increase the SSA.
引用
收藏
页数:10
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