挤压
3D打印
剂型
羟丙基纤维素
活性成分
材料科学
吡罗昔康
粒径
3d打印
纳米技术
赋形剂
墨水池
工艺工程
药物输送
化学工程
色谱法
聚合物
化学
生物医学工程
复合材料
医学
药理学
工程类
替代医学
病理
作者
Rathna Mathiyalagan,Erica Sjöholm,Sajana Manandhar,Satu Lakio,Jessica M. Rosenholm,Martti Kaasalainen,Xiaoju Wang,Niklas Sandler
标识
DOI:10.1016/j.ejps.2023.106497
摘要
Semi-solid extrusion (SSE) 3D printing enables flexible designs and dose sizes to be printed on demand and is a suitable tool for fabricating personalized dosage forms. Controlled Expansion of Supercritical Solution (CESS®) is a particle size reduction technology, and it produces particles of a pure active pharmaceutical ingredient (API) in a dry state, suspendable in the printing ink. In the current study, as a model API of poorly water-soluble drug, nanoformed piroxicam (nanoPRX) prepared by CESS® was accommodated in hydroxypropyl methylcellulose- or hydroxypropyl cellulose-based ink formulations to warrant the printability in SSE 3D printing. Importantly, care must be taken when developing nanoPRX formulations to avoid changes in their polymorphic form or particle size. Printing inks suitable for SSE 3D printing that successfully stabilized the nanoPRX were developed. The inks were printed into films with escalating doses with exceptional accuracy. The original polymorphic form of nanoPRX in the prepared dosage forms was not affected by the manufacturing process. In addition, the conducted stability study showed that the nanoPRX in the prepared dosage form remained stable for at least three months from printing. Overall, the study rationalizes that with nanoparticle-based printing inks, superior dose control for the production of personalized dosage forms of poorly water-soluble drugs at the point-of-care can be achieved.
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