Hot melt extrusion assisted additive manufacturing of mixed polymeric 3D printed metoprolol succinate extended-release tablets for controlled oral drug delivery

被引:2
作者
Ghatole, Shubham [1 ]
Dilip, Jannu [1 ]
Ashokbhai, Makka Krupali [1 ]
Vishwakarma, Himanshu [1 ]
Banerjee, Subham [2 ]
Kaity, Santanu [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmaceut, Kolkata 700054, W Bengal, India
[2] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmaceut, Gauhati 781101, Changsari, India
来源
CHEMICAL PHYSICS IMPACT | 2025年 / 10卷
关键词
Hot-melt extrusion; Three-dimensional printing (3DP); Controlled release metoprolol succinate; AMORPHOUS SOLID DISPERSIONS; FUSED FILAMENT FABRICATION; FORMULATION; MISCIBILITY;
D O I
10.1016/j.chphi.2024.100811
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study introduces an innovative methodology for fabricating extended-release metoprolol succinate (MS) tablets through the integration of Soluplus (R) and hydroxypropyl methylcellulose acetate succinate (HPMCAS) polymers, employing hot-melt extrusion (HME) and additive manufacturing technology. A carefully optimized polymer-plasticizer combination facilitated the production of extrudable filaments, which were subsequently used in three-dimensional printing (3DP) tablets via fused deposition modeling (FDM). The filaments were comprehensively characterized using tensile strength assessment, Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). At the same time, micro-computed tomography (mu CT) provided detailed analysis of the 3D-printed tablets. Filaments incorporating 10 % w/w citric acid as a plasticizer exhibited enhanced mechanical robustness, with tensile strength reaching 5.19 N, strain elongation of 29.2 %, and was found suitable for the fabrication of tablet dosage form with acceptable quality. Drug release , assessed in phosphate buffer at pH 6.8, revealed a controlled release profile, with 70 % of the active pharmaceutical ingredient (API) released over 6 h These results show the promise of using such techniques as platform technology for delivering similar categories of APIs. This developmental pathway can also be used for the fabrication of personalized medicines with adjustable drug release profiles.
引用
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页数:14
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