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

• Extrusion of drug-dispersed filaments using HME as a printing feedstock for AM. • Filaments mediate FDM-3D-printed tablets designed to tailor drug release properties. • Unique platform technology for tailored oral controlled-release drug formulation development. This study introduces an innovative methodology for fabricating extended-release metoprolol succinate (MS) tablets through the integration of Soluplus® 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 (FT-IR), and X-ray diffraction (XRD). At the same time, micro-computed tomography (µCT) 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.

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Publication Details

Journal
Chemical Physics Impact
Published
2024-12-27
DOI
https://doi.org/10.1016/j.chphi.2024.100811
Citations
3
Primary Topic
Additive Manufacturing and 3D Printing Technologies
Type
article
Field-Weighted Citation Impact
0.61
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article

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

Subham Banerjee, Santanu Kaity, Makka Krupali Ashokbhai, Jannu Dilip et al.
3 citations
Chemical Physics Impact
Additive Manufacturing and 3D Printing Technologies
0.61
article

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

Subham Banerjee, Santanu Kaity, Makka Krupali Ashokbhai, Jannu Dilip, Shubham Ghatole, Himanshu Vishwakarma
article en
3 citations

Abstract

• Extrusion of drug-dispersed filaments using HME as a printing feedstock for AM. • Filaments mediate FDM-3D-printed tablets designed to tailor drug release properties. • Unique platform technology for tailored oral controlled-release drug formulation development. This study introduces an innovative methodology for fabricating extended-release metoprolol succinate (MS) tablets through the integration of Soluplus® 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 (FT-IR), and X-ray diffraction (XRD). At the same time, micro-computed tomography (µCT) 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.

Chemical Physics ImpactVol. 10
National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN)
Good health and well-being
Openalex Percentile: Top 32%
Additive Manufacturing and 3D Printing Technologies
0.61
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