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3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release

The aim of the present work was to produce 3D-printed oral dosage forms with a sufficient drug dose displaying various release profiles. Hot-melt extrusion was utilized to produce drug-loaded feedstock material that was subsequently 3D-printed into 6, 8, and 10 × 2.5 mm tablets with 15% and 90% infi...

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Autores principales: Öblom, Heidi, Zhang, Jiaxiang, Pimparade, Manjeet, Speer, Isabell, Preis, Maren, Repka, Michael, Sandler, Niklas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373414/
https://www.ncbi.nlm.nih.gov/pubmed/30617660
http://dx.doi.org/10.1208/s12249-018-1233-7
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author Öblom, Heidi
Zhang, Jiaxiang
Pimparade, Manjeet
Speer, Isabell
Preis, Maren
Repka, Michael
Sandler, Niklas
author_facet Öblom, Heidi
Zhang, Jiaxiang
Pimparade, Manjeet
Speer, Isabell
Preis, Maren
Repka, Michael
Sandler, Niklas
author_sort Öblom, Heidi
collection PubMed
description The aim of the present work was to produce 3D-printed oral dosage forms with a sufficient drug dose displaying various release profiles. Hot-melt extrusion was utilized to produce drug-loaded feedstock material that was subsequently 3D-printed into 6, 8, and 10 × 2.5 mm tablets with 15% and 90% infill levels. The prepared formulations contained 30% (w/w) isoniazid in combination with one or multiple pharmaceutical polymers possessing suitable properties for oral drug delivery. Thirteen formulations were successfully hot-melt extruded of which eight had properties suitable for fused deposition modeling 3D printing. Formulations containing HPC were found to be superior regarding printability in this study. Filaments with a breaking distance below 1.5 mm were observed to be too brittle to be fed into the printer. In addition, filaments with high moisture uptake at high relative humidity generally failed to be printable. Different release profiles for the 3D-printed tablets were obtained as a result of using different polymers in the printed formulations. For 8 mm tablets printed with 90% infill, 80% isoniazid release was observed between 40 and 852 min. Drug release characteristics could further be altered by changing the infill or the size of the printed tablets allowing personalization of the tablets. This study presents novel formulations containing isoniazid for prevention of latent tuberculosis and investigates 3D printing technology for personalized production of oral solid dosage forms enabling adjustable dose and drug release properties. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1208/s12249-018-1233-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63734142019-03-01 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release Öblom, Heidi Zhang, Jiaxiang Pimparade, Manjeet Speer, Isabell Preis, Maren Repka, Michael Sandler, Niklas AAPS PharmSciTech Research Article The aim of the present work was to produce 3D-printed oral dosage forms with a sufficient drug dose displaying various release profiles. Hot-melt extrusion was utilized to produce drug-loaded feedstock material that was subsequently 3D-printed into 6, 8, and 10 × 2.5 mm tablets with 15% and 90% infill levels. The prepared formulations contained 30% (w/w) isoniazid in combination with one or multiple pharmaceutical polymers possessing suitable properties for oral drug delivery. Thirteen formulations were successfully hot-melt extruded of which eight had properties suitable for fused deposition modeling 3D printing. Formulations containing HPC were found to be superior regarding printability in this study. Filaments with a breaking distance below 1.5 mm were observed to be too brittle to be fed into the printer. In addition, filaments with high moisture uptake at high relative humidity generally failed to be printable. Different release profiles for the 3D-printed tablets were obtained as a result of using different polymers in the printed formulations. For 8 mm tablets printed with 90% infill, 80% isoniazid release was observed between 40 and 852 min. Drug release characteristics could further be altered by changing the infill or the size of the printed tablets allowing personalization of the tablets. This study presents novel formulations containing isoniazid for prevention of latent tuberculosis and investigates 3D printing technology for personalized production of oral solid dosage forms enabling adjustable dose and drug release properties. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1208/s12249-018-1233-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-01-07 /pmc/articles/PMC6373414/ /pubmed/30617660 http://dx.doi.org/10.1208/s12249-018-1233-7 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Öblom, Heidi
Zhang, Jiaxiang
Pimparade, Manjeet
Speer, Isabell
Preis, Maren
Repka, Michael
Sandler, Niklas
3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title_full 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title_fullStr 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title_full_unstemmed 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title_short 3D-Printed Isoniazid Tablets for the Treatment and Prevention of Tuberculosis—Personalized Dosing and Drug Release
title_sort 3d-printed isoniazid tablets for the treatment and prevention of tuberculosis—personalized dosing and drug release
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373414/
https://www.ncbi.nlm.nih.gov/pubmed/30617660
http://dx.doi.org/10.1208/s12249-018-1233-7
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