Author:
Öblom Heidi,Zhang Jiaxiang,Pimparade Manjeet,Speer Isabell,Preis Maren,Repka Michael,Sandler Niklas
Abstract
Abstract
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.
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics
Reference51 articles.
1. WHO. Global Tuberculosis Report 2017 [Internet]. World Health Organization. 2017. Available from:
http://apps.who.int/iris/bitstream/handle/10665/259366/9789241565516-eng.pdf;jsessionid=ABB149D89E3E1931D6E7577BE8525C0B?sequence=1
. Accessed 18 Aug 2018.
2. WHO. Latent tuberculosis infection Updated and consolidated guidelines for programmatic management [Internet]. 2018. Available from:
http://www.who.int/tb/publications/2018/latent-tuberculosis-infection/en/
. Accessed 18 Aug 2018.
3. Schaaf HS, Parkin DP, Seifart HI, Werely CJ, Hesseling PB, Van Helden PD, et al. Isoniazid pharmacokinetics in children treated for respiratory tuberculosis. Arch Dis Child. 2005;90(6):614–8.
4. EMA. Assessment report [Internet]. 2012. Available from:
http://www.ema.europa.eu/docs/en_GB/document_library/Report/2012/06/WC500128439.pdf
. Accessed 28 Aug 2018.
5. Bekker A, Schaaf HS, Seifart HI, Draper HR, Werely CJ, Cotton MF, et al. Pharmacokinetics of isoniazid in low-birth-weight and premature infants. Antimicrob Agents Chemother. 2014;58(4):2229–34.
Cited by
122 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献