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ABSTRACT: Purpose
A 3D printer was used to realise compartmental dosage forms containing multiple active pharmaceutical ingredient (API) formulations. This work demonstrates the microstructural characterisation of 3D printed solid dosage forms using X-ray computed microtomography (X?CT) and terahertz pulsed imaging (TPI).Methods
Printing was performed with either polyvinyl alcohol (PVA) or polylactic acid (PLA). The structures were examined by X?CT and TPI. Liquid self-nanoemulsifying drug delivery system (SNEDDS) formulations containing saquinavir and halofantrine were incorporated into the 3D printed compartmentalised structures and in vitro drug release determined.Results
A clear difference in terms of pore structure between PVA and PLA prints was observed by extracting the porosity (5.5% for PVA and 0.2% for PLA prints), pore length and pore volume from the X?CT data. The print resolution and accuracy was characterised by X?CT and TPI on the basis of the computer-aided design (CAD) models of the dosage form (compartmentalised PVA structures were 7.5?±?0.75% larger than designed; n?=?3).Conclusions
The 3D printer can reproduce specific structures very accurately, whereas the 3D prints can deviate from the designed model. The microstructural information extracted by X?CT and TPI will assist to gain a better understanding about the performance of 3D printed dosage forms.
SUBMITTER: Markl D
PROVIDER: S-EPMC5382186 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature
Markl Daniel D Zeitler J Axel JA Rasch Cecilie C Michaelsen Maria Høtoft MH Müllertz Anette A Rantanen Jukka J Rades Thomas T Bøtker Johan J
Pharmaceutical research 20161221 5
<h4>Purpose</h4>A 3D printer was used to realise compartmental dosage forms containing multiple active pharmaceutical ingredient (API) formulations. This work demonstrates the microstructural characterisation of 3D printed solid dosage forms using X-ray computed microtomography (XμCT) and terahertz pulsed imaging (TPI).<h4>Methods</h4>Printing was performed with either polyvinyl alcohol (PVA) or polylactic acid (PLA). The structures were examined by XμCT and TPI. Liquid self-nanoemulsifying drug ...[more]