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Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
by
Markl, Daniel
, Zeitler, J. Axel
, Müllertz, Anette
, Rantanen, Jukka
, Rasch, Cecilie
, Michaelsen, Maria Høtoft
, Rades, Thomas
, Bøtker, Johan
in
3-D printers
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Biopolymers
/ Chemistry, Pharmaceutical - methods
/ Computer-Aided Design
/ CT imaging
/ Dosage Forms
/ Drug delivery systems
/ Drug Delivery Systems - methods
/ Drug Liberation
/ Drugs
/ Halofantrine
/ Medical Law
/ Microstructure
/ Pharmaceutical Preparations - chemistry
/ Pharmacology/Toxicology
/ Pharmacy
/ Phenanthrenes - chemistry
/ Polyesters - chemistry
/ Polyvinyl alcohol
/ Polyvinyl Alcohol - chemistry
/ Porosity
/ Printing - methods
/ Printing, Three-Dimensional
/ Research Paper
/ Technology, Pharmaceutical - methods
/ Terahertz Imaging - methods
/ Tomography
/ Vehicles
/ X-Ray Microtomography - methods
/ X-Rays
2017
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Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
by
Markl, Daniel
, Zeitler, J. Axel
, Müllertz, Anette
, Rantanen, Jukka
, Rasch, Cecilie
, Michaelsen, Maria Høtoft
, Rades, Thomas
, Bøtker, Johan
in
3-D printers
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Biopolymers
/ Chemistry, Pharmaceutical - methods
/ Computer-Aided Design
/ CT imaging
/ Dosage Forms
/ Drug delivery systems
/ Drug Delivery Systems - methods
/ Drug Liberation
/ Drugs
/ Halofantrine
/ Medical Law
/ Microstructure
/ Pharmaceutical Preparations - chemistry
/ Pharmacology/Toxicology
/ Pharmacy
/ Phenanthrenes - chemistry
/ Polyesters - chemistry
/ Polyvinyl alcohol
/ Polyvinyl Alcohol - chemistry
/ Porosity
/ Printing - methods
/ Printing, Three-Dimensional
/ Research Paper
/ Technology, Pharmaceutical - methods
/ Terahertz Imaging - methods
/ Tomography
/ Vehicles
/ X-Ray Microtomography - methods
/ X-Rays
2017
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Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
by
Markl, Daniel
, Zeitler, J. Axel
, Müllertz, Anette
, Rantanen, Jukka
, Rasch, Cecilie
, Michaelsen, Maria Høtoft
, Rades, Thomas
, Bøtker, Johan
in
3-D printers
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Biopolymers
/ Chemistry, Pharmaceutical - methods
/ Computer-Aided Design
/ CT imaging
/ Dosage Forms
/ Drug delivery systems
/ Drug Delivery Systems - methods
/ Drug Liberation
/ Drugs
/ Halofantrine
/ Medical Law
/ Microstructure
/ Pharmaceutical Preparations - chemistry
/ Pharmacology/Toxicology
/ Pharmacy
/ Phenanthrenes - chemistry
/ Polyesters - chemistry
/ Polyvinyl alcohol
/ Polyvinyl Alcohol - chemistry
/ Porosity
/ Printing - methods
/ Printing, Three-Dimensional
/ Research Paper
/ Technology, Pharmaceutical - methods
/ Terahertz Imaging - methods
/ Tomography
/ Vehicles
/ X-Ray Microtomography - methods
/ X-Rays
2017
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Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
Journal Article
Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
2017
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Overview
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 (XμCT) and terahertz pulsed imaging (TPI).
Methods
Printing was performed with either polyvinyl alcohol (PVA) or polylactic acid (PLA). The structures were examined by XμCT 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 XμCT data. The print resolution and accuracy was characterised by XμCT 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 XμCT and TPI will assist to gain a better understanding about the performance of 3D printed dosage forms.
Publisher
Springer US,Springer,Springer Nature B.V
Subject
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Chemistry, Pharmaceutical - methods
/ Drug Delivery Systems - methods
/ Drugs
/ Pharmaceutical Preparations - chemistry
/ Pharmacy
/ Polyvinyl Alcohol - chemistry
/ Porosity
/ Technology, Pharmaceutical - methods
/ Vehicles
/ X-Ray Microtomography - methods
/ X-Rays
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