2018
DOI: 10.1016/j.ijpharm.2018.10.030
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Analytical aspects of printed oral dosage forms

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Cited by 36 publications
(16 citation statements)
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“…While it is easy to conduct API content analysis using well-established methods such as UV spectroscopy and HPLC analysis, these methods require the use of destructive sample preparation that is costly. Therefore, the API content analysis of the printed dosage forms should ideally be conducted using non-destructive, robust and fast methods (5). This is especially important in the future to realize on-demand and near the end-users pharmacoprinting of personalized medicine (6) or to integrate it in a continuous manufacturing setup (7,8) according to the emerging regulatory framework (9).…”
Section: Introductionmentioning
confidence: 99%
“…While it is easy to conduct API content analysis using well-established methods such as UV spectroscopy and HPLC analysis, these methods require the use of destructive sample preparation that is costly. Therefore, the API content analysis of the printed dosage forms should ideally be conducted using non-destructive, robust and fast methods (5). This is especially important in the future to realize on-demand and near the end-users pharmacoprinting of personalized medicine (6) or to integrate it in a continuous manufacturing setup (7,8) according to the emerging regulatory framework (9).…”
Section: Introductionmentioning
confidence: 99%
“…Especially for poorly soluble drugs, the composition of drug-loaded fluid should avoid the drug sedimentation which is the main cause of dose inaccuracy but should maintain the viscosity in a range acceptable for printing [108]. Moreover, several parameters (e.g., evaporation time, droplet size formation) have to be set-up to print homogenously the drug onto the subtract [117].…”
Section: D Printingmentioning
confidence: 99%
“…Therefore, dose verification prior to drug administration was considered a prerequisite. Colorimetric and spectroscopic techniques for the analysis of drug content in printed dosage forms are proposed methods for nondestructive quality control permitting real-time batch release [36,37]. For on-demand manufacturing purposes, either handheld, user-friendly analytical devices that are quick to operate or devices that are automated and integrated to the printers have to be incorporated to the production process in order to enable quick response times in hospital pharmacies.…”
Section: Main Findingsmentioning
confidence: 99%