2012
DOI: 10.1016/j.ijpharm.2012.02.011
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Fabrication of drug-loaded polymer microparticles with arbitrary geometries using a piezoelectric inkjet printing system

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Cited by 135 publications
(74 citation statements)
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“…Recent research in inkjet printed pharmaceuticals has focused on solutions (Alomari et al, 2015;Genina et al, 2013;Scoutaris et al, 2011;Sandler et al, 2011;Raijada et al, 2013;Lee et al, 2012;Acosta-Vélez et al 2017), nanosuspensions (Pardeike et al, 2011), and melts Zhu et al, 2013), each of which is primarily 2D. Reel to reel type flexographic (Raijada et al, 2013;Palo et al, 2015) printing, as well as inkjet printing in combination with electrospinning have also been utilized.…”
Section: Introductionmentioning
confidence: 99%
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“…Recent research in inkjet printed pharmaceuticals has focused on solutions (Alomari et al, 2015;Genina et al, 2013;Scoutaris et al, 2011;Sandler et al, 2011;Raijada et al, 2013;Lee et al, 2012;Acosta-Vélez et al 2017), nanosuspensions (Pardeike et al, 2011), and melts Zhu et al, 2013), each of which is primarily 2D. Reel to reel type flexographic (Raijada et al, 2013;Palo et al, 2015) printing, as well as inkjet printing in combination with electrospinning have also been utilized.…”
Section: Introductionmentioning
confidence: 99%
“…Low melting temperature PEG/naproxen mixtures Zhu et al, 2013;Hsu et al, 2015) have been reported for melt based inkjet applications in which crystalline domains of the drug could be affected by PEG coatings (Hsu et al, 2015), or controlled melt cooling . Lee et al successfully produced paxlitaxel loaded poly(lactic-co-glycolic acid) microparticles with various geometries (honeycombs, grids, rings and circles) and observed that the drug release rate was dependant on the surface area of the microparticles (Lee et al, 2012). However, these printing methods are limited in that the doses produced are films, often with an edible substrate incorporated into the dosage form.…”
Section: Introductionmentioning
confidence: 99%
“…The advancements in inkjet printing were based on the potential to print designed ratios of drugs and excipients as individual microdots onto an edible substrate. Two main inkjet dispensing systems have been investigated for pharmaceutical applications: thermal (23,25) or piezoelectric inkjet printers (26)(27)(28)(29).…”
mentioning
confidence: 99%
“…Ink jet printing requires the starting materials to possess certain characteristics mainly; particle size needs to be ˂1 µm to avoid clogging the printer head, viscosity needs to be ˂ 20 cP and surface tension between 30-70 mN/m for efficient flow (27,30). Ink jet printing is thus highly suitable for manufacturing drugs with low therapeutic doses, ideally in the microgram range, since they require a smaller area on the substrate.…”
mentioning
confidence: 99%
“…Inkjet bioprinting is widely explored in the field of tissue engineering due to their unique characteristics of noncontact printing, high-throughput efficiency, automation, versatility, resolution, and possibility of parallel printing. This technology has been used to print a variety of compounds in prescribed 2D patterns, including growth factors [119], proteins [5], polymers [85], nanoparticles [190] and drugs [94]. The capability of inkjet bioprinting to print mammalian cells with high accuracy, and little or even no reduction of cell viability, was also demonstrated using different cell types, such as embryonic rat motoneurons [206], human microvascular endothelial cells [34], mouse embryonic fibroblasts [194], and retinal ganglion cells [12].…”
Section: Inkjet Bioprintingmentioning
confidence: 99%