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Fabrication of printed drug-delivery systems

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Printing technologies specifically digital inkjet printing, offer possibilities in the production of individualized medicines. The main advantage of inkjet printing includes the ability to dispense uniform droplets in the picoliter range with high degree of accuracy to allow dose personalization. The pharmaceutical ink formulation has to be designed with respect to its viscosity and surface tension to guarantee continuous printing and high reproducibility of the forming droplets to allow dose uniformity. The aim of this paper is demonstrate the combined use of inkjet and flexographic printing to fabricate pharmaceutical solid dosage forms with controlled release properties of drug substances. Also the characterization of substrates and final drug-delivery systems is studied with various techniques and discussed.
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Document Type: Research Article

Publication date: 2013-01-01

More about this publication?
  • For more than 30 years, IS&T's series of digital printing conferences have been the leading forum for discussion of advances and new directions in 2D and 3D printing technologies. A comprehensive, industry-wide conference that brings together industry and academia, this meeting includes all aspects of the hardware, materials, software, images, and applications associated with digital printing systems?particularly those involved with additive manufacturing and fabrication?including bio-printing, printed electronics, page-wide, drop-on-demand, desktop and continuous ink jet, toner-based systems, and production digital printing, as well as the engineering capability, optimization, and science involved in these fields. In 2016, the conference changed its name formally to Printing for Fabrication to better reflect the content of the meeting and the evolving technology of printing.

    Please note: For purposes of its Digital Library content, IS&T defines Open Access as papers that will be downloadable in their entirety for free in perpetuity. Copyright restrictions on papers vary; see individual paper for details.

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