AI Article Synopsis

  • Inkjet printing could revolutionize personalized drug therapies using liposomes, but its effect on shear-sensitive materials is uncertain.
  • Researchers tested different liposome "inks" using commercial jetting technologies and analyzed their properties before and after printing.
  • Results showed that despite high shear forces during jetting, the liposome concentration and particle size distribution remained mostly unchanged, paving the way for future advancements in drug printing.

Article Abstract

Purpose: Inkjet printing has the potential to enable novel personalized and tailored drug therapies based on liposome and lipid nanoparticles. However, due to the significant shear force exerted on the jetted fluids, its suitability for shear-sensitive materials such as liposomes, has not been verified. We have conducted a proof-of-concept study to examine whether the particle concentration and size distribution of placebo liposomes are affected by common inkjet/dispensing technologies.

Methods: We have subjected three types of liposome-containing fluids ("inks") to two different commercial dispensing/jetting technologies, which are relevant to most drug printing approaches. The liposome jetting processes were observed in real-time using strobographic imaging techniques. The phospholipid concentrations and particle size distributions were determined before and after jetting via enzymatic colorimetric and dynamic light scattering methods, respectively.

Results: Our results have shown that the jetting dynamics of the liposome inks are well predicted by the established inkjet printing regime map based on their physical properties and the jetting conditions. Importantly, although significant shear forces were confirmed during jetting, the liposome concentrations and particle size distributions in the collected samples remain largely unaffected.

Conclusion: These findings, we believe, provide the essential proof-of-concept to encourage further development in this highly topical research area.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127480PMC
http://dx.doi.org/10.1007/s12247-022-09643-zDOI Listing

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