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Microfluidic-prepared, monodisperse, X-ray-visible, embolic microspheres for non-oncological embolization applications

  • Cyrus W. Beh
  • , Yingli Fu
  • , Clifford R. Weiss
  • , Charles Hu
  • , Aravind Arepally
  • , Hai-Quan Mao
  • , Tza-Huei Wang*
  • , Dara L. Kraitchman*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Embolotherapy using particle embolics is normally performed with exogenous contrast to assist in visualization. However, the exact location of the embolics cannot be identified after contrast washout. We developed a novel, pseudo-check valve-integrated microfluidic device, that partitions barium-impregnated alginate from crosslinking solution, thereby preventing nozzle failure. This enables rapid and continuous generation of inherently X-ray-visible embolic microspheres (XEMs) with uniform size. The XEMs are visible under clinical X-ray and cone beam CT both in vitro and in vivo. In particular, we demonstrated the embolization properties of these XEMs in large animals, performing direct intra-and post-procedural assessment of embolic delivery. The persistent radiopacity of these XEMs enables real-Time evaluation of embolization precision and offers great promise for non-invasive follow-up examination without exogenous contrast. We also demonstrated that bariatric arterial embolization with XEMs significantly suppresses weight gain in swine, as an example of a non-oncological application of embolotherapy. © The Royal Society of Chemistry 2020.
Original languageEnglish
Pages (from-to)3591-3600
JournalLab on a Chip
Volume20
Issue number19
Online published1 Sept 2020
DOIs
Publication statusPublished - 7 Oct 2020
Externally publishedYes

Funding

This work was supported by National Institutes of Health (NIH) R21/R33 HL089029 and R01 EB017615, American Heart Association (AHA) 16SDG30500010, and Maryland Stem Cell Research Fund 2011-MDSCRFII-0043. The authors thank Judy Mickey for assistance with the animal studies and Robert A Anders for histology evaluation.

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