Calibrated bioresorbable microspheres: a preliminary study on the level of occlusion and arterial distribution in a rabbit kidney model

J Vasc Interv Radiol. 2013 Oct;24(10):1567-75. doi: 10.1016/j.jvir.2013.06.009. Epub 2013 Aug 6.

Abstract

Purpose: To assess the level of occlusion and arterial distribution of calibrated bioresorbable microspheres (BRMS-I and BRMS-II) compared with tris-acryl gelatin microspheres (TGMS) after renal embolization.

Materials and methods: Six rabbits underwent renal embolization with 100-300 µm BRMS-I and TGMS; three rabbits received partial occlusion (group 1, n = 3), and three rabbits received total occlusion (group 2, n = 3). Four other rabbits received 100-300 µm BRMS-II (with higher cross-linking density than BRMS-I) in the left kidneys reaching total occlusion (group 3, n = 4). Coronal sections of the kidneys were histologically analyzed. Ease of injection, microsphere deformation, vessel sizes, and arterial distribution were assessed.

Results: The injection of BRMS-I, BRMS-II, and TGMS through microcatheters went smoothly without any clogging. In group 1, BRMS identification was easier than TGMS. In group 2, both BRMS-I and TGMS were observed in all three arterial levels (interlobar, arcuate, and interlobular arteries) without a significant difference (P = .84). BRMS-I were not significantly different from TGMS in the mean diameter of vessels occluded (197 µm ± 23 vs 158 µm ± 21, P = .25) or the microsphere deformation (8.85% ± 0.53% vs 11.80% ± 0.64%, P = .071). In group 3, the arterial distribution of BRMS-II was significantly different from BRMS-I and TGMS (P < .0001).

Conclusions: In occluding arteries, 100-300 µm BRMS-I were not significantly different from 100-300 µm TGMS. Arterial distribution of BRMS can be influenced by their cross-linking density.

Keywords: BRMS; D%; H&E; TGMS; bioresorbable microspheres; deformation percentage; hematoxylin and eosin; tris-acryl gelatin microspheres.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Flow Velocity / drug effects
  • Calibration
  • Embolization, Therapeutic / methods*
  • Gelatin Sponge, Absorbable / administration & dosage*
  • Gelatin Sponge, Absorbable / pharmacokinetics*
  • Hemostatics / administration & dosage
  • Hemostatics / pharmacokinetics
  • Kidney
  • Microspheres
  • Rabbits
  • Renal Artery / drug effects
  • Renal Artery / physiology*
  • Tissue Distribution
  • Treatment Outcome

Substances

  • Hemostatics