Toxins (Sep 2023)

Renal Embolization-Induced Uremic Swine Model for Assessment of Next-Generation Implantable Hemodialyzers

  • Jarrett Moyer,
  • Mark W. Wilson,
  • Thomas A. Sorrentino,
  • Ana Santandreu,
  • Caressa Chen,
  • Dean Hu,
  • Amy Kerdok,
  • Edward Porock,
  • Nathan Wright,
  • Jimmy Ly,
  • Charles Blaha,
  • Lynda A. Frassetto,
  • William H. Fissell,
  • Shant M. Vartanian,
  • Shuvo Roy

DOI
https://doi.org/10.3390/toxins15090547
Journal volume & issue
Vol. 15, no. 9
p. 547

Abstract

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Reliable models of renal failure in large animals are critical to the successful translation of the next generation of renal replacement therapies (RRT) into humans. While models exist for the induction of renal failure, none are optimized for the implantation of devices to the retroperitoneal vasculature. We successfully piloted an embolization-to-implantation protocol enabling the first implant of a silicon nanopore membrane hemodialyzer (SNMHD) in a swine renal failure model. Renal arterial embolization is a non-invasive approach to near-total nephrectomy that preserves retroperitoneal anatomy for device implants. Silicon nanopore membranes (SNM) are efficient blood-compatible membranes that enable novel approaches to RRT. Yucatan minipigs underwent staged bilateral renal arterial embolization to induce renal failure, managed by intermittent hemodialysis. A small-scale arteriovenous SNMHD prototype was implanted into the retroperitoneum. Dialysate catheters were tunneled externally for connection to a dialysate recirculation pump. SNMHD clearance was determined by intermittent sampling of recirculating dialysate. Creatinine and urea clearance through the SNMHD were 76–105 mL/min/m2 and 140–165 mL/min/m2, respectively, without albumin leakage. Normalized creatinine and urea clearance measured in the SNMHD may translate to a fully implantable clinical-scale device. This pilot study establishes a path toward therapeutic testing of the clinical-scale SNMHD and other implantable RRT devices.

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