AI Article Synopsis

  • Reliable large animal models for renal failure are essential for advancing renal replacement therapies (RRT) that can be used in humans.
  • This study introduced a novel embolization-to-implantation protocol that successfully integrated a silicon nanopore membrane hemodialyzer (SNMHD) into a swine model of renal failure.
  • The findings showed promising clearance rates for creatinine and urea using the SNMHD, suggesting potential for future clinical applications with fully implantable devices.*

Article Abstract

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/m and 140-165 mL/min/m, 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10536310PMC
http://dx.doi.org/10.3390/toxins15090547DOI Listing

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