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

Author:

Moyer Jarrett12,Wilson Mark W.1,Sorrentino Thomas A.1ORCID,Santandreu Ana1,Chen Caressa1,Hu Dean3,Kerdok Amy3,Porock Edward1,Wright Nathan12,Ly Jimmy12,Blaha Charles12,Frassetto Lynda A.1,Fissell William H.24,Vartanian Shant M.1,Roy Shuvo12ORCID

Affiliation:

1. Departments of Bioengineering & Therapeutic Sciences, Surgery, Medicine, and Radiology & Biomedical Imaging, University of California, San Francisco, CA 94143, USA

2. Silicon Kidney, San Ramon, CA 94583, USA

3. Outset Medical, San Jose, CA 95134, USA

4. Division of Nephrology & Hypertension, Vanderbilt University Medical Center, Nashville, TN 37232, USA

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/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.

Funder

NIH/NIDDK

NIH/NIBIB

Patsy Guglielmo

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

Reference51 articles.

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