Development of continuous implantable renal replacement: past and future.

Most of the 400,000+ patients in the United States with kidney failure depend on dialysis treatments in dedicated dialysis centers for 3 h to 5 h, usually 3 times a week, but they still suffer from accelerated cardiovascular disease and infections. Extended daily dialysis, for 6 to 8 hours every day, seems to be associated with better outcomes but would overwhelm the dialysis networks and severely limit patient activity. Technology to miniaturize and automate home dialysis will be necessary to offer extended daily dialysis to most dialysis patients. Miniaturization of existing hollow-fiber polymer membranes is constrained by requirements for high driving pressures for circulation and convective clearance. Recent advances in membrane technology based on microelectromechanical systems (MEMS) promise to enable the development of continuous implantable renal replacement therapy. Silicon nanoporous membranes with a highly monodisperse pore size distribution have been produced using protocols amenable to low-cost batch fabrication similar to those used to produce microelectronics. Hydraulic permeability of the flat-sheet membranes with critical pore sizes in the range of 8-100 nm has been measured to confirm that conventional fluid transport models are sufficiently accurate for predictive design for bulk liquid flow in an implantable hemofilter. Membrane biocompatibility was tested in vitro with human proximal tubule cells and revealed that silicon does not exhibit cytotoxicity, as evidenced by the formation of confluent cell layers with tight junctions and central cilia. Filtration characterization demonstrated that the nanoporous membranes exhibit size-dependent solute rejection in agreement with steric hindrance models. These advances in membrane technology are fundamentally enabling for a paradigm shift from an in-center to implantable dialysis system.

[1]  H D Humes,et al.  Tissue engineering of a bioartificial renal tubule assist device: in vitro transport and metabolic characteristics. , 1999, Kidney international.

[2]  S. M. MacKay,et al.  Replacement of renal function in uremic animals with a tissue-engineered kidney , 1999, Nature Biotechnology.

[3]  Christopher T. Chan,et al.  Regression of left ventricular hypertrophy after conversion to nocturnal hemodialysis. , 2002, Kidney international.

[4]  Anthony Atala,et al.  Tissue engineering, stem cells, and cloning: opportunities for regenerative medicine. , 2004, Journal of the American Society of Nephrology : JASN.

[5]  C. S. Chen,et al.  Geometric control of cell life and death. , 1997, Science.

[6]  Shuvo Roy,et al.  Differentiated Growth of Human Renal Tubule Cells on Thin-Film and Nanostructured Materials , 2006, ASAIO journal.

[7]  Mark E Meyerhoff,et al.  Polymers incorporating nitric oxide releasing/generating substances for improved biocompatibility of blood-contacting medical devices. , 2005, Biomaterials.

[8]  E. Mancini,et al.  Convective and adsorptive removal of beta2-microglobulin during predilutional and postdilutional hemofiltration. , 2005, Kidney international.

[9]  C Ronco,et al.  Nanoscale Modulation of the Pore Dimensions, Size Distribution and Structure of a new Polysulfone-Based High-Flux Dialysis Membrane , 2001, The International journal of artificial organs.

[10]  A. Fleischman,et al.  A System for Micro/Nano Fluidic Flow Diagnostics , 2005, Biomedical microdevices.

[11]  Véronique Sébille,et al.  Effect of Treatment With Low Doses of Hydrocortisone and Fludrocortisone on Mortality in Patients With Septic Shock , 2002 .

[12]  Ingrid Ledebo,et al.  Convective Dialysis Therapies, Current Status and Perspective , 2005, Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.

[13]  Y. Qiu,et al.  Biomimetic engineering of non-adhesive glycocalyx-like surfaces using oligosaccharide surfactant polymers , 1998, Nature.

[14]  J Ean,et al.  Efficacy and safety of recombinant human activated protein C for severe sepsis. , 2001, The New England journal of medicine.

[15]  G. Whitesides,et al.  Cell shape provides global control of focal adhesion assembly. , 2003, Biochemical and biophysical research communications.

[16]  C. Ronco,et al.  The Human Nephron Filter: Toward a Continuously Functioning, Implantable Artificial Nephron System , 2005, Blood Purification.

[17]  Feng Lin,et al.  The Incidence of End-Stage Renal Disease Is Increasing Faster than the Prevalence of Chronic Renal Insufficiency , 2004, Annals of Internal Medicine.

[18]  Christopher T. Chan,et al.  Quotidian dialysis – update 2005 , 2005, Current opinion in nephrology and hypertension.

[19]  G. Nesrallah,et al.  Calcium and phosphate balance with quotidian hemodialysis. , 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[20]  J. Díaz-Buxó,et al.  Home Hemodialysis and Remote Monitoring: Current Technology, Requirements and Capabilities , 2004, Blood Purification.

[21]  S. Jacobsen,et al.  Combined technological-clinical approach to wearable dialysis. , 1978, Kidney international. Supplement.

[22]  Hans-Dietrich Polaschegg,et al.  Continuous Renal Replacement Therapy for End-Stage Renal Disease , 2005 .

[23]  Alexander Papra,et al.  Characterization of ultrathin poly(ethylene glycol) monolayers on silicon substrates , 2001 .

[24]  Mehmet Toner,et al.  Blood-on-a-chip. , 2005, Annual review of biomedical engineering.

[25]  Y J Kim,et al.  Surface characterization and in vitro blood compatibility of poly(ethylene terephthalate) immobilized with insulin and/or heparin using plasma glow discharge. , 2000, Biomaterials.

[26]  C. Wanner,et al.  Beta2-microglobulin removal by extracorporeal renal replacement therapies , 2005 .

[27]  L. Moist,et al.  Patient quality of life on quotidian hemodialysis. , 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[28]  Edward F Leonard,et al.  Membraneless dialysis--is it possible? , 2005, Contributions to nephrology.

[29]  William F Weitzel,et al.  Initial clinical results of the bioartificial kidney containing human cells in ICU patients with acute renal failure. , 2004, Kidney international.

[30]  K. Leunissen,et al.  Pre-dilution on-line haemofiltration vs low-flux haemodialysis: a randomized prospective study. , 2005, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[31]  Humes Hd,et al.  Bioartificial kidney for full renal replacement therapy. , 2000 .

[32]  Edward F. Leonard,et al.  Dialysis without Membranes: How and Why? , 2004, Blood Purification.

[33]  Allen R Nissenson,et al.  Continuously functioning artificial nephron system: The promise of nanotechnology , 2005, Hemodialysis international. International Symposium on Home Hemodialysis.

[34]  Tejal A Desai,et al.  Nanoporous microsystems for islet cell replacement. , 2004, Advanced drug delivery reviews.

[35]  David Haber,et al.  Guide to clinical preventive services: a challenge to physician resourcefulness , 1993 .

[36]  B. Haraldsson,et al.  Glomerular size and charge selectivity in the rat as revealed by FITC-ficoll and albumin. , 2000, American journal of physiology. Renal physiology.