Literature DB >> 2439624

Molecular size dependence of peritoneal transport.

J K Leypoldt, H R Parker, R P Frigon, L W Henderson.   

Abstract

The nature of the barrier between blood and peritoneal dialysate was studied by determining peritoneal solute transport rates as a function of molecular size using neutral dextrans, polymers with different molecular weights but uniform chemical composition. Transport rates for creatinine, p-aminohippurate (PAH), and neutral dextran (3,000 to 50,000 daltons) were measured during peritoneal dialysis in the awake rabbit using sequential isotonic and hypertonic dialysis solutions. The permeability-area product (PA) for the peritoneum was determined from the dependence of the dialysate concentration on time during the isotonic exchange. The dependence of PA on molecular size showed no additional hindrance by the peritoneum as molecules of larger size were considered. By accounting for convective solute transport during the hypertonic exchange, the solute reflection coefficient (sigma) and PA were simultaneously determined. The values of PA for creatinine and PAH were similar to those determined during the isotonic exchange, and sigma values for creatinine and PAH were 0.18 +/- 0.20 and 0.14 +/- 0.14, respectively. Dextran sigma values (3,000 to 22,000 daltons) were near unity (0.9 to 1.0) and relatively independent of molecular size, suggesting substantial hindrance to convective transport for this size range. This work demonstrates that the paradoxical transport properties of an "open" diffusive yet "tight" convective peritoneal barrier are primarily reflective of the unique structural properties of this biologic tissue and are not related to test solute heterogeneity.

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Year:  1987        PMID: 2439624

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN: 0022-2143


  7 in total

1.  The effect of convection on bidirectional peritoneal solute transport: predictions from a distributed model.

Authors:  J K Leypoldt; L W Henderson
Journal:  Ann Biomed Eng       Date:  1992       Impact factor: 3.934

2.  Investigations into the route of uptake and pharmacokinetics of intraperitoneally-administered monoclonal antibodies: I. Transdiaphragmatic blockade of the terminal lymphatics in the rat.

Authors:  J S Barrett; R L Wahl; J G Wagner; R Brown; S J Fisher
Journal:  Cancer Immunol Immunother       Date:  1990       Impact factor: 6.968

3.  Transfer of liposomal drug carriers from the blood to the peritoneal cavity of normal and ascitic tumor-bearing mice.

Authors:  M B Bally; D Masin; R Nayar; P R Cullis; L D Mayer
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

Review 4.  Peritoneal changes in patients on long-term peritoneal dialysis.

Authors:  Raymond T Krediet; Dirk G Struijk
Journal:  Nat Rev Nephrol       Date:  2013-05-14       Impact factor: 28.314

5.  Ultrafiltration characteristics of glucose polymers with low polydispersity.

Authors:  John K Leypoldt; Catherine M Hoff; Dean Piscopo; Seraya N Carr; Jessica M Svatek; Clifford J Holmes
Journal:  Perit Dial Int       Date:  2012-11-01       Impact factor: 1.756

6.  Monitoring of the peritoneal membrane.

Authors:  Dirk G Struijk
Journal:  NDT Plus       Date:  2008-10

7.  Association of Plasma Uremic Solute Levels with Residual Kidney Function in Children on Peritoneal Dialysis.

Authors:  Lakshmi L Ganesan; Frank J O'Brien; Tammy L Sirich; Natalie S Plummer; Rita Sheth; Cecile Fajardo; Paul Brakeman; Scott M Sutherland; Timothy W Meyer
Journal:  Clin J Am Soc Nephrol       Date:  2021-07-07       Impact factor: 10.614

  7 in total

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