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20.06.2018 | Original article | Ausgabe 6/2018 Open Access

Clinical and Experimental Nephrology 6/2018

Biocompatibility of a new PD solution for Japan, Reguneal™, measured as in vitro proliferation of fibroblasts

Zeitschrift:
Clinical and Experimental Nephrology > Ausgabe 6/2018
Autoren:
Bart Dioos, Goedele Paternot, Rose-Marie Jenvert, Annick Duponchelle, Mark R. Marshall, Migaku Nakajima, Edward Ramirez Ganoza, James A. Sloand, Anders P. Wieslander
Wichtige Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s10157-018-1602-2) contains supplementary material, which is available to authorized users.

Abstract

Background

The aim of this study was to investigate in vitro biocompatibility of Reguneal™, a new bicarbonate containing peritoneal dialysis fluid (PDF) for Japan, and compare it with other PDFs available in that country.

Methods

We assessed basal cytotoxicity using in vitro proliferation of cultured fibroblasts, L-929, determining the quantity of living cells by the uptake of Neutral Red. Levels of ten glucose degradation products (GDPs) were measured by a validated ultrahigh-performance liquid chromatography method in combination with an ultraviolet detector. We compared inhibition of fibroblast cell growth between brands of PDF, adjusting for dextrose and GDP concentrations using random-effects mixed models.

Results

The results demonstrate that cytotoxicity of Reguneal™ is comparable to a sterile-filtered control and is less cytotoxic than most of the other PDFs, most of which significantly inhibited cell growth. As a “class effect”, increasing dextrose and GDP concentrations were non-significantly but positively associated with cytotoxicity. As a “brand effect”, these relationships varied widely between brands, and some PDFs had significant residual effects on basal cytotoxicity through mechanisms that were unassociated with either dextrose or GDP concentration.

Conclusion

Our study suggests that Reguneal™ is a biocompatible PDF. The results of our study also highlight that dextrose and GDPs are important for biocompatibility, but alone are not a complete surrogate. The results of our study need to be confirmed in other tissue culture models, and should lead to further research on determinants of biocompatibility and the effect of such PDFs on clinical outcomes.

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