Evidence map›Paper›PMID 30386465›Full record

ArticleWorld journal of hepatology2018

Experimental bio-artificial liver: Importance of the architectural design on ammonia detoxification performance.

María Dolores Pizarro, María Eugenia Mamprin, Lucas Damián Daurelio, Joaquín Valentín Rodriguez, María Gabriela Mediavilla

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Article in World journal of hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

María Dolores PizarroConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario S2002 LRK, Argentina.
María Eugenia MamprinConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario S2002 LRK, Argentina.
Lucas Damián DaurelioConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario S2002 LRK, Argentina.
Joaquín Valentín RodriguezConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario S2002 LRK, Argentina.
María Gabriela MediavillaConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario S2002 LRK, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determine the influence of the construction design over the biological component's performance in an experimental bio-artificial liver (BAL) device.

methodsTwo BAL models for liver microorgans (LMOs) were constructed. First, we constructed a cylindrical BAL and tested it without the biological component to establish its correct functioning. Samples of blood and biological compartment (BC) fluid were taken after 0, 60, and 120 min of perfusion. Osmolality, hematocrit, ammonia and glucose concentrations, lactate dehydrogenase (LDH) release (as a LMO viability parameter), and oxygen consumption and ammonia metabolizing capacity (as LMO functionality parameters) were determined. CPSI and OTC gene expression and function were measured. The second BAL, a "flat bottom" model, was constructed using a 25 cm

resultsThe cylindrical BAL showed a good exchange of fluids and metabolites between blood and the BC, reflected by the matching of osmolalities, and glucose and ammonia concentration ratios after 120 min of perfusion. No hemoconcentration was detected, the hematocrit levels remained stable during the whole study, and the minimal percentage of hemolysis (0.65% ± 0.10%) observed was due to the action of the peristaltic pump. When LMOs were used as biological component of this BAL they showed similar values to the ones obtained in a Normothermic Reoxygenation System (NRS) for almost all the parameters assayed. After 120 min, the results obtained were: LDH release (%): 14.7 ± 3.1 in the BAL and 15.5 ± 3.2 in the NRS (

conclusionIn this work, we demonstrate the importance of adapting the BAL architecture to the biological component characteristics to obtain an adequate BAL performance.

Indexed as

Ammonia detoxificationBio-artificial liverCarbamyl Phosphate Synthetase IDevice designOrnithine TranscarbamylaseRat liver microorgans

Identifiers

PMID30386465
PMCPMC6206149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.