Hydrogenology
Hydrogenology editorial study record

Quantification of dissolved H₂ and continuous monitoring of hydrogen-rich water for haemodialysis applications: an experimental study

Mouzakis FL, Khadka LB, Pereira da Silva M, Mottaghy K. · The International Journal of Artificial Organs. 2022;45(3):254–261.

PreclinicalOther formsPublished 2022
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Preclinical

Reported design

Two-run in-vitro closed-loop sensor and gas-exchange validation experiment

Research topic

Kidney and urinary health

Administration classification

Other forms

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Water and 0.9% saline circulating through a laboratory extracorporeal-style circuit; no patients, animals or blood were studied.

Sample

Two principal experimental runs plus additional paired-sensor and temperature/calibration comparisons; this was a device experiment rather than a biological sample.

Duration

Each concentration was held to steady state; the H₂ sensor required roughly 50 minutes to equilibrate.

Intervention

Pure cylinder H₂ was mixed with air and transferred across a membrane oxygenator into liquid flowing at 0.5 L/min.

Hydrogen form

H₂-only gas diluted with air — not Brown's gas and not inhalation.

H₂ specification

H₂ flow was 53±2 or 53±1 mL/min at H₂:air flow ratios 1:40, 1:20 and 1:10, producing about 2.7%, 5.3% and 10.5% H₂ inlet mixtures and target dissolved ranges relevant to dialysate.

H₂ flow

53 mL/min H₂ (reported uncertainty ±1–2 mL/min).

O₂ delivered with H₂

Air supplied the O₂; approximate air flows from the reported ratios were 2,120, 1,060 and 530 mL/min, but pure O₂ flow was not separately controlled.

Comparator

Oxygen-sensor partial-pressure readings and theoretical Henry/Dalton-law estimates, plus comparisons between contactless H₂ sensors/calibration temperatures.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Dissolved-H₂ sensor response, accuracy/reproducibility, temperature effects, theoretical agreement and response delay.

Reported result

Dissolved H₂ rose approximately linearly with feed concentration and paired devices broadly agreed at equilibrium. Important limitations were a roughly 50-minute lag, up to 30% early low-concentration divergence and increasing error at higher concentration/temperature. The article typesets equilibrium readings 47, 100 and 211 with a percent sign even though the defined sensor range and surrounding text use ppb; the units are therefore flagged as internally inconsistent.

Results-extraction completeness

The complete free PMC article, circuit methods, equations, figures and disclosures were checked for exact H₂ flow, air ratios, liquid versus gas flow, sensor results, unit inconsistency, limitations, funding and conflicts.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

In-vitro saline/water device study, only two principal runs, no blood/dialysis treatment, sensor not validated against gas chromatography and a likely unit-typesetting error. One author received Erasmus+/university support; authors reported no study funding and no conflicts.

Applies directly to

Analytical monitoring for H₂-enriched dialysate preparation; it provides no evidence of clinical dialysis benefit or patient safety.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 35075943 · DOI: 10.1177/03913988211070588

Publisher access

Free full article in PubMed Central.

Extraction basis

Complete PMC article and PubMed metadata; full-text extraction checked 9 August 2026.

Record revision

2026-08-10