Evidence map›Paper›PMID 40558473›Full record

ArticleBiosensors2025

MyμAlbumin: A Cutting-Edge Immunoturbidity-Based Device with Real-Time and Seamless Data Transmission for Early Detection of Chronic Kidney Disease at the Point of Care.

Wanna Chaijaroenkul, Napaporn Youngvises, Artitaya Thiengsusuk, Tullayakorn Plengsuriyakarn, Jakkrapong Suwanboriboon, Kridsada Sirisabhabhorn, Wanchai Meesiri, Kesara Na-Bangchang

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In one paragraph

Article in Biosensors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Wanna ChaijaroenkulGraduate Program in Bioclinical Sciences, Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand.
Napaporn YoungvisesDrug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University, Pathum Thani 12120, Thailand.
Artitaya ThiengsusukDrug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University, Pathum Thani 12120, Thailand.
Tullayakorn PlengsuriyakarnGraduate Program in Bioclinical Sciences, Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand.
Jakkrapong SuwanboriboonBangkok High Lab Co., Ltd., Bang Khen District, Bangkok 10220, Thailand.
Kridsada SirisabhabhornDepartment of Medical Technology Laboratory, Thammasat University Hospital, Pathum Thani 12120, Thailand.
Wanchai MeesiriBangkok High Lab Co., Ltd., Bang Khen District, Bangkok 10220, Thailand.
Kesara Na-BangchangGraduate Program in Bioclinical Sciences, Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand.

Funding

Chulabhorn International College of Medicine, Thammasat University F 4/2566National Research Council of Thailand (NRCT) N42A671041
6 · The paper itself

Abstract

Microalbuminemia, characterized by a urinary albumin concentration between 20 and 200 mg/L, is a critical marker in assessing the risk of chronic kidney disease (CKD), diabetic nephropathy, and various other chronic conditions. Previously, we developed and validated the MyACR point-of-care (PoC) device, which facilitates the monitoring of CKD progression through real-time data transmission, thus enhancing patient management. This device utilizes a spectrophotometric dye-binding assay to measure albumin and creatinine concentrations in urine samples, providing an albumin-to-creatinine ratio (ACR) result. In the present study, we introduced a refined version of the PoC device, MyμAlbumin, designed to offer a simple, accurate, specific, sensitive, and rapid method for detecting microalbumin in urine as an early indicator of CKD and related diseases. The measurement is based on a specific immunoturbidimetric assay in a microcuvette, using a total solution volume of 125 µL (n = 5 for each validation test). The MyμAlbumin device demonstrated excellent performance, achieving high accuracy (%DMV ≤ 4.67) and precision (%CV < 5) and a strong correlation (R

Indexed as

AlbuminuriaBiosensing TechniquesPoint-of-Care SystemsRenal Insufficiency, ChronicCreatinineEarly DiagnosisHumansNephelometry and TurbidimetryCreatininechronic kidney diseasemicroalbuminpoint-of-care (PoC) medical device

Identifiers

PMID40558473
PMCPMC12191223

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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.