Evidence map›Paper›PMID 42471438›Full record

ArticleMikrochimica acta2026

An integrated system of micromixers and microfluidic concentration gradient chips assisted drug screening over large concentration range.

Huanhuan Shi, Weizheng Xu, Ziwen Cheng, Chen Huang, Xinyi Wang, Shijie Qu, Rui Zhao, Derong Xu

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Article in Mikrochimica acta, 2026. 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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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

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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

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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.

Huanhuan ShiDepartment of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, 330052, People's Republic of China. shihuanhuancsu@126.com.
Weizheng XuDepartment of Biomedical Engineering, School of Instrument Science and Optical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, 330063, People's Republic of China.
Ziwen ChengDepartment of Biomedical Engineering, School of Instrument Science and Optical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, 330063, People's Republic of China.
Chen HuangDepartment of Biomedical Engineering, School of Instrument Science and Optical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, 330063, People's Republic of China.
Xinyi WangDepartment of Biomedical Engineering, School of Instrument Science and Optical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, 330063, People's Republic of China.
Shijie QuDepartment of Biomedical Engineering, School of Instrument Science and Optical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, 330063, People's Republic of China.
Rui ZhaoDepartment of Clinical Laboratory, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, 330052, People's Republic of China.
Derong XuJiangxi Institute of Translational Medicine, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, 330000, China. xudr@ncu.edu.cn.

Funding

Excellent Youth Fund for Jiangxi Provincial Natural Science Foundation 20242BAB22014National Natural Science Foundation of China 62461044Outstanding Youth Fund of Jiangxi Provincial Natural Science Foundation 20252BAC220010
6 · The paper itself

Abstract

There is an unmet need for a versatile platform that enables flexible multi-drug combination screening with a wide concentration range and automated operation. Accordingly, an automated multi-drug combination screening platform (ISMMCGs) integrating elliptical baffle micromixers (EBMixers) and three types of microfluidic concentration gradient (MCG) chips was developed. The EBMixer achieves > 90% mixing efficiency within a 40 mm channel (Re = 0-70), ensuring rapid uniform mixing. The MCG chips (linear, two-fold, ten-fold dilution), designed via the equivalent circuit method, spanning a four-order-of-magnitude concentration gradient (10⁻⁴-1). Automated switching via a micro-solenoid valve array enables "rough/fine/precise" screening. Validation with sodium fluorescein confirms gradient reliability; Screening experiments of vancomycin against MRSA demonstrate that this system can narrow the OD600-determined apparent MIC range down to 0.78-1.01 µg/mL, verifying the application potential of this platform in rapid screening of antimicrobial concentration ranges; and tigecycline-colistin sulfate combination screening for MDR-AB verifies the platform's flexibility for concentration-dependent combinatorial testing. This integrated platform addresses the limitations of traditional methods by balancing wide concentration coverage, multi-drug flexibility, and automation. It provides a refined, cost-effective tool for drug screening, facilitating the development of personalized treatment regimens and accelerating drug discovery processes, with broad applications in antimicrobial resistance research and pharmaceutical development.

Indexed as

Anti-Bacterial AgentsLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesDrug Evaluation, PreclinicalMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsVancomycinAnti-Bacterial AgentsVancomycinCombinatorial drug screeningConcentration gradientHigh-throughput screeningMicrofluidic chipMicromixer

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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.