ArticleAdvanced healthcare materials2026
Hepatocellular Carcinoma-on-a-Chip Based on Microfluidic Well Array for Personalized Drug Evaluation.
Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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.
Who cites it
1 citing paper in PubMed.
- Spatial architecture and dynamic surveillance: 3D bioprinting and microfluidics converge to overcome digestive malignancies.Hepatobiliary surgery and nutrition · 2026Article
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Authors and funding
4 authors.
Funding
Abstract
The high interpatient variability in hepatocellular carcinoma (HCC) poses a critical challenge to drug therapy, underscoring the need for personalized platforms that can assess therapeutic efficacy while capturing tumor heterogeneity. Here, we present a stereo microfluidic well array-based hepatocellular carcinoma-on-a-chip for one-stop individualized drug evaluation. We design the device with two modules for tumor spheroid formation and drug concentration gradient generation in a single platform. Using projection micro-stereolithography, the chip template is fabricated in a one-step process and subsequently molded in polydimethylsiloxane (PDMS). Controlled microfluidic flow in the chip enables precise cell loading into microwells, producing uniform-sized and high-viability HCC spheroids (∼2200 per chip) under dynamic culture conditions. Based on these features, this tumor-on-a-chip further supports high-throughput drug screening across tunable and multiple concentration gradients, validated with patient-derived HCC samples. Thus, this platform is capable of high-throughput generation of three-dimensional spheroids and multi-dose drug gradient exposure; it has already completed proof-of-concept studies for a drug screening platform based on microfluidic spheroids, laying the groundwork for subsequent translational research incorporating clinical data.
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Registered trials
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 Socratic graph.