ArticleBiomicrofluidics2018
A simple microdevice for single cell capture, array, release, and fast staining using oscillatory method.
Article in Biomicrofluidics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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
2 citing papers in PubMed.
- Periodic Flows in Microfluidics.Small (Weinheim an der Bergstrasse, Germany) · 2024Review
- A Resistance-Based Microfluidic Chip for Deterministic Single Cell Trapping Followed by Immunofluorescence Staining.Micromachines · 2022Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Microchips that perform single cell capture, array, and identification have become powerful tools for single cell studies, which can reveal precise underlying mechanisms among bulk cell populations. However, current single cell capture and on-chip immunostaining methods consume more time and reagent than desired. To optimize this technology, we designed a novel trap structure for single cell capture, array, and release, and meanwhile an oscillatory method was used to perform rapid on-chip cell immunostaining. The trap structure array used equal distribution of lateral flow to achieve single cell array in high velocity flows and decrease the risk of clogging. A length of glass capillary with a sealed bubble was inserted into the outlet so that it could act in a manner analogous to that of a capacitor in an RC circuit. By applying one periodic air pressure to the inlet, oscillation motion was generated, which significantly enhanced the on-chip reaction efficiency. In addition, the oscillation performance could be easily regulated by changing the length of the capillary. The trapped cells could maintain their positions during oscillation; hence, they were able to be tracked in real time. Through our trap microchip, 12
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.