Evidence map›Paper›PMID 39337729›Full record

ArticleMicromachines2024

Model-Based Optimization of Solid-Supported Micro-Hotplates for Microfluidic Cryofixation.

Daniel B Thiem, Greta Szabo, Thomas P Burg

Abstract read
In one paragraph

Article in Micromachines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Daniel B ThiemIntegrated Micro-Nano-Systems Laboratory, Technische Universität Darmstadt, 64283 Darmstadt, Germany.ORCID 0000-0003-4245-1750
Greta SzaboIntegrated Micro-Nano-Systems Laboratory, Technische Universität Darmstadt, 64283 Darmstadt, Germany.ORCID 0000-0002-3998-3425
Thomas P BurgIntegrated Micro-Nano-Systems Laboratory, Technische Universität Darmstadt, 64283 Darmstadt, Germany.

Funding

European Research Council 772441
6 · The paper itself

Abstract

Cryofixation by ultra-rapid freezing is widely regarded as the gold standard for preserving cell structure without artefacts for electron microscopy. However, conventional cryofixation technologies are not compatible with live imaging, making it difficult to capture dynamic cellular processes at a precise time. To overcome this limitation, we recently introduced a new technology, called microfluidic cryofixation. The principle is based on micro-hotplates counter-cooled with liquid nitrogen. While the power is on, the sample inside a foil-embedded microchannel on top of the micro-hotplate is kept warm. When the heater is turned off, the thermal energy is drained rapidly and the sample freezes. While this principle has been demonstrated experimentally with small samples (<0.5 mm

Indexed as

cooling ratecryofixationheat conduction modelvitrification

Identifiers

PMID39337729
PMCPMC11434347

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.