Evidence map›Paper›PMID 35626636›Full record

ArticleCells2022

Probing the Drug Dynamics of Chemotherapeutics Using Metasurface-Enhanced Infrared Reflection Spectroscopy of Live Cells.

Po-Ting Shen, Steven H Huang, Zhouyang Huang, Justin J Wilson, Gennady Shvets

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Metasurface-enhanced biomedical spectroscopy.Nanophotonics (Berlin, Germany) · 2025
    Review
  3. Article
  4. 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

5 authors at 1 institution in 1 country.

Po-Ting ShenSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0003-3321-4913
Steven H HuangSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-4753-1859
Zhouyang HuangDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0003-0335-2020
Justin J WilsonDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-4086-7982
Gennady ShvetsSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0001-8542-6753
Cornell University · US

Funding

Phenotypic assay for drug discovery and personalized medicine based on real-time vibrational spectroscopy enhanced by plasmonic metasurfacesR21CA251052 · NCI · CORNELL UNIVERSITY · PI SHVETS, GENNADY · 2020 to 2020
$599k
Inverted Spectroscopic Infrared Microscope (ISIM) for High Throughput Multi-Dimensional Cell AssaysR21GM138947 · NIGMS · CORNELL UNIVERSITY · PI SHVETS, GENNADY · 2021 to 2022
$439k
NCI NIH HHS R21 CA251052NIGMS NIH HHS R21 GM138947
6 · The paper itself

Abstract

Infrared spectroscopy has drawn considerable interest in biological applications, but the measurement of live cells is impeded by the attenuation of infrared light in water. Metasurface-enhanced infrared reflection spectroscopy (MEIRS) had been shown to mitigate the problem, enhance the cellular infrared signal through surface-enhanced infrared absorption, and encode the cellular vibrational signatures in the reflectance spectrum at the same time. In this study, we used MEIRS to study the dynamic response of live cancer cells to a newly developed chemotherapeutic metal complex with distinct modes of action (MoAs): tricarbonyl rhenium isonitrile polypyridyl (TRIP). MEIRS measurements demonstrated that administering TRIP resulted in long-term (several hours) reduction in protein, lipid, and overall refractive index signals, and in short-term (tens of minutes) increase in these signals, consistent with the induction of endoplasmic reticulum stress. The unique tricarbonyl IR signature of TRIP in the bioorthogonal spectral window was monitored in real time, and was used as an infrared tag to detect the precise drug delivery time that was shown to be closely correlated with the onset of the phenotypic response. These results demonstrate that MEIRS is an effective label-free real-time cellular assay capable of detecting and interpreting the early phenotypic responses of cells to IR-tagged chemotherapeutics.

Indexed as

Coordination ComplexesWaterPharmaceutical PreparationsSpectrophotometry, InfraredCoordination ComplexesPharmaceutical PreparationsWaterbiosensingcancer cellscancer drug discoverydrug dynamicsFTIRin vitrolabel-freemetal complexesmetasurface

Identifiers

PMID35626636
PMCPMC9139550
OpenAlexW4280619556

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.