Evidence map›Paper›PMID 42011529›Full record

ArticleAnalytical chemistry2026

Toward a Comprehensive Raman Analysis of Functional Cells With Structured Optical Traps.

Panchanil Sarmah, Vidya Rastapur, Ruchee Khanna, Aseefhali Bankapur

Abstract read
In one paragraph

Article in Analytical chemistry, 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

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

4 authors.

Panchanil SarmahManipal Institute of Applied Physics, Manipal Academy of Higher Education, Manipal 576104, India.ORCID 0009-0007-4864-1615
Vidya RastapurManipal Institute of Applied Physics, Manipal Academy of Higher Education, Manipal 576104, India.
Ruchee KhannaDepartment of Pathology, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
Aseefhali BankapurManipal Institute of Applied Physics, Manipal Academy of Higher Education, Manipal 576104, India.ORCID 0000-0001-9237-8980

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optically trapping RBCs with conventional Gaussian laser beams in physiological media and studying their properties have long been of interest, as it can be beneficial for understanding RBC-related disorders and their manifestations. An ever-ignored fact of such studies is that the point excitation spot of a tightly focused Gaussian beam inevitably probes only a small part of the cell's interior region, mostly the cytoplasm. More importantly, it omits key components of the cell membrane, thereby lagging behind information from one of the most crucial organs of RBCs. Recent donut- and line focus trapping using a focused vortex beam and an optical sheet, respectively, have proven capable of extracting information from cell membranes. However, the donut and line focus trapping are distinctly different from each other in probing RBCs, as the former is most exclusive, and the latter is most inclusive in excitation of the cell membrane. This study aims to establish a clear and distinctive capability of point, donut, and line focus trapping in deriving Raman spectroscopy signatures from RBCs. Principal component analysis highlighted these differences by classifying spectra based on dimensionally reduced characteristic spectral features. ANOVA identified the significance of the membrane contribution in shaping the Raman spectra obtained using donut and line focus trapping. Line focus trapping also revealed that the spectra are rich in information, particularly in the 1220-1290 cm

Indexed as

ErythrocytesOptical TweezersSpectrum Analysis, RamanHumansPrincipal Component Analysis

Identifiers

PMID42011529
PMCPMC13150814

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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 Socratic graph.