Evidence map›Paper›PMID 39185268›Full record

ArticleSmall science2024

Robust Synthesis of Targeting Glyco-nanoparticles for Surface Enhanced Resonance Raman Based Image-Guided Tumor Surgery.

Kunli Liu, A K M Atique Ullah, Aniwat Juhong, Chia-Wei Yang, Cheng-You Yao, Xiaoyan Li, Harvey L Bumpers, Zhen Qiu, Xuefei Huang

Abstract read
In one paragraph

Article in Small science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
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

9 authors.

Kunli LiuDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0003-1954-9776
A K M Atique UllahDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-4545-2663
Aniwat JuhongInstitute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-9115-9767
Chia-Wei YangDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-0950-5510
Cheng-You YaoInstitute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-6045-8676
Xiaoyan LiDepartment of Civil and Environmental Engineering, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-2649-7575
Harvey L BumpersDepartment of Surgery, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0001-6165-9261
Zhen QiuInstitute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0001-8790-8481
Xuefei HuangDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824 USA.ORCID 0000-0002-6468-5526

Funding

Homogeneous Heparan Sulfate Glycopeptides: Synthetic and Functional StudiesR01GM072667 · NIGMS · UNIVERSITY OF TOLEDO · PI HUANG, XUEFEI · 2005 to 2024
$5.1M
NIGMS NIH HHS R01 GM072667
6 · The paper itself

Abstract

Surface Enhanced Resonance Raman (SERS) is a powerful optical technique, which can help enhance the sensitivity of Raman spectroscopy aided by noble metal nanoparticles (NPs). However, current SERS-NPs are often suboptimal, which can aggregate under physiological conditions with much reduced SERS enhancement. Herein, a robust one-pot method has been developed to synthesize SERS-NPs with more uniform core diameters of 50 nm, which is applicable to both non-resonant and resonant Raman dyes. The resulting SERS-NPs are colloidally stable and bright, enabling NP detection with low-femtomolar sensitivity. An algorithm has been established, which can accurately unmix multiple types of SERS-NPs enabling potential multiplex detection. Furthermore, a new liposome-based approach has been developed to install a targeting carbohydrate ligand, i.e., hyaluronan, onto the SERS-NPs bestowing significantly enhanced binding affinity to its biological receptor CD44 overexpressed on tumor cell surface. The liposomal HA-SERS-NPs enabled visualization of spontaneously developed breast cancer in mice in real time guiding complete surgical removal of the tumor, highlighting the translational potential of these new glyco-SERS-NPs.

Indexed as

glyco-nanoparticlesimaging guided surgerysurface enhanced Raman spectroscopysynthesis

Identifiers

PMID39185268
PMCPMC11340905

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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 OpenQuestion graph.