Evidence map›Paper›PMID 40599579›Full record

ReviewRSC advances2025

An update on recent advances in fluorescent materials for fluorescence molecular imaging: a review.

Nkune Williams Nkune, Kave Moloudi, Blassan P George, Heidi Abrahamse

Abstract readReview
In one paragraph

Review in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Imaging of intranasal drug delivery to the brain: updated review 2.0.Drug delivery and translational research · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. MnOJournal of fluorescence · 2026
    Article
  12. Review
  13. Review
  14. 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

4 authors.

Nkune Williams NkuneLaser Research Centre, Faculty of Health Sciences, Doornfontein Campus, University of Johannesburg Johannesburg 2028 South Africa habrahamse@uj.ac.za.ORCID https://orcid.org/0000-0003-3746-707X
Kave MoloudiLaser Research Centre, Faculty of Health Sciences, Doornfontein Campus, University of Johannesburg Johannesburg 2028 South Africa habrahamse@uj.ac.za.
Blassan P GeorgeLaser Research Centre, Faculty of Health Sciences, Doornfontein Campus, University of Johannesburg Johannesburg 2028 South Africa habrahamse@uj.ac.za.ORCID https://orcid.org/0000-0002-7062-4412
Heidi AbrahamseLaser Research Centre, Faculty of Health Sciences, Doornfontein Campus, University of Johannesburg Johannesburg 2028 South Africa habrahamse@uj.ac.za.ORCID https://orcid.org/0000-0001-5002-827X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence molecular imaging (FMI) is a powerful imaging technique used primarily in biomedical research and clinical applications to visualize molecular and cellular processes of tumors and other diseases. FMI involves the use of fluorescent molecules (fluorophores) that absorb light at one wavelength and emit it at a longer wavelength. These fluorophores can be attached to specific molecules and markers (such as proteins, nucleic acids, or small molecules) in a biological sample. FMI typically offers non-radioactive and safe, real-time and higher spatial resolution compared to positron emission tomography (PET) for superficial tumors. Additionally, sensitivity and specificity of FMI for superficial tumors in better than PET is some cases. However, FMI and the materials used in molecular imaging (MI) have revolutionized biomedical research, diagnostics, and therapeutic monitoring. In contrast, despite their significant contributions, several challenges remain to be solved to improve the effective application of fluorescence-based techniques. These challenges are related to poor tissue penetration depth, background autofluorescence, photobleaching of fluorophores, low signal-to-noise ratio in deep tissues and the necessity for biocompatible and photostable probes. Hence, ongoing improvements in probe development, imaging technologies and analytical methods are required to overcome current challenges. Future advancements in fluorescence materials and imaging techniques hold promise for making MI more accurate, efficient and applicable for clinical and research scenarios. This review gives an overview of recent advances in the materials used in MI and findings of FMI. Finally, limitations of FMI are highlighted and recommendations for future research directions are proposed.

Identifiers

PMID40599579
PMCPMC12208293

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.