Evidence map›Paper›PMID 39211500›Full record

ArticleChemical science2024

Host-guest binding between cucurbit[8]uril and amphiphilic peptides achieved tunable supramolecular aggregates for cancer diagnosis.

Jie Niu, Jie Yu, Xuan Wu, Ying-Ming Zhang, Yong Chen, Zhilin Yu, Yu Liu

Abstract read
In one paragraph

Article in Chemical science, 2024. 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
–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

4 citing papers in PubMed.

  1. γ-Ray Regulated Host-Guest Molecular Recognition.Angewandte Chemie (International ed. in English) · 2026
    Article
  2. Review
  3. Peptide-Based Biomaterials as a Promising Tool for Cancer Radiotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  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

7 authors.

Jie NiuCollege of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University Tianjin 300071 P. R. China yuliu@nankai.edu.cn ymzhang@nankai.edu.cn.
Jie YuCollege of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University Tianjin 300071 P. R. China yuliu@nankai.edu.cn ymzhang@nankai.edu.cn.
Xuan WuSchool of Chemistry and Chemical Engineering, Yangzhou University Yangzhou Jiangsu 225002 P. R. China.
Ying-Ming ZhangCollege of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University Tianjin 300071 P. R. China yuliu@nankai.edu.cn ymzhang@nankai.edu.cn.
Yong ChenCollege of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University Tianjin 300071 P. R. China yuliu@nankai.edu.cn ymzhang@nankai.edu.cn.
Zhilin YuKey Laboratory of Functional Polymer Materials, Ministry of Education, State Key Laboratory of Medicinal Chemical Biology, Institute of Polymer Chemistry, College of Chemistry, Nankai University Tianjin 300071 P. R. China.ORCID https://orcid.org/0000-0002-7116-3304
Yu LiuCollege of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University Tianjin 300071 P. R. China yuliu@nankai.edu.cn ymzhang@nankai.edu.cn.ORCID https://orcid.org/0000-0003-0967-0919

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The manipulation of biocompatible supramolecular nanostructures at subcellular and cellular levels has become one of the increasingly significant topics but remains a formidable challenge in chemical and biological science. In this work, a controllable supramolecular aggregate based on host-guest competitive binding is elaborately constructed using cucurbit[8]uril, methionine-containing amphiphilic peptide, and perylene diimide, displaying

Identifiers

PMID39211500
PMCPMC11351706

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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.