Evidence map›Paper›PMID 39170981›Full record

ArticleNanoscale advances2024

Dynamic macromolecular material design: the versatility of cucurbituril over cyclodextrin in host-guest chemistry.

Jinnipha Pajoubpong, Collin M Mayhan, Ajaz Ahmad Dar, Alexander I Greenwood, Karoline C Klebba, Matthew L Cremer, Harshita Kumari

Abstract read
In one paragraph

Article in Nanoscale advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Jinnipha PajoubpongJames L. Winkle College of Pharmacy, University of Cincinnati 231 Albert Sabin Way Cincinnati OH 45267-0514 USA kumariha@ucmail.uc.edu.
Collin M MayhanJames L. Winkle College of Pharmacy, University of Cincinnati 231 Albert Sabin Way Cincinnati OH 45267-0514 USA kumariha@ucmail.uc.edu.
Ajaz Ahmad DarJames L. Winkle College of Pharmacy, University of Cincinnati 231 Albert Sabin Way Cincinnati OH 45267-0514 USA kumariha@ucmail.uc.edu.
Alexander I GreenwoodDepartment of Chemistry, University of Cincinnati Cincinnati Ohio 45221 USA.
Karoline C KlebbaHelias Catholic High School 1305 Swifts Hwy Jefferson City MO 65109 USA.
Matthew L CremerHelias Catholic High School 1305 Swifts Hwy Jefferson City MO 65109 USA.
Harshita KumariJames L. Winkle College of Pharmacy, University of Cincinnati 231 Albert Sabin Way Cincinnati OH 45267-0514 USA kumariha@ucmail.uc.edu.ORCID https://orcid.org/0000-0002-6861-0281

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The keto-enol tautomerism of avobenzone (AVO) is pivotal to its photostability, influenced by microenvironmental factors, such as, the type of solvent and complexation with macrocyclic compounds. This study explores the effect of host-guest complexation on AVO photostabilization, employing cucurbit[7]uril (CB[7]) and β-cyclodextrin (β-CD) to form inclusion complexes. CB[7] exhibits a higher affinity to the keto form of AVO, a UVC radiation absorber. The complexed keto form facilitates the regeneration of the enol form, reducing skin permeation. Spectroscopic and thermal analyses confirm 1 : 1 AVO-CB[7] and AVO-β-CD complex formation. Computational and MD simulations show that host-guest complex is favored over isolated AVO and β-CD or CB[7] molecules by 95-125 kJ mol

Identifiers

PMID39170981
PMCPMC11334980

What OpenQuestion holds

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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 OpenQuestion graph.