Evidence map›Paper›PMID 41693005›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

DNA as Drug Carrier: A Hydrophobic β-Cyclodextrin Channel in a Supramolecular Structure.

Giuseppina Raffaini

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. 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

1 author.

Giuseppina RaffainiDepartment of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di, Milano, Italy.ORCID https://orcid.org/0000-0003-3462-6514

Funding

ICSC-Centro Nazionale di Ricerca in High Performance Computing
6 · The paper itself

Abstract

The adsorption of drugs and their carriers onto double-stranded DNA is potentially significant for their transport and release within cells, and β-cyclodextrins (βCDs) complexed with therapeutic compounds represent promising drug delivery systems. However, the molecular mechanisms governing the formation and behavior of these supramolecular complexes on DNA structures remain poorly understood. Therefore, we employed molecular mechanics and molecular dynamics simulations at an atomistic level to examine the formation of inclusion complexes between βCDs and quercetin (an antioxidant flavonoid with anticancer properties), and their subsequent adsorption and self-aggregation on DNA structure. The adhesion process results from intermolecular interactions between the hydrophobic drugs included in βCD cavities, which create a uniquely ordered hydrophobic channel that wraps along the DNA grooves. This structure is further stabilized by hydrogen bonds between βCDs, forming a long-range ordered supramolecular structure over time, akin to a thread enveloping the DNA. This study provides insights into understanding supramolecular complexes involving DNA for potential drug delivery applications.

Indexed as

beta-CyclodextrinsDNADrug CarriersQuercetinAdsorptionHydrogen BondingHydrophobic and Hydrophilic InteractionsMolecular Dynamics Simulationbeta-CyclodextrinsDNADrug CarriersQuercetinadsorptionaggregationcyclodextrinsDNAdrug carriersupramolecular complexes

Identifiers

PMID41693005
PMCPMC12995853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.