Evidence map›Paper›PMID 40245266›Full record

ArticleThe Journal of organic chemistry2025

Rational Design of Supramolecular Receptors for Consistent Binding Affinities under High-Salinity Conditions.

Borja Gómez-González, Nuno Basílio, Belén Vaz, M Rita Paleo, F Javier Sardina, Moisés Pérez-Lorenzo, Luis García-Río

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2025. 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. Expansion of the Metal-Involving Noncovalent Interaction Repertoire: The Case of Pd(II) and Pt(II) Triel Bonding.Chemphyschem : a European journal of chemical physics and physical chemistry · 2026
    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.

Borja Gómez-GonzálezDepartment of Physical Chemistry, Universidade de Santiago de Compostela, Santiago de Compostela 15782, Spain.
Nuno BasílioLaboratório Associado para a Química Verde (LAQV), Rede de Química e Tecnologia (REQUIMTE), Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Caparica 2829-516, Portugal.ORCID 0000-0002-0121-3695
Belén VazCINBIO, Universidade de Vigo, Vigo 36310, Spain.ORCID 0000-0002-7900-1430
M Rita PaleoCenter for Research in Biological Chemistry and Molecular Materials (CIQUS), Universidade de Santiago de Compostela, Santiago de Compostela 15782, Spain.ORCID 0000-0002-0095-3931
F Javier SardinaDepartment of Organic Chemistry, Universidade de Santiago de Compostela, Santiago de Compostela 15782, Spain.ORCID 0000-0002-6758-0068
Moisés Pérez-LorenzoCINBIO, Universidade de Vigo, Vigo 36310, Spain.ORCID 0000-0002-7157-5966
Luis García-RíoDepartment of Physical Chemistry, Universidade de Santiago de Compostela, Santiago de Compostela 15782, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of water-soluble multicharged macrocycles has opened promising pathways in biomedical applications, enabling selective molecular recognition for therapeutic and diagnostic uses. Yet, traditional polyanionic and polycationic receptors often face performance limitations under realistic operating conditions. A major drawback is the natural tendency of these polycharged hosts to experience increasing screening effects as concentration rises due to self-ion pairing phenomena, which can reduce binding efficiency by several orders of magnitude. These issues are further intensified when polyionic receptors are used in high-salinity environments, typically used to replicate physiological settings, where the abundance of ions introduces additional screening effects that diminish the supramolecular affinity for a wide range of guests. This study presents a new approach that leverages zwitterionic synthetic receptors with rationally engineered architectures to overcome these challenges. By incorporation of specific structural features, self-ion pairing is eliminated, effectively making host concentration no longer a controlling factor in the thermodynamics of the complexation process. Additionally, these dual-charged hosts achieve self-contained stabilization, naturally shielding recognition sites from external ion interference under high-salinity conditions. Furthermore, the ability of these supramolecular hosts to encapsulate zwitterionic guests, a challenging task due to the strong solvation of these molecules in aqueous solution, adds significant value to the functional versatility of these macrocycles. Altogether, these findings represent a significant advancement in the design of stable and adaptable receptor systems for complex environments.

Indexed as

Macrocyclic CompoundsMacromolecular SubstancesMolecular StructureThermodynamicsMacrocyclic CompoundsMacromolecular Substances

Identifiers

PMID40245266
PMCPMC12133026

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.