Evidence map›Paper›PMID 42311478›Full record

ArticleACS applied polymer materials2026

Solute Diffusion in Styrenic Triblock Copolymer Organogels.

Kenneth P Mineart, Nicholas G DeVita, Ridwana Bashar

Abstract read
In one paragraph

Article in ACS applied polymer materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Kenneth P MineartDepartment of Chemical Engineering, Bucknell University, Lewisburg, Pennsylvania 17837, United States.ORCID https://orcid.org/0000-0003-2374-4670
Nicholas G DeVitaDepartment of Chemical Engineering, Bucknell University, Lewisburg, Pennsylvania 17837, United States.
Ridwana BasharDepartment of Chemical Engineering, Bucknell University, Lewisburg, Pennsylvania 17837, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gels composed of styrenic triblock copolymer and aliphatic solvent have been recently considered for use in transdermal drug delivery systems (TDDSs) due in part to their adhesive properties and nonpolar chemistry. Past research conducted on these block copolymer organogels has provided some formulation strategies to optimize their adhesiveness, drug retention, in vitro drug release, and in vivo delivery performance. However, the aforementioned studies' characterization of extrinsic properties and use of empirical modeling limit the generalizability of their outlined strategies. The current study presents solute diffusivity-an intrinsic material property-for various copolymer organogels including those with different copolymer molecular weights and concentrations, as well as several unique solutes. Furthermore, the gathered data sets are fitted with a theoretical model that accounts for the nanostructure of organogels including their impenetrable discrete domains (polystyrene) and continuous phase comprising solvated midblocks (poly-[ethylene-propylene] or poly-[ethylene-butylene]) and gel solvent. This model yields the hydrodynamic radius of the penetrant (i.e., solute molecules or aggregates) and its average rate of movement through a given gel. Interpretation of diffusivity values and model fit parameters suggests that copolymer concentration has a considerably stronger effect on solute diffusion than copolymer molecular weight. For example, increasing concentration from 5 wt% to 20 wt% yields a 50% reduction in solute diffusivity whereas molecular weight (at a fixed concentration) is observed to have a negligible impact. Our findings also highlight that solute aggregation behavior must be carefully considered when designing organogel-based TDDSs. The hydrodynamic radii of solutes employed do not correlate with their molecular weights (OA: 282.5 g/mol, 0.3 nm; SMO: 428.6 g/mol, 0.7 nm; AOT: 444.6 g/mol, 2.6 nm; STO: 957.5 g/mol, 0.8 nm), which stems from differing self-assembly behavior in the gel solvent. We anticipate that the presented results and analysis will enable more effective bottom-up design of block copolymer organogels for TDDSs.

Indexed as

block copolymerorganogelsSAXSsolute transportstructure–property relationships

Identifiers

PMID42311478
PMCPMC13270463

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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.