Evidence mapPaperPMID 42416097Full record

ArticleFood hydrocolloids for health2026

Ethanol-assisted fabrication of Casein-Ritonavir amorphous dispersions.

Deepika Sharma, Federico M Harte

Abstract read
In one paragraph

Article in Food hydrocolloids for health, 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
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Deepika SharmaDepartment of Food Science, The Pennsylvania State University, University Park, PA 16802, United States.
Federico M HarteDepartment of Food Science, The Pennsylvania State University, University Park, PA 16802, United States.ORCID 0000-0001-6822-0083

Funding

Milk Protein-Based Amorphous Solid Dispersion for Delivery of Hydrophobic APIsR21HD117135 · PENNSYLVANIA STATE UNIVERSITY, THE · 2025 to 2025
$428k
NICHD NIH HHS R21 HD117135
6 · The paper itself

Abstract

The study investigates the impact of ethanol content and temperature on the formation of casein-ritonavir amorphous dispersions, aiming to enhance the drug's effective solubility and delivery. Ritonavir, a poorly water-soluble crystalline antiviral medication, was combined with casein in aqueous ethanol solutions ranging from 0 to 60 % v/v ethanol and 60°C. Solubility tests revealed a sharp increase in ritonavir solubility in 50% ethanol, highlighting that reduced solvent polarity facilitates drug dispersion. After solvent removal, thermal analysis confirmed ritonavir-casein interaction leading to the formation of ritonavir amorphous dispersions. Microstructural analysis revealed a significant decrease in crystalline peaks and spectral shifts in the amide regions, particularly in ethanol-treated samples, indicating changes in the local microenvironment and noncovalent molecular associations of ritonavir within the casein matrix. Zeta potential measurements showed a consistent increase in negative surface charge (-45 mV to -60 mV) with increasing ethanol content during complex fabrication, indicating changes in surface charge characteristics and electrostatic dispersion stability. Therefore, these findings support the formation of stable, amorphous casein-ritonavir complexes with improved solubility and potential for oral delivery applications.

Indexed as

CaseinEthanol-assisted encapsulationHydrophobic drug deliveryRitonavir

Identifiers

PMID42416097
PMCPMC13340867

What Socratic holds

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Registered trials

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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 Socratic graph.