Evidence map›Paper›PMID 40407056›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2025

Curcumin-Loaded High-Charge Swelling Synthetic Mica: Characterization Studies and Stability under Stress Conditions.

María Del Mar Orta Cuevas, Ana Fernández Romero, Antonio M Rabasco Álvarez, Santiago Medina-Carrasco, María Luisa González-Rodríguez

Abstract read
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Article in Langmuir : the ACS journal of surfaces and colloids, 2025. 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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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

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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

María Del Mar Orta CuevasDepartment of Analytical Chemistry, Faculty of Pharmacy, Universidad de Sevilla, C/Profesor García, González 2, 41012 Sevilla, Spain.ORCID 0000-0001-6659-1518
Ana Fernández RomeroDepartment of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, Universidad de Sevilla, C/Profesor García, González 2, 41012 Sevilla, Spain.
Antonio M Rabasco ÁlvarezDepartment of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, Universidad de Sevilla, C/Profesor García, González 2, 41012 Sevilla, Spain.
Santiago Medina-CarrascoX-ray Laboratory, CITIUS, Universidad de Sevilla, Avenida Reina Mercedes, 4B, 41012 Sevilla, Spain.ORCID 0000-0003-1353-9331
María Luisa González-RodríguezDepartment of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, Universidad de Sevilla, C/Profesor García, González 2, 41012 Sevilla, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curcumin (Cur) is a bioactive compound with various pharmacotherapeutic effects. However, its limited solubility and stability pose challenges for therapeutic applications. Clay minerals, such as montmorillonite (MMT) and high-charge swelling synthetic micas, show promise as drug carriers due to their properties. This study aimed to obtain complexes with clay minerals that could enhance the stability of Cur. MMT, Na-Mica-4, and the latter organofunctionalized with 18-carbon alkylamines (C18-Mica-4) were used as support for Cur. Adsorption studies showed that Na-Mica-4 exhibited the highest percentage of adsorption (60%). Cur-Mica-4 complexes were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermal analysis (DSC and TGA), specific surface area (BET), pore size and volume determinations, and surface charge determination by zeta potential measurement. The effect of light on Cur and Cur-Mica-4 complexes was also evaluated. Forced degradation studies were performed under hydrolytic, oxidative, photolytic, and thermal conditions to assess the stability and degradation pathways. The FTIR spectra indicated that the enol tautomer mainly formed part of the complexes. BET analysis showed a reduced pore size after adsorption, indicating Cur immobilization. TGA and scanning electron microscopy (SEM) suggested degradation primarily occurring under exposure to sunlight, heat, and ultraviolet light. The effect of acidic and basic conditions on the Cur-Mica-4 complex was evaluated. Under acidic conditions, a decrease in the specific surface area of the complex was observed, suggesting the formation of larger configurational structures. An increase in the specific surface area with a smaller pore size was observed in the basic medium, possibly due to the formation of new structures in the clay minerals, supported by XRD results. These findings indicate that the pH of the medium can significantly influence the structure and stability of the Cur-Mica-4 complex, which could have important implications for its application in specific environments, such as drug delivery systems.

Identifiers

PMID40407056
PMCPMC12139042

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