Evidence map›Paper›PMID 41927965›Full record

ArticlePharmaceutical research2026

Development of a Novel Curcumin-Vanillic Acid Eutectic: Physicochemical Characterization, Antioxidant Activity, and Bioavailability Enhancement.

Jidnyasa Pantwalawalkar, Namdeo Jadhav, Sopan Nangare

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Article in Pharmaceutical research, 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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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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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jidnyasa PantwalawalkarDepartment of Pharmaceutics, Bharati Vidyapeeth College of Pharmacy, Kolhapur, 416013, Maharashtra State, India.
Namdeo JadhavDepartment of Pharmaceutics, Krishna Institute of Pharmacy, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad, 415539, Maharashtra State, India. nrjadhav18@rediffmail.com.
Sopan NangareDepartment of Pharmaceutics, Krishna Institute of Pharmacy, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad, 415539, Maharashtra State, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCurcumin, a well-known phyto-nutraceutical with broad therapeutic potential, faces critical formulation challenges, including poor aqueous solubility, low dissolution rate, and limited tablettability, leading to poor oral bioavailability and reduced therapeutic efficacy. This study presents a novel curcumin-vanillic acid eutectic system designed to overcome these limitations through a sustainable and green formulation approach.

methodsVanillic acid, a natural phenolic compound with potent antioxidant properties, was selected as a coformer based on in silico analysis demonstrating structural compatibility and potential therapeutic synergy with curcumin. The eutectic mixture was prepared via solvent-free solid-state grinding and characterized using X-ray diffraction, differential scanning calorimetry, Fourier-transform infrared spectroscopy, and proton/carbon nuclear magnetic resonance. Physicochemical, tablettability, and antioxidant properties were subsequently evaluated. DoE software was used to optimize the eutectic-based tablet formulation, followed by its pharmacokinetic evaluation.

resultSpectroscopic results supported eutectic formation, showing modifications in the solid-state characteristics of curcumin accompanied by a lower melting point. These modifications yielded significant improvements in solubility (tenfold, eightfold, and 11-fold in water, buffer pH 1.2, and buffer pH 6.8) and tablettability relative to pure curcumin. The eutectic also exhibited enhanced antioxidant activity (p < 0.05), which may be attributed to the combined intrinsic antioxidant properties of the drug and coformer compared to pure curcumin. DoE-optimized eutectic tablets suggested an enhanced bioavailability of curcumin compared to conventional curcumin tablets; however, warranting confirmation in a larger sample size.

conclusionOverall, the curcumin-vanillic acid eutectic represents a promising formulation approach for developing high-performance phyto-nutraceutical systems.

Indexed as

AntioxidantsCurcuminVanillic AcidAnimalsBiological AvailabilityCalorimetry, Differential ScanningChemistry, PharmaceuticalSolubilitySpectroscopy, Fourier Transform InfraredTabletsX-Ray DiffractionAntioxidantsCurcuminTabletsVanillic Acidcurcumineutectic mixturephyto-nutraceuticalsustainable formulationvanillic acid

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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.