Studies on solute–solute and solute–solvent interactions of quercetin and 7-hydroxy flavone with nicotinamide in hydro-ethanolic mixed solvents: bioflavonoid-HBD interactions by volumetric and acoustic analysis

The interaction between quercetin (QUE) <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mo>/</mml:mo></mml:math> 7-hydroxy flavone (7-HF) and nicotinamide (NAM) in drug formulations is an intriguing area of research due to their complementary biological effects. When used together, their combined actions can potentially offer synergistic therapeutic benefits. The objective of the present study is to analyze and interpret the types of interactions among various polar, non-polar, hydrophilic and hydrophobic parts of quaternary systems (QUE + water <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mo>+</mml:mo> <mml:mtext>ethanol</mml:mtext></mml:mrow> </mml:math> + NAM) and (7-HF + water <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mo>+</mml:mo> <mml:mtext>ethanol</mml:mtext></mml:mrow> </mml:math> + NAM) by volumetric and acoustic approach. The positive values of <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:msubsup><mml:mtext>V</mml:mtext> <mml:mrow><mml:mi>ϕ</mml:mi></mml:mrow> <mml:mn>0</mml:mn></mml:msubsup> </mml:math> exhibit an increasing trend with temperature, indicating that there is a significant solute-solvent interaction in the investigated solutions. Positive partial molar expansibilities demonstrate that QUE/7-HF promotes solute-solvent interactions in the system and functions as a structure former in aqueous solutions. The partial isentropic compressibility, <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:msubsup><mml:mtext>K</mml:mtext> <mml:mrow><mml:mtext>s</mml:mtext></mml:mrow> <mml:mn>0</mml:mn></mml:msubsup> </mml:math> values are higher in 7-HF than in QUE showing greater extent of molecular interactions in 7-HF. From the derived data, the types of solute-solvent and solute-solute interactions and the structural modifications of water molecules were interpreted as a result of the inclusion of QUE/7-HF (solute) and NAM (co-solute) in the solvation shells. This study may provide a better understanding regarding the stronger solute-solvent interactions and structure-building ability of QUE/7-HF + NAM in a hydro-ethanolic medium, which may further help develop a pharmaceutical formulation of their mixture.

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Journal
BMC Chemistry
Published
2025-04-26
DOI
https://doi.org/10.1186/s13065-025-01463-9
Citations
3
Primary Topic
Thermodynamic properties of mixtures
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article
Field-Weighted Citation Impact
2.16
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article

Studies on solute–solute and solute–solvent interactions of quercetin and 7-hydroxy flavone with nicotinamide in hydro-ethanolic mixed solvents: bioflavonoid-HBD interactions by volumetric and acoustic analysis

Sulochana Singh, L. N. Sahoo, Rupesh Kumar Pradhan, Monalisa Mohapatra
3 citations
BMC Chemistry
Thermodynamic properties of mixtures
2.16
article

Studies on solute–solute and solute–solvent interactions of quercetin and 7-hydroxy flavone with nicotinamide in hydro-ethanolic mixed solvents: bioflavonoid-HBD interactions by volumetric and acoustic analysis

Sulochana Singh, L. N. Sahoo, Rupesh Kumar Pradhan, Monalisa Mohapatra
article en
3 citations

Abstract

The interaction between quercetin (QUE) <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mo>/</mml:mo></mml:math> 7-hydroxy flavone (7-HF) and nicotinamide (NAM) in drug formulations is an intriguing area of research due to their complementary biological effects. When used together, their combined actions can potentially offer synergistic therapeutic benefits. The objective of the present study is to analyze and interpret the types of interactions among various polar, non-polar, hydrophilic and hydrophobic parts of quaternary systems (QUE + water <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mo>+</mml:mo> <mml:mtext>ethanol</mml:mtext></mml:mrow> </mml:math> + NAM) and (7-HF + water <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mo>+</mml:mo> <mml:mtext>ethanol</mml:mtext></mml:mrow> </mml:math> + NAM) by volumetric and acoustic approach. The positive values of <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:msubsup><mml:mtext>V</mml:mtext> <mml:mrow><mml:mi>ϕ</mml:mi></mml:mrow> <mml:mn>0</mml:mn></mml:msubsup> </mml:math> exhibit an increasing trend with temperature, indicating that there is a significant solute-solvent interaction in the investigated solutions. Positive partial molar expansibilities demonstrate that QUE/7-HF promotes solute-solvent interactions in the system and functions as a structure former in aqueous solutions. The partial isentropic compressibility, <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:msubsup><mml:mtext>K</mml:mtext> <mml:mrow><mml:mtext>s</mml:mtext></mml:mrow> <mml:mn>0</mml:mn></mml:msubsup> </mml:math> values are higher in 7-HF than in QUE showing greater extent of molecular interactions in 7-HF. From the derived data, the types of solute-solvent and solute-solute interactions and the structural modifications of water molecules were interpreted as a result of the inclusion of QUE/7-HF (solute) and NAM (co-solute) in the solvation shells. This study may provide a better understanding regarding the stronger solute-solvent interactions and structure-building ability of QUE/7-HF + NAM in a hydro-ethanolic medium, which may further help develop a pharmaceutical formulation of their mixture.

BMC ChemistryVol. 19(1)
Sambalpur University (IN), Siksha O Anusandhan University (IN)
Openalex Percentile: Top 14%
Thermodynamic properties of mixtures
2.16
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