2016
DOI: 10.13005/ojc/320330
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Identification and Characterization of Solid Binary System of Quercetin-Nicotinamide

Abstract: Preparation of binary system quercetin-nicotinamide and the solubility evaluation have been conducted in this study. Binary system was prepared by solvent evaporation technique and physical mixture was used as comparison. The aim of this study is to analyze the type of interaction and to investigate the solubility of quercetin-nicotinamide produced. Identification of binary system interaction were done using Powder X-ray diffraction (PXRD), Differential Thermal Analysis (DTA), Infrared spectroscopy (IR), Scann… Show more

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Cited by 11 publications
(11 citation statements)
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“…Meanwhile, eutectic mixtures and solid solutions do not change the PXRD patterns of the mixture. [17,18] Figure 4 shows the PXRD patterns of fenofibric acid, syringic acid, and the eutectic mixture. The PXRD patterns of fenofibric acid and syringic acid are similar to those reported in a recent study by Anggraini et.…”
Section: Resultsmentioning
confidence: 99%
“…Meanwhile, eutectic mixtures and solid solutions do not change the PXRD patterns of the mixture. [17,18] Figure 4 shows the PXRD patterns of fenofibric acid, syringic acid, and the eutectic mixture. The PXRD patterns of fenofibric acid and syringic acid are similar to those reported in a recent study by Anggraini et.…”
Section: Resultsmentioning
confidence: 99%
“…Nicotinamide and picolinic acid co-crystals of quercetin were also reported [ 38 ]. The properties of the solid binary system between quercetin and nicotinamide including the melting point, solubility and physical morphology were reported to be different from the physical mixture of quercetin-nicotinamide [ 39 ]. These studies suggest that co-crystallization could be occurring between flavonoids and the different molecules that have functional groups which could be forming bonds with them, then altering the properties of the compounds.…”
Section: Discussionmentioning
confidence: 99%
“…One of the factors that affect the solubility of a drug is particle size. Microparticles formation is one of the most potential approach to increase the bioavailability of lipophilic drugs by reducing the particle size [6]. Microparticles increase drug bioavailability by increasing the total surface area of drug particles [7].…”
Section: Introductionmentioning
confidence: 99%