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Thin-layer chromatography (TLC) after development at (a) visible light, (b) 254 nm, (c) 366 nm, and (d) after spraying with 10% methanolic KOH reagent (A = rhein sample before purification, B = rhein sample after purification, C = rhein standard, and D = residue from the CHCl 3 layer).

Thin-layer chromatography (TLC) after development at (a) visible light, (b) 254 nm, (c) 366 nm, and (d) after spraying with 10% methanolic KOH reagent (A = rhein sample before purification, B = rhein sample after purification, C = rhein standard, and D = residue from the CHCl 3 layer).

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Rhein is used as an active ingredient in laxatives in medicinal herbal products and is a chemical marker for quality control purposes. Thus, a simple and effective method for the optimized extraction of a high amount of rhein from the fruit pulp of Cassia fistula was investigated using ultrasonic-assisted extraction (UAE). The response surface meth...

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Context 1
... chromatography was used to check the purified rhein. As depicted in Figure 8a, samples A and B showed the same yellow spot as the rhein standard (C) in visible light. All three spots had the same Rf value of 0.32, so the two yellow spots from A and B were identified as rhein. ...
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... same chromatogram was detected under ultraviolet light. At 254 nm (Figure 8b), the rhein spot of samples A-C quenched the fluorescence of the TLC plate, which led to dark spots. Sample D showed other compounds which were separated from rhein. ...
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... impurities of sample A fluoresced at 366 nm (Figure 8c), while the rhein spots appeared as a beige-brownish color, which was in accordance with the literature [29]. Rhein had an Rf value of 0.32, while the Rf values of the impurities ranged between 0.41 and 0.90. ...
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... the UV-Vis examination, the TLC was sprayed with 10% methanolic KOH reagent to test the Borntraeger reaction. The rhein spots interacted with the spraying reagent and the color changed immediately from yellow to a pinkish color in visible light (Figure 8d). ...
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... chemical structure was confirmed by 1 H-and 13 C-NMR (Figure 10a,b) Thin-layer chromatography was used to check the purified rhein. As depicted in Figure 8a, samples A and B showed the same yellow spot as the rhein standard (C) in visible light. All three spots had the same R f value of 0.32, so the two yellow spots from A and B were identified as rhein. ...
Context 6
... same chromatogram was detected under ultraviolet light. At 254 nm (Figure 8b), the rhein spot of samples A-C quenched the fluorescence of the TLC plate, which led to dark spots. Sample D showed other compounds which were separated from rhein. ...
Context 7
... impurities of sample A fluoresced at 366 nm (Figure 8c), while the rhein spots appeared as a beige-brownish color, which was in accordance with the literature [29]. Rhein had an R f value of 0.32, while the R f values of the impurities ranged between 0.41 and 0.90. ...
Context 8
... the UV-Vis examination, the TLC was sprayed with 10% methanolic KOH reagent to test the Borntraeger reaction. The rhein spots interacted with the spraying reagent and the color changed immediately from yellow to a pinkish color in visible light (Figure 8d). ...

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... 41 Cassia fistula consists of Rhein, an anthraquinone, that acts as a laxative was extracted using ultrasound from the fruit pulp, wherein a yield twice the conventional decoction method was obtained from the UAE-optimized Central Composite Design (CCD). 42 Polysaccharides from Trametes orientalis were also extracted using ultrasonic-microwave assisted extraction for hepatoprotection. 43 Enzymatic extraction of β carotene from orange peel waste was performed using ultrasound (20 kHz, 500 W) as the pectinase enzyme results in increased penetration of the solvent into cell walls. ...
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... Many advantages of ultrasonic -assisted extraction including lower processing time, less thermal damage, being a cost-effective approach, and increment of product quality, have made widespread attention used for the extraction of natural products. Actually, due to the high cavitation effect of ultrasonic waves, this extraction method requires less time and is highly efficient as well, providing a high extraction rate under low-temperature conditions [34,42,43]. Low-temperature extraction conditions prevent the degradation of lutein that occurs at high temperatures, thus improving the extraction rate. ...
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... Various parts of CF have been found to have anticancer activities (11)(12)(13)(14). Rhein is one of the main active components, which have been found in various parts of CF (12,(15)(16)(17)(18)(19)(20). For anticancer activity, rhein, an active compound isolated from the CF flower extract, showed cytotoxicity on colon cancer cells (COLO 320DM) in concentrationand time-dependent manners (12). ...
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... As a positive control, diclofenac diethylamine was used at concentrations of 0.25-2.5 µg/mL. The dose-response curve was used to determine the sample solution concentrations for 50% inhibition (IC 50 ). Each sample was tested in triplicate. ...
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... alcohol (8.7%).eugenol (25.0%), limonene (11.0%), (E)-phytol (21.5%), linalool (9.9%),camphor (13.5%), salicyl alcohol (10.4%), in seed 5 compounds-hydroxymethylfurfural, (2'S)-7-hydroxy-2-(2'hydroxypropyl)-5methylchromone 5-(2-hydroxyphenoxymethyl) furfural, (2'S)-7-hydroxy-5-hydroxymethyl-2-(2'-hydroxypropyl) chromone, benzyl 2-hydroxy-3,6-dimethoxybenzoate, and benzyl 2βO-dglucopyranosyl-3,6-dimethoxybenzoate, and two oxyanthraquinones, chrysophanol and chrysophanein. In Bark 27 compounds1-hexacosanol, 1-octacosanol, oleic acid, palmitic acid, stearic acid, eight long-chain hydrocarbons, heptacosyleicosanate, glyceryl-1tetraeicosanoate; three sterols, linoleic acid, β-sitosterol , citreorosein,, βsitosteryl-3-Oone triterpene, lupeol , eight anthraquinones, chrysophanol , stigmasterol, emodin, Dglucopyranoside, physcion, , ziganein, rhein methyl ester 1,4,5trihydroxyanthraquinone, coumarins, isoscopoletin , scopoletin ; and 2,4-dihydroxybenzaldehyde two chromones, 2,5dimethyl-7-hydroxychromone ,2,5-dimethyl-7-methoxychromone ; three aromatic compounds, vanillic acid, isovanillic acid , [4]. ...
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... Carla Cirillo [25] has reviewed the most common botanical laxatives such as senna, cascara, frangula, aloe, and rhubarb and their use in the treatment of constipation. In addition, the active ingredients in botanical products can also be used to alleviate constipation, such as Rhein extracted from Cassia fistula pod pulp is used as an active ingredient in laxatives [26]. Yan et al. [27] confirmed that aqueous extracts of Herba Cistanche promoted intestinal motility in loperamide-induced constipation rats by ameliorating the interstitial cells of Cajal. ...
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... Molecules 2019, 24, x FOR PEER REVIEW 2 of 12 which is a new technology that has attracted widespread attention in the extraction of natural products [17][18][19]. Low temperature extraction conditions prevent the instability of zeaxanthin and lutein that occurs at high temperatures, thus improving the extraction rate. ...
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