2021
DOI: 10.3390/antiox10081218
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Almond (Prunus dulcis cv. Casteltermini) Skin Confectionery By-Products: New Opportunity for the Development of a Functional Blackberry (Rubus ulmifolius Schott) Jam

Abstract: This work proposes for the first time a model for reusing almond (Prunus dulcis cv. Casteltermini from Sicily, Southern Italy) skin to formulate a new functional blackberry (Rubus ulmifolius Schott) jam. For this purpose, blackberries were analysed fresh and as jam, traditionally prepared with a minimum fruit amount of 80%. Different percentages of almond skin (20, 15, and 10% w/w) were added to jam. The phytochemical profile of enriched jam was investigated by LC-ESI/LTQOrbitrap/MS analyses. Anthocyanins, hyd… Show more

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Cited by 23 publications
(51 citation statements)
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“…Citrus aurantium EOs and their mixes were screened for their radical scavenging activity by using 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) tests [ 42 ]. Briefly, a solution of ABTS radical was obtained by mixing 7 mM ABTS solution with 2.45 mM K 2 S 2 O 8 .…”
Section: Methodsmentioning
confidence: 99%
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“…Citrus aurantium EOs and their mixes were screened for their radical scavenging activity by using 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) tests [ 42 ]. Briefly, a solution of ABTS radical was obtained by mixing 7 mM ABTS solution with 2.45 mM K 2 S 2 O 8 .…”
Section: Methodsmentioning
confidence: 99%
“…FRAP test is based on the reaction that involves 2,4,6-tripyridyl-s-triazine-Fe 3+ complex (TPTZ/Fe 3+ ). Briefly, a mixture namely FRAP reagent, consisting of 40 mM HCl, 20 mM FeCl 3 , and 0.3 M acetate buffer at pH 3.6, was prepared [ 42 ]. EO at concentration of 2.5 mg/mL in MeOH (100 μL) was mixed with FRAP reagent and water.…”
Section: Methodsmentioning
confidence: 99%
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“…To assess the potential anti-obesity effects of pomelo EOs and their mixes, the activity of porcine pancreatic lipase (type II) (EC 3.1.1.3) activity was measured using p -nitrophenyl octanoate as a substrate [ 54 ]. The EOs were mixed with the enzyme solution (1 mg/mL in water), 0.005 M of p -nitrophenyl octanoate solution, and Tris-HCl buffer (pH = 8.5).…”
Section: Methodsmentioning
confidence: 99%
“…Both α-amylase and α-glucosidase are involved in carbohydrate digestion and have been recognised as targets for postprandial hyperglycaemia modulation [ 55 ]. For the α-amylase-inhibitory assay, a starch solution of α-amylase enzyme (EC 3.2.1.1) and colorimetric reagent were prepared [ 54 ]. Pomelo oils were added to the starch solution and left to react with the enzyme.…”
Section: Methodsmentioning
confidence: 99%