Rutin as a standard y = 0.0118x+0.0023, (R2 = 0.9995). The linear relationship between absorbance and flavonoids content ranged from 15?5 mg/mL. TFC was then expressed as rutin equivalents (RE), in mg RE per g DW.Materials and Methods Sample collection and pretreatmentLeaves of C. cyrtophyllum were collected at a very limited scale (2 kg) surrounding the Dead Crater Garden on Hainan Island, China. The People’s Republic of China issued the specific permissions are required from authority of plant collection in a protected area of land, but not a national geological garden. The location we collect our plant materials is a national geological garden and the author was not obliged to have any permissions. This work did not involve endangered or protected species, the species C. cyrtophyllum is a common plant growing nearby the curbside. Leaves were selected, washed thoroughly in potable water, and then dried for 36 h using a hot air oven at 60uC. Dried leaves were then powdered using a herb disintegrator (118 Swing, Zhejiang, China) and subsequently sieved (20 mesh).DPPH radical scavenging capacity measurementThe radical scavenging ability of 2,2′-diphenyl-b-picrylhydrazyl (DPPH) was estimated by a method adapted from Sharififar et al [20]. Thus, an aliquot of extract (0.1 mL) was added to 3.9 mL of ethanolic DPPH (60 mM). The mixture was shaken vigorously and left to stand at room temperature for 30 min in the dark and absorbance was measured at 517 nm. The free radical scavenging activity was calculated as follows: ?? RSA Ablank {Nobiletin chemical information Asample =Ablank |100 where Ablank was the absorbance of the control reaction (containing all reagents except the test compound), and Asample was the absorbance of the test 1662274 compound.UAE with C. cyrtophyllumUltrasonic-assisted extraction (UAE) were performed in in a digitally controlled ultrasonic device (Model XO-5200DTD, 200 W, 40 kHz; Nanjing Xian’ou Instruments Manufacture Company Ltd., China). Working frequency was fixed at 40 kHz. The extraction variables were selected according to Thoo et al [16]. Dried leaves of C. cyrtophyllum (5 g) were get Madrasin extracted twice with the required solvent, temperature, and time. Extracts were then filtered and the filtrate was prepared with a constant volume (250 ml) using 60 ethanol for estimation of phenolics and antioxidant measurements through various chemical assays. Each extraction was performed in duplicate and all analyses were performed in triplicate.ABTS radical scavenging capacity measurementFree radical scavenging capacity using a stable ABTS radical was performed according to Thoo et al [16]. with some modifications. The ABTS radical solution was produced by gently mixing 10 mL of 7 mM ABTS solution and 10 mL of 2.45 mM potassium persulfate solution. This was allowed to stand in the dark at room temperature for 12?6 h. The ABTS radical solution was adjusted with ethanol to an absorbance of 0.7 (60.02) at 734 nm before usage. Extract (100 ml) or ethanol (100 ml, control) was added to 3.9 mL ABTS radical solution and allowed to react for 30 min until a stable absorbance was obtained. The decrease in absorbance at 734 nm was measured against a blank (ethanol). Antioxidant activity of ABTS radical scavenging capacity was calculated as a scavenging percentage: ?? RSA Ablank {Asample =Ablank |100 where Ablank was the absorbance of the control reaction(containing all reagents except the test compound), and Asample was the absorbance of the test compound.TPC measuremen.Rutin as a standard y = 0.0118x+0.0023, (R2 = 0.9995). The linear relationship between absorbance and flavonoids content ranged from 15?5 mg/mL. TFC was then expressed as rutin equivalents (RE), in mg RE per g DW.Materials and Methods Sample collection and pretreatmentLeaves of C. cyrtophyllum were collected at a very limited scale (2 kg) surrounding the Dead Crater Garden on Hainan Island, China. The People’s Republic of China issued the specific permissions are required from authority of plant collection in a protected area of land, but not a national geological garden. The location we collect our plant materials is a national geological garden and the author was not obliged to have any permissions. This work did not involve endangered or protected species, the species C. cyrtophyllum is a common plant growing nearby the curbside. Leaves were selected, washed thoroughly in potable water, and then dried for 36 h using a hot air oven at 60uC. Dried leaves were then powdered using a herb disintegrator (118 Swing, Zhejiang, China) and subsequently sieved (20 mesh).DPPH radical scavenging capacity measurementThe radical scavenging ability of 2,2′-diphenyl-b-picrylhydrazyl (DPPH) was estimated by a method adapted from Sharififar et al [20]. Thus, an aliquot of extract (0.1 mL) was added to 3.9 mL of ethanolic DPPH (60 mM). The mixture was shaken vigorously and left to stand at room temperature for 30 min in the dark and absorbance was measured at 517 nm. The free radical scavenging activity was calculated as follows: ?? RSA Ablank {Asample =Ablank |100 where Ablank was the absorbance of the control reaction (containing all reagents except the test compound), and Asample was the absorbance of the test 1662274 compound.UAE with C. cyrtophyllumUltrasonic-assisted extraction (UAE) were performed in in a digitally controlled ultrasonic device (Model XO-5200DTD, 200 W, 40 kHz; Nanjing Xian’ou Instruments Manufacture Company Ltd., China). Working frequency was fixed at 40 kHz. The extraction variables were selected according to Thoo et al [16]. Dried leaves of C. cyrtophyllum (5 g) were extracted twice with the required solvent, temperature, and time. Extracts were then filtered and the filtrate was prepared with a constant volume (250 ml) using 60 ethanol for estimation of phenolics and antioxidant measurements through various chemical assays. Each extraction was performed in duplicate and all analyses were performed in triplicate.ABTS radical scavenging capacity measurementFree radical scavenging capacity using a stable ABTS radical was performed according to Thoo et al [16]. with some modifications. The ABTS radical solution was produced by gently mixing 10 mL of 7 mM ABTS solution and 10 mL of 2.45 mM potassium persulfate solution. This was allowed to stand in the dark at room temperature for 12?6 h. The ABTS radical solution was adjusted with ethanol to an absorbance of 0.7 (60.02) at 734 nm before usage. Extract (100 ml) or ethanol (100 ml, control) was added to 3.9 mL ABTS radical solution and allowed to react for 30 min until a stable absorbance was obtained. The decrease in absorbance at 734 nm was measured against a blank (ethanol). Antioxidant activity of ABTS radical scavenging capacity was calculated as a scavenging percentage: ?? RSA Ablank {Asample =Ablank |100 where Ablank was the absorbance of the control reaction(containing all reagents except the test compound), and Asample was the absorbance of the test compound.TPC measuremen.
