Table 6.
Extract | Antioxidant method | Finding | Reference |
---|---|---|---|
crude nutmeg extract in methanol 2.4 μL/mL |
The 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay and the β-carotene-linoleic acid assay. |
DPPH assay result showed that eugenol followed by methoxyeugenol had higher activity than BHT. While isoeugenol had higher activity than α–tocopherol. β-carotene-linoleic acid assay, the showed α-tocopherol had higher antioxidant activities than BHT and isoeugenol, followed by methoxyeugenol and the weakest activity was eugenol. |
Kim,et al., 2010 |
acetone, ethanol, methanol, butanol, and water extract of nutmeg | The DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging activity of the various extract (0.025–2 mg/mL) or BHT (0.025–1.0 mg/mL) was measured using the method of Brand-Williams, Cuvelier, and Berset. BHT was used as positive control. |
The acetone extract showed 93.12 ± 1.48 mg gallic acid equivalents (GAE)/100 g dry weight total phenolic content, DPPH scavenging activity of 63.04 ± 1.56 %, chelating activity of 64.11 ± 2.21 % and 74.36 ± 1.94 % inhibition of β-carotene bleaching, at 1 mg/mL extract concentration | Gupta, Bansal, Babu, & Maithil, 2013 |
Nutmeg extracted by acetone | DPPH radical scavenging capacity | DPPH radical scavenging capacity of the acetone extract as well as its fractions was comparatively lower than that of green pepper phenolics. | Chatterjee et al., 2007 |
Essential oil and oleoresins (ethanol, ethyl acetate, and iso-propyl alcohol) of Myristica fragrans | scavenging effect on DPPH, reducing power, and chelating effect was determined. | The essential oil and ethanol oleoresin showed better activity compared to other tested oleoresins and synthetic antioxidants, butylated hydroxyl anisole and butylated hydroxyl toluene. | Kapoor et al., 2013 |
Six isolated compounds from nutmeg seed of Myristica fragrans licarin-B, dehydrodiisoeugenol malabaricone B, malabaricone C, β-sitosterol, and daucosterol. | Antioxidant activities of the isolated compounds were studied using oil stability index (OSI), reducing power, ABTS scavenging, and DPPH scavenging methods. |
The results showed that Malabaricone C is an efficient antioxidant agent which exhibits a stronger antioxidant activity than the commonly used synthetic antioxidants in all studied methods | Hou, Wu, Wang, & Weng, 2012 |
essential oil from nutmeg seed. |
The antioxidant activity was examined by DPPH assay using spectrophotometric. | The nutmeg essential oil showed a good antioxidant activity after incubation (EC50 = 1.35 ± 0.003 mg/ml) | Nikolic et al., 2021 |
Methanol extract potential of flesh, seed and mace of nutmeg (Myristica fragrans Houtt) |
(DPPH), ferric-reducing antioxidant power (FRAP), ferrous ion chelating activity and antioxidant activity assay in a linoleic acid system with ferrothiocyanate reagent (FTC). | Flesh, seed, and mace extract well inhibit the linoleic peroxidation. Tannin, flavonoid and terpenoid were found in seed and mace extract, whereas flesh extract contains flavonoid and terpenoid. | Assa, Widjanarko, Kusnadi, & Berhimpon, 2014 |
Polyphenol extracts of nutmeg. | O brine-shrimp lethality assay, phytotoxicity test, DPPH, and superoxide anion radical scavenging as well as BSA-glucose antiglycation assay | Nutmeg extract exhibited a cytotoxic and phytotoxic potential with LD50 of 4359.70 and 1490 μg/mL respectively. | Kazeem, Akanji, Hafizur, & Choudhary, 2012 |
Methanol and acetone extract of nutmeg | Phenol content & radical scavenging activity were measured quantitatively using (DPPH) (µPADs) methods | The extract contains a high concentration of phenolic compounds (0.6217 mg/ml) and the DPPH assay for acetone extract indicated a high amount of antioxidant compounds. | (Orabi et al., 2022) |