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Analisis Fitokimia Berbasis GC-MS dan Evaluasi Aktivitas Antioksidan Metode DPPH dari Ekstrak Etanol dan N-Heksan Daun Bidara (Ziziphus mauritiana Lam.) Maharani Zahra; Rahma Yulia; Syarifah Nadia; Bunga Rimta Barus
Journal of Pharmaceutical and Sciences JPS Volume 9 Nomor 2 (2026)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v9i2.1146

Abstract

Background: The increasing public interest in herbal medicine which is safer and rarely causes side effects has made people use more natural ingredients as a source of bioactive compounds. One promising plant is the bidara leaf (Ziziphus mauritiana Lam.), known for its rich supply of secondary metabolites, including alkaloids, flavonoids, glycosides, and terpenoids, which boast pharmacological benefits, especially in their role as antioxidants. Objective: This research is conducted to determine the phytochemical compounds and examine the antioxidant potential of bidara leaf extracts prepared with ethanol and n-hexane, using experimental method. Methods: The extraction was done through maceration using 96% ethanol and n-hexane as solvents, and then we analyzed the phytochemicals via phytochemical screening and GC-MS. For checking antioxidant activity, we used the DPPH method, which involved figuring out the maximum wavelength, the operating time, measuring absorbance, and calculating the IC50 value. Results: From the phytochemical analysis, it turned out that ethanol extracts of bidara leaves feature a richer array of bioactive compounds, including alkaloids, flavonoids, glycosides, and terpenoids or steroids, in contrast to the n-hexane extracts, which only include alkaloids, glycosides, and terpenoids or steroids. Analysis using GC-MS identified that the ethanol extract was dominated by fatty acid ester compounds, including methyl palmitate and methyl oleate, while the n-hexane extract contained non-polar compounds such as squalene and tetratetracontane. Through the DPPH approach, the antioxidant activity of ethanol and n-hexane extracts was demonstrated by IC₅₀ values of 4.488 µg/mL and 7.54 µg/mL, respectively, both of which are classified as very strong, although still lower than vitamin C, which has an IC₅₀ of 2.47 µg/mL. Conclusion: The analysis indicates that the ethanol extract exhibits stronger antioxidant activity compared to the n-hexane extract.
Skrining Fitokimia, Analisis GC-MS, dan Aktivitas Antioksidan (Metode DPPH) Ekstrak Etanol Daun Sirih Cina (Peperomia Pellucida (L.) Kunth) Putri Nurjannah; Rahma Yulia; Syarifah Nadia
Journal of Pharmaceutical and Sciences JPS Volume 9 Nomor 2 (2026)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v9i2.1562

Abstract

Introduction: Peperomia pellucida (L.) Kunth, commonly known as Chinese betel leaf, is a medicinal plant widely used in traditional medicine for various ailments. The plant is reported to contain diverse secondary metabolites with potential pharmacological activities, including antioxidant properties. However, comprehensive information on its phytochemical constituents and antioxidant potential remains limited, particularly for extracts of Indonesian origin. Objective: This study aimed to determine the phytochemical profile, chemical constituents, and antioxidant activity of the ethanol extract of P. pellucida leaves. Methods: Dried leaf powder (100 g) was extracted by maceration using 96% ethanol (1:10 w/v) for 3 × 24 hours at room temperature. Phytochemical screening was conducted using standard qualitative tests for alkaloids, flavonoids, glycosides, saponins, steroids/terpenoids, and tannins. Chemical composition was analyzed using Gas Chromatography-Mass Spectrometry (GC-MS). Antioxidant activity was evaluated using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical-scavenging assay, with IC₅₀ values determined by linear regression analysis. Vitamin C served as the positive control. Results: The extraction yielded a concentrated ethanol extract of 11.8% (w/w). Phytochemical screening revealed the presence of flavonoids, glycosides, saponins, and terpenoids/steroids, while alkaloids and tannins were not detected. GC-MS analysis identified 14 chromatographic peaks, with major compounds including methyl hexadecanoate (14.12%), methyl 9-octadecenoate (13.61%), and triacontanoic acid. The ethanol extract exhibited very strong antioxidant activity with an IC₅₀ value of 41.47 µg/mL, compared to vitamin C (IC₅₀ = 4.083 µg/mL). The linear regression equation for the extract was y = 0.4291x + 32.2016 (R² = 0.9985). Conclusion: The ethanol extract of P. pellucida leaves contains various secondary metabolites and demonstrates very strong antioxidant activity. Although GC-MS analysis was predominantly characterized by fatty acid esters, the observed bioactivity likely results from synergistic contributions of multiple bioactive constituents. Further studies employing LC-MS/MS are recommended to identify specific compounds responsible for the antioxidant activity and to quantitatively determine total phenolic and flavonoid contents to establish their correlation with the observed bioactivity.