TY - JOUR
T1 - Arginase inhibitory activity of stem bark extracts of Caesalpinia tortuosa roxb
AU - Najid, Amirah
AU - Elya, Berna
AU - Noviani, Arikadia
N1 - Publisher Copyright:
© 2018 The Authors. Published by Innovare Academic Sciences Pvt Ltd.
PY - 2018/12
Y1 - 2018/12
N2 - Objective: This study aimed to evaluate the arginase inhibitory activity of Caesalpinia tortuosa Roxb. stem bark extracts. Methods: C. tortuosa Roxb. stem bark extracts were obtained through reflux extraction using n-hexane, ethyl acetate, and methanol and their inhibitory activity against arginase was measured using a microplate reader at 430 nm. Active extracts were subjected to phytochemical analysis and based on the qualitative phytochemical analysis, quantitative data regarding flavonoid and phenolic contents were obtained. The total flavonoid content of active extracts was determined using AlCl3 colorimetric method, and the phenolic content was determined using Folin-Ciocalteu method. Results: Ethyl acetate and methanol extracts of C. tortuosa Roxb. inhibited activity of arginase with IC50 values of 33.81 and 11.58 µg/mL, respectively, nor-NOHA acetate as standard drug inhibited arginase with IC50 values of I3.77 µg/mL. Both active extracts contained saponins, tannins, and flavonoids. Ethyl acetate and methanol extracts showed a total flavonoid content of 7.41 mgQE/g and 5.05 mgQE/g and total phenolic content of 27.55 mgGE/g and 17.16 mgGE/g, respectively. Methanol extracts had a higher inhibitory activity than ethyl acetate extracts despite having flavonoid and phenolic content, thereby suggesting no correlation between arginase inhibitory activity and flavonoid or phenolic content. Conclusion: Ethyl acetate and methanolic extracts of C. tortuosa Roxb. stem barks containing flavonoids, tannins, and saponins displayed arginase inhibitory activity, and no correlation was observed between arginase inhibitory activity and flavonoid and phenolic content.
AB - Objective: This study aimed to evaluate the arginase inhibitory activity of Caesalpinia tortuosa Roxb. stem bark extracts. Methods: C. tortuosa Roxb. stem bark extracts were obtained through reflux extraction using n-hexane, ethyl acetate, and methanol and their inhibitory activity against arginase was measured using a microplate reader at 430 nm. Active extracts were subjected to phytochemical analysis and based on the qualitative phytochemical analysis, quantitative data regarding flavonoid and phenolic contents were obtained. The total flavonoid content of active extracts was determined using AlCl3 colorimetric method, and the phenolic content was determined using Folin-Ciocalteu method. Results: Ethyl acetate and methanol extracts of C. tortuosa Roxb. inhibited activity of arginase with IC50 values of 33.81 and 11.58 µg/mL, respectively, nor-NOHA acetate as standard drug inhibited arginase with IC50 values of I3.77 µg/mL. Both active extracts contained saponins, tannins, and flavonoids. Ethyl acetate and methanol extracts showed a total flavonoid content of 7.41 mgQE/g and 5.05 mgQE/g and total phenolic content of 27.55 mgGE/g and 17.16 mgGE/g, respectively. Methanol extracts had a higher inhibitory activity than ethyl acetate extracts despite having flavonoid and phenolic content, thereby suggesting no correlation between arginase inhibitory activity and flavonoid or phenolic content. Conclusion: Ethyl acetate and methanolic extracts of C. tortuosa Roxb. stem barks containing flavonoids, tannins, and saponins displayed arginase inhibitory activity, and no correlation was observed between arginase inhibitory activity and flavonoid and phenolic content.
KW - Arginase inhibition
KW - Caesalpinia tortuosa
KW - Phytochemical screening
KW - Total flavonoids
KW - Total phenolics
UR - http://www.scopus.com/inward/record.url?scp=85071833257&partnerID=8YFLogxK
U2 - 10.22159/ijap.2018.v10s1.27
DO - 10.22159/ijap.2018.v10s1.27
M3 - Article
AN - SCOPUS:85071833257
SN - 0975-7058
VL - 10
SP - 130
EP - 132
JO - International Journal of Applied Pharmaceutics
JF - International Journal of Applied Pharmaceutics
IS - Special Issue 1
ER -