ANTIOXIDANT ACTIVITIES OF DIFFERENT POLARITY EXTRACTS FROM THREE ORGANS OF MAKRUT LIME (CITRUS HYSTRIX DC) AND CORRELATION WITH TOTAL FLAVONOID, PHENOLIC, CAROTENOID CONTENT

Authors

  • Irda Fidrianny School of Pharmacy Bandung Institute of Technology
  • Yurika Johan School of Pharmacy Bandung Institute of Technology
  • Sukrasno - School of Pharmacy Bandung Institute of Technology

Abstract

ABSTRACT
Objectives: The objectives of this research were to study antioxidant activities from various extracts of three organs of makrut lime (Citrus hystrix)
using two methods of antioxidant assays, which were 2,2-diphenyl-1-picrylhydrazyl (DPPH) and cupric ion reducing antioxidant capacity (CUPRAC);
and correlation of total flavonoid, phenolic, and carotenoid content in various extracts of three organs of makrut lime with IC50 of DPPH antioxidant
activities and EC50 of CUPRAC capacities.
Methods: Extraction was performed by reflux apparatus using different polarity solvents. The extracts were evaporated using rotary evaporator.
Antioxidant capacities were tested using DPPH and CUPRAC assays. Determination of total phenolic, flavonoid and carotenoid content performed by
ultraviolet-visible and their correlation with IC50 of DPPH scavenging activities and EC50 of CUPRAC capacities were analyzed by Pearson's method.
Results: Ethyl acetate stem extract of makrut lime (ST2) had the lowest IC50 of DPPH scavenging activity 0.6 μg/ml and the lowest EC50 of CUPRAC
capacity 123 μg/ml. N-hexane stem extract of makrut lime (ST1) had the highest total flavonoid content (8.7 g QE/100 g), ethyl acetate stem extract
(ST2) contained the highest total phenolic content (TPC) (8.3 g gallic acid equivalent /100 g and total carotenoid content (1.8 g BE/100 g).
Conclusions: There was negatively high correlation between TPC in peel and stem extracts of makrut lime with their IC50 of DPPH scavenging activity.
EC50 of CUPRAC capacity of leaves, peel and stem extracts of makrut lime had negative and high correlation with their total flavonoid and carotenoid
content. IC50 of DPPH scavenging activities in leaves, peel and stem extracts of makrut lime had no linear result with EC50 of CUPRAC capacities.
Keywords: Antioxidant, 2,2-diphenyl-1-picrylhydrazyl, Cupric ion reducing antioxidant capacity, Organs, Makrut lime, Flavonoid, Phenolic, Carotenoid.

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References

REFERENCES

Londoño JL, Lima VR, Lara O, Gil A, Pasa TB, Arango GJ, et al.

Clean recovery of antioxidant flavonoids from citrus peel: Optimizing

an aqueous ultrasound-assisted extraction method. Food Chem

;119(1):81-7.

Thaipong K, Boonprakob U, Crosby K, Zevallos LC, Byrne DH.

Comparison of ABTS, DPPH, FRAP, and ORAC assays for estimating

antioxidant activity from guava fruit extracts. J Food Compost Anal

;19:669-75.

Xu BJ, Chang SK. A comparative study on phenolic profiles and

antioxidant activities of legumes as affected by extraction solvents.

J Food Sci 2007;72(2):S159-66.

Lindley MG. The impact of food processing on antioxidants in vegetable

Table 1: Pearson’s correlation coefficient of IC50 of DPPH scavenging activities, EC50 of CUPRAC capacities and TFC, TPC, TCC in various

organs extracts of makrut lime

Pearson’s correlation coefficient (r)

TFC TPC TCC EC50 CUPRAC LE EC50 CUPRAC PE EC50 CUPRAC ST

IC50 DPPH LE −0.014 −0.08 −0.316 0.259

IC50 DPPH PE 0.278 −0.89** 0.838** −0.421

IC50 DPPH ST 0.65** −0.986** −0.214 −0.364

EC50 CUPRAC LE −0.931** 0.921** −0.996**

EC50 CUPRAC PE −0.968** 0.016 −0.845**

EC50 CUPRAC ST −0.936** 0.366 −0.83**

TFC: Total flavonoid content, TPC: Total phenolic content, TCC: Total carotenoid content, DPPH: 2,2-diphenyl-1-picrylhydrazyl, CUPRAC: Cupric ion reducing

antioxidant capacity

Asian J Pharm Clin Res, Vol 8, Issue 4, 2015, 239-243

Fidrianny et al.

oils, fruits and vegetables. Trends Food Sci Technol 1998;9:336-40.

Prasad MP, Rajkumar RA. In vitro antioxidant assay of citrus species

using DPPH method. Indian J Adv Plant Res 2014;1(4):1-3.

Ghasemi K, Ghasemi Y, Ebrahimzadeh MA. Antioxidant activity,

phenol and flavonoid contents of 13 citrus species peels and tissues.

Pak J Pharm Sci 2009;22(3):277-81.

Khatua S, Roy T, Acharya K. Antioxidant and free radical scavenging

capacity of phenolic extract from Russula laurocerasi. Asian J Pharm

Clin Res 2013;6(4):156-60.

Fidrianny I, Utari P, Ruslan K. Evaluation of antioxidant capacities,

flavonoid, phenolic, carotenoid content from various extracts of four

kinds Brassica herbs. Int J Pharm Pharm Sci 2014;6(2):268-72.

Samuagam L, Sia CM, Akowuah GA, Okechukwu PN, Yim HS. The

Effect of extraction conditions on total phenolic content and free radical

scavenging capacity of selected tropical fruits’ peel. Health Environ J

;4(2):80-102.

Pellegrini N, Serafini M, Colombi B, Rio DD, Salvatore S. Total

antioxidant capacity of plant food, beverages and oils consumed

in Italy assessed by three different in vitro assays. J Am Coll Nutr

;133:2812-9.

Tachakittirungrod S, Okonogi S, Chowwanapoonpohn S. Study

on antioxidant activity of certain plants in Thailand: Mechanism

of antioxidant action of guava leaf extract. Food Chem 2007;103:381‑8.

Apak R, Güçlü K, Demirata B, Ozyürek M, Celik SE, Bektasoglu B,

et al. Comparative evaluation of various total antioxidant capacity

assays applied to phenolic compounds with the CUPRAC assay.

Molecules 2007;12(7):1496-547.

Souri E, Amin G, Farsan H, Barazandeh TM. Screening antioxidant

activity and phenolic content of 24 medicinal plants extracts. DARU J

Pharm Sci 2008;16:83-7.

Fidrianny I, Harnovi M, Insanu M. Evaluation of antioxidant activities

from various extracts of sweet orange peels using DPPH, Asian J Pharm

Clin Res 2014;7(3):186-90.

Prakash NK, Bhuvaneswari S, Sripriya N, Prameela L, Bhagya R,

Radhika B, et al. Antioxidant activity of common plants of northern

Tamil Nadu, India. Int J Pharm Pharm Sci 2014;6(4):128-32.

Blois MS. Antioxidant determination by the use of stable free radicals.

Nature 1958;181:1199-2000.

Bedawey AA. Characteristics of Antioxidant Isolated from Some Plants

Sources. Cairo: Shibin El-Kom; 2010. p. 1-11.

Chang CC, Yang MH, Wen HM, Chern JC. Estimation of total flavonoid

content in propolis by two complementary colorimetric methods.

J Food Drug Anal 2002;10:178-82.

Pourmorad F, Hosseinimehr SJ, Shahabimajd N. Antioxidant activity,

phenol and flavonoid content of some selected Iranian medicinal plants.

Afr J Biotechnol 2006;5(11):1142-5.

Ghafar MF, Prasad KN, Weng KK, Ismail A. Flavonoid, hesperidine,

total phenolic contents and antioxidant activities from Citrus species.

Afr J Biotechnol 2010;9(3):326-30.

Li XC, Wang XZ, Chen DF, Chen SZ. Antioxidant activity and

mechanism of protochatechuic acid in vitro. J Funct Food Health Dis

;1:232-44.

Ling LT, Palanisamy UD. Review: Potential antioxidants from tropical

plants. In: Valdez B, editor. Food Industrial Processes-Methods. Kuala

Lumpur: In Tech; 1999. p. 64-72.

Heim KE, Tagliaferro AR, Bobilya DJ. Flavonoid antioxidants:

Chemistry, metabolism and structure-activity relationships. J Nutr

Biochem 2002;13(10):572-84.

Hayat K, Hussain S, Abbas S, Farooq U, Ding B, Xia S, et al. Optimized

microwave-assisted extraction of phenolic acids from Citrus mandarin

peels and evaluation of antioxidant activity in vitro. Sep Purif Technol

;70(1):63-70.

Huang D, Ou B, Prior RL. The chemistry behind antioxidant capacity

assays. J Agric Food Chem 2005;53:1841-56.

Published

01-07-2015

How to Cite

Fidrianny, I., Y. Johan, and S. -. “ANTIOXIDANT ACTIVITIES OF DIFFERENT POLARITY EXTRACTS FROM THREE ORGANS OF MAKRUT LIME (CITRUS HYSTRIX DC) AND CORRELATION WITH TOTAL FLAVONOID, PHENOLIC, CAROTENOID CONTENT”. Asian Journal of Pharmaceutical and Clinical Research, vol. 8, no. 4, July 2015, pp. 239-43, https://mail.innovareacademics.in/journals/index.php/ajpcr/article/view/6592.

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