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Volume 7, Issue 5 (Suppl)
J Biotechnol Biomater
ISSN: 2155-952X JBTBM, an open access journal
Biotechnology 2017
November 13-14, 2017
November 13-14, 2017 Osaka, Japan
19
th
World Congress on
Biotechnology
Effect of solvent system on the extraction of phenolic compounds and antioxidant capacity of
Gloriosa
superb
L.
Amit Bahukhandi, Anjali Barola, I D Bhatt and R S Rawal
GB. Pant National Institute of Himalayan Environment and Sustainable Development, India
G
loriosa superba
Linn. (Family: Colchicaceae), commonly known as Malabar glory lily; Kalihari; Glory lily is grown in
semi-shade open areas. The species is distributed throughout temperate zone of India, Burma, Malaysia, SriLanka at
an altitude of 2100 m above sea level. In India, it is found in southern parts to the mid hill zones of Himachal Pradesh,
Jammu Kashmir, Uttar Pradesh and Uttarakhand. The species is brilliant wavy-edged yellow and red flowers. The plants have
reported richest sources of colchicine and gloriosine. Recently, colchicine is reported prime importance for its possible use in
cancer treatment. The species has been reported to use in the Indian and Chinese system of medicine for its analgesic, anti-
inflammatory, antimicrobial and antitumor properties. In addition, it is used in the treatment of snake bite, skin diseases, fever,
inflammation and respiratory disorders by local communities. The rhizome and its paste is used for the treatment of colic,
paralysis, chronic ulcer, bruises, sprains and considered useful in promoting labor and expulsion of placenta. The essential oil
of the species is used in cosmetic industries. Therefore, rhizome portion of
Gloriosa superba
was sampled and analyzed for
polyphenolic and antioxidant capacity in different solvent system and for harnessing maximum potential. Results revealed a
significant variation (p<0.05) in analyzed parameters among solvent systems. Total phenolic content ranged between 0.54-
1.35 mg GAE/g; flavonoid 0.66-185 mg QE/g; flavonol 0.33-1.03 mg QE/g and tannins 1.08-3.47 mg TAE/g dry weight and
maximum exhibited in methanolic solvent. Similarly, antioxidant activities were determined
in vitro
assays varied significantly
(ABTS 2.67-4.09; NO 2.26-4.05; DPPH 1.24-4.58 and OH 0.14-041 mM AAE/100 g dry weight). Among different solvent
types, methanolic extract was recorded best for harnessing maximum antioxidant potential; however, highest reducing
antioxidant power (0.54 mM AAE/100 g dry weight) was found in acetone. Total phenolic content showed significant (p<0.05)
positive relationship with flavonoid (r=0.905); tannin (r=0.914) and antioxidant activity (ABTS-r=0.967; NO-r=0.994;
p<0.01; OH-r=0.927; p<0.05, respectively). Likewise, flavonol showed strong correlation (p<0.01) with tannin (r=0.978) and
hydroxyl radical scavenging antioxidant activity (r=0.971). Tannin positively correlated (p<0.05) with antioxidant activity
(ABTS-r=0.892; NO-r=0.914; OH-r=0.971; p<0.01, respectively). The results of the present study are indicative of the fact that
the species possess polyphenolic content and antioxidant activity and therefore, can be a source of natural antioxidant. Solvents
with moderate polarity such as methanol and acetone showed higher polyphenolics and antioxidant activity, therefore, can be
utilized for harnessing maximum polyphenolics content.
amit.bahukhandi@gmail.comJ Biotechnol Biomater 2017, 7:5 (Suppl)
DOI: 10.4172/2155-952X-C1-083