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Volume 4

Toxicology: Open Access

ISSN: 2476-2067

Toxicology Congress 2018

March 12-14, 2018

March 12-14, 2018 Singapore

14

th

World Congress on

Toxicology and Pharmacology

The anti-proliferative activity of

Coriandrum sativum

alcoholic extract on HCT-116 and MCF-7 cell lines

Eugenia Dumitrescu

1

, Florin Muselin

1

, Roxana Popescu

2

, Tulcan Camelia

1

, Andreia Chirila

1

and Romeo T Cristina

1

1

Banat’s University of Agriculture and Veterinary Medicine, Romania

2

Univesity of Medicine and Pharmacy, Romania

Statement of the Problem:

It is known that vegetal extracts can generate

positive responses in stages of several patho-processes. The anti-oxidant;

protection against DNA damage and cancer activities of

Coriandrum

sativum

were intensely studied in the last decade. Our research envisaged

the polyphenolic compounds’ structure and the anti-proliferative biologic

activity of

C. sativum

10% alcoholic extract against HCT-116 and MCF-7

cell lines.

Methodology:

The

C. sativum

extract was obtained respecting the Romanian

Pharmacopoeia 10

th

edition, the plant being lyophilized (with Ilshin

Kryptonstraat 11, 6718WR EBE lyophilisator to -55 oC, 5 mTorr pressure

and 24 hours lyophilization time). The polyphenols were determined by LC-MS and the

in vitro

evaluation effects by the MTT

proliferation test, using HCT116 (colorectal carcinoma) and MCF7 (mammary adenocarcinoma). The cells were seed as: 2×10

4

(MCF7) and 1×10

4

(HCT) in 96 well plates. The lyophilized extracts were suspended in specific culture medium being obtained

a 300 mg/mL

C. sativum

stock solution. From this, different test concentrations were prepared by dilution (300, 200, 100 and

respectively 50 mcg/mL).

Result & Conclusion:

As a following, after 24 hours from the exposure, using HCT-116 and MCF-7 cell lines it was observed

that the cellular proliferation reduced, this being correlated to dose and the alterations of cell morphology to the groups studied;

to great extract doses, apoptotic and necrotic alterations were observed, both for HCT and MCF cells; the IC50, representing

concentration to which a marker substance is reducing the tissues viability with 50% after a fixed time exposure period wasn’t

observed for the cell lines used in this test; the chromatographic analysis of

C. sativum

alcoholic extract evidenced the presence

of the polyphenolic compounds, the greatest concentrations were ascertained for epicatechin (77.083 mcg/mL) and rutin

(30.279 mcg/mL), substances with known hard anti-oxidant proprieties.

References

1. Rayar A, Manivannan R (2015)

In Vitro

Cytotoxicity Activity of Phytochemicals Isolated from

Coriandrum sativum Linn

.

in Selected Cell Lines.

Journal of Pharmacy and Biological Sciences

; 10(3): 38-48.

2. AL Snafi A E (2014) The Pharmacological importance and chemical constituents of

Arctium lappa

: A review.

International

Journal for Pharmaceutical Research Scholars

; 3(1-1): 663-670.

3. Kumar R S, Balasubramanian P, Govindaraj P, Krishnaveni T (2014) Preliminary studies on phytochemicals and

antimicrobial activity of solvent extracts of

Coriandrum sativum L.

roots (Coriander).

Journal of Pharmacognosy and

Phytochemistry

; 2(6): 74-78.

4. Nithya T G, Sumalatha D (2014) Evaluation of

in vitro

anti-oxidant and anticancer activity of

Coriandrum sativum

against

human colon cancer HT-29 cell lines.

International Journal of Pharmacology and Pharmacy Science

; 6(2): 421-424.

5. Tang E L, Rajarajeswaran J, Fung S Y, Kanthimathi M S (2013) Antioxidant activity of

Coriandrum sativum

and protection

against DNA damage and cancer cell migration.

BMC Complementary and Alternative Medicine

; 13: 347.

Biography

Eugenia Dumitrescu has her expertise in the veterinary field, reproductive toxicology, heavy metals, phyto-therapy and oxidative stress in animals. She is an

Associate Professor at the Faculty of Veterinary Medicine at Banat’s University of Agriculture and Veterinary Medicine, Romania.

cris_tinab@yahoo.com

Eugenia Dumitrescu et al., Toxicol Open Access 2018, Volume 4

DOI: 10.4172/2476-2067-C1-006