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Pharma & Clinical Pharmacy Congress 2016

November 07-09, 2016

Volume 5 Issue 4(Suppl)

Clin Pharmacol Biopharm

ISSN: 2167-065X CPB, an open access journal

conferenceseries

.com

November 07-09, 2016 Las Vegas, Nevada, USA

4

th

International

Pharma & Clinical Pharmacy Congress

Clin Pharmacol Biopharm 2016, 5:4(Suppl)

http://dx.doi.org/10.4172/2167-065X.C1.023

Molecular mechanism investigation of a novel Ruthenium (II) complex inhibits proliferation of

human esophageal squamous cell carcinoma

Jianguo Lin, Liubin Guo, Gaochao Lv and Ling Qiu

Jiangsu Institute of Nuclear Medicine, China

H

igh toxicity acquired resistance and serious side effects, prompting the search for novel compounds for cancer treatment.

Recently, a Ruthenium (II) complex [Ru (p-cymene)(L)Cl2] (L = 1,3-bis(4-(tert-butyl)benzyl)-1H-imidazol-3-ium

chloride) , which named L-4, has been synthesized and characterized. The purpose of this study was to investigate the effects

of L-4 against human esophageal squamous carcinoma (ESCC) cell line EC109. Different methods to determine the apoptotic

pathways triggered by L-4 in EC109 cells were investigated by using flow cytometry, Hoechst 33258 staining, Caspases

activation, mitochondria functioning, generation of reactive oxygen species (ROS) and western-blotting techniques. Results

showed that a dose- and time-dependent reduction occurred in cell viability after exposure to L-4 in EC109 cells. The flow

cytometry analysis showed that L-4 induced cell cycle arrest at G2/M phase in EC109 cells, concomitant to p53 and p21 up-

regulation and Cyclin D1 down-regulation. L-4 also induced ROS-dependent and mitochondria-mediated apoptosis in EC109

cells by targeting the glutathione reductase, leading to generation of ROS, Ca2+ overloading, increase of Bax/Bcl-2 ratio, loss

of MMP, release of cytochrome c into the cytosol, and then activation of Caspase-3/-9. Whereas, ROS scavengers, N-acetyl-

L-cysteine, significantly attenuated the effects of L-4 on reduction of cell viabilities, activity of GR, generation of ROS, loss

of MMP, the dysfunction of mitochondria and induction of apoptosis. The preliminary results suggest that the Ruthenium

(II) complex, L-4, inhibits EC109 cells proliferation via blocking cell cycle progression and inducing ROS-dependent and

mitochondria-mediated apoptosis, and deserves further investigation as a new chemotherapeutic strategy for patients with

esophageal cancer.

linjianguo@jsinm.org

Formulation of hand sanitizer gel using the semi-purified flavonoids from the outer coverings of

the red creole variety of

Allium cepa

Linn of family Alliaceae

John Paul T Toting, Jemimaiah R Arceo, Romalyn A Joson, Yasmine D L Tobias, Jan Karlo T Ecalne, Cecilia D Santiago and Regina A Jazul

Centro Escolar University, Philippines

T

his research focuses on the formulation of hand sanitizer gel using the semi-purified flavonoids from the outer coverings

of the Red creole variety of

Allium cepa

L. fam. Alliaceae. This study utilizes the experimental method of research. The

agar cup diffusion method was used in determining the antibacterial activity of formulation with 40% semi-purified extract as

compared to the two (2) locally available leading hand sanitizer brands.

Staphylococcus aureus, Escherichia coli, Pseudomonas

aeruginosa, Micrococcus luteus, Enterobacter aerogenes, Proteus vulgaris, Salmonella typimurium, Klebsiella pneumoniae,

Bacillus subtilis

and

Bacillus cereus

were utilized as test organisms. The formulation exhibited antibacterial activity against

8 of 10 bacteria used in the experiment, while Brand A exhibited antibacterial activity against 1 of 10 bacteria and brand B

manifested an antibacterial activity against 4 out 10 of bacteria utilized in the microbial assay. Moreover, based on the result

of the primary skin irritation test, the formulation is perceptibly not capable of causing irritation to the skin when applied

topically. The researchers recommends that thorough investigation of the semi-purified flavonoid extract using instrumental

method of analysis and isolation of the pure flavonoid should be conducted in order to determine the specific flavonoid that

exhibits the antibacterial activity.

jptoting@aol.com