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4th EucheMs chemistry congress

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Poster Session 2<br />

s1109<br />

chem. Listy 106, s257–s1425 (2012)<br />

Poster session 2 - Analytical Chemistry<br />

P - 0 4 9 4<br />

deterMinAtion of CAdMiuM By AdSorPtive<br />

StriPPinG voLtAMMetry uSinG PyroCAteChoL<br />

vioLet CheLAtinG AGent<br />

A. AhMAd 1 , A. ALdABAh 1 , A. ALMAiuf 1<br />

1 King Saud University, Chemistry, AlRiyadh, Saudi Arabia<br />

The adsorptive collection of Cd (II) complex with<br />

pyrocatechol violet ligand, coupled with the square wave<br />

voltammetric technique, yields a very sensitive electroanalytical<br />

procedure for the determination of cadmium in various industrial<br />

samples. The optimized experimental conditions include:<br />

supporting electrolyte (carbonate buffer), pH (9.5), pyrocatechol<br />

violet concentration (1.5?10-5 moll-1 ), accumulation time (30 s),<br />

accumulation potential (0.0 V), scan rate (200 mV s-1 ), pulse<br />

amplitude (0.05 V) and SW frequency (50 Hz). The monitored<br />

stripping voltammetric current was linear over the range of<br />

7.5?10-8 –1.75?10-7 moll-1 and the detection limit was 0.66 ppb.<br />

The relative standard deviation was calculated as 1.02% (n =10)<br />

for 1?10-7 mol l-1 Cd(II) and the obtained electrochemical signal<br />

was stabile for up to 120 minutes. Possible interferences by either<br />

co-existing metal ions or other chelating agents were also<br />

investigated. The applicability of the developed method for the<br />

determination of Cd element was assessed by the analysis of<br />

various industrial and environmental samples. The accuracy of<br />

the obtained voltammetric analytical results was validated by<br />

comparing with that obtained by atomic absorption spectrometry<br />

and conducting the necessary statistical evaluation.<br />

Keywords: Electro<strong>chemistry</strong>; Voltammetry; Cadmium;<br />

4 th <strong>EucheMs</strong> <strong>chemistry</strong> <strong>congress</strong><br />

P - 0 4 9 5<br />

deterMinAtion of PKA vALue of irinoteCAn<br />

uSed for treAtMent of CoLoreCtAL CAnCer<br />

By reverSed PhASe Liquid ChroMAtoGrAPhy<br />

B. AKMeSe 1 , S. SAnLi 2 , n. SAnLi 2<br />

1 Hitit University Faculty of Science and Arts, Chemistry,<br />

Corum, Turkey<br />

2 Usak University Faculty of Science and Arts, Chemistry, Usak,<br />

Turkey<br />

Email: bdhylcn@hotmail.com<br />

Colorectal cancer, also called coloncancer or large bowel<br />

cancerincludes cancerous growths in the colon, rectum and<br />

appendix. It is the thirdmost common form of cancer and the second<br />

leading cause of cancer-related deathin the Western world [1] .<br />

Colorectal cancer is the third mostcommon form of cancer appears<br />

in our country and it can also occur in everyage, but above the<br />

90% of the patients are more than 40 years old [2] . Recently,<br />

combined active drugs in the treatment of colorectal cancer was<br />

usedbecause of more efficiently destroy the tumor cells in the<br />

standard therapy forpatients. Irinotecanwhich is one of the drugs<br />

for this purpose, an antineoplastic drug usedintravenously in the<br />

treatment of advanced colorectal cancer. It is isolatedfrom<br />

Camptotheca acuminata which issitotiksik a tree that grows in<br />

China [3] .<br />

The ionization constant is an importantphysico-chemical<br />

parameter of a drug and the knowledge of this parameter is<br />

offundamental importance in a wide range of applications and<br />

research areas. Inthis study pK values of irinotecan were<br />

a<br />

determined and the effectof the mobile phase composition on the<br />

ionization constant was studied bymeasuring the pK at different<br />

a<br />

acetonitrile-water mixtures, 35,40,45, 50 % (v/v) using LC-UV<br />

method.<br />

references:<br />

1. A. S. Sameer, S. Abdullah, M. Z. Banday, N. Syeed,<br />

M. A. Siddiqi,International Journal of Genetics<br />

andMolecular Biology, 2010, 2(6), 101–111.<br />

2. C. Smith and J. A. Butler, Diseases ofthe Colon & Rectum,<br />

1989, 32, 843–846.<br />

3. W. Zhang, G. E. Dutschman, X. Li, M. Ye, Y.C. Cheng,<br />

Journal of Chromatography B,2009, 877, 3038–3044.<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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