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II International Symposium on Carbon for Catalysis ABSTRACTS

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PP-<str<strong>on</strong>g>II</str<strong>on</strong>g>-1<br />

FUNCTIONALIZATION OF CARBON NANO BALL FOR BIO-MEDICAL<br />

APPLICATIONS<br />

Abdi S.H.R., Liu Zhen-Xue, Park Y<strong>on</strong>g-Ki, Park Seung-Kyu 1 , Lee Chul Wee<br />

Advanced Chemical Technology Divisi<strong>on</strong>, Korea Research Institute of Chemical Technology,<br />

Daeje<strong>on</strong> 305-600, Korea<br />

1 LG Household & Health Care Research Park, Daeje<strong>on</strong> 305-343, Korea<br />

e-mail : chulwee@krict.re.kr<br />

Carb<strong>on</strong> nano balls (CNBs) are basically hollow core mesoporous shell structures with specific<br />

surface area of 1,230m 2 /g and the total pore volume 1.27 cm 3 /g as determined by nitrogen<br />

BET adsorpti<strong>on</strong> measurements [1,2] have attracted much attenti<strong>on</strong> <strong>for</strong> potential applicati<strong>on</strong>s<br />

in many fields of science and engineering [3]. Drawing parallel with carb<strong>on</strong> nano tubes<br />

(CNTs) it would be interesting to investigate the utility of CNBs <strong>for</strong> its applicati<strong>on</strong> as carrier<br />

<strong>for</strong> drug delivery [4]. The task of drug delivery can be accomplished by means of either<br />

physical adsorpti<strong>on</strong> of the drug <strong>on</strong>to CNB or by chemical modificati<strong>on</strong> of CNB i.e., through<br />

functi<strong>on</strong>alizati<strong>on</strong> [5]. The later has been found to be better in terms of better c<strong>on</strong>trolled release<br />

of the drug than <strong>for</strong>mer where the release of the drug can be fast and unc<strong>on</strong>trolled.<br />

In this report we disclose the functi<strong>on</strong>alizati<strong>on</strong> of CNBs by oxidati<strong>on</strong> route and its<br />

modificati<strong>on</strong> with 1-docosanol, a known antiviral l<strong>on</strong>g chain alcohol [6]. In a simple synthetic<br />

step the CNBs were oxidized with dilute sulfuric acid nitric acid mixture at 80 o C <strong>for</strong> 18 h <strong>for</strong><br />

generati<strong>on</strong> of carboxyl groups <strong>on</strong> the surface of CNBs. The oxidized material was treated with<br />

thi<strong>on</strong>yl chloride followed by its interacti<strong>on</strong> with 1-docosanol <strong>for</strong> its chemical linkage with<br />

CNBs through ester linkage (Scheme-1). The oxidized material and 1-docosanol supported<br />

CNB (CNB-1D) were characterized by elemental analysis, 1 H and 13 C NMR, XPS and SEM<br />

analysis. The biological activity of the CNB-1D is in progress and would be communicated in<br />

due course.<br />

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