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Proceedings of the International Cyanide Detection Testing Workshop

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cyanide hydratase converts <strong>the</strong> toxic<br />

cyanide into non-toxic products for<br />

measurement<br />

<strong>the</strong> combination <strong>of</strong> enzymes makes<br />

<strong>the</strong> system highly specifi c<br />

<strong>the</strong>re is no need for vigorous sample<br />

pre-treatment<br />

no use <strong>of</strong> hazardous chemicals<br />

To take this work a step fur<strong>the</strong>r, Mak et al.<br />

(Mak, Yanase et al., 2005) used <strong>the</strong> microbial<br />

sensor system to measure cyanide levels in<br />

marine fi sh. They exposed fi sh to sub-lethal<br />

doses <strong>of</strong> 10 μM potassium cyanide in seawater<br />

for 15 minutes and <strong>the</strong>n transferred <strong>the</strong> fi sh<br />

to clean seawater for recovery. After different<br />

recovery times (0-180 minutes), fi sh were<br />

tested for residual cyanide using <strong>the</strong> biosensor<br />

system. Results are expected in a forthcoming<br />

publication (Mak et al., in prep).<br />

<strong>Cyanide</strong> <strong>Testing</strong> Protocols Used in Non-<br />

Fish Settings<br />

Because <strong>of</strong> <strong>the</strong> fact that cyanide is a toxic poison<br />

and <strong>the</strong> fact that it can be an environmental<br />

pollutant, <strong>the</strong>re is a large scientifi c literature<br />

on cyanide detection.<br />

Table 1 summarizes <strong>the</strong> most common<br />

cyanide detection tests as well as advantages<br />

and disadvantages <strong>of</strong> each test. Table 2<br />

presents a sampling <strong>of</strong> cyanide detection tests<br />

in human, fi sh, and mouse blood, urine, and<br />

tissue samples. In addition, Table 2 presents<br />

some publications reporting on a variety <strong>of</strong><br />

cyanide detection tests.<br />

It is interesting to note that <strong>the</strong>re is a large<br />

amount <strong>of</strong> activity in <strong>the</strong> U.S. federal<br />

government to develop rapid cyanide<br />

detection in humans in order to prepare for<br />

a potential bioterrorist attack using cyanide.<br />

It is possible to explore <strong>the</strong>se methods and<br />

experts to fi nd avenues through which to<br />

102<br />

improve <strong>the</strong> current cyanide detection system<br />

for marine fi sh.<br />

The current method used to test cyanide<br />

concentrations in fish employs <strong>the</strong> Ion<br />

Selective Electrode (ISE) methodology. This<br />

method is not highly sensitive and it is subject<br />

to a tremendous amount <strong>of</strong> interference<br />

with samples found in seawater. Tables 1 and<br />

3 present a wide range <strong>of</strong> methodologies,<br />

each with varying degrees <strong>of</strong> cost, sensitivity,<br />

and potential effectiveness for marine fi sh<br />

samples.<br />

Because cyanide breaks down so quickly in<br />

fi sh, it may be necessary to develop a test<br />

that measures a by-product <strong>of</strong> cyanide. Some<br />

<strong>of</strong> <strong>the</strong> possibilities to explore in this arena<br />

include:<br />

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Thiocyanate. Thiocyanate is a<br />

non-toxic by-product <strong>of</strong> cyanide<br />

degradation.<br />

O<strong>the</strong>r biological by-products such as:<br />

o formate (Mak, Law et al.,<br />

2005)<br />

o a cyanide/hemoglobin adduct<br />

(Kobeleski, pers. com.)<br />

o2-aminothiazoline-4- carboxylic acid (ATCA)<br />

(Logue, Kirschten et al.,<br />

2005)<br />

o a gill protein that is changed<br />

upon cyanide exposure (Chu,<br />

Liu et al., 2001)<br />

Cytochrome oxidase — dose-related<br />

reductions in cytochrome c oxidase<br />

activity were detected in various<br />

organs <strong>of</strong> rats exposed to oral doses<br />

<strong>of</strong> potassium cyanide (Ikegaya,<br />

Iwase et al., 2001). This marker was<br />

suggested as a method <strong>of</strong> diagnosis<br />

for samples taken within two days<br />

post-mortem.

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