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Proceedings of the International Cyanide Detection Testing Workshop

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existing cyanide detection methods used<br />

in fi sh samples. The aim was to answer <strong>the</strong><br />

following questions: (1) is <strong>the</strong> current cyanide<br />

detection method appropriate and effective<br />

and (2) what kinds <strong>of</strong> improvements can<br />

be done to achieve a higher sensitivity and<br />

accuracy? (Mak, Yanase et al., 2005).<br />

The results indicate that <strong>the</strong> current method<br />

could not measure cyanide concentration<br />

below 1 × 10 -5 m. However, much lower<br />

cyanide concentration in seawater was<br />

enough to suffocate a 500 g marine food<br />

fi sh (Mak, Yanase et al., 2005). Therefore,<br />

<strong>the</strong> researchers concluded that <strong>the</strong> cyanide<br />

detection method currently used was not<br />

sensitive enough for <strong>the</strong> determination <strong>of</strong><br />

cyanide traces in post cyanide-exposed fi sh. In<br />

o<strong>the</strong>r words, <strong>the</strong>se results indicate <strong>the</strong> amount<br />

<strong>of</strong> cyanide necessary to kill fi sh is well below<br />

<strong>the</strong> amounts that can reliably be determined<br />

using <strong>the</strong> existing procedures (Mak, Yanase et<br />

al., 2005).<br />

Ultimately, an effective cyanide detection test<br />

will include <strong>the</strong> following criteria:<br />

•<br />

•<br />

•<br />

•<br />

•<br />

•<br />

Sufficient sensitivity to detect low<br />

quantities <strong>of</strong> cyanide in marine fish<br />

hours and perhaps up to days after<br />

exposure<br />

Ability to distinguish between<br />

background levels <strong>of</strong> cyanide exposure<br />

versus concentrations resulting from<br />

illegal fi shing practices<br />

Use <strong>of</strong> technology that is available in<br />

countries where marine fi sh collection<br />

occurs<br />

Ability to detect cyanide exposure<br />

prior to metabolic processing by fi sh<br />

Technology that is possible for use by<br />

non-specialized fi eld staff<br />

Ability to replicate <strong>the</strong> procedure in<br />

many locations<br />

101<br />

•<br />

•<br />

•<br />

Ability for rapid reporting <strong>of</strong><br />

results to industry and government<br />

representatives<br />

Affordable costs<br />

The ability to test fi sh at <strong>the</strong> location<br />

<strong>of</strong> import country — which could<br />

take place several weeks after original<br />

exposure to cyanide<br />

It may be necessary to develop a hybrid<br />

approach that utilizes a less sensitive screening<br />

method in <strong>the</strong> fi eld. Field-based test samples<br />

that indicate a positive result for cyanide<br />

use can be followed up with more sensitive<br />

and verifi able lab-based tests done on <strong>the</strong><br />

same fi sh sample. The techniques that are<br />

appropriate in <strong>the</strong> fi eld include colorimetric<br />

and some bioassay procedures. If <strong>the</strong> test<br />

includes chromatography-related methods<br />

such as gas chromatography and high<br />

performance liquid chromatography/mass<br />

spectrometry, it will be necessary to conduct<br />

this work in a laboratory.<br />

Preliminary Work to Improve <strong>Cyanide</strong><br />

<strong>Detection</strong> in Fish<br />

Mak and Law (Mak, Law et al., 2005)<br />

conducted preliminary experiments to<br />

develop a biosensor system and satisfy <strong>the</strong><br />

necessary detection criteria. Their methods<br />

include <strong>the</strong> pretreatment <strong>of</strong> cyanide with<br />

cyanide hydrolase and <strong>the</strong>n detection by<br />

spectrophotometric formate sensor. The<br />

researchers report that <strong>the</strong> system has a<br />

detection limit at 7.3 μmol/l although<br />

<strong>the</strong>oretically it is possible to increase <strong>the</strong><br />

sensitivity <strong>of</strong> <strong>the</strong> biosensor by injecting a<br />

larger volume <strong>of</strong> <strong>the</strong> pre-incubated sample<br />

(i.e. more formate) into <strong>the</strong> measuring cell.<br />

The researchers identify <strong>the</strong> following<br />

advantages <strong>of</strong> this system over o<strong>the</strong>r potential<br />

cyanide detection tests:

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