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Proceedings of the International Cyanide Detection Testing Workshop

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The Cyantesmo paper changes color from<br />

light green to dark blue depending on <strong>the</strong><br />

concentration <strong>of</strong> hydrogen cyanide liberated.<br />

Several papers have been published using<br />

Cyantesmo paper. Flinger et al. (1992) used<br />

it as a screening tool to detect <strong>the</strong> presence<br />

<strong>of</strong> cyanide liberated from blood samples.<br />

Relia et al. (2004) evaluated <strong>the</strong> method<br />

with concentrations <strong>of</strong> cyanide ion ranging<br />

from 0.25 to 30 mg/L (ppm). The test strips<br />

demonstrated incrementally increasing deep<br />

blue color changes over a progressively longer<br />

portion <strong>of</strong> <strong>the</strong> test strip in less than fi ve minutes<br />

for each concentration <strong>of</strong> cyanide including<br />

1, 3, 10, and 30 mg/L. The concentrations <strong>of</strong><br />

0.25, 0.5, and 0.75 mg/L required more than<br />

two hours to begin demonstration <strong>of</strong> a color<br />

change.<br />

It is recommended that <strong>the</strong> FDA protocol be<br />

evaluated as a screening tool for <strong>the</strong> detection<br />

<strong>of</strong> cyanide in fi sh tissue samples near <strong>the</strong><br />

point <strong>of</strong> collection in exporting countries.<br />

The procedure will require <strong>the</strong> use <strong>of</strong> regional<br />

testing laboratories. It has <strong>the</strong> advantage that<br />

many samples can be analyzed at low cost.<br />

BioSensors<br />

Mak et al. (2005a) presented a summary <strong>of</strong><br />

various papers that have developed biosensors<br />

for detecting cyanide ion. Most <strong>of</strong> <strong>the</strong> methods<br />

are dependent on measuring chemical reaction<br />

products based on enzymatic reactions (e.g.,<br />

formate production from action <strong>of</strong> cyanide<br />

hydratase, cytochrome oxidase inhibition,<br />

peroxidase inhibition, rhodanese and sulphite<br />

oxidase reactions). There is also a microbial<br />

sensor, and <strong>the</strong> measurement <strong>of</strong> oxygen<br />

uptake by bacteria. There are efforts being<br />

made to link <strong>the</strong> enzymatic reactions to<br />

potentiometers to measure <strong>the</strong> enzymatic<br />

reaction as changes in electrical potentials.<br />

The idea is to create a microprobe (containing<br />

<strong>the</strong> enzymes) that would be inserted into <strong>the</strong><br />

blood to give a reading based on a change in<br />

Figure 1. Sealed test tubes used by <strong>the</strong> U.S. Food and Drug Administration to detect <strong>the</strong> presence <strong>of</strong> cyanide<br />

in foodstuffs using Cyantesmo paper suspended above an acidifi ed sample. Image provided by Dr. Fred Fricke,<br />

USFDA.<br />

48

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