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TECHNOLOGY DIGEST - Draper Laboratory

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B. anthracis spores. This would be beneficial as it would<br />

allow distinction between B. subtilis or other spores from<br />

B. anthracis. Additionally, we further demonstrate the ability<br />

of the DMS to detect chemical weapon agent simulants.<br />

Pyrolysis was used as the sample introduction method for<br />

the DMS, which uses thermal energy to break apart chemical<br />

bonds. [45] The fragmentation of the sample will be<br />

characteristic of the relative strengths of the bonds in the<br />

original molecule. The maximum known detectable particle<br />

size for the DMS is about 500 Daltons (0.5 kDa) based<br />

on previous results (data not shown). We tested several<br />

pyrolysis methods to ensure that the spores were broken<br />

down sufficiently for detection by the DMS. Based on the<br />

SDS-PAGE results shown, the spores were fragmented<br />

completely at temperatures above 650°C. However, it is<br />

important to note that the spores were also completely<br />

fragmented at the lower temperature 550°C when this<br />

temperature was held for 10 s. The fragmentation thus<br />

seems to be dependent not only on temperature, but also<br />

on the time at which this temperature is held. This allows<br />

flexibility in determining an optimal pyrolysis condition to<br />

use for DMS analysis. The knowledge of various pyrolysis<br />

conditions that ensure adequate fragmentation for DMS<br />

analysis is important not only for these experiments, but<br />

for any field setups in the future that use pyrolysis as a<br />

sample introduction method.<br />

We examined the response of the DMS to pyrolyzed<br />

spores. We chose to use a lower pyrolysis temperature and<br />

extend it over a longer period of time in an attempt to<br />

ensure fragmentation of the spores to particles well under<br />

the detection limit of the gel, but also without complete<br />

destruction of any characteristics of these molecular fragments.<br />

The DMS spectra shown in Figure 4 demonstrate the ability<br />

of the DMS to distinguish the spores from the sterile<br />

water in which they are suspended. Significant peaks are<br />

marked with numbers 1-5. Peaks 1, 3, and 4 appear to be<br />

correlated with the presence of spores and could potentially<br />

mark the presence of specific biomarkers. In fact, it<br />

seems that these peaks may also be concentration-dependent,<br />

as their magnitude appears to increase proportionally<br />

to the number of spores present in the sample. The spectra<br />

for the spores can be distinguished from that of the<br />

water in which they were resuspended.<br />

We also demonstrate the use of the DMS for chemical<br />

weapons agents. MS was used as a simulant nerve agent.<br />

The DMS produces a clear spectrum for MS at concentration<br />

levels as low as 45 ppt, as shown in Figures 5a and 5b.<br />

Another compound, DMMP, was used as a simulant blister<br />

agent. A unique DMS spectrum is obtained for this compound<br />

when compared with the one obtained for MS.<br />

When a mixture of these two compounds was analyzed, the<br />

resultant spectrum showed features of both compounds.<br />

38<br />

Detection of Biological and Chemical Agents Using Differential Mobility Spectrometry (DMS) Technology<br />

This experiment shows that the specificity of the DMS<br />

enables the detection of multiple chemical warfare agents<br />

simultaneously.<br />

CONCLUSIONS<br />

In view of the growing concern over terrorism, there is a<br />

need for a sensor that can detect trace amounts of chemical<br />

or biological warfare agents to minimize the potential<br />

impact of such a release on the public. Such a sensor<br />

would aid the government in the defense against chemical<br />

and biowarfare attacks; an early alert to such an attack<br />

could save many lives. It would also aid the public health<br />

sector in the treatment of biowarfare victims by speeding<br />

diagnosis based on the identification of the particular<br />

agent delivered. To service both industries, such a sensor<br />

must be portable, inexpensive, sensitive, and able to detect<br />

multiple biological or chemical agents.<br />

<strong>Draper</strong> <strong>Laboratory</strong> has designed a sensor that fits these<br />

characteristics, the DMS. Sionex Corporation is a <strong>Draper</strong><br />

spin-off company created to commercialize and market<br />

this new device. The DMS has several advantages over<br />

other types of detectors. It is small, extremely sensitive,<br />

and relatively inexpensive. Not only are conventional ion<br />

mobility spectrometers much larger and more expensive,<br />

they also operate with short pulses of ions. In comparison,<br />

the DMS analyzes continuously-introduced ions with<br />

nearly 100% of the “tuned” ions reaching the detector.<br />

Also, as the electric fields required to filter the ions are on<br />

the order of 10,000 V/cm, the DMS actually benefits from<br />

miniaturization; by reducing the gap dimensions to the<br />

order of 500 µm, the voltages required for ion filtering are<br />

easily achievable. Mass spectrometers are larger and more<br />

expensive. They also require an inert environment for<br />

detection, whereas the DMS operates at atmospheric pressure.<br />

A portable hand-held DMS unit is already a reality<br />

and further miniaturization is possible.<br />

We have demonstrated the utility of the DMS to detect<br />

potential biological and chemical warfare agents. The DMS<br />

is a sensitive, hand-held device that can detect multiple<br />

biological and chemical agents, even in the presence of<br />

interferents. Furthermore, these devices can be manufactured<br />

using mass production techniques, significantly<br />

lowering their cost. The DMS identified a unique, repeatable<br />

spectrum for B. subtilis spores, used as a surrogate for<br />

B. anthracis spores. The concentrations shown here as<br />

being detected easily are very low for the reagentless and<br />

fast (less than 5 min) class of sensors. Even at such low<br />

concentrations, the spores can be distinguished from the<br />

water in which they are resuspended. This sensor with the<br />

detection capacity currently shown could be used initially<br />

as a trigger device, where a warning would be given if a<br />

signal that looks similar to that resulting from the presence<br />

of spores is discovered. In the future, however, if we can<br />

show the ability to detect lower concentrations than

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