TECHNOLOGY DIGEST - Draper Laboratory
TECHNOLOGY DIGEST - Draper Laboratory
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