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1.
Sci Rep ; 13(1): 2634, 2023 02 14.
Article in English | MEDLINE | ID: mdl-36788326

ABSTRACT

Vibrational spectroscopies offer great potential for standoff detection of chemical and biological warfare agents, avoiding contamination to the operator and equipment. Among them, particularly promising is Coherent anti-Stokes Raman scattering (CARS) spectroscopy, using synchronized pump/Stokes laser pulses to set up a vibrational coherence of target molecules at a laser focus, which is read by further interaction with a probe pulse, resulting in the emission of a coherent beam detectable at a distance. CARS has previously demonstrated the capability to detect bacterial spores based on the Raman spectrum of the characteristic molecule calcium dipicolinate (CaDPA); however, a complex and bulky laser technology, which is only suitable for a laboratory environment, was employed. Here we develop a broadband CARS setup based on a compact, industrial grade ytterbium laser system. We demonstrate high signal-to-noise ratio detection of Bacillus atrophaeus spores at a concentration of 105 cfu/mm2, at a standoff distance of 1 m, and an acquisition time of 1 s. Our system, which combines chemical specificity and sensitivity along with improved ruggedness and portability, paves the way to a new generation of instruments for real-world standoff detection of chemical and biological threats.


Subject(s)
Spectrum Analysis, Raman , Spores, Bacterial , Spectrum Analysis, Raman/methods , Lasers , Vibration
2.
Toxins (Basel) ; 12(12)2020 12 08.
Article in English | MEDLINE | ID: mdl-33302573

ABSTRACT

Ricin, produced from the castor beans of Ricinus communis, is a cytotoxin that exerts its action by inactivating ribosomes and causing cell death. Accidental (e.g., ingestion of castor beans) and/or intentional (e.g., suicide) exposure to ricin through the oral route is an area of concern from a public health perspective and no current licensed medical interventions exist to protect from the action of the toxin. Therefore, we examined the oral toxicity of ricin in Balb/C mice and developed a robust food deprivation model of ricin oral intoxication that has enabled the assessment of potential antitoxin treatments. A lethal oral dose was identified and mice were found to succumb to the toxin within 48 h of exposure. We then examined whether a despeciated ovine F(ab')2 antibody fragment, that had previously been demonstrated to protect mice from exposure to aerosolised ricin, could also protect against oral intoxication. Mice were challenged orally with an LD99 of ricin, and 89 and 44% of mice exposed to this otherwise lethal exposure survived after receiving either the parent anti-ricin IgG or F(ab')2, respectively. Combined with our previous work, these results further highlight the benefit of ovine-derived polyclonal antibody antitoxin in providing post-exposure protection against ricin intoxication.


Subject(s)
Antitoxins/administration & dosage , Disease Models, Animal , Gastrointestinal Tract/drug effects , Ricin/administration & dosage , Ricin/toxicity , Administration, Oral , Animals , Antitoxins/isolation & purification , Ricinus communis/toxicity , Chemical Warfare Agents/isolation & purification , Chemical Warfare Agents/toxicity , Dose-Response Relationship, Drug , Female , Gastrointestinal Tract/pathology , Mice , Mice, Inbred BALB C , Ricin/isolation & purification , Sheep , Sheep, Domestic , Treatment Outcome
3.
Electrophoresis ; 26(6): 1144-54, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15704246

ABSTRACT

We report the development of a hand-held instrument capable of performing two simultaneous microchip separations (gel and zone electrophoresis), and demonstrate this instrument for the detection of protein biotoxins. Two orthogonal analysis methods are chosen over a single method in order to improve the probability of positive identification of the biotoxin in an unknown mixture. Separations are performed on a single fused-silica wafer containing two separation channels. The chip is housed in a microfluidic manifold that utilizes o-ring sealed fittings to enable facile and reproducible fluidic connection to the chip. Sample is introduced by syringe injection into a septum-sealed port on the device exterior that connects to a sample loop etched onto the chip. Detection of low nanomolar concentrations of fluorescamine-labeled proteins is achieved using a miniaturized laser-induced fluorescence detection module employing two diode lasers, one per separation channel. Independently controlled miniature high-voltage power supplies enable fully programmable electrokinetic sample injection and analysis. As a demonstration of the portability of this instrument, we evaluated its performance in a laboratory field test at the Defence Science and Technology Laboratory with a series of biotoxin variants. The two separation methods cleanly distinguish between members of a biotoxin test set. Analysis of naturally occurring variants of ricin and two closely related staphylococcal enterotoxins indicates the two methods can be used to readily identify ricin in its different forms and can discriminate between two enterotoxin isoforms.


Subject(s)
Electrophoresis, Microchip/methods , Microfluidic Analytical Techniques/methods , Toxins, Biological/isolation & purification , Electrophoresis, Microchip/instrumentation , Enterotoxins/isolation & purification , Equipment Reuse , Miniaturization , Ricin/isolation & purification , Ricinus/chemistry , Sensitivity and Specificity , Staphylococcus aureus
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