This invention relates to chemical analysis, and more particularly to liquid extraction surface sampling for chemical analysis.
The field of chemical analysis has been assisted by the use of liquid extraction surface sampling. Liquid extraction-based surface sampling mass spectrometry (MS) employing spatially resolved confined liquid/solid extraction of the analyte(s) of interest from a surface is becoming an established analysis methodology. The increased use of this methodology is due in part to the realization that this sampling method provides unrivaled sensitivity compared to other ambient surface sampling techniques. Examples of such systems are shown in U.S. Pat. No. 8,084,735 to Kertesz et al; U.S. Pat. No. 8,384,020 to Jesse et al.; U.S. Pat. No. 8,486,703 to Van Berkel et al.; U.S. Pat. No. 8,637,813 to Van Berkel et al.; U.S. Pat. No. 8,519,330 to Van Berkel et al.; U.S. Pat. No. 8,497,473 to Kertesz et al.; U.S. Pat. No. 8,742,338 to Van Berkel et al.; and U.S. Pat. No. 6,803,566 to Van Berkel et al.; and U.S. Publication Nos. 2012/0053065 to Van Berkel et al.; 2011/0284735 to Van Berkel et al.; 2012/0304747 to Van Berkel et al.; 2014/0096624 to ElNaggar et al.; 2013/0294971 to Van Berkel et al.; 2014/0216177 to Van Berkel et al.; and 2014/0238155 to Van Berkel et al. In addition, spatially resolved, confined liquid solid/extraction of surface has been coupled with high performance liquid chromatography (HPLC) separation utilizing a wall-less liquid microjunction probe surface sampling concept to allow transfer of the sampled material for post-sampling processing (V. Kertesz, G. J. Van Berkel. Liquid microjunction surface sampling coupled with high-pressure liquid chromatography-electrospray ionization-mass spectrometry for analysis of drugs and metabolites in whole-body thin tissue sections. Anal. Chem. 2010, 82, 5917-5921; V. Kertesz, G. J. Van Berkel. Automated liquid microjunction surface sampling-HPLC-MS/MS analysis of drugs and metabolites in whole-body thin tissue sections. Bioanal. 2013, 5, 819-826; G. J. Van Berkel, V. Kertesz. Continuous-flow liquid microjunction surface sampling probe connected on-line with high-performance liquid chromatography/mass spectrometry for spatially resolved analysis of small molecules and proteins. Rapid Commun. Mass Spectrom. 2013, 27, 1329-1334). The best spatial resolution achieved was about 500 μm.
Recently a single capillary liquid junction extraction/ESI emitter named scanning probe electrospray ionization (SPESI) was introduced for surface analysis purposes. See U.S. Pat. No. 8,710,436 to Otsuka; U.S. Publication Nos. 2014/0070088 to Otsuka; US 2013/0341279 to Otsuka et al.; 2014/0070089 to Otsuka; U.S. 2014/0070093 to Otsuka; U.S. 2014/0070094 to Otsuka; U.S. 2014/0072476 to Otsuka; and 2013/0334030 to Otsuka et al.; Otsuka et al. Imaging mass spectrometry of a mouse brain by tapping-mode scanning probe electrospray ionization. Analyst, 2014, 139, 2336-2341; and Otsuka et al.; Scanning probe electrospray ionization for ambient mass spectrometry. Rapid Commun. Mass Spectrom. 2012, 26, 2725-2732. This geometry eliminates the aspiration/emitter capillary that is a primary factor in the ultimate resolution of any dual capillary, liquid junction surface sampling probe. A single capillary is used to supply solvent to form a liquid junction between the capillary and a sample surface. A bias voltage is applied to the solvent to generate an ESI from liquid that pools at the top of the capillary via capillary action and the force of the applied electric field. In the version most suitable for imaging, spontaneous vibration of the probe itself (termed tapping-mode) created an alternate liquid junction surface sampling/non-contact ESI situation at a rate of greater than 100 Hz. Data presented by Otsuka and coworkers indicated a sampling spot size and lane scan width of approximately 150 μm. As surface sampling probes become smaller and direct spraying from the probe is accomplished there is a need for a way to incorporate post-sampling sample processing to obtain more chemical information. The elimination of the aspiration capillary from these systems requires a different system to handle the extract.
The disclosures of the above-identified patents and publications are incorporated fully by reference.
A system for sampling a surface includes a surface sampling probe comprising a solvent liquid supply conduit and a distal end, and a sample collector for suspending a sample collection liquid adjacent to the distal end of the surface sampling probe. A first electrode provides a first voltage to solvent liquid at the distal end of the surface sampling probe. The first voltage produces a field sufficient to generate an electrospray plume at the distal end of the surface sampling probe. A second electrode provides a second voltage. The second electrode is positioned to produce a plume-directing field sufficient to direct the components of the electrospray plume generated at the distal end of the surface sampling probe to the suspended sample collection liquid. The second voltage is less than the first voltage in absolute value. A voltage supply system supplies the voltages to the first electrode and the second electrode. The first electrode can apply the first voltage directly to the solvent liquid.
The system can further include a driver for moving the distal end of the surface sampling probe between at least a surface-adjacent position and a surface-remote position. The voltage system can supply an electrospray generating voltage to the first electrode when the surface sampling probe is in the surface-remote position, and can supply a non-electrospray generating voltage difference when the surface sampling probe is in the surface-adjacent position. The driver can oscillate the distal end of the surface sampling probe between the surface-adjacent position and the surface-remote position at between 1 Hz and 100 MHz.
The second electrode can be electrically connected to the sample collector. The second electrode can be positioned such that the second voltage is applied to the sample collection liquid. The second electrode can include electrospray plume-directing structure for directing the movement of the charged droplets and ions of the electrospray plume toward the sample collector. The second electrode can be a plate and the plume-directing structure can be an opening in the plate. The plate and the plume-directing opening can be interposed between and not connected to the sample collector and the distal end of the probe when the probe is in the surface-remote position.
The system can include at least a third electrode for providing a third voltage. The third electrode can be positioned remotely to the second electrode. The third voltage can produce a plume-directing field that is supplemental to the plume directing field of the second electrode. The second electrode can be located remotely to the sample collector and positioned at a distance from the distal end of the surface sampling probe. The third electrode can be positioned at greater distance to the distal end of the surface sampling probe. A fourth electrode can be connected to the sample collector. A plume-directing voltage can be applied to the fourth electrode.
The surface sampling probe can include a probe body having a liquid inlet and a liquid outlet, and a liquid extraction tip. A solvent delivery conduit receives solvent liquid from the liquid inlet and delivers the solvent liquid to the liquid extraction tip. An open liquid extraction channel can extend across an exterior surface of the probe body from the liquid extraction tip to the liquid outlet. An electrospray emitter tip is in liquid communication with the liquid outlet of the liquid extraction surface sampling probe.
The electrospray-generating field can be at least 108 V/m. The field at the distal end of the surface sampling probe can be at least 108 V/m.
The surface-adjacent position can be less than 1 mm from the sample surface. The surface-remote position can be between 1 μm and 5 cm from the sample surface.
The driver can include a mechanical relay. The driver can include a piezoelectric device. The driver can include an atomic force microscopy cantilever system.
The system can further include a pump for pumping solvent through the conduit to the surface, and for withdrawing solvent from the surface through the conduit. The sample collection liquid can be suspended statically. The sample collection liquid can be suspended dynamically. The sample collector can include a sample collection liquid suspension opening, a sample collection liquid supply conduit communicating with the suspension opening, and a sample collection liquid removal conduit communicating with the suspension opening. The rate of supply of collection liquid can be balanced with the rate of removal such that the sample collection liquid passes the suspension opening to receive charged droplets and ions from the surface sampling probe but does not exit the probe through the suspension opening, and is removed through the removal conduit.
The system can further include at least one separation device for separating samples in the sample collection liquid. The separation device can include at least one selected from the group consisting of liquid chromatography, solid phase extraction, high pressure liquid chromatography (HPLC), ultra pressure liquid chromatography (UPLC), capillary electrophoresis, ion mobility spectrometry and differential mobility spectrometry.
The system can include a mass spectrometer for analyzing samples from the sample collection liquid. The mass spectrometer can include at least one selected from the group consisting of sector MS, time-of-flight MS, quadrupole mass filter MS, three-dimensional quadrupole ion trap MS, linear quadrupole ion trap MS, Fourier transform ion cyclotron resonance MS, orbitrap MS, and toroidal ion trap MS.
A method for analyzing a surface can include the steps of providing a surface sampling probe comprising a solvent liquid supply conduit and a distal end; positioning a sample collector for suspending a sample collection liquid adjacent to the distal end of the surface sampling probe; applying a first voltage to the distal end of the surface sampling probe, the first voltage producing a field sufficient to generate an electrospray plume at the distal end of the surface sampling probe; applying a second voltage to an electrode positioned such that electrospray generated charged droplet and ions at the distal end of the surface sampling probe are directed to the suspended sample collection liquid, the second voltage being less than the first voltage (in absolute value) and sufficient to direct the electrospray plume to the sample collector; and collecting the plume components in the sample collection liquid of the sample collector.
There are shown in the drawings embodiments that are presently preferred it being understood that the invention is not limited to the arrangements and instrumentalities shown, wherein:
A system for sampling a surface is shown in
Solvent liquid exits the distal end 12 of the probe 14 and contacts sample 16 on support surface 18. A liquid microjunction can be formed between the distal end 12 of the probe 14 and the sample 16. The voltage that is applied to the solvent liquid by a voltage application unit 30 is sufficient to generate an electrospray plume of the solvent liquid and sample. The position and voltage of the second electrode 46 is sufficient to direct the plume components through the space indicated by arrow 66 to the sample collection liquid 22. The position of the second electrode 46 can vary. In the example shown in
The system can further include a driver for moving the distal end 12 of the surface sampling probe 14 between at least a surface-adjacent position and a surface-remote position. There is shown in
The suspension of the sample collection liquid refers to the fact that the sample collection liquid is maintained out of direct contact with the sample surface or the probe. The sample collection liquid can be maintained either statically, for example suspended as a drop, or dynamically in which the sample collection liquid is flowed but is at some point available to receive charged droplets and gas phase ions from the electrospray plume and remains out of contact with the sample surface or the probe. The adjacent positioning of the sample collection liquid means that the liquid is suspended at a distance where the electrospray plume will reach the sample collection liquid without substantial dissipation of the plume into the surrounding atmosphere. The distal end of the probe refers to a portion of the probe that is nearer to the point of the probe where the solvent exits the probe than where the solvent enters the probe. The second voltage is equal to or less than the first voltage. Less can mean 1-100 V, or more, in absolute value. The term plume directing field refers to the ability of this field to steer the electrospray plume in the direction of the sample collection liquid such that the probability of the plume components contacting and being trapped in the sample collection liquid is greater than the probability would be without the field.
The voltage system can supply an electrospray generating voltage to the first electrode when the surface sampling probe is in the surface-remote position, and can supply a non-electrospray generating voltage when the surface sampling probe is in the surface-adjacent position. There is shown in
The second electrode can be positioned remotely from the sample collector and can direct the electrospray plume to the sample collection liquid. The second electrode can include a plume-directing structure for directing the movement of the plume components toward the sample collector. There is shown in
The system can include at least a third electrode for providing a third voltage, as shown in
Multiple electrodes can be utilized in order to finely control the plume-generating and directing fields, and the interplay among these fields. Such a system is shown in
Many orientations between the sample collector and the probe are possible. One such orientation is shown in
There is shown in
The electrospray plume generating field is selected for the particular solvent/analyte system and quantitative factors such as analyte concentration and distance to the sample collector. The plume generating field can be at least 108 V/m. The voltage at the distal end of the surface sampling probe can be sufficient to generate a field of at least 108 V/m.
The surface adjacent position can be less than 1 mm from the sample surface. The surface-remote position can be between 1 μm and 5 cm from the sample surface.
The solvent and sample collection liquid can be the same or different compositions. Examples of suitable sampling solvents include all those that can be electrosprayed, with or without additives like acids or bases or various salts, including among others methanol, ethanol, isopropanol, water, acetonitrile, and chloroforms either neat or in various combinations. Examples of suitable sample collection liquids include various combinations of the same solvents that might be used to sample the surface but also solvents not typically use with electrospray including dimethylsulfoxide (DMSO) and dimethylformamide (DMF) or even very nonpolar solvents like hexane and toluene.
The driver can include a mechanical relay. The driver can include a piezoelectric device. The driver can include an atomic force microscopy cantilever system. Other driver systems are possible.
The system can further include a pump for pumping solvent through the conduit to the surface, and for withdrawing solvent from the surface through the conduit. The sample collection liquid can be suspended statically. The sample collection liquid can be suspended dynamically. The sample collector can include a sample collection liquid suspension opening, a sample collection liquid supply conduit communicating with the suspension opening, and a sample collection liquid removal conduit communicating with the suspension opening. The rate of supply of collection liquid can be balanced with the rate of removal such that the sample collection liquid passes the suspension opening to receive charged droplets and ions from the surface sampling probe but does not exit the probe through the suspension opening and is removed through the removal conduit.
There is shown in
The system can further include at least one separation device for separating samples in the sample collection liquid. The separation device can include at least one selected from the group consisting of liquid chromatography, solid phase extraction, high pressure liquid chromatography (HPLC), ultra pressure liquid chromatography (UPLC), capillary electrophoresis, ion mobility spectrometry and differential mobility spectrometry.
The system can include a mass spectrometer for analyzing samples from the sample collection liquid. The mass spectrometer can include at least one selected from the group consisting of sector MS, time-of-flight MS, quadrupole mass filter MS, three-dimensional quadrupole ion trap MS, linear quadrupole ion trap MS, Fourier transform ion cyclotron resonance MS, orbitrap MS, and toroidal ion trap MS.
A method for analyzing a surface can include the steps of providing a surface sampling probe comprising a solvent liquid supply conduit and a distal end; positioning a sample collector for suspending a sample collection liquid adjacent to the distal end of the surface sampling probe; applying a first voltage at the distal end of the surface sampling probe, the first voltage producing a field sufficient to generate an electrospray at the distal end of the surface sampling probe; applying a second voltage to an electrode positioned such that electrospray plume generated at the distal end of the surface sampling probe is directed to the suspended sample collection liquid, the second voltage being less than the first voltage (in absolute value) and sufficient to direct the plume components to the sample collector; and collecting the plume components in the sample collection liquid of the sample collector.
Ranges: throughout this disclosure, various aspects of the invention can be presented in a range format. It should be understood that the description in the range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range for example, 1, 2, 2.7, 3, 4, 5, 5.3 and 6. This applies regardless of the breadth of the range.
This invention can be embodied in other forms without departing from the spirit or essential attributes thereof, and accordingly, reference should be had to the following claims to determine the scope of the invention.
This invention was made with government support under contract No. DE-AC05-00OR22725 awarded by the U.S. Department of Energy. The government has certain rights in this invention.
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Number | Date | Country | |
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20160126080 A1 | May 2016 | US |