The invention relates generally to electrospray ionization of a sample to be analyzed. The invention is generally useful in providing an ion source for an analyzer such as a mass spectrometer.
Electrospray ionization refers to a method of providing ionized molecules from a liquid sample. The electrospray ionization process generates highly-charged droplets from the liquid sample. As solvent evaporates from the droplets, gas phase ions representative of the species contained in the liquid sample are generated. The ions are then introduced into an analyzer (e.g. a mass spectrometer) via an ion-sampling interface coupled to the analyzer.
In operation, an electrospray is produced when a sufficient electrical potential difference Vinlet is applied between the inlet 112 of the ion-sampling interface 106 and the fluid at the tip of the spray needle 104 to generate a concentration of electric field lines emanating from the tip of the spray needle 104. When a positive voltage Vinlet is applied at the inlet 112 of the ion-sampling interface 106 relative to the tip of the spray needle 104, the electric field causes negatively-charged ions in the fluid to migrate to the surface of the fluid at the tip of the spray needle 104. Conversely, a negative voltage Vinlet applied at the inlet 112 of the ion-sampling interface 106 relative to the tip of the spray needle 104 will result in positively-charged ions in the fluid migrating to the surface of the fluid at the tip of the spray needle 104. Once the ions are at the surface of the fluid, small charged droplets 116 under the influence of the electric field are urged by electrostatic forces towards the inlet 112 of the ion-sampling interface 106. Solvent rapidly evaporates from the droplets 116, leaving ions 118 from the analyte drawn to and through the inlet 112 of the ion-sampling interface 106 and into the passage of the ion guide. The ions 118 typically are delivered from the ion-sampling interface 106 to a mass spectrometer for analysis.
Conventional electrospray ion sources, such as shown in
In an orthogonal electrospray ion source 102b, such as shown in
Although the orthogonal design works well, further improvements are sought.
The invention addresses the aforementioned deficiencies in the art, and provides novel electrospray apparatus and methods. In an embodiment in accordance with the invention, an electrospray apparatus includes a nozzle defining an exit orifice, an entrance orifice, and a first passage extending from the entrance orifice to the exit orifice, the nozzle defining a nozzle axis. The electrospray apparatus further includes an interface defining an inlet, an outlet, and a second passage extending from the inlet to the outlet, the interface defining an interface axis. The interface is disposed such that the inlet is adjacent the exit orifice and the interface axis is in transverse relation to the nozzle axis; wherein an angle formed between the nozzle axis and the interface axis is between about 75 degrees and about 105 degrees. The interface is operable to receive a voltage from an interface voltage source. An auxiliary electrode disposed in operable relation to the exit orifice is operable to receive a voltage from an auxiliary voltage source, and is also operable to modulate an electric field at the exit orifice. The electrospray apparatus is operable to define an ion pathway followed by ions enroute from the exit orifice to the inlet, and the auxiliary electrode is disposed outside the ion pathway.
In an embodiment the interface comprises a housing defining an opening disposed adjacent the inlet, wherein the housing defines a lumen for transporting a gas, the lumen in fluid communication with the opening.
In some embodiments, the auxiliary electrode is disposed such that an angle of less than 15 degrees is subtended between the auxiliary electrode and the interface axis, said angle having its vertex at the inlet. In other embodiments, the auxiliary electrode is disposed such that an angle of less than 15 degrees is subtended between the auxiliary electrode and the nozzle axis, said angle having its vertex at the exit orifice.
The auxiliary electrode in some embodiments is a disk electrode; in other embodiments, the auxiliary electrode is a pin electrode; and in still other embodiments, the auxiliary electrode is an ‘L’ shaped electrode. In yet another embodiment, the auxiliary electrode has a convex cylindrical surface having a central axis, the central axis parallel to the nozzle axis.
The invention further provides a method of converting a liquid solute sample into ionized molecules. The method includes introducing a liquid solute sample into an apparatus according to the invention and applying an interface voltage to the interface and an auxiliary voltage to the auxiliary electrode. The applied interface voltage and auxiliary voltage are sufficient to subject the sample at the exit orifice and the inlet to an electric field, whereby the sample is discharged from the exit orifice in the form of droplets, the electric field effective to produce ionized molecules from the droplets and urge the ionized molecules towards the inlet. In particular embodiments, the method further includes applying a housing potential to the housing.
Additional objects, advantages, and novel features of this invention shall be set forth in part in the descriptions and examples that follow and in part will become apparent to those skilled in the art upon examination of the following specifications or may be learned by the practice of the invention. The objects and advantages of the invention may be realized and attained by means of the instruments, combinations, compositions and methods particularly pointed out in the appended claims.
These and other features of the invention will be understood from the description of representative embodiments of the method herein and the disclosure of illustrative apparatus for carrying out the method, taken together with the Figures, wherein
To facilitate understanding, identical reference numerals have been used, where practical, to designate corresponding elements that are common to the Figures. Figure components are not drawn to scale.
Before the invention is described in detail, it is to be understood that unless otherwise indicated this invention is not limited to particular materials, reagents, reaction materials, manufacturing processes, or the like, as such may vary. It is also to be understood that the terminology used herein is for purposes of describing particular embodiments only, and is not intended to be limiting. It is also possible in the present invention that steps may be executed in different sequence where this is logically possible. However, the sequence described below is preferred.
It must be noted that, as used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “an insoluble support” includes a plurality of insoluble supports. In this specification and in the claims that follow, reference will be made to a number of terms that shall be defined to have the following meanings unless a contrary intention is apparent.
For purposes of describing spatial relationships in embodiments of the application, the following are defined:
An ion pathway is defined as the path followed by ions enroute from the exit orifice to the inlet during normal operation of the electrospray apparatus according to the current invention. It should be noted that the ion pathway is still defined for the apparatus even if no ions are actively being generated (e.g. the apparatus is turned off).
“Upstream” and “downstream” as used herein refer to the typical flow of an ion through an apparatus in accordance with the present invention. The ion starts at the entrance orifice (as an as-yet-un-ionized species in solution), passing through the first passage to the exit orifice, it passes into an electrosprayed droplet which evaporates to result in the de-solvated ion urged toward the inlet, through the second passage to the outlet. Upstream references a location relatively earlier in the ion's journey (or in the same general direction), and downstream references a location later in the ion's journey (or in the same general direction).
A nozzle axis is the center axis of the nozzle.
A nozzle plane is a plane that is perpendicular to the nozzle axis and intersects the nozzle axis at the exit orifice.
An interface axis is the center axis of the interface.
An interface plane is a plane that is perpendicular to the interface axis and intersects the interface axis at the inlet.
Transverse, as used to describe a spatial relationship between two items (e.g. two axes), indicates that the two items are oriented in a generally crosswise orientation. The items need not cross at right angles to be in transverse relation, but in particular embodiments, the two items cross at an angle of greater than about 45 degrees and less than about 135 degrees, and in more typical embodiments, the angle is greater than about 75 degrees and less than about 105 degrees.
As shown in
The term “passage”, as used in this application herein with respect to the second passage, means “ion guide” in any form whatsoever. It is possible that the passage is of such short length relative to the opening diameter that it may be called an orifice. Other ion guides, including capillaries, which are or may come to be used, can operate in the invention. The configurations herein are not meant to be restrictive, and those skilled in the art will see possible configurations not specifically mentioned here but which are included in the teaching and claims of this invention. In particular, the voltages mentioned herein are typically measured relative to ground unless specifically mentioned otherwise. The nozzle (or spray needle) is assumed to be connected to ground unless otherwise specifically indicated. One of ordinary skill in the art of mass spectroscopy will realize that the voltages may be measured relative to various other points without altering the basic functionality of the system. Further, it will be readily apparent to the ordinarily skilled practitioner of the art that the apparatus may be operated to yield anions or cations, and the disclosure of operation for one is generally sufficient to describe operation for the other.
Referring now to the Figures,
The auxiliary electrode 140 is a conductive circular plate made of, for instance, stainless steel, gold platted steel, brass or other chemically stable surface. The diameter of the plate is about in the same dimension as the inlet 112, for instance 5 to 15 mm and more typically 6 to 10 mm. The thickness of electrode is more or less arbitrary, but typically about 1 mm.
The auxiliary electrode 140 is placed about 4 to 20 mm away from the inlet 112 depending on the size of the nozzle 134. For a nanoliter spray tip, the distance is about 4 to 12 mm and more typically 5 to 10 mm. The nozzle 134 is about in the center of the auxiliary electrode 140 and inlet 112, preferably slightly closer to the inlet 112. For instance, if the distance between the inlet 112 and auxiliary electrode 140 is 7 mm, the distance between the nozzle 134 and the inlet 112 is about 3 mm, or the distance between the nozzle and the auxiliary electrode 140 is 4 mm.
The voltage applied to the auxiliary electrode 140 is about the same as that applied to the inlet 112. The voltage may be more positive or slightly more negative. In case it is more positive, it typically does not exceed 50% of the inlet voltage and in case more negative, not exceed 10%. For instance, for positive ion detection, a voltage of −2000 V is applied to the inlet 112, the voltage applied to the auxiliary electrode 140 will not be higher than −1000 V and not lower than −2200 V. This rule is also applied to the negative ion, but with opposite polarity.
In the embodiment shown in
Further Examples:
The auxiliary electrode 140 can be made with various shapes in the proper dimension providing similar or slightly modified electrical fields for electrospray. The electrode of the each shape is optimized in its geometric and electric dimension to obtain optimal spray. In
In a further embodiment, a planar auxiliary electrode 140 is placed perpendicular and opposite to the nozzle 134 as shown in
In some embodiments, the auxiliary electrode is disposed such that an angle of less than 15 degrees is subtended between the auxiliary electrode and the interface axis, said angle having its vertex at the inlet. In other embodiments, the auxiliary electrode is disposed such that an angle of less than 15 degrees is subtended between the auxiliary electrode and the nozzle axis, said angle having its vertex at the exit orifice.
The auxiliary electrode in some embodiments is a disk electrode; in other embodiments, the auxiliary electrode is a pin electrode; and in still other embodiments, the auxiliary electrode is an ‘L’ shaped electrode. In yet another embodiment, the auxiliary electrode has a convex cylindrical surface having a central axis, the central axis parallel to the nozzle axis.
The invention further provides a method of converting a liquid solute sample into ionized molecules. The method includes introducing a liquid solute sample into an apparatus according to the invention and applying an interface voltage to the interface and an auxiliary voltage to the auxiliary electrode. The applied interface voltage and auxiliary voltage are sufficient to subject the sample at the exit orifice and the inlet to an electric field, whereby the sample is discharged from the exit orifice in the form of droplets, the electric field effective to produce ionized molecules from the droplets and urge the ionized molecules towards the inlet. In particular embodiments, the method further includes applying a housing potential to the housing, wherein the voltage on the housing is about 80% to about 100% of the voltage on the inlet of the interface; in a particular embodiment, the voltage applied to the housing and the inlet is from the same voltage source, e.g. the interface source.
The practice of the present invention will employ, unless otherwise indicated, conventional techniques of synthetic organic chemistry, biochemistry, molecular biology, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.
The Examples herein are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to perform the methods and use the compositions disclosed and claimed herein. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc.) but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C. and pressure is at or near atmospheric. Standard temperature and pressure are defined as 20° C. and 1 atmosphere.
While the foregoing embodiments of the invention have been set forth in considerable detail for the purpose of making a complete disclosure of the invention, it will be apparent to those of skill in the art that numerous changes may be made in such details without departing from the spirit and the principles of the invention. Accordingly, the invention should be limited only by the following claims.
All patents, patent applications, and publications mentioned herein are hereby incorporated by reference in their entireties.