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1 enables the separation of isotopologues with ion mobility spectrometry.
2 e high-performance liquid chromatography and ion mobility spectrometry.
3 is and resolution of isomers, including from ion mobility spectrometry.
4 sequently analyzed by means of tandem MS and ion mobility spectrometry.
5 ime scales, and can readily be combined with ion mobility spectrometry.
6 e investigated using electrospray ionization ion mobility spectrometry.
7 l information for spectral interpretation in ion mobility spectrometry.
8 als and analyzed using multicapillary column ion-mobility spectrometry.
12 imination of oligosaccharide isomers by both ion mobility spectrometry and tandem mass spectrometry.
13 ng or steering beams of charged particles in ion mobility spectrometry and time-of-flight mass spectr
14 te the use of coupled liquid chromatography, ion mobility spectrometry, and mass spectrometry (LC-IMS
18 ing wave, trapped, and high-field asymmetric ion mobility spectrometry, are evaluated for their abili
19 This work demonstrates the first example of ion mobility spectrometry at pressures above ambient.
20 chains of insulin, were characterized using ion mobility spectrometry-based mass spectrometry and at
21 vitamin D from its inactive epimer; however, ion mobility spectrometry can distinguish the epimer pai
23 ation of OzID in a high-pressure region, the ion-mobility spectrometry cell, of a contemporary quadru
24 his article introduces the concept of chiral ion mobility spectrometry (CIMS) and presents examples d
26 eparation and analysis of the products using ion mobility spectrometry coupled to conventional mass s
27 by liquid chromatography with traveling-wave ion mobility spectrometry coupled to high resolution mas
28 rpentine ultralong path and extended routing ion mobility spectrometry coupled to mass spectrometry (
29 rk explores the capabilities of differential ion mobility spectrometry coupled to tandem mass spectro
33 s tissue extraction followed by differential ion mobility spectrometry (DMS) mass spectrometry for an
34 estion (PD) is demonstrated using drift tube ion mobility spectrometry (DTIMS) coupled with linear io
35 ) can be directly calculated from drift tube ion mobility spectrometry (DTIMS) data, measurements mad
36 rtcomings of atmospheric pressure drift tube ion mobility spectrometry (DTIMS) is its intrinsically l
37 rrors were all within 1-2% of the drift tube ion mobility spectrometry (DTIMS) measurements, with low
41 increase in applications of native mass and ion mobility spectrometry, especially for the study of p
44 lity to mass spectrometry makes differential ion mobility spectrometry (FAIMS) a powerful tool for is
45 d intensity (E) in field asymmetric waveform ion mobility spectrometry (FAIMS) analyses was doubled t
46 Microchip-based field asymmetric waveform ion mobility spectrometry (FAIMS) analyzers featuring a
47 miniaturized high-field asymmetric waveform ion mobility spectrometry (FAIMS) and mass spectrometry
48 Strong orthogonality between differential ion mobility spectrometry (FAIMS) and mass spectrometry
51 trategy using high-field asymmetric waveform ion mobility spectrometry (FAIMS) coupled to the Orbitra
52 lication of a high-field asymmetric waveform ion mobility spectrometry (FAIMS) device as an interface
53 d aerodynamic high-field asymmetric waveform ion mobility spectrometry (FAIMS) device into the phosph
54 a chip-based high-field asymmetric waveform ion mobility spectrometry (FAIMS) device to image metabo
55 We show that high-resolution differential ion mobility spectrometry (FAIMS) employing helium-rich
57 e benefits of high field asymmetric waveform ion mobility spectrometry (FAIMS) for mass spectrometry
58 e benefits of high-field asymmetric waveform ion mobility spectrometry (FAIMS) for proteomics have be
59 coupled with high field asymmetric waveform ion mobility spectrometry (FAIMS) for top-down protein a
60 key application of field asymmetric waveform ion mobility spectrometry (FAIMS) has been in selectivel
62 ass spectrometric analysis, field asymmetric ion mobility spectrometry (FAIMS) has previously been us
63 he utility of high-field asymmetric waveform ion mobility spectrometry (FAIMS) in quantitative bioana
65 d to MS via a high-field asymmetric waveform ion mobility spectrometry (FAIMS) interface to evaluate
69 turized ultra high field asymmetric waveform ion mobility spectrometry (FAIMS) is used for the select
71 e coupling of high-field asymmetric waveform ion mobility spectrometry (FAIMS) separation into the LE
74 s, differential or field asymmetric waveform ion mobility spectrometry (FAIMS) was implemented at or
76 lity spectrometry (field asymmetric waveform ion mobility spectrometry (FAIMS)) is emerging as a broa
77 t coupling of high field asymmetric waveform ion mobility spectrometry (FAIMS), also known as differe
78 demonstrate that high field asymmetric wave ion mobility spectrometry (FAIMS), also known as differe
79 eferred to as high-field asymmetric waveform ion mobility spectrometry (FAIMS), is a rapidly advancin
80 I-MS) coupled with field asymmetric waveform ion mobility spectrometry (FAIMS), predictive metabolic
81 itching using high-field asymmetric waveform ion mobility spectrometry (FAIMS), we identified multipl
85 lity spectrometry (field asymmetric waveform ion mobility spectrometry, FAIMS) employing H2/N2 gas mi
86 e states by the new approach of differential ion mobility spectrometry (field asymmetric waveform ion
88 at shows the potential of gas chromatography-ion mobility spectrometry for early detection of ventila
89 s that depend on the drift times measured by ion mobility spectrometry for repeating units released a
90 the continued development and application of ion mobility spectrometry for the distinction and resolu
93 /HS isomers may be resolved by gated-trapped ion mobility spectrometry (gated-TIMS) with negligible s
94 to study the potential of gas chromatography-ion mobility spectrometry (GC-IMS) to differentiate lact
95 The dual separation in gas chromatography-ion mobility spectrometry generates complex multi-dimens
96 ue termed high asymmetric longitudinal field ion mobility spectrometry (HALF-IMS), which allows separ
99 findings allow for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strat
100 cisely localize d-amino acids in peptides by ion mobility spectrometry (IMS) analysis of mass spectro
101 This strategy was developed by combining ion mobility spectrometry (IMS) and collision-induced di
102 trace chemical detection techniques such as ion mobility spectrometry (IMS) and differential mobilit
104 cedure, based on the combined application of Ion Mobility Spectrometry (IMS) and Infrared Spectroscop
106 e analytical separation techniques including ion mobility spectrometry (IMS) and liquid chromatograph
107 T) electrospray ionization (ESI) paired with ion mobility spectrometry (IMS) and mass spectrometry (M
108 ation (vt-ESI) technique in combination with ion mobility spectrometry (IMS) and mass spectrometry (M
109 rature electrospray ionization combined with ion mobility spectrometry (IMS) and mass spectrometry (M
110 y, and their conformations were probed using ion mobility spectrometry (IMS) and Monte Carlo minimiza
112 ncreasingly involve gas-phase separations by ion mobility spectrometry (IMS) and particularly differe
113 qualitative and quantitative capabilities of ion mobility spectrometry (IMS) as a comprehensive and p
114 rrival time distributions (ATDs) recorded by ion mobility spectrometry (IMS) can often be interpreted
118 elationship between the output signal of the ion mobility spectrometry (IMS) detector and the concent
119 ctures for lossless ion manipulations (SLIM) ion mobility spectrometry (IMS) device capable of switch
121 mplexity in the absence of any solvent using ion mobility spectrometry (IMS) followed by MS detection
122 ar gas chromatography (GC) column coupled to ion mobility spectrometry (IMS) has been explored to cla
131 MD) simulations, mass spectrometry (MS), and ion mobility spectrometry (IMS) in positive ion mode.
132 developed for detecting heavy metals via the ion mobility spectrometry (IMS) in the negative mode.
133 owever, both tandem spectrometry (MS(2)) and ion mobility spectrometry (IMS) indicated structural dif
134 o substrates suitable for calibration of the ion mobility spectrometry (IMS) instruments currently de
139 ry within trace detection techniques such as ion mobility spectrometry (IMS) is an area of intense in
141 Native mass spectrometry (MS) coupled with ion mobility spectrometry (IMS) is emerging as an import
142 etection of black powder (BP) by stand-alone ion mobility spectrometry (IMS) is full of challenges.
145 Detection by mass spectrometry (MS) and/or ion mobility spectrometry (IMS) is traditionally difficu
147 ion cross section (CCS) values obtained from ion mobility spectrometry (IMS) measurements were recent
153 F separation fields normally associated with ion mobility spectrometry (IMS) or differential mobility
154 olome of live microglial cells by drift-tube ion mobility spectrometry (IMS) quadrupole time-of-fligh
155 produced can be dispersed again in a second ion mobility spectrometry (IMS) region prior to addition
156 ork, we demonstrate the advantages of adding ion mobility spectrometry (IMS) separation to existing L
157 ributions are extensively compared to recent ion mobility spectrometry (IMS) studies reported in the
158 ect of space charge on the performance of an Ion Mobility Spectrometry (IMS) system becomes more impo
161 xamined employing mass spectrometry (MS) and ion mobility spectrometry (IMS) techniques in combinatio
163 mance liquid chromatography (chip-HPLC) with ion mobility spectrometry (IMS) via fully integrated ele
166 es (extra virgin, virgin and lampante) using Ion Mobility Spectrometry (IMS) was improved by replacin
167 rich gases has recently enabled differential ion mobility spectrometry (IMS) with a resolving power u
172 two-dimensional gas chromatography (GCxGC), ion mobility spectrometry (IMS), and capillary electroph
173 yed a combination of mass spectrometry (MS), ion mobility spectrometry (IMS), and molecular dynamics
176 ns, including isotopomers and isobars, using ion mobility spectrometry (IMS), specifically, the field
178 e, store, and eject ions in conjunction with ion mobility spectrometry (IMS), which elevated the char
179 itional gas-phase separation dimension using ion mobility spectrometry (IMS), which is a method in wh
181 ically around a few microseconds or less for ion mobility spectrometry (IMS)-based separations on the
183 ion allows for comparison of two-dimensional ion mobility spectrometry (IMS)-MS data sets in a pixel-
197 ncreasing the efficiency of multidimensional ion mobility spectrometry (IMS-IMS) measurements (as def
200 oices include liquid chromatography (LC) and ion-mobility spectrometry (IMS), in which separation tak
204 neumonia we determined if gas chromatography-ion mobility spectrometry is able to detect 1) ventilato
209 where mass-selected structural studies using ion-mobility spectrometry mass spectrometry (IMS-MS) cou
210 ay ionization-high field asymmetric waveform ion mobility spectrometry-mass spectrometry (ESI-FAIMS-M
211 for interrogation by electrospray ionization-ion mobility spectrometry-mass spectrometry (ESI-IMS-MS)
213 ated as a shift reagent for multidimensional ion mobility spectrometry-mass spectrometry (IMS-IMS-MS)
218 trospray ionization and analyzed by combined ion mobility spectrometry-mass spectrometry (IMS-MS) tec
219 we report a high-throughput method based on ion mobility spectrometry-mass spectrometry (IMS-MS) tha
221 inum coordination, have been investigated by ion mobility spectrometry-mass spectrometry (IMS-MS).
222 es in multidimensional liquid chromatography-ion mobility spectrometry-mass spectrometry (LC-IMS-MS)
223 esults suggested that paper spray ionization-ion mobility spectrometry-mass spectrometry (PSI-IMS-MS)
224 ere, we assess the ability of tandem-trapped ion mobility spectrometry-mass spectrometry (tandem-TIMS
226 phy (LC) followed by high resolution trapped ion mobility spectrometry-mass spectrometry (TIMS-MS) wa
228 en/deuterium back exchange (HDX) and trapped ion mobility spectrometry-mass spectrometry (TIMS-MS).
229 shown here experimentally by traveling wave ion mobility spectrometry-mass spectrometry (TWIMS-MS) o
230 amyloid intermediates using a combination of ion mobility spectrometry-mass spectrometry and gas-phas
232 hormone as a model protein, the potential of ion mobility spectrometry-mass spectrometry as a tool to
233 thermore, we demonstrate the ease with which ion mobility spectrometry-mass spectrometry can guide th
234 loride ions using a novel technique coupling ion mobility spectrometry-mass spectrometry with infrare
236 es of molecular species using traveling wave ion-mobility spectrometry-mass spectrometry (TWIMS-MS) i
237 taneously using a prototype multidimensional ion mobility spectrometry/mass spectrometry spectrometry
239 termined by a novel, portable, field-capable ion mobility spectrometry method described herein and en
240 gnals were detected by multicapillary column ion-mobility spectrometry, of which 44 could be identifi
241 s challenge, we developed a drift tube-based ion mobility spectrometry-Orbitrap mass spectrometer (IM
242 Oversampling Selective Accumulation Trapped Ion Mobility Spectrometry (OSA-TIMS) when coupled to ult
247 loid-beta oligomers by mass spectrometry and ion mobility spectrometry, revealing functionally releva
248 present work, selected accumulation trapped ion mobility spectrometry (SA-TIMS) is coupled to Fourie
249 que combination of preseparation and trapped ion mobility spectrometry separation in the negative ion
251 ein, we report on the use of high-resolution ion mobility spectrometry separations in structures for
252 powder were also analyzed by two stand-alone ion mobility spectrometry systems, yielding an average r
253 n using electrospray ionization-differential ion mobility spectrometry-tandem mass spectrometry (ESI-
255 lity to separate isotopes by high-resolution ion mobility spectrometry techniques is considered as a
257 the peptide-crown complexes are separated by ion mobility spectrometry, the ions can be collisionally
259 el analytical method based on hybrid trapped ion mobility spectrometry-time-of-flight mass spectromet
262 recursor ions are accumulated in the trapped ion mobility spectrometry (TIMS) cells and separated acc
263 the Traveling Wave (TWIMS), and the Trapped Ion Mobility Spectrometry (TIMS) coupled to mass spectro
264 light (Q-TOF) mass spectrometer with trapped ion mobility spectrometry (TIMS) enables a >250% increas
267 on liquid chromatography coupled to trapped ion mobility spectrometry (TIMS) for separation and tand
268 the combination of MALDI-2 with the trapped ion mobility spectrometry (TIMS) functionality of the in
273 which we have termed Transversal Modulation Ion Mobility Spectrometry (TM-IMS), utilizes only electr
274 The potential of a Transversal Modulation Ion Mobility Spectrometry (TMIMS) instrument for protein
275 troduced based on the transversal modulation ion mobility spectrometry (TMIMS) technique, which provi
279 we describe how to integrate traveling-wave ion mobility spectrometry (TWIMS) into traditional LC-MS
281 rift time determination using traveling wave ion mobility spectrometry (TWIMS) of poorly resolved or
282 CCS calibration accuracy with traveling wave ion mobility spectrometry (TWIMS) separations in structu
283 the more recently introduced traveling wave ion mobility spectrometry (TWIMS) technique are usually
284 Although the hyphenation of traveling-wave ion mobility spectrometry (TWIMS) with high-resolution q
285 (UPLC-IM-TOFMS), integrating traveling wave ion mobility spectrometry (TWIMS) with negative electros
287 pid screening method based on traveling-wave ion-mobility spectrometry (TWIMS) combined with tandem m
288 llisions in PF IMS compared to uniform field ion mobility spectrometry (UF IMS) for equivalent operat
290 Here, using mass spectrometry coupled with ion mobility spectrometry, we demonstrate the conformati
297 The combination of field asymmetric waveform ion mobility spectrometry with liquid chromatography-mas
299 onstrate the application of corona discharge ion mobility spectrometry with orthogonal acceleration t
300 rformance is compared to conventional linear ion mobility spectrometry, with and without a radioactiv