ライフサイエンスコーパス: electrospray

1 pared with those obtained by direct infusion electrospray.

2 ating problems with electric fields, such as electrosprays.

3 chain omega-3 polyunsaturated fatty acids by electrospraying.

4 techniques, encompassing electrospinning and electrospraying, allow the generation of fibres and part

5 that were analyzed in positive and negative electrospray and the diastereoisomers ephedrine and pseu

6 Multiple modes of atomization in electrosprays are affected by viscosity, surface tension

7 We have developed an electrospray-assisted device for quantitative low-volume

8 t amount of sample and from that same tip an electrospray can be directed into a mass spectrometer.

9 nformation space of any molecule that can be electrosprayed can now be explored.

10 y and oxidative stability of fish oil-loaded electrosprayed capsules were studied by Electron Spin Re

11 Electrosprayed capsules with dextran as main biopolymer

12 es, was studied by mobility measurements via electrospray charge reduction with a differential mobili

13 Different electrospray conditions were tested and the morphology a

14 Electrospray deposition (ESD) applies a high voltage to

15 In this work electrospray deposition (ESD) has been exploited as a no

16 process for micro-coatings, a self-limiting electrospray deposition (SLED) method has recently been

17 Gas-phase electrophoresis employing a nano-electrospray differential mobility analyzer (nES DMA), a

18 onditions is formed by clustering inside the electrospray droplet, but <=5.6% and ~0.6% of serine exi

19 on of organic solvents strongly enhanced the electrospray efficiency in microflow-LC-MS experiments a

20 cal contact, and a monolithically integrated electrospray emitter was developed.

21 ed at the interface of the Taylor cone in an electrospray emitter with a large orifice, thus allowing

22 lity spectrometry (IMS) via fully integrated electrospray emitters is introduced.

23 Electrospraying (ES) dissolved viral particles, followed

24 data analysis pipelines for deconvolution of electrospray (ESI) mass spectra containing multiple char

25 olymers by suitable conventional methods and electrospraying for all polymers.

26 ion, and co-/multi-axial electrospinning and electrospraying) for the development of peptide and prot

27 s because it measures and separates proteins electrosprayed from solution on the basis of charge and

28 suspect analyses with liquid chromatography/electrospray/high-resolution mass spectrometry (LC/ESI/H

29 overcome some of these limitations based on electrospray hyphenated with Quadrupole Orbitrap mass sp

30 d as an additive to the sheath liquid of the electrospray interface (ESI), generated a highly efficie

31 mino acids were directly introduced into the electrospray interface of a trapped ion mobility-mass sp

32 ges were collected at the Taylor cone of the electrospray interface, enabling simultaneous and robust

33 are isolated by mass-selective, soft-landing electrospray ion beam deposition and imaged by low-tempe

34 nding graphene were prepared by soft-landing electrospray ion beam deposition, which allows chemical-

35 nfirmed by circular dichroism, (1)H NMR, and electrospray ion mobility-mass spectrometry studies.

36 Using native nano-electrospray ionisation ion mobility-mass spectrometry (

37 Desorption electrospray ionisation mass spectrometry (DESI-MS) can

38 maintains its activity after undergoing the electrospray ionisation process and deposition and the f

39 on chromatography, and liquid chromatography-electrospray ionisation tandem mass spectrometry (LC-ESI

40 (electron impact-EI) and ambient ionisation (electrospray ionisation-ESI) techniques were also examin

41 Desorption electrospray ionisation-mass spectrometry imaging (DESI-

42 solid-phase dispersion (DVUA-MSPD) and UHPLC-electrospray ionization (+)-quadrupole time-of-flight ma

43 cal imaging of small molecules by desorption electrospray ionization (DESI) - MS of a complete swine

44 erstate the tremendous utility of desorption electrospray ionization (DESI) and its various configura

45 er desorption ionization (MALDI), desorption electrospray ionization (DESI) and secondary ion mass sp

46 Here, we apply desorption electrospray ionization (DESI) mass spectrometry (MS) im

47 the use of a HT platform based on desorption electrospray ionization (DESI) MS for the label-free stu

48 ntation of this method for online desorption electrospray ionization (DESI) MS imaging of FA isomers

49 ew chemical imaging capability in desorption electrospray ionization (DESI) MSI, which enables cell-t

50 Desorption electrospray ionization (DESI), easy ambient sonic-spray

51 In this study, desorption electrospray ionization (DESI)-mass spectrometry (MS) im

52 Desorption electrospray ionization (DESI)-MSI defined regions of a

53 the soft ionization capability of extractive electrospray ionization (EESI) and the ultrahigh mass re

54 metal particles in situ using an extractive electrospray ionization (EESI) source coupled to a high-

55 inities correlate with stronger responses in electrospray ionization (ESI(-)) and longer retention ti

56 rmance liquid chromatography (UPLC)/negative electrospray ionization (ESI(-))/quadrupole time-of-flig

57 To facilitate electrospray ionization (ESI) and produce high-quality m

58 However, conventional native electrospray ionization (ESI) can disrupt labile interac

59 o the gas phase from charged droplets during electrospray ionization (ESI) continue to be controversi

60 sted laser desorption ionization (MALDI) and electrospray ionization (ESI) for both spatial imaging a

61 Using electrospray ionization (ESI) Fourier transform ion cycl

62 ze the internal energies of ions produced by electrospray ionization (ESI) have chiefly relied upon b

63 Electrospray ionization (ESI) high resolution accurate m

64 ed to high-resolution mass spectrometry with electrospray ionization (ESI) in negative mode for the c

65 Electrospray ionization (ESI) in positive mode yielded s

66 Electrospray ionization (ESI) in-source fragmentation (I

67 nstrument includes a dual polarity high-flux electrospray ionization (ESI) interface, a tandem electr

68 the self-aspiration process intrinsic of the electrospray ionization (ESI) interface.

69 Electrospray ionization (ESI) is often affected by coron

70 parameters that influence the sensitivity of electrospray ionization (ESI) mass spectrometry.

71 orr) to significantly enhance performance in electrospray ionization (ESI) MS.

72 Electrospray ionization (ESI) operating in the negative

73 ate the utility of variable-temperature (vT) electrospray ionization (ESI) paired with ion mobility s

74 The nonlinear signal response of electrospray ionization (ESI) presents a critical limita

75 med in the heating capillary of the modified electrospray ionization (ESI) source, while for MALDI im

76 solution produce higher charge states during electrospray ionization (ESI) than their natively folded

77 myloid assembly process, we have used native electrospray ionization (ESI) together with ion mobility

78 tter, this method is compared to traditional electrospray ionization (ESI) under saline and neat cond

79 Native MS is usually performed by electrospray ionization (ESI) with its soft ionization p

80 atly increase the sensitivity achieved using electrospray ionization (ESI) with MS.

81 he extracts were analyzed by direct infusion electrospray ionization (ESI) with no previous chromatog

82 licates in three different ionization modes (electrospray ionization (ESI)(+), ESI(-), and atmospheri

83 etic organic reaction monitoring largely use electrospray ionization (ESI), or other related atmosphe

84 DOM analysis commonly utilizes electrospray ionization (ESI), while some have implement

85 uefied CO(2) to the mobile phase provided an electrospray ionization (ESI)-friendly and "superchargin

86 , Fourier transform infrared (FTIR) studies, electrospray ionization (ESI)-mass spectra, and Job's pl

87 When metabolites are analyzed by electrospray ionization (ESI)-mass spectrometry, they ar

88 Electrospray ionization (ESI)-MS analysis revealed that

89 in salmon muscle tissue were conducted using electrospray ionization (ESI)-MS/MS in a triple quadrupo

90 gh performance liquid chromatography (UHPLC)-electrospray ionization (ESI)-quadrupole time of flight

91 aching comparable ion abundances to those of electrospray ionization (ESI).

92 nts that modulate the charge acquired during electrospray ionization (ESI).

93 mentation mode in both positive and negative electrospray ionization (ESI).

94 c acid (PDPA) reagent dianions generated via electrospray ionization (ESI).

95 s achieved for continuous ion sources [e.g., electrospray ionization (ESI)].

96 he combination of fiber-based laser ablation electrospray ionization (f-LAESI) with 21 T Fourier tran

97 two soft ionization sources, that is, heated electrospray ionization (HESI) and nano-ESI for the anal

98 , infrared, matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mass spectrometry (

99 ss infrared matrix assisted laser desorption electrospray ionization (IR-MALDESI) mass spectrometry i

100 trate a unique combination of laser ablation electrospray ionization (LAESI) coupled with a 21 tesla

101 photoionization (LAAPPI) and laser ablation electrospray ionization (LAESI) mass spectrometry imagin

102 Infrared (IR) laser ablation-remote-electrospray ionization (LARESI) platform coupled to a t

103 Nanospray desorption electrospray ionization (nano-DESI) and other ambient io

104 The development of nanospray desorption electrospray ionization (nano-DESI) has enabled the robu

105 patial resolution using nanospray desorption electrospray ionization (nano-DESI) mass spectrometry, a

106 aimed to develop and incorporate a secondary electrospray ionization (SESI) setup in combination with

107 chromatography tandem mass spectrometry with electrospray ionization (UHPLC-ESI-MS/MS) method has bee

108 re investigated using a variable temperature electrospray ionization (vt-ESI) technique in combinatio

109 t acquired on a liquid chromatography-heated electrospray ionization [LC-HESI(-)] Orbitrap instrument

110 to study the tautomers of nucleobases using electrospray ionization and anion spectroscopy.

111 rgy deposition is as low as or lower than in electrospray ionization and micropulsed plasma ionizatio

112 spectrometry: negative and positive ion mode electrospray ionization and negative and positive ion mo

113 with other label-free MS methods, including electrospray ionization and solid state MALDI, as well a

114 Electrospray ionization applied to solutions generated u

115 Variable-temperature electrospray ionization combined with ion mobility spect

116 ed-phase liquid chromatography with negative electrospray ionization coupled to either an orbital-tra

117 isomeric trisaccharides were reported using electrospray ionization coupled to trapped ion mobility

118 interaction liquid chromatography, and nano-electrospray ionization coupled with high-resolution tan

119 The CCSs were obtained using a native electrospray ionization drift tube ion mobility-Orbitrap

120 titative with the aid of in silico predicted electrospray ionization efficiencies and this allows dir

121 For the first time, the electrospray ionization efficiency (IE) scales in positi

122 Electrospray ionization emitters with tip sizes between

123 diagnostic ions (DIs) generated in positive electrospray ionization for 57 amino acid standard compo

124 graphy tandem mass spectrometry method using electrospray ionization for the determination of seven m

125 alyzed in positive and negative ion modes by electrospray ionization Fourier transform ion cyclotron

126 izes this high Pu affinity subfraction using electrospray ionization Fourier transform ion cyclotron

127 ion method was combined with direct infusion electrospray ionization Fourier transform-ion cyclotron

128 ultra-high-performance liquid chromatography-electrospray ionization high resolution mass spectrometr

129 ier-transform infrared spectroscopy (FT-IR), electrospray ionization high-resolution accurate-mass ta

130 applying liquid chromatography interfaced to electrospray ionization high-resolution mass spectrometr

131 nal ion chromatography separation coupled to electrospray ionization high-resolution mass spectrometr

132 ect flow injection analysis (FIA) coupled to electrospray ionization high-resolution mass spectrometr

133 d chromatography, detected via negative mode electrospray ionization high-resolution MS, and their fr

134 gh-resolution Q-TOF equipped with ETD and an electrospray ionization interface consisting of a glass

135 In this paper, laser ablation electrospray ionization ion mobility time-of-flight mass

136 Electrospray ionization is the primary interface used to

137 romatography coupled to photodiode array and electrospray ionization mass detectors (UHPLC/PDA/ESI-MS

138 xplores the application of catch-and-release electrospray ionization mass spectrometry (CaR-ESI-MS) f

139 as surrogates for GSLs for catch-and-release-electrospray ionization mass spectrometry (CaR-ESI-MS)-b

140 use of accelerated reactions with desorption electrospray ionization mass spectrometry (DESI-MS) as a

141 phase microextraction (SPME) with desorption electrospray ionization mass spectrometry (DESI-MS) for

142 omponents that adapt a commercial Desorption Electrospray Ionization Mass Spectrometry (DESI-MS) imag

143 ethod using metabolic analysis by desorption electrospray ionization mass spectrometry (DESI-MS) imag

144 Desorption electrospray ionization mass spectrometry (DESI-MS) is a

145 s spectrometry (DART-MS) and direct infusion electrospray ionization mass spectrometry (DI-ESI-MS) we

146 Electrospray ionization mass spectrometry (ESI-MS) analy

147 ir ease of reactant and product detection by electrospray ionization mass spectrometry (ESI-MS) and t

148 A multipronged electrospray ionization mass spectrometry (ESI-MS) appro

149 uce CUPRA-ZYME, a versatile and quantitative electrospray ionization mass spectrometry (ESI-MS) assay

150 al approach, which combines the proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay

151 3) sulfonates are major products detected by electrospray ionization mass spectrometry (ESI-MS) at pH

152 ere we describe capillary microsampling with electrospray ionization mass spectrometry (ESI-MS) for t

153 cRn affinity liquid chromatography (LC) with electrospray ionization mass spectrometry (ESI-MS) in na

154 Electrospray ionization mass spectrometry (ESI-MS) is a

155 e, capillary electrophoresis (CE) coupled to electrospray ionization mass spectrometry (ESI-MS) is im

156 While electrospray ionization mass spectrometry (ESI-MS) is th

157 Herein, we describe the potency of electrospray ionization mass spectrometry (ESI-MS) to st

158 ed (IR) laser ablation sampling with offline electrospray ionization mass spectrometry (ESI-MS) was u

159 ess and the coupling of the IEF syringe with electrospray ionization mass spectrometry (ESI-MS), a BG

160 Electrospray ionization mass spectrometry (ESI-MS), on t

161 ss spectrometry (AEMS) setup for contactless electrospray ionization mass spectrometry (ESI-MS)-based

162 ar magnetic resonance spectroscopy (NMR) and electrospray ionization mass spectrometry (ESI-MS).

163 ter droplets based on direct detection using electrospray ionization mass spectrometry (ESI-MS).

164 SAXS), pair distribution function (PDF), and electrospray ionization mass spectrometry (ESI-MS).

165 roscopic methods, and 3) in the gas phase by electrospray ionization mass spectrometry (ESI-MS).

166 A high-performance liquid chromatography/electrospray ionization mass spectrometry (HPLC-ESI-MS)

167 e squarate radical anion has been studied by electrospray ionization mass spectrometry (including col

168 The PCI-IS assisted liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) me

169 (AMS), high-resolution nanospray desorption electrospray ionization mass spectrometry (nano-DESI/HRM

170 xidation incorporated into the standard nano-electrospray ionization mass spectrometry (nanoESI-MS) w

171 mal titration calorimetry (ITC), native nano-electrospray ionization mass spectrometry (native nESI-M

172 ) and ultraperformance liquid chromatography/electrospray ionization mass spectrometry (UPLC/ESI-MS).

173 Liquid chromatography/negative electrospray ionization mass spectrometry [LC/(-)ESI-MS]

174 xcitation in the deep-UV spectral region and electrospray ionization mass spectrometry after the firs

175 identification of CF by combining desorption electrospray ionization mass spectrometry and a machine-

176 Electrospray ionization mass spectrometry is used extens

177 to 5-fold) and consistent enhancement in the electrospray ionization mass spectrometry signal (ESI-MS

178 e application of EC-ESI/MS (Electrochemistry/ElectroSpray Ionization Mass Spectrometry) in the presen

179 he yeast Kluyveromyces lactis, with nanoflow electrospray ionization mass spectrometry, and mapped in

180 orescence resonance energy transfer-melting, electrospray ionization mass spectrometry, dialysis equi

181 pectroscopy, hydrogen evolution experiments, electrospray ionization mass spectrometry, nuclear magne

182 ich were characterized by X-ray diffraction, electrospray ionization mass spectrometry, UV-vis, (1)H

183 Liquid chromatography with electrospray ionization mass spectrometry-based metabolo

184 des using normal phase liquid chromatography-electrospray ionization mass spectrometry.

185 ultra-high performance liquid chromatography/electrospray ionization mass spectrometry.

186 UV-vis, and fluorescence spectroscopies and electrospray ionization mass spectrometry.

187 ables direct and high-throughput coupling to electrospray ionization mass spectrometry.

188 For the negative electrospray ionization mode (ESI(-)), an RP-18e-HPLC co

189 Through desorption electrospray ionization MS imaging (DESI-MSI), specific

190 , analytical ultracentrifugation, and native electrospray ionization MS, we show that LC8 forms a pre

191 sed approaches such as liquid chromatography/electrospray ionization multiple reaction monitoring mas

192 nted miniaturized reactor with an integrated electrospray ionization needle to a mass spectrometer.

193 The optimized electrospray ionization parameters (high cone gas flow,

194 ultrahigh-performance liquid chromatography electrospray ionization quadrupole-Orbitrap (UHPLC/ESI Q

195 theoretical method to calculate the relative electrospray ionization sensitivities of hydrazones of o

196 nection of multiple microchip outlets to the electrospray ionization source of a mass spectrometer is

197 14 h followed by analysis with a commercial electrospray ionization source that produces larger (~60

198 es are coupled with a temperature-controlled electrospray ionization source to follow the structural

199 lytes in preparation for ionization using an electrospray ionization source.

200 Direct infusion electrospray ionization spectrometry, also known as shot

201 We showed by electrospray ionization spray MS that the Escherichia co

202 ots containing mercury were characterized by electrospray ionization tandem mass spectrometry (ESI-MS

203 matography (HILIC) coupled to a negative-ion electrospray ionization tandem mass spectrometry (ESI-MS

204 analysis of glycerophospholipids via direct electrospray ionization tandem mass spectrometry (ESI-MS

205 liquid chromatography-diode array detection-electrospray ionization tandem mass spectrometry (HPLC-D

206 rformance liquid chromatography coupled with electrospray ionization tandem mass spectrometry.

207 nts were identified by liquid chromatography-electrospray ionization tandem mass spectrometry.

208 The CC extract was characterized by electrospray ionization with high-resolution time-of-fli

209 us morphologies were tested using desorption electrospray ionization with plastic objects coated by 2

210 nvironment (charged nanodroplet generated by electrospray ionization) to the solvent-free peptide ion

211 ed using electrospray ionization, desorption electrospray ionization, and low temperature plasma ioni

212 es, and two coffee types were measured using electrospray ionization, desorption electrospray ionizat

213 aporated and ionized using negative ion mode electrospray ionization, transferred into a linear quadr

214 ulting MALDI-ISD MS data is complementary to electrospray ionization-based MS/MS sequencing readouts,

215 rofile of the pitomba fruit peel and pulp by electrospray ionization-Fourier transform-mass spectrome

216 Using electrospray ionization-high resolution mass spectrometr

217 SSA applications using liquid chromatography/electrospray ionization-high resolution-mass spectrometr

218 host-guest complex has been characterized by electrospray ionization-high-resolution mass spectrometr

219 We demonstrate that desorption electrospray ionization-imaging mass spectrometry (DESI-

220 In this study, we combined PET, desorption electrospray ionization-mass spectrometry (DESI-MS), non

221 rison of IMS with fluorescence detection and electrospray ionization-mass spectrometry (ESI-MS) allow

222 Here, we combine nano-electrospray ionization-mass spectrometry (ESI-MS) and n

223 + H + Na](2+) ions acquired by positive-ion electrospray ionization-mass spectrometry (ESI-MS).

224 ed by high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS)

225 ult of symbiosis, we utilized laser ablation electrospray ionization-mass spectrometry (LAESI-MS) for

226 ments when compared to liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) vi

227 The molecular method PCR/electrospray ionization-mass spectrometry (PCR/ESI-MS) c

228 The recent development of desorption electrospray ionization-mass spectrometry imaging (DESI-

229 by graphitized carbon liquid chromatography-electrospray ionization-mass spectrometry.

230 in-source fragments in liquid chromatography-electrospray ionization-mass spectrometry.

231 LC-electrospray ionization-MS quantification of products an

232 Here, we used desorption electrospray ionization-MSI (DESI-MSI) and bespoke chemo

233 d by ultra-performance liquid chromatography/electrospray ionization-quadruple time of flight mass sp

234 tes from complex biological samples prior to electrospray ionization-tandem mass spectrometry (ESI-MS

235 ed on high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (HPLC-E

236 w elution volumes, nanoliquid chromatography-electrospray ionization-tandem mass spectrometry (nano-L

237 ultrahigh-performance-liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-

238 s and high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry of the

239 cking and confirmed by liquid chromatography-electrospray ionization-tandem mass spectrometry studies

240 n and High-Performance Liquid Chromatography Electrospray Ionization-Tandem Mass Spectrometry.

241 and the mechanism was probed by using online electrospray ionization-tandem mass spectrometry.

242 cyclic forms using capillary electrophoresis-electrospray ionization-time-of-flight mass spectrometry

243 di Sarconi beans performed by flow injection-electrospray ionization-ultrahigh resolution mass spectr

244 are detected by the mass spectrometer after electrospray ionization.

245 mass spectrometry signal suppression during electrospray ionization.

246 mely, multiply charged proteins generated by electrospray ionization.

247 mass spectrometry with positive and negative electrospray ionization.

248 ) and [keto-amino-H] (KAN1(-) ), produced by electrospray ionization.

249 said analytes into the mass spectrometer via electrospray ionization.

250 positive and negative ionization modes using electrospray ionization.

251 RapidFire-mass spectrometry (MS) assay using electrospray ionization.

252 Immobilized peptide arrays and nanoflow LC-electrospray ionization/MS of Nav1.6 reveal potential si

253 h volatile salts at neutral pH combined with electrospray-ionization mass spectrometry (SEC-ESI-MS) i

254 the reaction solution is characterized using electrospray-ionization mass spectrometry combined with

255 ultivation systems with ultrahigh resolution electrospray-ionization mass spectrometry with its exqui

256 y parallel analysis of tissue extracts using electrospray-ionization MS.

257 phase high-performance liquid chromatography-electrospray-ionization tandem mass spectrometry (HPLC-E

258 Electrohydrodynamic spraying (electrospraying) is a versatile tool for liquid atomizat

259 A large fraction of ions observed in electrospray liquid chromatography-mass spectrometry (LC

260 the CB7.FcG(+) complex was also confirmed by electrospray mass spectrometric (ESI MS) experiments.

261 Electrospray mass spectrometry (ESMS) exhibits high-thro

262 ss spectrometry (ICP-MS) and high resolution electrospray mass spectrometry (HR-ESI-MS) allowed the i

263 ere readily identified using direct infusion electrospray mass spectrometry and high-performance liqu

264 ing mode, the electric field degenerates the electrospray mechanism into a microdripping mode that ca

265 In fact, electrospinning and electrospraying methods are promising techniques to fabr

266 lathin release profiles at pH 7.4 with ES100 electrosprayed nanoparticles having the slowest (p < 0.0

267 Overall, ES100 electrosprayed nanoparticles showed the most favourable

268 as-phase as a single-charged species, a nano electrospray (nES) process followed by drying of nanodro

269 Here, a unique electrospraying-netting technique is used to create spid

270 Electrospray of a solution containing hexose and a lithi

271 s compatible with both native and denaturing electrospray, operates with a throughput of up to 15 s/s

272 interaction liquid chromatography (HILIC) - electrospray-OrbitrapMS.

273 This article reviews the effects of electrospraying parameters in production of monodisperse

274 Electrosprayed particles/electrospun fibres are easily p

275 Meanwhile the electrospray process in Type B system is more stable tha

276 To enhance the microflow-LC-MS electrospray process of complex proteomic samples, we te

277 ar imperfections in the DMA response and the electrospraying process suggest that the real width of t

278 Electrospraying produced more favourable results than co

279 Electrospray produces at least one structure that reacts

280 and scaled-up production of electrospun and electrosprayed protein delivery systems are discussed.

281 This electrospray provided the driving force to quantitativel

282 formance liquid chromatography coupled to an electrospray quadrupole time-of-flight mass spectrometer

283 yl dipeptides were identified using infusion electrospray quadrupole time-of-flight mass spectrometry

284 raphy (GC) column are coupled to a secondary electrospray (SESI) ion source, so the adsorption sampli

285 , which is the fundamental reason for Type B electrospray system to perform better.

286 electrode arrangement was applied in Type A electrospray system, and for Type B, an additional ring

287 ets was theoretically calculated for the two electrospray systems.

288 sity was theoretically calculated in the two electrospray systems.

289 acellular Trolox-based liquid chromatography-electrospray-tandem mass spectrometry (LC-ESI-MS/MS) met

290 the recent state of art for electrospinning/electrospraying techniques.

291 We use electrospray to easily functionalize the surface of a su

292 isolated molecules or complexes after their electrospray transfer to the gas phase.

293 ncentration measurement uncertainties is the electrospray transmission efficiency.

294 Finally, our data indicate that when electrosprayed under native conditions, protein ions pos

295 ion volumes using our spray-capillary as the electrospray voltage, capillary ID, and column length we

296 Stable electrospray was achieved through a chemically etched ti

297 In this work an electrohydrodynamic process (electrospray) was used to produce beta-carotene loaded n

298 The encapsulation of broccoli extract, by electrospraying, was performed with the purpose of evalu

299 oline liposomes, within a WPC matrix through electrospraying, were developed and used as delivery veh

300 Electrosprayed WPI-based nanocapsules can be used for th