ライフサイエンスコーパス: iontophoresis

1 set was faster than could be reproduced with iontophoresis.

2 nts of human interstitial fluid extracted by iontophoresis.

3 Rabbits were killed 5 days after iontophoresis.

4 f magnitude greater than that seen following iontophoresis.

5 en delivered across the skin with the aid of iontophoresis.

6 ty of concentrations delivered by controlled iontophoresis.

7 h duration was evaluated following histamine iontophoresis.

8 7 mug/g in epi-on, and 15.0 +/- 5.1 mug/g in iontophoresis.

9 olonged recovery of barrier disrupted due to iontophoresis.

10 ites of mature adult-born GCs following NMDA iontophoresis.

11 izable groups to render propofol amenable to iontophoresis.

12 e immediate vicinity of the neurons by micro-iontophoresis.

13 eness of activating presynaptic receptors by iontophoresis.

14 ock adrenergic function, was administered by iontophoresis.

15 ically, by local intradermal injection or by iontophoresis.

16 Application of iontophoresis (0.5mA/cm(2)) to SCD-propofol solution enh

17 Prolonged AMPH iontophoresis (2-3 min; 5-30 nA) inhibited both spontane

18 crease in the average pain rating during ATP iontophoresis (22.7 +/- 3.1) compared with pre-capsaicin

19 (alpha) in vivo has been tetramethylammonium iontophoresis, a technically challenging method develope

20 des that had been transdermally delivered by iontophoresis across hairless mouse skin.

21 In this study, we investigated whether iontophoresis across the intestine can be utilized to im

22 vidual cells with Lucifer Yellow dextran via iontophoresis and by analyzing patterns of fluorescence

23 Iontophoresis and pressure ejection were employed to loc

24 on, agonists and antagonists were applied by iontophoresis and single neurone activity was recorded e

25 To study this, we use glutamate iontophoresis and synaptic stimulation to position pairs

26 ncentration in samples collected via reverse iontophoresis and the results compared well to those obt

27 ng pain, which began within 20 s of starting iontophoresis and was maintained for several minutes.

28 f solvent into the skin, which is induced by iontophoresis and which contributes significantly to the

29 reactivity, using laser Doppler imaging with iontophoresis, and arterial stiffness, using pulse wave

30 hat transscleral iontophoresis, transcorneal iontophoresis, and intravitreal injection deliver ions t

31 compare transscleral and transcorneal ocular iontophoresis, and monitor the distribution of a probe i

32 Amethocaine, tetracaine, iontophoresis, and the S-caine patch, a product on the h

33 An iontophoresis approach was implemented to explore the ef

34 cular reactivity (laser Doppler imaging with iontophoresis), arterial stiffness (pulse wave velocity

35 cular reactivity (laser Doppler imaging with iontophoresis), arterial stiffness [pulse wave velocity,

36 presents a proof of principle for intestinal iontophoresis as a novel method for oral protein deliver

37 eyes) were included; 11 studies compared non-iontophoresis-assisted transepithelial with epithelium-o

38 noparticles, and integrated with modules for iontophoresis-based sweat induction, microfluidic sweat

39 hree types of stimuli (electrical, glutamate iontophoresis, bath-applied kainate) produced biphasic f

40 popular in the clinical setting (pilocarpine iontophoresis being a prominent exception).

41 ed to reactivate by transcorneal epinephrine iontophoresis, but others were not induced.

42 sing conventional wrist-strapped devices and iontophoresis can be cumbersome, particularly for infant

43 ntal fluorescent profiles to demonstrate how iontophoresis can generate near-uniform concentration di

44 carboplatin delivered by Coulomb-controlled iontophoresis (CCI; 14 mg/mL carboplatin, 5.0 mA/cm(2),

45 rget sites of ion delivery in the eye during iontophoresis, compare transscleral and transcorneal ocu

46 rinic M1 receptors (M1Rs) in the dlPFC using iontophoresis coupled with single-unit recordings from a

47 , but this effect can easily be caused by an iontophoresis current artifact.

48 nstant current transscleral and transcorneal iontophoresis (current density, 10 mA/cm(2)) was perform

49 lls) were randomized to EGP-437 delivered by iontophoresis (days 0 and 7) or self-administered PA 1%

50 ered the ion into the vitreous, transcorneal iontophoresis delivered the ion into the anterior chambe

51 Whereas transscleral iontophoresis delivered the ion into the vitreous, trans

52 T-ionto CL was performed using an iontophoresis device with dextran-free 0.1% riboflavin-5

53 Patients were randomized into 1 of 4 iontophoresis dose groups (1.6, 4.8, 10.0, or 14.0 mA-mi

54 Stressomic integrates iontophoresis-driven sweat extraction with bursting valv

55 ACh iontophoresis either excited or inhibited striatal and a

56 Carbon fibre-based reverse iontophoresis electrodes were fabricated and used instea

57 hloride concentrations are unperturbed, GABA iontophoresis elicits spikes and increases excitability

58 Transdermal administration by iontophoresis (enhanced transport via the skin using the

59 Transscleral and transcorneal iontophoresis experiments were conducted with the electr

60 In vitro reverse iontophoresis experiments were performed to extract Li(+

61 ate for the first time power generation from iontophoresis extracts obtained from pig skin.

62 Subsequently, with paired recordings and iontophoresis, first at spatially aligned site-pairs in

63 acetylcholine (ACh) (endothelium dependent) iontophoresis, flicker-light-induced retinal vasodilatat

64 electrophoresis for controllable release and iontophoresis for directional penetration.

65 ntly delivered into and across the sclera by iontophoresis for drug delivery.

66 Iontophoresis-generated sweat pH from regions of activel

67 earable-like technology integrates a reverse iontophoresis glucose extraction capability with an enzy

68 up was about 2-fold greater than that of the iontophoresis group (50.5 +/- 5.3 mug/g and 23.6 +/- 2.5

69 al enhancers, noncavitational ultrasound and iontophoresis have also resulted in clinical products; t

70 While pressure ejection and iontophoresis have been used to deliver picoliter volume

71 Corneal cross-linking transepithelial iontophoresis imbibition yielded greater and deeper ribo

72 laser-Doppler flowmetry (LDF) combined with iontophoresis in 15 low-flow POTS patients, 17 normal-fl

73 ed extracellular single-unit recordings with iontophoresis in awake animals.

74 ity, single-unit recording was combined with iontophoresis in awake, unrestrained rats.

75 Adaptation of adjunct strategies (e.g., iontophoresis in conjunction with CPE) has shown signifi

76 for sustained drug delivery in transscleral iontophoresis in vitro.

77 ned electrophysiologically and marked by dye iontophoresis in vivo.

78 -437 (dexamethasone phosphate formulated for iontophoresis) in patients with noninfectious anterior u

79 NE iontophoresis inhibited spontaneous firing and decreased

80 A wearable and miniaturized iontophoresis interface is an excellent solution to over

81 The challenge remains in devising an iontophoresis interface that can extract sufficient amou

82 ough realizing an electrochemically enhanced iontophoresis interface, integrated in a wearable sweat

83 ability to reactivate following epinephrine iontophoresis into the cornea.

84 Iontophoresis is a promising technology that can substan

85 Iontophoresis is now established as one of the methods o

86 With this information, quantitative iontophoresis is possible for electrochemically inactive

87 ximum increase in calcein fluorescence after iontophoresis is proportional to the aqueous volume into

88 Iontophoresis is the movement of charged molecules in so

89 irment using microneedles (MNs) coupled with iontophoresis (ITP) may broaden the range of drugs suita

90 low-mediated dilatation (FMD), laser Doppler iontophoresis (LDI), and digital volume pulse (DVP).

91 nanoparticulates, liposomes, or transscleral iontophoresis may provide the solution.

92 t-source paradigm, realized in the real-time iontophoresis method using tetramethylammonium, as well

93 onditions, we used the established real-time iontophoresis method with tetramethylammonium (TMA(+)) t

94 A miniaturized carbachol gel-based iontophoresis module autonomously induces localized swea

95 bition with epi-on (n = 3), epi-off (n = 3), iontophoresis (n = 3), and saline exposure (control; n =

96 erm systemic exposure to dexamethasone after iontophoresis; no nonocular systemic corticosteroid-medi

97 odilation in the forearm skin in response to iontophoresis of 1% acetylcholine chloride (Ach) (endoth

98 putative pyramidal cells were attenuated by iontophoresis of 5-HT2A antagonists, which primarily pro

99 ecording of reflectance properties following iontophoresis of a potent vasoconstrictor, noradrenaline

100 es, measured using laser Doppler imaging, to iontophoresis of acetylcholine (ACh) and sodium nitropru

101 n the dorsal foot in response to heating and iontophoresis of acetylcholine (endothelium-dependent) a

102 on, as assessed by laser Doppler imaging and iontophoresis of acetylcholine and localized heating.

103 esponses in the fingers were assessed during iontophoresis of acetylcholine and sodium nitroprusside,

104 ase in skin blood flow induced following the iontophoresis of ACh and to investigate possible contrib

105 ood cell flux (P < 0.001) in response to the iontophoresis of ACh minus the response to ACh vehicle w

106 kin perfusion (P < 0.001) in response to the iontophoresis of ACh minus the response to ACh vehicle w

107 in perfusion (P < 0.001) in response to the iontophoresis of ACh vehicle was significantly inhibited

108 Conversely, iontophoresis of acid over a wide range of skin temperat

109 significantly inhibited the pain induced by iontophoresis of acid, suggesting an involvement of acid

110 Iontophoresis of ACPD had different effects in different

111 hermal burn, and the pain ratings during the iontophoresis of adenosine triphosphate (ATP) and acid.

112 Iontophoresis of alpha4beta2-nAChR agonists also enhance

113 Iontophoresis of alpha4beta2-nAChR agonists increased th

114 activity in cortical layer 2 was silenced by iontophoresis of AMPA and NMDA receptor antagonists.

115 We compared the sweat response to iontophoresis of an alpha-adrenergic agent (phenylephrin

116 of NMDARs and AMPARs in working memory using iontophoresis of antagonists in the PFC of monkeys remem

117 Iontophoresis of ATP caused an increase in blood flow, a

118 ation of presynaptic purinergic receptors by iontophoresis of ATP decreased evoked IPSC amplitudes an

119 Persistent iontophoresis of ATP led to desensitization within 12 mi

120 Iontophoresis of ATP produced a higher pain rating than

121 Interictal spikes (IISs) were induced with iontophoresis of bicuculline methiodide in rat neocortex

122 e modulation (IPM) before, during, and after iontophoresis of bicuculline, an antagonist to the inhib

123 Iontophoresis of Ca2+ at various membrane potentials all

124 Following iontophoresis of CtB into the PVN, retrogradely labeled

125 ter infection, rabbits received transcorneal iontophoresis of epinephrine.

126 and spontaneous firing could be inhibited by iontophoresis of ergometrine (9/10 cells), sumatriptan (

127 ning retrogradely labeled cells following LC iontophoresis of Fluoro-Gold and anterograde LC labeling

128 puts, single-unit recording was coupled with iontophoresis of GLU and GABA in rats under two conditio

129 Iontophoresis of glutamate NMDA receptor agonists increa

130 tivity also decreases the response to direct iontophoresis of glutamate onto postsynaptic receptors.

131 lectrodes combined with pressure ejection or iontophoresis of ions from a micropipette to quantify di

132 ny change in intracellular calcium following iontophoresis of l-aspartate or two-photon uncaging of g

133 Iontophoresis of l-aspartate, an NMDAR agonist, onto bas

134 Iontophoresis of L-glutamate or vasopressin into the vic

135 In ambulant rats, iontophoresis of low concentrations of dopamine (DA) enh

136 ses to the chemoreflex excitation and direct iontophoresis of N-methyl-D-aspartic acid (NMDA) but wit

137 arbors in layer IV of area 17 were filled by iontophoresis of Phaseolus lectin into lamina A of the l

138 (cRCF) was recorded in dorsal finger during iontophoresis of phenylephrine (PE) or clonidine (0.5 mm

139 logical methods and was visibly marked using iontophoresis of pontamine sky blue dye.

140 We found that transdermal iontophoresis of protons consistently caused moderate pa

141 We used a novel technique, iontophoresis of protons, to investigate acid-induced pa

142 essed this issue by examining the effects of iontophoresis of selective receptor ligands on prefronta

143 lcium imaging, extracellular recordings, and iontophoresis of serotonin (5-HT) receptor antagonists i

144 in perfusion (P < 0.001) in response to the iontophoresis of SNP vehicle was significantly inhibited

145 In addition, iontophoresis of the alpha-2 agonist clonidine, footshoc

146 archistriatum were therefore investigated by iontophoresis of the anterograde tracer Phaseolus vulgar

147 on-specific effect of the drug, since (1) co-iontophoresis of the D2 antagonist YM 09151-2 antagonize

148 ropic glutamate agonist ACPD was examined by iontophoresis of the drugs close to the cell body.

149 Inactivating a single barrel by iontophoresis of the GABA(A) agonist muscimol abolished

150 Reactivating a single barrel by iontophoresis of the GABA(A) antagonist bicuculline whil

151 Iontophoresis of the GABAA agonist muscimol (MUS) into t

152 l-N (G)-nitro-l-arginine methyl ester, while iontophoresis of the NO donor sodium nitroprusside elimi

153 nd LC stimulation mimicked the effects of NE iontophoresis on spontaneous activity.

154 ts demonstrate the importance of the reverse iontophoresis operation and validate the sensor specific

155 Masking was maintained with placebo iontophoresis or eye drops.

156 Likewise, repetitive iontophoresis (or puffs) of glutamate (or AMPA) onto the

157 r, and sweating in response to acetylcholine iontophoresis over the calf and forearm.

158 ion in the aqueous and vitreous humor after iontophoresis, passive delivery, and intravitreal inject

159 Surprisingly, the elevated dye iontophoresis persists in shaking B mutants that elimina

160 ly unexpected and highly robust neuronal dye iontophoresis phenotype in the well mapped giant fiber (

161 le of autonomous sweat induction at rest via iontophoresis, precise microfluidic sweat sampling contr

162 The iontophoresis process involves delivery of stimulating a

163 Iontophoresis produced no meaningful increase in deliver

164 o using insulin-loaded mucoadhesive patches, iontophoresis produced profound hypoglycemia (63% blood

165 or agonist, applied by either superfusion or iontophoresis, produced an atropine-sensitive increase o

166 e during and after iontophoresis, such as in iontophoresis protocol and device testing.

167 With the present transscleral iontophoresis protocol, the ion penetrated the sclera an

168 that had compared transepithelial CXL using iontophoresis provided no conclusive evidence of an adva

169 smic and occurs due to a highly elevated dye iontophoresis rate.

170 ectrode system for ISF extraction by reverse iontophoresis (RI), a printed three-electrode amperometr

171 nvestigation indicates that the tattoo-based iontophoresis-sensor platform holds considerable promise

172 sweat sampling for over 2 days from a single iontophoresis session, eliminating the need for physical

173 Understanding how FMRP regulates iontophoresis should reveal new molecular factors underp

174 Five hours post-iontophoresis, sites were irradiated with broad-band yel

175 ion was measured before and during carbachol iontophoresis stimulated accommodation, a total of seven

176 probe compounds in the eye during and after iontophoresis, such as in iontophoresis protocol and dev

177 transepithelial corneal cross-linking using iontophoresis (T-ionto CL) and standard corneal cross-li

178 During iontophoresis, the current delivered into the eye was mo

179 resolving perhaps the greatest limitation of iontophoresis, the inability to determine the concentrat

180 For transcorneal iontophoresis, the ion penetrated the cornea and filled

181 lutinin and cholera toxin B were injected by iontophoresis through a single glass micropipette and de

182 circuit and battery to delivery this drug by iontophoresis through the surface of the skin, microflui

183 esulted in clinical products; the ability of iontophoresis to control delivery rates in real time pro

184 Here we have used iontophoresis to deliver ATP to the forearm skin of volu

185 investigational PCA transdermal system using iontophoresis to deliver fentanyl provided postsurgical

186 We used iontophoresis to eject small amounts of glutamate recept

187 We used single-unit recording coupled with iontophoresis to examine impulse activity and responses

188 This study used glutamate iontophoresis to identify regions that may be involved i

189 lied to a site pretreated with bretylium via iontophoresis to inhibit noradrenergic neurotransmission

190 Single-unit recording was combined with iontophoresis to monitor basal impulse activity of dorsa

191 With MRI, it was shown that transscleral iontophoresis, transcorneal iontophoresis, and intravitr

192 Forty of 42 randomized patients received an iontophoresis treatment in 1 qualifying eye and complete

193 zero within 28 days, after only receiving 1 iontophoresis treatment.

194 Iontophoresis uses a current to eject solution from the

195 Iontophoresis uses electricity to deliver solutes into l

196 To address this, a method called controlled iontophoresis was developed which employs a carbon-fiber

197 rovascular reactivity to local acetylcholine iontophoresis was measured.

198 Afterwards histamine iontophoresis was performed and skin blood flow and itch

199 cy was established, transcorneal epinephrine iontophoresis was performed.

200 Moreover, NMDA iontophoresis was sufficient to induce the formation of

201 Using iontophoresis, we demonstrated that ET-1 is a potent, pa

202 Using iontophoresis, we developed a rapid and quantifiable sys

203 The current pathways during iontophoresis were mainly from the electrode into the ey

204 -200 ms) activation of mGluRs with aspartate iontophoresis were suppressed by superfusion of agonists

205 es above the pore opening is observed during iontophoresis, which is a consequence of the separation