ライフサイエンスコーパス: QCM

1 QCM application allows rapid trypsin activity evaluation

2 QCM temperature ramping experiments identified domains o

3 QCM-D astonishingly proved to be more sensitive and reli

4 QCM-D monitoring of L-Tym interaction with the aptamer m

5 QCM-D results show that motility is a critical factor in

6 QCM-D results suggest that during adhesion of the hydrop

7 QCM-D sensors functionalized with anti-CD63 antibodies f

8 10(4) M(-1) s(-1) and k(off) = 0.024 s(-1) (QCM-D).

9 The developed 100MHz QCM immunosensor strongly improves sensitivity in biosen

10 s were compared with those reported for 9MHz QCM, analytical parameters clearly showed an improvement

11 The coupling of LSPR nanostructures and a QCM allows optical spectra and QCM resonant frequency sh

12 We have identified a QCM-D signature characteristic of morphological modifica

13 cyanate ([OMIm][SCN]), onto the surface of a QCM-D transducer.

14 It is hypothesized that a QCM can be used in its flow injection mode to monitor th

15 For aPTT we report for the first time that a QCM-D (Quartz Crystal Microbalances with Dissipation) ba

16 Rituximab to the cells were studied using a QCM biosensor.

17 RNA gene was amplified and hybridized with a QCM immobilized probe.

18 acoustic layer thickness (determined with a QCM).

19 A series of additional QCM experiments, in which the effects of CH3OH, CO3(2-),

20 a polydimethylsiloxane wall between adjacent QCM electrodes on a quartz substrate to form inverted-me

21 A are separately immobilized on two adjacent QCM electrodes, which are subsequently blocked with BSA

22 ce glycans were quantified with both AFM and QCM techniques that revealed the presence of various gly

23 As a result, QCM-D and QCM apparatuses can be used to follow NS1 recognition an

24 Combined SPR/EIS and QCM-D/EIS measurements revealed that during EIS the gold

25 range of 0.01-10microgmL(-1) by both QCM and QCM-D.

26 ometric interference spectroscopy (RIfS) and QCM is developed to simultaneously analyze adsorption of

27 uctures and a QCM allows optical spectra and QCM resonant frequency shifts to be recorded simultaneou

28 fies the conventional combination of SPR and QCM and has the potential to be miniaturized for applica

29 In contrast to SPR and QCM-D, repeatable EIS measurements were not possible at

30 As QCM research with cells has been rather limited in succe

31 These studies confirm that cell-based QCMs can detect early events in intrinsic apoptosis and

32 in the range of 0.01-10microgmL(-1) by both QCM and QCM-D.

33 ease of water that can be easily detected by QCM-D.

34 ing process, and their separate detection by QCM-D.

35 geneous deposit by spray coating followed by QCM measurements at multiharmonic frequencies to ensure

36 tion boundary of the shear wave generated by QCM.

37 toward oxygen reduction was investigated by QCM and electrochemical techniques.

38 sitivity and short detection time offered by QCM-based biosensors are attractive for the early detect

39 .5x10(-3) U mL(-1) obtained by the "classic" QCM method).

40 comparison with the anti-H5 antibody coated QCM immunosensor, the hydrogel QCM aptasensor lowered th

41 ency response of a bare and a bilayer-coated QCM-D crystal during linear temperature variation.

42 loped aptamer hydrogels, hydrogel III coated QCM aptasensor achieved the highest sensitivity with the

43 Time-dependent binding of FN to SAM-coated QCM crystals occurred in at least two phases: initial ra

44 mmunosensors surpassed those of conventional QCM and SPR, closely approaching the most sensitive ELIS

45 ment in sensitivity relative to conventional QCM sensors.

46 nstrate an alternative strategy for creating QCM-based sensor arrays by use of a single sensor to pro

47 that fits instantaneous, overtone-dependent QCM data on (delta/a, -Deltaf/n) coordinates where delta

48 The newly developed QCM system provides a valuable tool for the dynamic char

49 The developed QCM nanosensor was successfully used to examine red yeas

50 The developed QCM-based method for assessing and studying release of o

51 Quartz crystal microbalance dissipation (QCM-D) measurements showed that only Cr(3+) adsorbed ont

52 st, quartz crystal microbalance-dissipation (QCM-D) measurements performed with equivalent samples we

53 and quartz crystal microbalance-dissipation (QCM-D) measurements.

54 nal quartz crystal microbalance-dissipation (QCM-D) setup with a reflection-mode localized surface pl

55 uartz crystal microbalance with dissipation (QCM)-based viscosity measurements were used to study cho

56 uartz crystal microbalance with dissipation (QCM-D) and fluorescence microscopy.

57 uartz crystal microbalance with dissipation (QCM-D) and magnetic contrast neutron reflectrometry (MCN

58 uartz crystal microbalance with dissipation (QCM-D) experiments were conducted to measure the deposit

59 uartz Crystal Microbalance with Dissipation (QCM-D) measurements confirmed the successful modificatio

60 uartz crystal microbalance with dissipation (QCM-D) measurements or an automated flow-through immunoa

61 uartz crystal microbalance with dissipation (QCM-D) measurements to maximize the increase in reflecti

62 uartz-crystal microbalance with dissipation (QCM-D) resolved the formation of a stable complex betwee

63 uartz crystal microbalance with dissipation (QCM-D) technique for the real-time detection of the earl

64 uartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify int

65 on gold surfaces using QCM with dissipation (QCM-D) to obtain frequency and dissipation changes durin

66 uartz crystal microbalance with dissipation (QCM-D), and a rear stagnation point flow (RSPF) system w

67 uartz-crystal microbalance with dissipation (QCM-D), as well as density-functional theory (DFT) to ob

68 uartz crystal microbalance with dissipation (QCM-D).

69 uartz crystal microbalance with dissipation (QCM-d).

70 uartz crystal microbalance with dissipation (QCM-D).

71 uartz crystal microbalance with dissipation (QCM-D).

72 rtz Crystal Microbalance with Dissipation'' (QCM-D) has been applied, while the acoustic assays namel

73 of 2:3:12 spin coated onto a dual electrode QCM.

74 ion were also studied providing the enhanced QCM signals, in particular with Ca(2+), further indicati

75 In this work a cheaper silver fabricated QCM was developed to identify both single and mixed infe

76 ion of the two devices were 0.1mugmL(-1) for QCM-D and 0.32mugmL(-1) for QCM.

77 0.1mugmL(-1) for QCM-D and 0.32mugmL(-1) for QCM.

78 superior suitability of chemFN coatings for QCM research, and provide real-time QCM-D data from cell

79 r electrochemical sensor and 50 cells/mL for QCM sensor), a widened logarithmic range of detection (i

80 a biomimetic surface imprinting strategy for QCM studies of D1R-ligand binding and presented a new me

81 be efficiently modulated, tuned and used for QCM biosensing and quantification.

82 tical performance achieved by high frequency QCM immunosensors surpassed those of conventional QCM an

83 an be used to extract shape information from QCM measurement data.

84 d versatile high fundamental frequency (HFF) QCM immunosensor has successfully been developed and tes

85 sensitivity was exhibited by the 100MHz HFF-QCM carbaryl immunosensor.

86 The IgG and HSA QCM sensors only show frequency shift responses to their

87 e results showed that the developed hydrogel QCM aptasensor was capable of detecting target H5N1 viru

88 tibody coated QCM immunosensor, the hydrogel QCM aptasensor lowered the detection limit and reduced t

89 repeatability of the prepared LOV-imprinted QCM nanosensor make them intriguing for use in QCM senso

90 The imprinted QCM sensor was validated according to the ICH guideline

91 Herein, the strategies employed in QCM-based biosensors for the detection of infectious dis

92 ints using a cocktail of acrylic monomers in QCM measurements.

93 n outline of the future scope of research in QCM-based diagnostics.

94 M nanosensor make them intriguing for use in QCM sensors.

95 studies demonstrated no frequency change in QCMs with untreated cells or without cells but NaN3.

96 ectin onto silicon oxide surfaces, including QCM crystals pre-coated with silicon oxide.

97 ctrical testing results show that individual QCM signal is unaffected by those of adjacent channels u

98 We interpreted QCM-D signals using a theoretical approach by calculatin

99 ghts in favor of the use of the non invasive QCM-D technique for quickly probing the cancer cell sens

100 The HPV-58 detection was compared among LAMP-QCM, conventional LAMP and nested PCR in 50 cervical can

101 on (LAMP) technique with QCM, called as LAMP-QCM, for detection of high-risk human papillomavirus vir

102 The integrated LAMP-QCM system has improved the detection limit up to ten ti

103 The positive rate of LAMP-QCM was higher than that of conventional LAMP with 100%

104 The liquid-phase LAMP-QCM prototype comprised the frequency counter, a tempera

105 Quartz crystal microbalance (QCM) and attenuated total reflection infrared (ATR-IR) s

106 analyses using Quartz-Crystal Microbalance (QCM) and Differential Scanning Fluorimetry (DSF) are con

107 onitored with a quartz crystal microbalance (QCM) and electrochemical impedance measurements.

108 e-based method, Quartz Crystal Microbalance (QCM) and paper based detection of lateral flow biosensor

109 real time using quartz crystal microbalance (QCM) and verified findings with localized surface plasmo

110 microarray and quartz crystal microbalance (QCM) approach for the analysis of carbohydrate-mediated

111 gold fabricated quartz crystal microbalance (QCM) as a post-PCR method of malaria diagnosis.

112 reports a novel Quartz Crystal Microbalance (QCM) based method that can quantitatively analyze the in

113 urfaces using a quartz crystal microbalance (QCM) biosensor was developed, in which binding events ta

114 bandwidth of a quartz crystal microbalance (QCM) contacting these layers.

115 DNA (47bp) to a quartz crystal microbalance (QCM) device in a suspended way and predicted correctly t

116 ency monitoring quartz crystal microbalance (QCM) devices, have good clinical utility as fast diagnos

117 arch, including quartz crystal microbalance (QCM) experiments involving cells.

118 e (LSPR) into a quartz crystal microbalance (QCM) for studying biochemical surface reactions.

119 ecent years the quartz crystal microbalance (QCM) has seen an impressive evolution from a film-thickn

120 ts pertinent to quartz crystal microbalance (QCM) investigation of nanoparticle adsorption kinetics w

121 A quartz crystal microbalance (QCM) is a highly sensitive device to detect such interac

122 The quartz crystal microbalance (QCM) is a label-free, biosensing system that has, in the

123 act angle and a quartz crystal microbalance (QCM) is elucidated.

124 Quartz crystal microbalance (QCM) is frequently used to investigate adsorption of nan

125 Quartz crystal microbalance (QCM) measurements performed in parallel confirmed the di

126 s of flavors by quartz crystal microbalance (QCM) measurements.

127 ted-temperature quartz crystal microbalance (QCM) method we call microscale thermogravimetric analysi

128 Quartz crystal microbalance (QCM) methodology has been adopted to unravel important f

129 cular imprinted quartz crystal microbalance (QCM) nanosensor, LOV imprinted poly(2-hydroxyethyl metha

130 ive analysis of quartz crystal microbalance (QCM) response for heterogeneous loads consisting of nano

131 PCR process on quartz crystal microbalance (QCM) sensor and to increase the sensitivity, isothermal

132 A quartz crystal microbalance (QCM) sensor platform was used to develop an immunosensor

133 cular imprinted quartz crystal microbalance (QCM) sensor was prepared by fabricating a self-assemblin

134 ional (5-20MHz) quartz crystal microbalance (QCM) sensors remains an unsolved challenging task.

135 A quartz crystal microbalance (QCM) study is performed to confirm the interaction betwe

136 an experimental Quartz Crystal Microbalance (QCM) study of tuning interfacial friction and slip lengt

137 opillars with a quartz crystal microbalance (QCM) substrate to form a two-degree- of-freedom resonanc

138 Quartz crystal microbalance (QCM) systems have emerged as a robust biosensing platfor

139 s, based on the quartz crystal microbalance (QCM) technique, focused on the high surface coverage reg

140 metry (DPV) and quartz crystal microbalance (QCM) techniques are used for DNA sensing on DOPE-AuNP na

141 approach using quartz crystal microbalance (QCM) to measure emissions of additives to water from pol

142 e method uses a quartz crystal microbalance (QCM) to measure the change in the mass of the active lay

143 We used a quartz crystal microbalance (QCM) to show that tripod-bound Concanavalin A retains it

144 metry (DPV) and quartz crystal microbalance (QCM) to verify the changes in currents.

145 trochemical and Quartz Crystal Microbalance (QCM) transducers and by using the direct pili-mannose bi

146 ments, based on Quartz Crystal Microbalance (QCM) was developed, analytically characterized and descr

147 py (SMFS) and a quartz crystal microbalance (QCM) were respectively employed to probe interfacial cha

148 e combined with quartz crystal microbalance (QCM), both applied to quantify the molecular interaction

149 croscope (SEM), quartz crystal microbalance (QCM), contact angle (CA) and attenuated total reflectanc

150 A-mannan using quartz crystal microbalance (QCM), cost and time efficient system for biosensor analy

151 cal techniques, quartz crystal microbalance (QCM), Fourier transform infrared (FT-IR) spectroscopy, a

152 Using quartz crystal microbalance (QCM), it was revealed that S. oneidensis biofilm formati

153 was studied by quartz crystal microbalance (QCM), surface plasmon resonance (SPR) and X-ray photoele

154 onitoring using quartz crystal microbalance (QCM), thereby relating the shifts in its frequency and m

155 (D1R) by using quartz crystal microbalance (QCM).

156 termined with a quartz crystal microbalance (QCM).

157 ing gold-coated quartz-crystal-microbalance (QCM) sensors.

158 g a dissipation crystal quartz microbalance (QCM-D) together with microscopy to understand the mechan

159 ressure grown on Quartz Crystal Microbalance-QCM electrodes for which the non-specific absorption of

160 dual-electrode quartz crystal microbalances (QCM).

161 Quartz crystal microbalances (QCMs) have been used in the literature for mass sensitiv

162 ed onto 20 MHz quartz crystal microbalances (QCMs) to form the gas piezoelectric sensors.

163 e (SPR), and quartz crystal microgravimetry (QCM).

164 Such we obtained one D1R-MIP-QCM electrode, whereas the other electrode carried the n

165 a novel use of a polymer composite modified QCM as a chemical sensor at high temperatures.

166 onality of AL-BSA nanofibers, these modified QCM surfaces were directly activated by glutaraldehyde (

167 gold nanoparticles versus monolayer modified QCMs.

168 ) and without energy dissipation monitoring (QCM).

169 al Microbalance with Dissipation monitoring (QCM-D) and EIS.

170 al microbalance with dissipation monitoring (QCM-D) and fluorescence scanning.

171 al microbalance with dissipation monitoring (QCM-D) and microscale thermophoresis (MST) we have been

172 al microbalance with dissipation monitoring (QCM-D) and microscopy-based cell counting were used to q

173 al microbalance with dissipation monitoring (QCM-D) and second harmonic generation (SHG) using solid-

174 al microbalance with dissipation monitoring (QCM-D) biosensor functionalized with a supported lipid b

175 al microbalance with dissipation monitoring (QCM-D) for the enantioselective detection of a low molec

176 al microbalance with dissipation monitoring (QCM-D) measurements.

177 al microbalance with dissipation monitoring (QCM-D) studies.

178 al microbalance with dissipation monitoring (QCM-D) to directly detect the gel-fluid phase transition

179 al microbalance with dissipation monitoring (QCM-D) to investigate binding and assembly of perforin o

180 al microbalance with dissipation monitoring (QCM-D) to separate and individually observe deposition m

181 al microbalance with dissipation monitoring (QCM-D) was used to evaluate changes in the noncovalent i

182 al microbalance with dissipation monitoring (QCM-D) was used to study the effect of particle surface

183 al microbalance with dissipation monitoring (QCM-D) where TRIM21 and TROVE2 autoantigens were covalen

184 aneous frequency and dissipation monitoring (QCM-D) with a double aim, specifically, as investigative

185 al microbalance with dissipation monitoring (QCM-D), surface plasmon resonance (SPR), atomic force mi

186 al microbalance with dissipation monitoring (QCM-D), to detect exosomes by exploiting their surface p

187 al microbalance with dissipation monitoring (QCM-D), we determine the affinity constant, KD, of the m

188 al microbalance with dissipation monitoring (QCM-D), which enabled the label-free, real-time detectio

189 al Microbalance with Dissipation monitoring (QCM-D).

190 al microbalance with dissipation monitoring (QCM-D).

191 al microbalance with dissipation monitoring (QCM-D).

192 al microbalance with dissipation monitoring (QCM-D).

193 al microbalance with dissipation monitoring (QCM-D).

194 to verify the detection results from MZOnano-QCM.

195 odified quartz crystal microbalance (MZOnano-QCM) biosensor to dynamically monitor antimicrobial effe

196 The MZOnano-QCM biosensor provides a promising technology enabling d

197 The MZOnano-QCM showed 4-times more sensitivity over ZnOnano-QCM and

198 cytostatic drug effects whereas the MZOnano-QCM was able to accurately detect the drug effects.

199 The MZOnano-QCM was applied to detect the effects of ampicillin and

200 higher-number overtones produce a negligible QCM signal.

201 This novel QCM approach involves capture of NTHi on lectin-derivati

202 We built novel QCMs as toxicity biosensors incorporating living cells.

203 urface contact which resulted in the obvious QCM responses opposite to that of activation, and propor

204 he challenges to the clinical application of QCM-based biosensors are highlighted, along with an outl

205 of the adsorbed mass solely on the basis of QCM-D results is not possible, but additional informatio

206 Thus, the real time capability of QCM and its simplicity of operation are shown to be high

207 Furthermore, in situ combination of QCM-D with spectroscopic ellipsometry unambiguously demo

208 The harmonic-dependence of QCM-D measurements suggested that a population of the ca

209 s a serious problem in the interpretation of QCM experiments.

210 l step in the quantitative interpretation of QCM results obtained on thin samples with in-plane struc

211 ple and viable method for the preparation of QCM bioactive surfaces, featuring variable protein bindi

212 was attached on the modified gold surface of QCM chip.

213 rogel was immobilized on the gold surface of QCM sensor using a self-assembled monolayer method.

214 des in real time was efficiently achieved on QCM chips thin-coated with tailored ionic liquid TIL 1.

215 ng monolayer formation of allylmercaptane on QCM chip surface for selective determination of lovastat

216 s or canine macrophages were equilibrated on QCM crystal surfaces until stable oscillation frequencie

217 ne) (ppST-EG) thin-layers have been grown on QCM electrodes.

218 spun AL-BSA infrastructure sensing layers on QCM surfaces.

219 -bovine serum albumin (AL-BSA) nanofibers on QCM surfaces.

220 Immobilizing particles on QCM sensors also enriches the range of applications for

221 f our knowledge, this is the first report on QCM VSAs, as well as an experimental sensor array, that

222 In parallel, QCM bacteria-chips were developed for the analysis of le

223 Finally, we perform QCM experiments using cells on both surfaces which demon

224 The plasma ppST QCM electrodes present a higher adsorption of Concanaval

225 stability and repeatability of the prepared QCM nanosensor were studied.

226 As crystallization growth progressed, QCM-D revealed inversions between negative and positive

227 no-QCM and over 10-times better than regular QCM.

228 As a result, QCM-D and QCM apparatuses can be used to follow NS1 reco

229 The combined RIfS-QCM successfully detected the adsorption of proteins wit

230 Moreover, the RIfS-QCM revealed differential adsorption of the vesicles on

231 The results demonstrate that the RIfS-QCM serves as a useful tool to quantitatively analyze mo

232 a novel quartz crystal microbalance sensor (QCM).

233 The anti-hIgG and hIgG binding results show QCM-P achieved an eightfold improvement in sensitivity r

234 ic area demonstrated that the malaria silver QCM could identify both false negative and misdiagnosis

235 Validation showed that malaria silver QCM had high diagnostic potency.

236 Thus, the malaria silver QCM is accurate, precise, rapid, cheap, and field applic

237 The malaria silver QCM is stable at tropical temperature for up to 6 months

238 The analysis cost of malaria silver QCM was $1/sample and analysis time was 30 min after blo

239 Since QCM-D is sensitive to the whole mass of the sensing laye

240 ere grown on the top electrode of a standard QCM using metal-organic chemical-vapor deposition (MOCVD

241 m a two-degree- of-freedom resonance system (QCM-P).

242 ted in order to show for the first time that QCM experiments can quantitatively measure the deformati

243 The QCM crystal surface was modified with a variety of sorpt

244 The QCM sensor showed excellent sensitivity and specificity

245 termination by using electrochemical and the QCM method.

246 zed, respectively, and then were used as the QCM sensor coating material.

247 frameworks that incorporate slippage at the QCM surface electrode or alternatively at the surface of

248 ibody-antigen recognition effect on both the QCM and LSPR has been analyzed and discussed.

249 However, the physicochemical analysis by the QCM alone often leads to overestimation of the actual ad

250 tration is in the range of 0.5-4.5 nM by the QCM method.

251 The swollen hydrogel was monitored by the QCM sensor in terms of decreased frequency.

252 tachment behavior, which was detected by the QCM.

253 In contrast, the QCM detects physicochemical characteristics of the adsor

254 We differentiate the QCM's frequency response to changes in the droplet conta

255 tion, the binding affinity obtained from the QCM-P device for anti-hIgG and hIgG proteins was found i

256 irmed, especially the abrupt decrease in the QCM wet mass with the particle coverage and the overtone

257 Larger frequency change in the QCM-D signal was observed for cells with larger spread a

258 the adhesion LPS versus GSL vesicles in the QCM-D, with the latter exhibiting 50% higher adhesion to

259 gle polymer thin film coatings increased the QCM response by 1-2 orders of magnitude, while operating

260 pth, a is the particle radius, Deltaf is the QCM frequency shift, and n is the overtone number.

261 ded to perforin already on the membrane, the QCM-D response changes significantly, indicating that pe

262 The normalized frequency shift of the QCM device together with the microscopic observation of

263 rovide readers an overview of the use of the QCM for examination of cell-substrate adhesion.

264 The performance of the QCM immunosensor developed using sandwich assay by utili

265 ttability alterations of gold surface of the QCM owing to ion valency/concentration changes using sta

266 cant impact on the frequency response of the QCM regardless of the droplet size.

267 e expressions furnish the upper limit of the QCM signal, which can be attained for a sensor providing

268 the functionalization and activation of the QCM surface, prior to antibody immobilization.

269 e an effect on the frequency response of the QCM when the droplet height is on the order of the visco

270 the most important practical aspects of the QCM-based cell study including data acquisition and anal

271 ion of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled.

272 From a correlation of the QCM-D results with the structural characterization it is

273 edle-shaped crystals grow as clusters on the QCM sensor's surface, not in uniform layers.

274 ophobic and superhydrophilic surfaces on the QCM substrates.

275 and employing either elelctrochemical or the QCM method.

276 DNA base pairs for two acoustic sensors, the QCM and Love-wave devices operating at a frequency of 35

277 ated to determine the dry coverage using the QCM measurements.

278 nation of vapor phase analytes utilizing the QCM.

279 y contributed to the EIS spectra whereas the QCM-D response was still repeatable.

280 e which indicated SLB formation, whereas the QCM-D signals detected a significant loss in net acousti

281 While the QCM-D and LSPR signals both detected mass uptake arising

282 he extent of liposome deformation, while the QCM-D measurements yield a more complex response that is

283 With the QCM setup, the association and dissociation rate constan

284 HSA layers on GO was also examined with the QCM-D.

285 The sensitivity of these QCM-P devices was evaluated by measuring mass changes fo

286 azide (NaN3) (25-100 mM) was added to these QCMs while continuously collecting crystal oscillation f

287 oplatforms were evaluated using flow-through QCM technology, as well as hemagglutination inhibition a

288 ings for QCM research, and provide real-time QCM-D data from cells subjected to an actin depolymerizi

289 The model was applied to QCM measurement data pertaining to the adsorption of 34

290 ovoking thus a greater decrease of the total QCM crystal mass compared with the non charged substrate

291 Using QCM-D crystals modified with a photo-activatable RGD pep

292 silica nanoparticles on gold surfaces using QCM with dissipation (QCM-D) to obtain frequency and dis

293 enriches the range of applications for which QCM can be exploited, especially in colloid science.

294 While QCM-D is a powerful technique for label-free, real-time

295 y AFM topography and phase images along with QCM-D.

296 The theoretical results are confronted with QCM and atomic force microscopy measurements of positive

297 othermal amplification (LAMP) technique with QCM, called as LAMP-QCM, for detection of high-risk huma

298 ollowed by quartz crystal microbalance with (QCM-D) and without energy dissipation monitoring (QCM).

299 If NaN3 was added to either cell type within QCMs, 5 to 8 min later increases in oscillation frequenc

300 showed 4-times more sensitivity over ZnOnano-QCM and over 10-times better than regular QCM.