ライフサイエンスコーパス: zero-order

1 A one-compartment model with zero-order absorption and allometric scaling best descri

2 A 1-compartment model with zero-order absorption and allometric scaling best descri

3 ontrolling processes are here described by a zero-order analytical model aimed at assessing how plant

4 of L( *), Hue angle and Chroma values fitted zero order and first order kinetic, respectively.

5 ons were above 4x PA-IC(90) for 90 days with zero-order and diffusion-controlled absorption, respecti

6 alpha-tocopherol (AT) degradation followed a zero-order and first-order kinetic model, respectively,

7 ic models were fit to DO microprofiles using zero-order and first-order kinetics with both zero and n

8 ws us to define precisely the conditions for zero-order and first-order product formation.

9 r-interactive algorithm quickly corrects for zero-order and first-order variation of phase with frequ

10 ations of the intersecting states, which are zero-order approximations to the diabatic states.

11 mass >95% when modelling only variables with zero-order associations with preferences, but only 90% w

12 l at lower concentrations but transitions to zero-order at concentrations > 0.3 M.

13 ves from first-order at low concentration to zero-order at high concentration, and this is consistent

14 [alkyne] at lower alkyne concentrations, and zero-order at higher [alkyne].

15 presence of the gauge field and observe the zero-order chiral Landau level with one-way propagation.

16 ired patients with schizophrenia, in which a zero-order correlation was obtained.

17 ols (N = 107) using a MANCOVA and calculated zero-order correlations with the discriminant function f

18 nd 2 (5 mol %) in DCE at 40 degrees C led to zero-order decay of 1 to approximately 80% conversion (k

19 A zero-order ( degrees Brix, fructose, glucose), a first-o

20 Comparing these models with the observed zero-order dependence in bicarbonate and simulated inter

21 volution reaction (OER), consistent with the zero-order dependence of Pi on the OER current density;

22 (<8 microM) O(2) concentrations and exhibits zero-order dependence on *NO concentration.

23 he reaction is photon-limited and exhibits a zero-order dependence on amine, azide, and photocatalyst

24 er dependences on aryl bromide and amine and zero-order dependence on base.

25 tadiene to form Diels-Alder product 3 with a zero-order dependence on diene.

26 droxide concentrations and the transition to zero-order dependence on hydroxide at high concentration

27 r dependence on DCI enzyme concentration and zero-order dependence on inhibitor concentration; and (i

28 first-order kinetics, but yields an apparent zero-order dependence on initial substrate concentration

29 at higher concentrations of ethylene, and a zero-order dependence on the concentration of Cu(II) oxi

30 of the polymerization rate on the epoxide, a zero-order dependence on the cyclic anhydride, and a fir

31 s reveal a first-order dependence on 1 and a zero-order dependence on the cyclic anhydrides.

32 e nearly unimolecular dependent on aluminum, zero-order dependent on substrate, and inversely depende

33 ins a conventional fluorescence image in the zero-order diffracted light and a fluorescence spectral

34 ndergo slow thermal dissociation to NO, with zero-order dissociation observed at both -15 and 23 degr

35 Zero-order drug delivery systems have the potential to o

36 not show recrystallisation and maintained a zero-order drug release for variable 3DP infill patterns

37 crystal, ensuring sustained, adjustable and zero-order drug release kinetics.

38 ellular domains, has been transformed into a zero-order drug-delivery platform.

39 also exhibit enhanced sensitivity due to the zero-order effect, raising the question whether both phe

40 le, give rise to ultrasensitivity, including zero-order effects, multisite phosphorylation, and compe

41 ms, compared to a lag of 15-28 d followed by zero-order elimination kinetics in the spiked systems.

42 Random fluctuations in the zero-order excited-state energy of the MOPVs (disorder)

43 acious when eluted from stents in a constant zero order fashion as this maximizes the duration of elu

44 concentrations, and there are terms that are zero order, first order, and second order in hydroxide i

45 d using various mathematical models such as, zero order, first order, Higuchi model and Peppas model.

46 Zero-order, first-order and two-phase models were utiliz

47 order in initial catalyst concentration, and zero-order for the terminal alkyne.

48 The reaction is first order in amine and zero order in 1:1 base--ligand complex.

49 studies reveal that hydroamination rates are zero order in [amine substrate] and first order in [cata

50 The exchange is dissociative and zero order in [COE].

51 1, first order in the haloalkylcarborane and zero order in [Nu(-)], and the elimination appears to be

52 of AB catalyzed by 3 is first order in 3 and zero order in AB.

53 der in catalyst and chlorenium ion donor and zero order in alkenoic acid substrate under syntheticall

54 es are near first order in H(2)O(2) and near zero order in all other species, including H(2)O.

55 t order in both catalyst and aryl halide and zero order in base and amine.

56 lf-reactions catalyzed by the holoenzyme are zero order in cobalamin, so rate constants for reactions

57 Apo-MnSOD metallation kinetics are "gated", zero order in metal ion for both the native Mn2+ and a n

58 ion to be first order in gold and allene and zero order in nucleophile.

59 reveal anomalous concentration dependences (zero order in o-CF(3)-phenylacetic acid concentration, z

60 in o-CF(3)-phenylacetic acid concentration, zero order in oxygen pressure, and negative orders in bo

61 reaction of a representative aryl bromide is zero order in PhCN.

62 rs, exhibiting an induction period and being zero order in PhI.

63 D exchange, a rate law first order in Ru and zero order in phosphine, and kinetic deuterium isotope e

64 talyst and butylene oxide concentrations but zero order in phthalic anhydride and, where it is presen

65 t low [PPh(3)], the reaction rate was nearly zero order in PPh(3), but reactions at high [PPh(3)] rev

66 sis followed by a much slower region that is zero order in superoxide and due to a product inhibition

67 u(R,R)-Ph-bis(oxazoline)]OTf(2) catalyst and zero order in TEMPO.

68 tion of 1-azido-4-phenylbutane (S1) revealed zero order in the azide substrate and first order in bot

69 be the cyclization of the substrate that is zero order in the concentration of the iodoarene precata

70 phthalic anhydride and, where it is present, zero order in THF.

71 to be first order in the borane catalyst and zero order in ylide.

72 cyclization is first-order in [catalyst] and zero-order in [alkynyl alcohol], as observed in the intr

73 .9 (9.7) eu, while the reaction kinetics are zero-order in [amine] and first-order in both [catalyst]

74 he rate law is first-order in [catalyst] and zero-order in [aminodiene].

75 tively; at higher [H(2)], the rates approach zero-order in [H(2)].

76 (one-half-order in both [1] and [AIBN], and zero-order in [O(2)]).

77 he rate law is first-order in [catalyst] and zero-order in [substrate] over approximately one half-li

78 '' = eta(5)-Me(4)C(5)) shows the reaction is zero-order in [thiol], first-order in [1a], first-order

79 ct to the carboxylate, while the reaction is zero-order in acridinium catalyst, consistent with anoth

80 ignard reagent, first-order in catalyst, and zero-order in alkyl halide.

81 rocess to be first-order in [InCl(3)](0) and zero-order in both [BnOH](0) and [NEt(3)](0).

82 Assessment of the reaction kinetics showed zero-order in both the aziridine species and the aryl br

83 be first-order in N(2)O partial pressure and zero-order in C(3)H(8) partial pressure, consistent with

84 dependence on H(2) partial pressure and are zero-order in H(2)O and O(2) partial pressures.

85 nversion to phenyl pinacolborane (PhBpin) is zero-order in HBpin concentration.

86 er in initial zirconacycle concentration and zero-order in incoming phosphine (k(obs) = 1.4(2) x 10(-

87 st-order in N,N-di-t-butyldiaziridinone (1), zero-order in olefin, and first-order in total Cu(I) cat

88 first-order in hydrosilane and B(C6F5)3 but zero-order in phosphine.

89 The enamine formation is zero-order in proline and oxazolidinones, which excludes

90 monstrated that the catalytic cyclization is zero-order in substrate and first-order in catalyst.

91 The reaction was zero-order in substrate, when the concentration of olefi

92 -order in di-tert-butyldiaziridinone (5) and zero-order in the olefin.

93 action order was determined for iodobenzene (zero order), indole (first order), and the catalyst (fir

94 oincident with the start of a 2 microg/kg/hr zero-order infusion.

95 For X = I or F, zero-order kinetic behavior is observed, while for X = C

96 te and catalyst combination, deviations from zero-order kinetic behavior reflect competitive product

97 Zero-order kinetic equations were used to determine kine

98 t Mg dissolution to Mg(2+) followed mostly a zero-order kinetic rate law for both Mg anode materials,

99 depended on initial solution pH, following a zero-order kinetic regression.

100 In the catalytic process, zero order kinetics are observed on both reaction substr

101 contrast to NDMA, a transition from first to zero order kinetics was not observed for the other nitro

102 Dose related pharmacokinetics with near zero order kinetics was observed for up to 6 weeks in ra

103 nd all the data showed good correlation with zero order kinetics.

104 at achieves multi-day drug release with near zero-order kinetics and efficient delivery.

105 y at very low C(3)H(8) partial pressures and zero-order kinetics at higher C(3)H(8) partial pressures

106 and, in contrast to previous work indicating zero-order kinetics in both.

107 Zero-order kinetics observed by NMR, indicated a shelf-l

108 cose declined linearly with time, confirming zero-order kinetics of hepatocyte respiration.

109 d degradation, with betalain changes fitting zero-order kinetics over 120 days.

110 owed that two of the compounds decomposed by zero-order kinetics under neutral conditions.

111 temperature can effectively be modeled using zero-order kinetics when nitrate concentrations are >2 m

112 enolics and a-tocopherol decreased following zero-order kinetics with a higher susceptibility in unst

113 ics and alpha-tocopherol decreased following zero-order kinetics with a higher susceptibility in unst

114 appearance of both TPCPGa and DPMNCPGa obeys zero-order kinetics with rate constants (k) having a lin

115 ated (MWH) reaction displays very pronounced zero-order kinetics, displaying a much higher reaction r

116 t and phenanthrene was mineralized following zero-order kinetics, due to bioavailability limitations.

117 stituted cyclopropenes were found to present zero-order kinetics, indicating their rapid single addit

118 pening polymerization of the OCAs, exhibited zero-order kinetics, suggesting that the polymerization

119 e rate of oxidation from the expected pseudo-zero-order kinetics, we can detect and characterize loca

120 (1) produces *Cl and added alcohols exhibit zero-order kinetics.

121 the reaction process exhibits overall pseudo zero-order kinetics.

122 ormation with hydroxycinnamic acids followed zero-order kinetics.

123 reduction/oxidation reactions, which display zero-order kinetics.

124 n into glioblastoma cells that proceeds with zero-order kinetics.

125 nt capacity (ABTS, DPPH) decreased following zero-order kinetics; gamma-tocopherol showed the stronge

126 nt capacity (ABTS, DPPH) decreased following zero-order kinetics; y-tocopherol showed the strongest d

127 ely associated with status allocation at the zero-order level.

128 ation noise, unwanted diffractive orders and zero-order light.

129 of LNG to 5.8 +/- 0.5% and achieved roughly zero-order LNG release for 6.2 +/- 0.1 months in vitro.

130 leotides with the frequencies predicted by a zero order Markov chain determined by the codon bias of

131 nisms using both Markov chain analysis and a zero-order Markov method.

132 discrimination indicated better fit for the zero order model than the first order model which was he

133 predicting nitrate concentrations between a zero-order model and the other multispecies reactive tra

134 Overall, kinetic analysis showed an apparent zero-order model fit for the change in the colour (L( *)

135 B system and were kinetically described by a zero-order model.

136 at the inhibited complex responsible for the zero-order phase in the catalysis by Mn-SOD of superoxid

137 sembled that of the enzyme in the inhibited, zero-order phase of the catalyzed disproportionation of

138 actions, supporting a mechanism in which the zero-order phase results from product inhibition.

139 It is proposed that the zero-order process reflects a cyclization of this interm

140 The zero-order rate constant at 37 degrees C was the same fo

141 The pH dependence of apparent zero-order rate constants fit best a model in which a si

142 Zero-order rate constants for artificial honey with adde

143 Fitted zero-order rate constants ranged from 50 to 510 mg L(-1)

144 dependence on aziridine aldehyde dimer and a zero-order rate dependence on all other reagents have be

145 orders of magnitude and grew according to a zero-order rate law.

146 ng electrolyte), ECD resulted in an apparent zero-order rate of 30 mumol L(-1).h(-1), whereas rates o

147 ciation rates of NADH approached an apparent zero-order rate with increasing NADH concentrations at p

148 mergence of a greatly inhibited catalysis of zero-order rate.

149 e of chi-p53 nanoparticles and Dox at a near zero-order rate.

150 To ensure drug release at zero-order rates, empirical and theoretical modelling ha

151 atalytic oxidation process was observed as a zero-order reaction in terms of the concentration of the

152 This process exhibits pseudo-zero-order reaction kinetics and a temperature dependenc

153 h quickly tapers off and falls into a pseudo-zero-order reaction.

154 se followed by a linear, steady-state pseudo-zero-order reaction.

155 exhibited a strong product inhibition with a zero-order region of superoxide decay slower by 10-fold

156 first-order dependence on [fluoroarene] and zero-order relationship with respect to [R(3)SiH].

157 ll films displayed a significant duration of zero order release kinetics.

158 DPV, PTV, and LNG elicited zero-order release kinetics in vitro in simulated vagina

159 olled release of the molecules studied, with zero-order release kinetics under infinite sink conditio

160 contraceptive and antiretroviral (ARV) with zero-order release kinetics.

161 Remarkably, zero-order release of atenolol was achieved from FAU (Si

162 w covers strategies being employed to attain zero-order release or alter traditionally first-order re

163 80-2010) was dedicated to the development of zero-order release systems, self-regulated drug delivery

164 acking with rate-limiting drug elution--near zero-order release was three-fold more efficient at depo

165 To achieve zero-order release, we developed a novel core-shell MN p

166 ctions between silk and drug molecules, near-zero order sustained release may be achieved through dif

167 irteen participants used discrete movements (zero order system) as well as more sustained control act

168 s first-order during an induction period and zero-order thereafter indicating that the mechanism incl

169 ly used in current practice such as Tikhonov zero-order, Tikhonov first-order and L1 first-order regu

170 ved by measuring changes in the ratio of the zero order to first order peak intensity, with a sensiti

171 scosity is achieved by monitoring changes in zero order to first order peak separation in the far-fie

172 ymmetric Fano resonances are observed in the zero-order transmission spectra using an incoherent ligh

173 idth at half maximum (FWHM) of ~15 nm in the zero-order transmission using an incoherent white light

174 ystems with single-enzyme biochemistry using zero-order ultrasensitivity as an example.

175 contrast to the conditions often required by zero-order ultrasensitivity, perhaps the most well known

176 As a result of the classic mechanism of zero-order ultrasensitivity, we find that biosensor acti

177 in [C(3)H(8)] and [catalyst] are essentially zero-order under all conditions, with the former implyin

178 ke and uptake and conversion conditions were zero-order with no detectable lag or burst periods.

179 respect to chloroarene, and the reaction was zero-order with respect to chloroarene.

180 It has been found that this opening is zero-order with respect to PNA, indicating that the init