ライフサイエンスコーパス: MEKC

1 10(4) were obtained in the SDS micro-CGE and MEKC separation dimensions, respectively, for the invest

2 to provide a complementary method to CZE and MEKC for the separation of specific types of solutes tha

3 y IR and NMR spectroscopies, whereas CZE and MEKC were applied to evaluate their purity and to invest

4 nic chiral polymeric surfactants in MEKC and MEKC-MS.

5 nd separated using a combination of tITP and MEKC.

6 sources of congeneric relationships between MEKC retention and log Po/w.

7 astereomers of some of them, was achieved by MEKC in an acidic BGE (500 mM acetic acid [pH 2.54] and

8 kaline background electrolytes (BGEs) and by MEKC in acidic and alkaline BGEs containing a pseudostat

9 ounds in the training set were determined by MEKC, while the K(mw) of the aliphatic solutes were esti

10 bicide spiked in lake water was separated by MEKC and detected by ultraviolet absorption.

11 ly labeled substrates followed by an on-chip MEKC separation of the reaction products from the substr

12 lar electrokinetic capillary chromatography (MEKC) and the high sensitivity of fluorescence detection

13 lar electrokinetic capillary chromatography (MEKC).

14 s in micellar electrokinetic chromatography (MEKC) can be improved significantly.

15 e of micellar electrokinetic chromatography (MEKC) coupled to inductively coupled plasma-mass spectro

16 and micellar electrokinetic chromatography (MEKC) in fused silica capillary with an inner roughened

17 , in micellar electrokinetic chromatography (MEKC) is directly related to solute partition coefficien

18 and micellar electrokinetic chromatography (MEKC) is discussed here.

19 sive micellar electrokinetic chromatography (MEKC) method with UV detection was used to determine sev

20 wing micellar electrokinetic chromatography (MEKC) separations in a 19.6-cm-long serpentine channel,

21 r 74 micellar electrokinetic chromatography (MEKC) systems taken from the literature.

22 sing Micellar Electrokinetic Chromatography (MEKC) to estimate the octanol-water partition coefficien

23 e to micellar electrokinetic chromatography (MEKC) to monitor extracellular dopamine concentration in

24 ) in micellar electrokinetic chromatography (MEKC) using sodium dodecyl sulfate (SDS) and fused silic

25 , in micellar electrokinetic chromatography (MEKC) using the simple relationship k = K(mw)phi, where

26 and micellar electrokinetic chromatography (MEKC) were used as the separation modes for the first an

27 Micellar electrokinetic chromatography (MEKC) which separates PB-labeled amino acids by their hy

28 ling micellar electrokinetic chromatography (MEKC) with electrospray mass spectrometry initiates the

29 and micellar electrokinetic chromatography (MEKC) with laser-induced fluorescence detection was expl

30 and micellar electrokinetic chromatography (MEKC) with subsequent off-line identification of the sep

31 and micellar electrokinetic chromatography (MEKC), containing sodium dodecyl sulfate, applies the pr

32 s by micellar electrokinetic chromatography (MEKC), two-dimensional correlation analysis resolved all

33 and micellar electrokinetic chromatography (MEKC).

34 n by micellar electrokinetic chromatography (MEKC).

35 with micellar electrokinetic chromatography (MEKC).

36 s in micellar electrokinetic chromatography (MEKC).

37 ) to micellar electrokinetic chromatography (MEKC).

38 n by micellar electrokinetic chromatography (MEKC).

39 ) in micellar electrokinetic chromatography (MEKC).

40 and flavonoids has been developed combining MEKC and DAD detection.

41 In comparison with conventional MEKC, only a small portion of the capillary is filled wi

42 s of a modified Environmental Kuznets Curve (MEKC), which postulates the coevolution of fossil fuel C

43 y with laser-induced fluorescence detection (MEKC-LIF) making it possible to detect superoxide found

44 elution peaks unseparable by one-dimensional MEKC, demonstrating the utility of 2D correlation in sep

45 ecyl sulfate to the separation buffer (i.e., MEKC) resulted in peak splitting for all four serogroups

46 lications, and advantages of partial-filling MEKC are similarly addressed.

47 ons between conventional and partial-filling MEKC in terms of separation efficiency and resolution of

48 or of triazine herbicides in partial-filling MEKC.

49 initiates the development of partial-filling MEKC.

50 performing the separation in partial-filling MEKC.

51 te numbers of 230000 and 40000 in the first (MEKC) and second (CE) dimensions, respectively, correspo

52 c chromatography-laser induced fluorescence (MEKC-LIF) method was developed using sodium dodecylbenze

53 e electric field strengths were 200 V/cm for MEKC and 2400 V/cm for CE.

54 by a gated valve onto a separate column for MEKC analysis.

55 The use of Ag(I) addition in MEKC is also applied to the separation of various other

56 e results using Ag(I) as buffer additives in MEKC are also compared to studies utilizing a mixed coun

57 a priori prediction of retention behavior in MEKC from solute structure.

58 ship for prediction of retention behavior in MEKC is examined.

59 the retention times (thus chromatograms) in MEKC can be predicted from the calculated retention fact

60 coefficient can be accurately determined in MEKC for a given micellar pseudostationary phase.

61 This means that retention factor in MEKC can be predicted for solutes with known micelle-wat

62 Retention mechanisms in MEKC separations can also be manipulated by the addition

63 he addition of Ag(I) on the elution range in MEKC is also investigated.

64 The stacking strategy in MEKC was applied to metabolic stability studies of small

65 ying anionic chiral polymeric surfactants in MEKC and MEKC-MS.

66 from the antibody and analyzed by microchip MEKC.

67 corporated a 30-mm SDS micro-CGE and a 10-mm MEKC dimension length.

68 A new MEKC-MS/MS method was developed for the determination of

69 ir of sulfonamides was achieved under normal MEKC conditions.

70 The use of MEKC as the separation mode significantly increased the

71 After careful optimization, MEKC-ICP-MS was used to separate engineered nanoparticle

72 The optimized MEKC conditions (45 mM CHAPSO, pH 6 at 5 degrees C) effe

73 With the use of the PNAA-MEKC method, PCR products of 88, 134, 216, and 447 bases

74 A sensitive MEKC-mass spectrometry (MS) method is developed for one

75 able and remained fluorescent under standard MEKC conditions for peptide and protein separations.

76 The MEKC broadly captures the historic FFCO(2)-NO(x) dynamic

77 The MEKC separation buffer consisted of 30 mM phosphate, 6.5

78 ion with the electrophoresis run time in the MEKC dimension being 10 s.

79 bicides were achieved without optimizing the MEKC conditions.

80 In addition, the tITP/MEKC method was combined with capillary isoelectric focu

81 Using MEKC to separate the dialysate samples allowed aspartate

82 sal concentrations for these compounds using MEKC were 1.9 +/- 0.2, 4.1 +/- 0.2, 4.6 +/- 0.7, 2.6 +/-

83 conductivity detection were performed using MEKC, in which the carrier electrolyte contained the ani

84 Various MEKC background electrolyte (BGE) solutions were prepare

85 n plug into a capillary that was filled with MEKC background solution.