ライフサイエンスコーパス: micropore

1 thick and contain a network of 0.5-nanometer micropores.

2 y due to desorption of chemicals from narrow micropores.

3 intergranular pores and the H(2) residing in micropores.

4 area and pore volume, respectively) is from micropores.

5 upon MN length, number, and occlusion of the micropores.

6 e the penetration of liquid through putative micropores.

7 er in between bran particles and probably in micropores.

8 layer and continuous water provision through micropores.

9 iquor is subsequently soaked off through the micropores.

10 erived carbon, with a narrow distribution of micropores.

11 ient) with the fraction of porosity in small micropores.

12 is attributed to the microenvironment of the micropores.

13 d survival in migration through constraining micropores.

14 sorbed, both to exterior surfaces and within micropores.

15 hibition of mesopore collapse, and therefore micropore accessibility, as the basis for the extraordin

16 s, nanopores in the range of 2 nm and below (micropores, according to IUPAC classification) are usual

17 Containment within small micropores also protects clusters against thermal sinter

18 the interface between a single ion-selective micropore and aqueous solutions is quantitatively invest

19 This paper describes synthetic micropore and nanotube membranes that mimic the function

20 ities that allow CO2 gas molecules to access micropores and adsorb effectively.

21 Here, in cancer cell migration through rigid micropores and in passive pulling into micropipettes, lo

22 arbons was characterized for the presence of micropores and macropores, when obtained from highly cro

23 The presence of interconnected micropores and mesopores is responsible for the enhanced

24 The unique nanoarchitectures with rich micropores and mesopores, as well as the high surface ar

25 of water molecules from the surfaces of coal micropores and mesopores.

26 only in CD34(+) cells, but migration through micropores and nuclear flexibility in micropipette aspir

27 erlayer macropores, narrowly distributed 7 A micropores, and ever most polar pore walls.

28 for solution sampling from biological cells, micropores, and other microscopic objects.

29 NaA micropore apertures restrict access to encapsulated clus

30 ti-channel device which utilized solid-state micropores array assembly for simultaneous measurement o

31 T-1 crystals and contained partially ordered micropores as well as disordered mesopores.

32 e Pd nanoparticles controlled by the zeolite micropores, as elucidated by competitive adsorption and

33 trolite) irreversibly inserts xenon into its micropores at 1.7 GPa and 250 degrees C, while Ag(+) is

34 are observed: (1) minor sorption effects in micropores at low pressures; (2) capillary condensation

35 ns are increasingly desorbed from the carbon micropores at the negative electrode, while at the posit

36 deformability is reduced in sepsis but that micropore bulk-filtration methods may not be appropriate

37 ulatory disturbances in sepsis have prompted micropore bulk-filtration studies of red blood cell (RBC

38 Solid-state micropores can characterize each cell in a sample provid

39 The ionic current across each micropore channel was continuously monitored and recorde

40 eaks and TEM images that reveal well-ordered micropore channels.

41 lored, and we report for the first time that micropore closure is delayed in elderly subjects in a ma

42 Micropore closure was measured with impedance spectrosco

43 In addition to a large micropore contribution to the surface area, mesopores ar

44 distinctive advection domain, macropores and micropores created in silicon substrate.

45 s combining mesopores (d >/= 20 A) and large micropores (d = 10-20 A), due to the overlap of pore-fil

46 This interfacial micropore defect formation becomes more prominent with i

47 The present result shows the formation of micropore defects in the interface region of the PEDOT:P

48 d carbon samples with well-aligned, straight micropores demonstrate high specific capacitance of up t

49 The measured micropore diffusion coefficient for CO2 in Cu-BTC is 1.7

50 tal size aids in the accurate measurement of micropore diffusion coefficients.

51 h the high external surface area and reduced micropore diffusion length, account for higher reaction

52 These micropore dimensions are relevant for many valuable chem

53 nt membrane-like Matrigel on a polycarbonate micropore filter was evoked by vasoactive intestinal pep

54 d with a cell transit analyzer (containing a micropore filter with 30 identical, 8-microm diameter po

55 ctic mobility, assessed by migration through micropore filters without Matrigel, and in situ MMP acti

56 did not respond to VIP by chemotaxis through micropore filters without or with a top layer of basemen

57 The migration of RNK-16 cells across micropore filters, without or with a layer of Matrigel,

58 en CLL cells were separated from the MSCs by micropore filters.

59 were osmotically fragile, and ektacytometry/micropore filtration measurements demonstrated reduced d

60 cal behavior was tested using a computerized micropore filtration system (CTA) and a laser-diffractio

61 MN deformation behavior was investigated via micropore filtration, using the cell transit analyzer.

62 hell membranes (CSEMs) consisting of natural micropores function well as a polysulfide reservoir in L

63 rug delivery), as well as calculation of the micropore half-life.

64 ites vs. placebo, suggesting slower rates of micropore healing.

65 e involvement of subclinical inflammation in micropore healing.

66 However, despite being extremely beneficial, micropores impose restrictions on the mass transport of

67 Square arrays of 100 micropores in 130 mum thick borosilicate glass coverslip

68 ct the rate of ionic diffusion in the carbon micropores in an effort to understand supercapacitor cha

69 suggesting that despite the vast numbers of micropores in shale, the micropores will be unavailable

70 ow-noise properties of bilayer recordings on micropores in Teflon AF films were exploited to record t

71 t ionic liquids spontaneously wet the carbon micropores in the absence of any applied potential and t

72 icroscopy showed that NaOH steeping produced micropores in the cell walls and light microscopy reveal

73 ng powdered allergen and adjuvants into many micropores in the epidermis.

74 It is most likely caused by the lack of micropores in the polymer structures.

75 nation via vaccine delivery into an array of micropores in the skin, instead of bolus injection at a

76 orresponding swollen material; the amount of micropores increased with increasing rigidity and size o

77 DB2 at the subnuclear DNA damage foci within micropore irradiated cells.

78 Using micropore irradiation, we demonstrate that large amounts

79 Filtration through micropores is frequently used to assess red blood cell d

80 ca or carbon nanospheres with size-selective micropores is presented.

81 sults indicate that the surface chemistry in micropores is tunable thereby influencing the selectivit

82 sfer limitation due to the small size of the micropores (less than 1 nm).

83 ent, or replacement of framework atoms), the micropore level (e.g. template removal and functionalisa

84 ent the first human study demonstrating that micropore lifetime can be extended following MN treatmen

85 man proof-of-concept study demonstrates that micropore lifetime can be prolonged with simple topical

86 ), and contained a significant population of micropores (< or =20 A).

87 t monolith had relatively large fractions of micropores (<2 nm, 11.9%) and mesopores in the range fro

88 y (cell-on-cell) or indirectly (separated by micropore membrane)] designed to interrogate the interpl

89 F)-positive cells separated by 0.4-mum-thick micropore membranes from stromal cells), indicating a pa

90 T(g)), sorption of TCE is well-described by micropore models, with enthalpies of sorption characteri

91 bution increases, making a portion of closed micropore network accessible.

92 le-sites anchored on the internal surface of micropores of a microporous silicate exhibit high select

93 Ion migration through the micropores of the flow electrodes was facilitated in par

94 enotype of the endothelial cells through the micropores of the membrane and their spread morphology o

95 The micropores of the MOF crystals embedded within a semiper

96 showed that slow diffusion occurs within the micropores of the sol-gel films which could be modeled a

97 ated metal centers and two distinct types of micropores, one of which is lined by CrO4 (2-) (CROFOUR)

98 ur, compared with its counterparts with only micropores or bimodal micro/mesopores.

99 ondensation reactions also occur within tiny micropores or defects in the topmost layer.

100 ined and arrange themselves according to the micropore pattern.

101 timated pore size that can contribute to the micropore peak is estimated to be around 2.4 nm.

102 The chemical shift of the micropore peak is observed to evolve with changing press

103 Organic open frameworks with well-defined micropore (pore dimensions below 2 nm) structure are att

104 However, rapid healing of the micropores prevents further drug delivery, blunting the

105 structure, with no detectable interspaces or micropores; probiotic inclusion did not significantly ch

106 Here we show that the mordenite micropores provide a perfect confined environment for th

107 terial with a periodic arrangement of narrow micropores, shows an increase in isosteric enthalpy with

108 This ease of the micropore size adjustment and the attained degree of str

109 se after bioconversion, while the accessible micropore size distribution increases, making a portion

110 Both inaccessible meso-/micropore size distributions decrease after bioconversio

111 e average pore diameter increases, while the micropore surface area increases with pore volume decrea

112 tment, which is confirmed by the increase of micropore surface area.

113 Micropore Teflon diffusion chambers were implanted subcu

114 skin-impermeable drugs by creating transient micropores that bypass the barrier function of the skin.

115 vitro inhibited macrophage migration through micropores that mimic features of dense 3D tissue.

116 lly owing to the formation of ultraselective micropores that selectively exclude the bulkier CH4 mole

117 both small (<0.7 nm) and large (0.7-1.0 nm) micropores, the former enhancing selectivity and the lat

118 By creating laser-generated micropores through the epidermis, we targeted a model pr

119 e synthetic protocols and the ability of NaA micropores to sieve reactants based on molecular size.

120 scutaneous immunotherapy via laser-generated micropores to subcutaneous injection.

121 s of magnitude is possible by minimizing the micropore tortuosity.

122 t of measurement and as the cells passed the micropores, tumor cells showed distinctive current block

123 e titration confirm the expected decrease of micropore volume and increase in external surface area f

124 This means that a particular surface area or micropore volume can be precisely tuned.

125 Increasing their micropore volume could further improve their already exc

126 ith a continuously tuneable surface area and micropore volume over a wide range can be prepared.

127 This increased micropore volume results from the opening of some of the

128 yte applications, the importance of matching micropore volume to sulfide loading and cycling rate is

129 and sorbent; this results in ca. 10% higher micropore volume with limited impact on its thermal stab

130 trend regularly with N2 or CO2 surface area, micropore volume, mesopore volume, H/C ratio, O/C ratio,

131 graphite due to the higher surface area and micropore volume.

132 r intensity, while a higher surface area and micropores volume were important for removing phenolic a

133 ciency was related to their surface area and micropores volume.

134 t properties such as large surface areas and micropore volumes, that favor a high adsorption capacity

135 The defects in the silica layer of the micropore wall enable the creation of an electric pathwa

136 The MO adsorbed in the micropores was strongly adsorbed and difficult to remove

137 ion, provided that distances between any two micropores were sufficient.

138 that the heel was mainly built up in narrow micropores which can be occupied or blocked by some of t

139 n of the total permeable area created by the micropores (which would approximate the area available f

140 holder from single crystalline silicon with micropores, which carries up to thousands of crystals an

141 f adsorbed and non-adsorbed molecules within micropores, which experience significantly different che

142 y and structure of these thermally regulated micropores, which is crucial to systematic engineering o

143 the vast numbers of micropores in shale, the micropores will be unavailable for storage for geologic

144 was fabricated in silicon in series with two micropores with 2 and 100 microm diameters.

145 nificantly dependent on the volume of narrow micropores with a pore size of less than 0.8 nm rather t

146 rd, accessible method for the fabrication of micropores with diameters from 2 to 800 micro m in films

147 simulate red cell motion through cylindrical micropores with diameters of 3.6, 5, and 6.3 microns, an

148 PIMs contain interconnected regions of micropores with high gas permeability but with a level o

149 d nitrogen-doped active carbons exhibit rich micropores with high surface area and high nitrogen cont

150 (-1)) that arise almost entirely (>90%) from micropores, with an oxygen-rich nature.

151 Two binding energies are present in the micropores, with the lower, more dominant one being on t

152 he thin inorganic barriers of interconnected micropores within deep-sea vents.

153 aker ionic interactions are allowed to enter micropores without sacrificing the power density.