ライフサイエンスコーパス: nanoshell

1 phoretic motility driven by an asymmetric Au nanoshell.

2 istinct at various positions within a single nanoshell.

3 LSPR at different positions within a single nanoshell.

4 the SM-SERS fluctuations from single silver nanoshells.

5 ibe mobility of lipid molecules in these 1-D nanoshells.

6 h a mean size much smaller than that of gold nanoshells.

7 mbedded within the walls of porous Al(2)O(3) nanoshells.

8 mmiscible elements into single phase ceramic nanoshells.

9 (NPs) can spontaneously organize into porous nanoshells.

10 physical cross-links formed in the imprinted nanoshells.

11 facilitate deep glandular penetration of the nanoshells.

12 iodegradability by doping iron(III) into the nanoshells.

13 plasmon absorption (LSPR) of individual gold nanoshells.

14 The nanoshells accumulated within the intracranial cTVT, sug

15 The formation of a PANI nanoshell allows dynamic modulation of the dielectric en

16 escent nanoparticles, gold nanoparticles and nanoshells, among others.

17 -shift by 3.0 nm per methylene unit for gold nanoshells and 0.2 nm per methylene unit for solid collo

18 rom two types of nanoparticle substrates: Au nanoshells and Au nanorods.

19 age to normal brain tissue in the absence of nanoshells and compensate for variability in the accumul

20 es a scalable strategy to produce mesoporous nanoshells and proposes an in situ functionalization mec

21 d description of NPs reveal the emergence of nanoshells and some of their stabilization mechanisms.

22 After conjugating the TSDP onto gold nanoshells and upon NIR illumination, the increased temp

23 to mesoscale chains, sheets, supraparticles, nanoshells, and nanostars.

24 Metal nanoshells are a class of nanoparticles with tunable opt

25 Porous, electrically interconnected copper nanoshells are conformally deposited around the silicon

26 muc-Si based solar cells while the plasmonic nanoshells are formed by a combination of silica and gol

27 Highly symmetric nanoshells are found in many biological systems, such as

28 Au and Ag nanoshells are investigated as substrates for surface-en

29 results seem to suggest that the individual nanoshells are not smooth and well-defined, but are rath

30 plasmon resonances of a concentric metallic nanoshell arise from the hybridization of primitive plas

31 that spontaneously assemble in a continuous nanoshell around a template of a carbon nanotube wrapped

32 ototypical tunable plasmonic particles, gold nanoshells, as well as approximately 2-fold higher X-ray

33 Our model of nanoshell assembly shows that the spontaneous curvature

34 wed the effectiveness and selectivity of the nanoshell-assisted thermal ablation.

35 through tissue is optimal, a distribution of nanoshells at depth in tissue can be used to deliver a t

36 ciency of near infrared resonant silica-gold nanoshells (AuNSs) and benchmarked this against the heat

37 duced release are distinctly observable from nanoshell-based complexes, with light-triggered release

38 ve laser-induced release of docetaxel from a nanoshell-based DNA host complex showed increased cell d

39 econd pulsed laser, lapatinib release from a nanoshell-based human serum albumin protein host complex

40 ect ratio SiGe nanowire (NW) with a metallic nanoshell cap.

41 Aggregation of antibody/nanoshell conjugates with extinction spectra in the near

42 In particular, the nanoshells core radius and metal thickness, the periodic

43 s (polystyrene nanoparticle core with silver nanoshells covalently conjugated to HSA antibodies), and

44 Controls treated without nanoshells demonstrated significantly lower average temp

45 ation of the plasmons of the inner and outer nanoshells determines the resonant frequencies of the mu

46 ew type of nanostructures feature a metallic nanoshell directly coupled to the crystalline semiconduc

47 a spheres in the absence of metal, the metal nanoshells displayed an enhanced emission intensity, sho

48 Cells without nanoshells displayed no loss in viability after the same

49 Doxorubicin-loaded hollow gold nanoshells (Dox@PEG-HAuNS) increase the efficacy of phot

50 , carboxysomes, exosomes, vacuoles and other nanoshells easily self-assemble from biomolecules such a

51 urrent, we investigate the role of plasmonic nanoshells, embedded within a ultrathin microcrystalline

52 The resulting thin palladium nanoshells exhibit enhanced catalytic activity and high

53 ition, the surface plasmon resonance of gold nanoshells exhibited a much more sensitive response towa

54 f [(89) Zr]-labeled hollow mesoporous silica nanoshells filled with porphyrin molecules, for effectiv

55 We find that SERS enhancements on nanoshell films are dramatically different from those ob

56 enhancements as large as 2.5 x 10(10) on Ag nanoshell films for the nonresonant molecule p-mercaptoa

57 With Pd islands grown on Au nanoshell films, this reaction can be followed in situ u

58 sis and application of aptamer-modified gold nanoshells for photothermal therapy (PTT).

59 ared to conventional ~150nm silica core gold nanoshells for photothermal therapy of triple negative b

60 xperimental observation of SERS inside metal nanoshells for the first time.

61 ies, the use of inert, inorganic silica-gold nanoshells for the treatment of a widely prevalent and r

62 nd glands, followed by wiping of superficial nanoshells from skin surface and exposure of skin to nea

63 imit of detection (LoD) for silica-core gold nanoshells (GNSs) preloaded in nitrocellulose (NC) membr

64 cal trial in which laser-excited gold-silica nanoshells (GSNs) were used in combination with magnetic

65 Gold nanoshells have been synthesized by reacting aqueous HAu

66 nique physico-chemical properties of protein nanoshells help define their structure and morphology, a

67 are tethered to plasmon-resonant hollow gold nanoshells (HGN) tuned to absorb light from 650-950 nm.

68 ic stem cells is developed using hollow gold nanoshells (HGNs) and near-infrared (NIR) light.

69 ed within seconds by irradiating hollow gold nanoshells (HGNs) with a near-infrared (NIR) pulsed lase

70 d theoretically using Mie scattering for the nanoshells (i.e., nanoshells with silica cores approxima

71 cacy of ultrasonically-delivered silica-gold nanoshells in inducing photothermal disruption of sebace

72 The LSPR spectra of single nanoshells in several different solvents were also exami

73 ted as a function of 2n(2) (or 2epsilon) for nanoshells in six different solvents, a linear relations

74 nsate for variability in the accumulation of nanoshells in tumor.

75 Human breast carcinoma cells incubated with nanoshells in vitro were found to have undergone phototh

76 y predicted by stretching and flattering the nanoshells into a plate-like capsule while retaining the

77 Upon delivery of the nanoshells into the follicles and glands, followed by wi

78 mum requirements for the formation of closed nanoshells is a necessary step toward engineering of nan

79 poly(ethylene glycol) (PEG) adsorbates on Au nanoshells is determined by exploiting the surface-enhan

80 n of a single layer of 50-nm-thick spherical nanoshells is equivalent to a 1-mum-thick planar nc-Si f

81 d plasmonic droplet with functionalized gold nanoshells is then deposited at an overlapping spot and

82 This was accomplished using gold nanoshells, layered dielectric-metal nanoparticles whose

83 mportantly we demonstrate that the EC(50) of nanoshell loaded GEM can be suppressed but fully restore

84 and exposure of skin to near-infrared laser, nanoshells localized in the follicles absorb light, get

85 Importantly, the LSPR of individual nanoshells measured by the NIR-MSI microscope agrees wel

86 es used for detection consist of gold-silica nanoshells modified with a two-component mixed monolayer

87 tructures including gold/silver nanospheres, nanoshells, nanoflowers, and nanostars were synthesized

88 ng constructs such as dendrimers, liposomes, nanoshells, nanotubes, emulsions and quantum dots, these

89 We have also prepared multiple-walled nanoshells/nanotubes (or nanoscale Matrioshka) with a va

90 he visualization of therapeutically relevant nanoshell (NS) concentrations at the tumor site.

91 The synthesis of hollow Ag nanoshells (NSs) with tunable plasmon bands in the visib

92 ate the hollow metal nanocrystals, producing nanoshells of increased diameters and decreased thicknes

93 Cu core can be selectively etched to obtain nanoshells of the platinum-group metal components, leadi

94 the core and the formation of crystalline Si nanoshells on the outside.

95 electrostatic layer-by-layer deposition of a nanoshell onto the microspheres, and finally by their di

96 ved by surface plasmon heating with metallic nanoshells or nanoparticles, which have inherently narro

97 following subheadings: Au nanorods (NRs), Au nanoshells, other Au-related nanomaterials, graphene oxi

98 Such enhanced sensitivities should make gold nanoshells particularly useful as optical probes for che

99 The resulting porous phospholipid nanoshells (PPNs) are potentially useful for a range of

100 The band gap emission of fabricated nanoshells, ranging from 15 to 30 nm in diameter, has re

101 4 W/cm2) in solid tumors treated with metal nanoshells reached average maximum temperatures capable

102 ields at the surface of smooth and roughened nanoshells reveal that surface roughness contributes onl

103 of a dsDNA self-assembled monolayer on an Au nanoshell SERS substrate provide information concerning

104 igh enhancements and large active area of Au nanoshell SERS substrates, the transparency of Raman spe

105 een conjugated to near-infrared-absorbing Au nanoshells (SiO2 core, Au shell), each forming a light-r

106 We also discovered that the nanoshell structure can significantly enhance the therma

107 The organometallic polymers with nanoshell structure were confirmed by using FT-IR, UV-vi

108 her the removal of iron(III) from the silica nanoshell structure would facilitate its degradation.

109 ng-gallery resonant modes inside a spherical nanoshell structure.

110 nced Raman scattering response of individual nanoshell substrates.

111 ropose a general route to produce mesoporous nanoshell-supported nanocatalysts by in situ decoration

112 all molecular spacers coadsorbed onto the Au nanoshell surface to "raise" the DNA molecules yields a

113 thiols, a mixed monolayer is prepared on the nanoshell surface with the ability to recognize low conc

114 DNA aptamer self-assembled monolayers on Au nanoshell surfaces provides a direct, label-free detecti

115 than an extended "mushroom" configuration on nanoshell surfaces.

116 e new strategies in faceted nanoparticle and nanoshell synthesis, and provide insight into the molecu

117 to depend on the shape and morphology of the nanoshells, these results seem to suggest that the indiv

118 proof of concept for the passive delivery of nanoshells to an orthotopic tumor where they induce a lo

119 ne, and deferiprone, were found to cause the nanoshells to degrade on the removal of iron(III) within

120 cleotides were covalently bound on the metal nanoshells to hybridize with the target miRNA-486 molecu

121 use of spherical shape-deformable polymeric nanoshells to regulate the anisotropic growth of Ag nano

122 By tuning the nanoshells to strongly absorb light in the near infrared

123 ing the ability of the NIR absorption by the nanoshells to sufficiently drive this transition.

124 We use ~150nm silica-gold nanoshells, tuned to absorb near-IR light and near-IR la

125 Additionally, the silica-gold nanoshells used were designed to have a peak extinction

126 id metal nanoparticles to hollow metal oxide nanoshells via a nanoscale Kirkendall process-for exampl

127 th near-infrared (NIR) absorbing silica-gold nanoshells was designed as a platform for pulsatile deli

128 ngle dose of near-IR (NIR)-absorbing, 150-nm nanoshells was infused i.v. and allowed time to passivel

129 Nanoshells were coated with thiol-capped poly(ethylene g

130 These metal nanoshells were composed of silica spheres with encapsul

131 The surface plasmon peaks of these gold nanoshells were considerably red-shifted as compared to

132 ty and longer lifetime, the conjugated metal nanoshells were isolated distinctly from the cellular au

133 max)/fwhm)(2) values of LSPR for single gold nanoshells were plotted as a function of 2n(2) (or 2epsi

134 When the iron(III)-doped, silica nanoshells were submerged in fetal bovine and human seru

135 In this study, fluorescent metal nanoshells were synthesized as a molecular imaging agent

136 NIR-absorbing hollow gold nanoshells were synthetized and conjugated with anti-MUC

137 To obviate this problem, silica nanoshells were tested for enhanced biodegradability by

138 he important case of a four-layer concentric nanoshell, where the hybridization of the plasmons of th

139 e envisaged the integration of GEM with gold nanoshells which constitute an interesting class of nano

140 For a nanoshell with an offset core, the reduction in symmetry

141 gnostics in the future: 1) application of Au nanoshells with a magnetic core (MP@silica@Au); 2) use o

142 signal was enhanced 43 times integrating Au nanoshells with a magnetic core compared to the biosenso

143 application of anti-PSA antibody modified Au nanoshells with a magnetic core for enrichment of PSA fr

144 silica@Au); 2) use of surface plasmons of Au nanoshells with a magnetic core for spontaneous immobili

145 d 70.9 nm per refractive index unit for gold nanoshells with a mean diameter of 50 nm and wall thickn

146 ing Mie scattering for the nanoshells (i.e., nanoshells with silica cores approximately 800 nm in dia

147 thod for the synthesis of Prussian blue (PB) nanoshells with tunable size using miniemulsion peripher