ライフサイエンスコーパス: nanoshell

1 istinct at various positions within a single nanoshell.

2 LSPR at different positions within a single nanoshell.

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

4 physical cross-links formed in the imprinted nanoshells.

5 facilitate deep glandular penetration of the nanoshells.

6 (NPs) can spontaneously organize into porous nanoshells.

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

8 plasmon absorption (LSPR) of individual gold nanoshells.

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

10 The nanoshells accumulated within the intracranial cTVT, sug

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

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

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

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

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

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

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

18 Metal nanoshells are a class of nanoparticles with tunable opt

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

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

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

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

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

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

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

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

27 Our model of nanoshell assembly shows that the spontaneous curvature

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

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

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

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

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

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

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

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

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

37 Controls treated without nanoshells demonstrated significantly lower average temp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 Gold nanoshells have been synthesized by reacting aqueous HAu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

83 4 W/cm2) in solid tumors treated with metal nanoshells reached average maximum temperatures capable

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

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

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

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

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

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

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

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

92 nced Raman scattering response of individual nanoshell substrates.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 These metal nanoshells were composed of silica spheres with encapsul

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

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

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

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

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

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

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

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

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

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

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