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1 CeO2, as well as the polymer coating alone (nanocapsule).
2 t step toward development of a biocompatible nanocapsule.
3 l disruption to the overall structure of the nanocapsule.
4 of discrete nickel-seamed pyrogallol[4]arene nanocapsules.
5 additional shell covalently connected to the nanocapsules.
6 terior as well as exterior properties of the nanocapsules.
7 lysis of dye-sensitized, lipid-vesicle based nanocapsules.
8 and specifically functionalized to generate nanocapsules.
9 chondrocytes which were pretreated with the nanocapsules.
10 l does not affect the fluorescence of poly A nanocapsules.
11 elf-assembles to form hierarchically ordered nanocapsules.
12 nterior of gallium-seamed pyrogallol[4]arene nanocapsules.
13 ht-induced release of DHEA from targeted DNA nanocapsules.
14 mechanisms into two different, well-defined nanocapsules: (1) pH-induced assembly yielded 28 nm viru
15 th Sleeping Beauty transposase in hyaluronan nanocapsules and injected them intravenously into hemoph
18 idate the interplay between chondrocytes and nanocapsules and their therapeutic effect, we pursued a
19 teraction between adenine moieties of Poly A nanocapsules and thymine/uracil does not affect the fluo
20 solution, we can entrap charged molecules in nanocapsules and trigger the release of encapsulated con
21 ocytes did not show any adverse effects upon nanocapsule application and coherent anti-Stokes Raman s
24 payload release from these plasmon resonant nanocapsules are independently controlled using a pulsed
27 t to functional beverages, but protein-based nanocapsules are unstable around the isoelectric point o
28 n gold nanorod (AuNR)-encapsulated graphitic nanocapsule (AuNR@G), a photothermal agent, through pi-p
29 The aim of this study was to produce bixin nanocapsules by the interfacial deposition of preformed
33 n the nanometer-thin shells of hollow porous nanocapsules can regulate the transport of charged molec
35 , we show a novel delivery platform based on nanocapsules consisting of a protein core and a thin per
37 tudy has also demonstrated that CeO2 NPs and nanocapsules containing Nile red are able to traverse th
39 is challenge, we present here a single siRNA nanocapsule delivery technology, which is achieved by en
40 of curcumin is improved dramatically in such nanocapsules demonstrating that nanotechnology could be
41 MS-DE or PDMS-DC) were encapsulated into the nanocapsules during the miniemulsion process and their r
44 s studies on utilizing polymeric vesicles as nanocapsules, fabrication of tunable molecular pathways
45 and characterized self-assembling lipid-core nanocapsules for coencapsulation of two poorly soluble n
46 mes offers a promising functionality to tune nanocapsules for encapsulating and releasing fluorescent
47 hnology not only demonstrates the use of UOx nanocapsules for hyperuricemia management, but also prov
48 ing hyaluronan- and asialoorosomucoid-coated nanocapsules, generated using dispersion atomization, to
51 ork of nickel-seamed hexameric metal-organic nanocapsules has been synthesized by connecting the tail
52 e report self-assembled intertwining DNA-RNA nanocapsules (iDR-NCs) that efficiently delivered synerg
53 in we describe a nucleic acid functionalized nanocapsule in which nucleic acid ligands are assembled
54 reassembly could enable application of these nanocapsules in drug delivery and in nanomaterials synth
57 Rationally designed non-covalent protein nanocapsules incorporating copper-free "click chemistry"
59 ternal cavity and sufficient dynamicity, the nanocapsule is able to recognize and encapsulate large a
60 de new functionality to the microcapsule and nanocapsule is layer-by-layer deposition of functional s
62 work shows that surface functionalization of nanocapsules is an effective and innovative method of co
63 luidic platform for the synthesis of complex nanocapsules is presented via a controlled self-assembly
65 ed and/or expanded, that possess extra-large nanocapsule-like cages, high porosity, and potential for
68 combining a cell-targetable, icosahedral DNA-nanocapsule loaded with photoresponsive polymers, we sho
69 In this work, we utilized polymeric magnetic nanocapsules (m-NCs) for magnetic targeting in tumors an
71 -of-concept encapsulation of HRP through PSS nanocapsules may pave the way for alternative signal enh
72 report the use of stable magnetic graphitic nanocapsules (MGNs), for in situ targeted magnetic reson
74 d for hyperuricemia treatment, as-formed UOx nanocapsules, n(UOx), exhibits enhanced stability, more
76 Cl) embedded with an acid-responsive DNase I nanocapsule (NCa) was developed for targeted cancer trea
78 ssibility, we encapsulated HAs in lipid-core nanocapsules (NCs) based on a biodegradable and biocompa
80 An original oral formulation of docetaxel nanocapsules (NCs) embedded in microparticles elicited i
86 ammation affects the clearance of 50nm lipid nanocapsules, or is exacerbated by their pulmonary admin
87 different biomaterial types, pegylated lipid nanocapsules, polyvinyl acetate (PVAc) and polystyrene n
90 tor dyes were entrapped in vesicle-templated nanocapsules prepared by copolymerization of tert-butyl
97 s, manipulation, and assembling of plasmonic nanocapsule SERS sensors for high-sensitivity biochemica
98 given quantity of antibody, the bioconjugate nanocapsules showed 30 times greater sensitivity and a s
101 vourable colloidal properties), silica-based nanocapsules (SNCs) with a size cutoff of approximately
103 re, we report the discovery of a enantiopure nanocapsule that is formed through the self-assembly of
104 Vaults are self-assembled ribonucleoprotein nanocapsules that consist of multiple copies of three pr
105 into the system resulted in the formation of nanocapsules that were cleaved under specific conditions
107 ffraction structure of a dimeric zinc-seamed nanocapsule using a mixed pyrogallol/resorcinol[4]arene
108 this information, we were able to design new nanocapsules using ternary mixtures of lipid and cholest
110 cavitands were shown to form supramolecular nanocapsules via assembly around a range of guest molecu
113 und 100% of encapsulation efficiency and the nanocapsules were considered physically stable during 11
114 silencing target of HIV therapy, CCR5-siRNA nanocapsules were delivered into 293T cells and successf
116 earance and whole body distribution of lipid nanocapsules were unaffected by the presence of acute lu
117 nitroxide was incarcerated into an octa acid nanocapsule, which was confirmed by 1H NMR and EPR spect
118 e siRNA molecule within a degradable polymer nanocapsule with a diameter around 20 nm and positive su
120 amines in the polymerization, we endowed the nanocapsules with efficient cell-transduction and suffic
123 ion with chloroauric acid, forming graphitic nanocapsules with significant surface-enhanced Raman sig
124 nyl groups, we obtained nanosized core-shell nanocapsules with the enzyme as the core and a cross-lin
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