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1 otion of an optically levitated, underdamped microparticle.
2 -end regions and to a capture probe-magnetic microparticle.
3 e collapse near a gallium-based liquid-metal microparticle.
4 a delivery of miR-23a-and miR-155-containing microparticles.
5 sein digest using 70 mug of magnetic Ti-IMAC microparticles.
6 ethylsiloxane microfabricated patches to fix microparticles.
7  poly(vinylpolypyrrolidone), and polystyrene microparticles.
8 ees C were the optimal conditions for OLE-SA microparticles.
9 , p = 0.029), compared to the acellular bone microparticles.
10 beads by moderate addition of self-propelled microparticles.
11 id metal microdroplets and metallic magnetic microparticles.
12 s only the superficial ORP was released from microparticles.
13 otential bioavailability from OLE and OLE-SA microparticles.
14 tions of the acoustophoretic response of the microparticles.
15 oscillating shell composed largely of silica microparticles.
16  (TLR) ligands, using biodegradable, polymer microparticles.
17 the formation of ceramide and the release of microparticles.
18 tion, characterization and quantification of microparticles.
19  of intricate arrays of droplets, cells, and microparticles.
20 S/DNA NP loading and encapsulation within ZN microparticles.
21 tection of those walkers by substrate-coated microparticles.
22  an important class of biomedically relevant microparticles.
23 is the broad size distribution of biological microparticles.
24 pes of surface patterns in these pollen-like microparticles.
25 uantifications on irregularly shaped uranium microparticles.
26 /min, respectively, to continuously generate microparticles.
27  heterogeneous loads consisting of nano- and microparticles.
28  and detection scheme using barcoded polymer microparticles.
29  approach is applied to isolate a mixture of microparticles (1.1, 3.2, and 5 mum in diameter) into di
30 sment of novel and economically manufactured microparticle adjuvants, namely strontium-doped hydroxya
31       We suggest that this membrane-mediated microparticle aggregation is a reason behind reported lo
32 other active components are not required for microparticle aggregation.
33 ne microparticles compared to acellular bone microparticles alone.
34  potato, and cereal starch granules from the microparticle analysis and milk protein from the proteom
35  of diet in mid-19th-century Ireland through microparticle and proteomic analysis of human dental cal
36 st protocol of poly(lactic-co-glycolic) acid microparticles and a replication-defective herpes simple
37 4.7 macrophage cells upon the uptake of both microparticles and B. anthracis Sterne 34F2 spores.
38 thod to size dependently control movement of microparticles and cells in paper using surface acoustic
39 d physical changes experienced by individual microparticles and exploration of the role of pH in the
40 (mu(EP)((3))), for four types of polystyrene microparticles and four cell strains.
41 ly aligned, electrospun microfibers with the microparticles and further demonstrate that the substrat
42 ally engineered rheology crucially depend on microparticles and microfibers with tunable shape, size,
43  demonstrated as a novel platform to produce microparticles and microfibers with tunable size, shape,
44 only able to shrink larger elements (such as microparticles and microfibers) into micro/nano-elements
45  modulate the pharmacological performance of microparticles and mitigate the initial burst release.
46 dy how a short-ranged adhesive force between microparticles and model lipid membranes causes membrane
47 ings were contaminated with carbon and steel microparticles and stressed using a 17 kW continuous-wav
48  from the surface roughness arising from the microparticles and the chemical cue offered by the fatty
49 lease of catalytic DNA walkers from hydrogel microparticles and the detection of those walkers by sub
50 s and specialized for the capture of luminal microparticles and their delivery to underlying immune c
51 ensuring its overlap with the functionalized microparticles and ultimately yielding enhanced detectio
52 hear stress-induced increase in CD31+/CD41b- microparticles, and improved FMD after accounting for th
53 the formulation of printlets, nanoparticle-, microparticle-, and nanofiber-based delivery systems for
54                                              Microparticle architecture, as determined by scanning el
55 ring coefficients and contrast factor of the microparticles are determined, and in a sensitivity anal
56                                              Microparticles are formed in stored pRBCs over time and
57                                   The silica microparticles are functionalized with branched polyethy
58                                              Microparticles are guided to and pushed into microwells
59 nlinear material characteristics of aluminum microparticles are investigated through precise single p
60                                              Microparticles are lipid bilayer-enclosed vesicles produ
61  the microparticle surface when the magnetic microparticles are transferred to a polymerase chain rea
62 y activated tissue-infiltrating PMNs release microparticles armed with proinflammatory microRNAs (miR
63                                  Large-scale microparticle arrays (LSMAs) are key for material scienc
64 crowell-based approach to create large-scale microparticle arrays with complex motifs.
65 is study was to design and evaluate hydrogel microparticles as a carrier for sustained pulmonary deli
66 liver CTX conjugated with OCT in the form of microparticles as a GIT-targeted SSTR therapy.
67 t the properties and results of Ac-DEX nano-/microparticles as well as the use of the polymer in othe
68 aracterization of surface morphology of PLGA microparticles, as it is a manifestation of the formulat
69 ulations and electrochemical measurements on microparticles at ultramicroelectrodes to explore this e
70 e applicability of this system to enrich the microparticles based on the inertial focusing mechanism
71                                              Microparticle-based delivery of TLR9 ligands might serve
72  of a bioresorbable mineral coating improves microparticle-based transfection of plasmid DNA lipoplex
73 flow-mediated dilation (FMD) and circulating microparticles before and after 20 minutes of experiment
74 ple method for producing donut-shaped starch microparticles by adding ethanol to a heated aqueous slu
75 2O2 formation in aqueous suspensions of FeS2 microparticles by monitoring, in real time, the H2O2 and
76 oping (<1 at%) render quasi-metallic silicon microparticles by substitutional doping and increase lit
77                                     Metallic microparticles can acquire remarkable nanoscale morpholo
78 mino acid (UAA) incorporation, these protein microparticles can also be photo-crosslinked and stably
79                 We show that chitosan-coated microparticles can lyse human cells and capture the rele
80 tic surface reactions can be used to deliver microparticle cargo to specified regions in microchamber
81 ex changes, including changes in circulating microparticles, cell-free DNA, and neutrophil extracellu
82 ere, we fabricate a synthetic cell-mimicking microparticle (CMMP) that recapitulates stem cell functi
83 dhesive; anti-inflammatory effects of chitin microparticles (CMPs; 1- to 10-mum diameters) have been
84          To prepare the biohybrid motors, Mg microparticles coated with titanium dioxide and poly(l-l
85 mesenchymal stromal cells (MSCs)-seeded bone microparticles compared to acellular bone microparticles
86 orrelation between the capture level and the microparticles concentration in solution, two calibratio
87                     A dispersion of magnetic microparticles confined at the air-liquid interface and
88 een applied to demonstrate that the obtained microparticles consist of a triuranium octoxide phase.
89 e therapeutic utility of an immunomodulatory microparticle containing natural TLR9 ligand (MIS416).
90                         Spray dried hydrogel microparticles containing biodegradable sodium carboxyme
91 an increase in the mayonnaise viscosity when microparticles containing chia and pumpkin seeds oil wer
92 t, on the successful addition of spray-dried microparticles containing roasted coffee oil, to soluble
93 avenous injection, but numerous cell-derived microparticles continued to circulate in blood.
94              The different subpopulations of microparticles could be determined via their capture ont
95                        Chitosan-Zein Nano-in-Microparticles (CS-ZN-NIMs), consisting of core Chitosan
96               Highly radioactive cesium-rich microparticles (CsMPs) released from the Fukushima Daiic
97 icroparticles, while the moisture content of microparticles decreased with desolvation and increased
98 abled delivery of large permeants, including microparticles, deep into colonic tissue ex vivo.
99                                              Microparticle delivery and release of NAMPT inhibitor at
100 very was found to depend on size, with large microparticles demonstrating negligible clearance from t
101                                 Accordingly, microparticles dispersed in fluids are rapidly focused t
102 dressed by introducing a mixture of tungsten microparticles dispersed within a LM matrix (LM-W) that
103  stamping, direction- and track-programmable microparticle/droplet transport, and smart magnetic micr
104             The changes in morphology of the microparticles during different phases of the in vitro r
105 Previous studies have shown that circulating microparticles during P. vivax acute attacks are indirec
106 functionalized colloids (fluorescent polymer microparticles, dye-labeled protein on gold nanoparticle
107  drive controlled aggregation of polystyrene microparticles, either through reversible coiled-coil in
108 application of controlled forces on a single microparticle embedded in an individual cell of an embry
109 73), tissue factor (TF), endothelial-derived microparticle (EMP) numbers and phenotype, and platelet
110 othelial function, we quantified endothelial microparticles (EMPs) and endothelial progenitor cells (
111 ated that Cavin-2 is secreted in endothelial microparticles (EMPs) and is required for EMP biogenesis
112                                  Endothelial microparticles (EMPs) are endothelium-derived submicron
113                                  Endothelial microparticles (EMPs) are involved in various cardiovasc
114               Here we combined biodegradable microparticles encapsulating Rapa (Rapa MPs) with vaccin
115  the concept of a micropatterned surface for microparticle entrapment, featuring high-aspect-ratio el
116                                    ATRA-PLLA microparticles exerted its efficacy likely through degra
117                                          The microparticles exhibited a higher gelatinization tempera
118  Indeed, EVs (a terminology that encompasses microparticles, exosomes, and apoptotic bodies) are emer
119 MIP layer grafted from the surface of silica microparticles following a RAFT (reversible addition-fra
120 were explored for their ability to fix solid microparticles for drug-release applications, using tetr
121 , so that formed NPs adhered to the mannitol microparticles for easy isolation and immediate dispersi
122 imple yet versatile approaches to synthesize microparticles for mechanosensing, tissue engineering, d
123 gradable bilayer MN arrays containing nano - microparticles for targeted and sustained intradermal dr
124 hesis, aptly designed for the formulation of microparticles for vaccines and immune modulation.
125 mers and a mechanistic understanding of PLGA microparticles formation.
126                     The spray dried hydrogel microparticles formulation can be considered as a potent
127 y of this chip for generating pharmaceutical microparticle formulations, we generated 5-9 um polycapr
128 iformity) increased from 1.24 to 3.1 for the microparticles generated at the homogenization speed of
129 h confirmed treatment-naive sarcoidosis with microparticles generated from Mycobacterium abscessus ce
130 red proteins (IDPs), we have created complex microparticle geometries, including porous particles, co
131 the antigen-presenting cell-targeting glucan microparticle (GP) vaccine delivery system.
132     The results demonstrated that formulated microparticles had a mean geometric particle size betwee
133                                        These microparticles had a spherical morphology, presented goo
134                                    ATRA-PLLA microparticles had good biocompatibility, and significan
135 hape and irregular size, and the lyophilized microparticles had irregular shape and size.
136                                 The atomized microparticles had spherical shape and irregular size, a
137 in films of a composite of nafion and carbon microparticles have been deposited on nonconducting subs
138 ng the shape and/or composition of catalytic microparticles; however, the ability to design particle
139                                              Microparticle image velocimetry allowed mapping of the f
140 speed of the microdroplets is measured using microparticle image velocimetry.
141 r additional testing with a chemiluminescent microparticle immunoassay.
142 ontent, and the generation of three types of microparticles (iMP) that expressed platelet markers, tu
143               Over the years, nanoparticles, microparticles, implants of poly(D,l-lactide-co-glycolid
144  intensity in SC while, for IC, all loads of microparticles improved aroma intensity.
145 hat exploits electrochemical sintering of Zn microparticles in aqueous solutions at room temperature.
146 ration of the spray dried inhalable hydrogel microparticles in comparison to orally administered Viag
147 nonreciprocal effective interactions between microparticles in complex plasmas were published in 1995
148                    The directed transport of microparticles in microfluidic devices is vital for effi
149 ind reported long retention times of polymer microparticles in organisms.
150 r-based SAW approach to trap and concentrate microparticles in paper and release them when required,
151 ith sufficient spatial resolution to resolve microparticles in tablets is essential to ensure high qu
152  texture was not affected by the presence of microparticles in the mayonnaise in all formulations tes
153  of endothelial cell apoptosis (CD31+/CD41b- microparticles) in COPD patients, but not age-matched co
154 logy using micron-scale ellipsoidal magnetic microparticles, in both cases using light-sheet fluoresc
155        In hypertensive patients, endothelial microparticles indeed contained higher levels of NOX5-bu
156 sure did not induce platelet aggregation, TF microparticle induction, or TF on granulocytes or eosino
157 ing pro-inflammatory effector T cells, these microparticles inhibited destructive hypersensitivity re
158                                    The solid microparticle is more convenient for storage and transpo
159                           The density of the microparticles is determined by using a neutrally buoyan
160 on, and from this the compressibility of the microparticles is inferred.
161                 Transfusion of aged pRBCs or microparticles isolated from aged blood into mice caused
162  in mice receiving transfusions of pRBCs and microparticles isolated from these units.
163 es for shape-based separation and sorting of microparticles like microplastics, cells, and crystal po
164  platform is introduced, employing magnesium microparticles loaded within the microneedle patch, as t
165 udy showed that inhaled spray dried hydrogel microparticles (M6) formulation had significantly higher
166 e study were also studied for three types of microparticles made with different PLGA concentrations a
167 rug loading (DL) from 27.4% to 31.7% for the microparticles made with the homogenization speed of 200
168 munications, microscopy, quantum optics, and microparticle manipulation.
169      In the presence of these mineral-coated microparticles (MCMs), we observed up to 4-fold increase
170                            Here we show that microparticle-mediated intratumoral delivery of NAMPT in
171                                              Microparticle-mediated local inhibition of NAMPT modulat
172 mulation of anti-cancer drugs, and ATRA-PLLA microparticles might be a promising targeted drug for HC
173                               Megakaryocytic microparticles (MkMPs), the most abundant MPs in circula
174           Here, we demonstrate that platinum microparticles move spontaneously in solutions of hydrog
175 duced inflammatory response of two polymeric microparticle (MP) EPO-R76E sustained release formulatio
176                                              Microparticles (MPs) are cell-cell communication vesicle
177                                  Circulating microparticles (MPs) are elevated in many cardiovascular
178                                  Circulating microparticles (MPs) are major mediators in cardiovascul
179                                        Blood microparticles (MPs) are small membrane vesicles (50-100
180                                              Microparticles (MPs) are submicron extracellular vesicle
181                                              Microparticles (MPs) are submicron-sized shed membrane v
182 as therefore to assess the exposure of PS on microparticles (MPs) as well as on endothelial and blood
183 llular Hb obtained from RBCs and RBC-derived microparticles (MPs) from the blood of 23 SCD patients (
184                                              Microparticles (MPs) have emerged as a surrogate marker
185 in NPs encapsulated within gastro-protective microparticles (MPs) made from alginate and chitosan tha
186  rats, as well as ligand-decorated synthetic microparticles (MPs) to examine the role of integrin alp
187                    Production of blood-borne microparticles (MPs), 0.1-1 um diameter vesicles, and in
188 -deleted mice, which had reduced circulating microparticles (MPs), supported accelerated tumor growth
189          In various cardiovascular diseases, microparticles (MPs), the membrane-derived vesicles rele
190 nant GET-RUNX2 protein) encapsulated in PLGA microparticles (MPs), we demonstrate that human mesenchy
191 ine ligand 2 (CCL2) using controlled-release microparticles (MPs).
192 drug (vitamin D3, VD3)-loaded PLGA nano- and microparticles (NMP) were prepared by a single emulsion
193 that it depends neither on the nature of the microparticles nor that of the excitation; rather, angul
194                             The stability of microparticles of Bordo grape skin aqueous extract, prod
195                            Ligand-conjugated microparticles of iron oxide (MPIO) have the potential t
196 netic resonance imaging using antibody-based microparticles of iron oxide targeting P-selectin.
197 re determined for NIST homogeneous spherical microparticles of K411 glass and compared to certified o
198 unctionalize the surface of a substrate with microparticles of natural fatty acids at a controllable
199 m) but not by chitosan (deacetylated chitin) microparticles, oligosaccharide chitin, or glucosamine.
200  growth factors in delivery vehicles such as microparticles or nanoparticles.
201                                          The microparticle particle formation was not due to the ICL
202 ovel microchannel architectures for designed microparticle patterning.
203 nd create injectable pulsatile drug-delivery microparticles, pH sensors, and 3D microfluidic devices
204                             Platelet-derived microparticles (PMPs) are associated with enhancement of
205 FM) to quantify and qualify platelet-derived microparticles (PMPs), on the whole nano-to micro-meter
206  that release was more greatly influenced by microparticle porosity, and hence surface area, than by
207  single intravitreous injection of sunitinib microparticles potently suppresses choroidal neovascular
208 ity of developing an inhaled nanoparticle-in-microparticle powder formulation was ascertained.
209                                  Endothelial microparticles prevent lipid-induced endothelial damage
210 ize of poly(D,L-lactide-co-glycolide) (PLGA) microparticles produced by diverse microfluidic systems
211                                 Injection of microparticles produced in vitro from Jurkat cells resul
212                                              Microparticles produced using Arabic and cashew gums sho
213                                              Microparticles produced using cashew gum were more hygro
214 elinase activity, ceramide accumulation, and microparticle production during pRBC storage.
215 Here, the authors show that VEGF-immobilized microparticles prolong survival of endothelial progenito
216         Intravitreous injection of sunitinib microparticles provides a promising approach to achieve
217  studied the electromigration of polystyrene microparticles ranging in size from 2 to 6.8 mum, three
218 rin polymerization, platelet activation, and microparticle release were increased in venovenous extra
219 s a novel mechanism whereby membrane-derived microparticles released by tissue infiltrating PMNs (PMN
220               Many applications of nano- and microparticles require molecular functionalization.
221 ntravitreous injection in rabbits, sunitinib microparticles self-aggregate into a depot that remains
222  in venules, generated tissue factor-bearing microparticles, shortened plasma-clotting times, and inc
223  to conventionally dried powders, PGSS-dried microparticles showed lower primary and secondary oxidat
224  formulated drug-loaded spray dried hydrogel microparticles showed promising in-vitro and in-vivo res
225                   Thus, the chitosan/xanthan microparticles showed the best potential for practical a
226            In this case, the chitosan/pectin microparticles showed the best release profile.
227                           Moreover ATRA-PLLA microparticles significantly enhanced the efficacy of AT
228                     The PEI-decorated silica microparticles (SiO2@PEI MPs) were characterized using s
229 he properties of the microparticles, such as microparticle size distributions, surface and internal m
230 e conjugated to discoidal silicon mesoporous microparticles (SMP) to enhance accumulation of these ag
231                       Simultaneously, starch microparticles (SMP) were also obtained, which were sign
232  biodegradable polymer to generate sunitinib microparticles specially formulated to self-aggregate in
233  molecules could penetrate easier within the microparticles, substantially increased their solubility
234 sing parameters affect the properties of the microparticles, such as microparticle size distributions
235 sing carboxylic acid-functionalized magnetic microparticles supported onto screen-printed carbon elec
236 bound DNA can be amplified directly from the microparticle surface when the magnetic microparticles a
237  nonreciprocal effective interaction between microparticles suspended a radio-frequency produced plas
238 ection process that involves centrifuging of microparticles suspended in different density solutions,
239                                    Then, the microparticles swelled to form smooth surfaces.
240 nufacturing process, and characterization of microparticle systems.
241 e assemblies of the ever-increasing range of microparticle systems.Self-assembled systems are normall
242               Active colloids are a class of microparticles that 'swim' through fluids by breaking th
243  wherein systemically injected cells release microparticles that accumulate in the BM.
244 e matrix is dispersed with liquid metal (LM) microparticles that are used to tailor the thermal and e
245 duce hemodynamically active, proinflammatory microparticles that cause intrahepatic inflammation, vas
246 , radiolabelled molecules, nanoparticles, or microparticles that either naturally accumulate in or ar
247 e cancer trap is composed of hyaluronic acid microparticles that have good cell and tissue compatibil
248 ing method using amine-functionalized silica microparticles that is effective under varying operating
249 lcohol matrix filled with poly(acrylic acid) microparticles that mimics functional properties and bio
250 the potential use of these solid lipid-based microparticles, the release kinetics of a model drug (pi
251 d characterize their formulation into porous microparticles through spontaneous emulsification withou
252 e the immunomodulatory role of tumor-derived microparticles (TMPs)-extracellular vesicles shed from t
253 ybridized the cryogels with calcium peroxide microparticles to controllably produce bactericidal hydr
254 scence-encoded polystyrene core/silica shell microparticles to create a site for competitive binding
255 te the potential for using antibiotic-loaded microparticles to effectively treat chronic UTIs.
256 to a faster shell formulation, enabling PLGA microparticles to entrap more naltrexone into the struct
257 h, it is critical to chemically characterize microparticles to identify whether particles are indeed
258 s can be used for the selective targeting of microparticles to infected tissue(s).
259 nsional patterned polymer surfaces and solid microparticles, to create patterns of iridescent colour
260 m pyrophosphate dihydrate, as well as silica microparticles, triggered cell necrosis involving PPIF-d
261                                Compared with microparticle unchallenged PBMCs, total NF-kappaB and p-
262 s found in developed granulomas comparing to microparticle unchallenged PBMCs.
263 e latter effect is especially pronounced for microparticles under the soft contact regime, where the
264  aqueous suspension of silver orthophosphate microparticles under UV illumination, in the presence of
265                  Contactless manipulation of microparticles using acoustic waves holds promise for ap
266 riboflavin-loaded whey protein isolate (WPI) microparticles, using desolvation and then spray drying.
267 -survival approach based on VEGF-immobilized microparticles (VEGF-MPs).
268  accessibility of methods for characterizing microparticles via Raman spectroscopy, we created an app
269 suspensions is measured as a function of the microparticle volume fraction, and from this the compres
270                          The average size of microparticles was 14.1+/-0.3mum with holes of an averag
271                        ORP from both OLE and microparticles was degraded to hydroxytyrosol under colo
272                        The uniformity of the microparticles was found to be related to the viscosity
273     The average diameter of resistant starch microparticles was in the range of 45.53-49.29mum.
274           The crystalline arrangement of the microparticles was of a V-type single helix.
275                                      As PLGA microparticles went through structural changes, the surf
276                                 The obtained microparticles were analysed by SEM, XRD and DSC.
277 ol)-poly(lactic-co-glycolic acid) (PEG-PLGA) microparticles were engineered to release TGF-beta1, Rap
278                                              Microparticles were engineered to sustainably release TG
279 one-loaded poly(lactide-co-glycolide) (PLGA) microparticles were prepared using an in-line homogeniza
280  release site and release characteristics of microparticles were readily adjusted by varying the etha
281                             The donut-shaped microparticles were stable for more than 18months and ca
282 yphosphate (TPP), further encapsulated in ZN microparticles, were formulated using a water-in-oil emu
283 icated micropillars, and the diameter of the microparticles, were investigated.
284 ked clusters using thermally expandable soft microparticles, whereby the self-assembling process is r
285 by the release of large numbers of activated microparticles which coat leukocytes.
286 1 directly and as a component of circulating microparticles, which activated synovial fibroblasts in
287 influenced the morphology of the spray-dried microparticles, while the moisture content of microparti
288           The in-line approach produced PLGA microparticles with a highly reproducible size distribut
289 sing commercially available polystyrene (PS) microparticles with a size comparable to cancer cells.
290 le material for the development of probiotic microparticles with adequate physicochemical properties
291  we show an unusual phenomenon that tin (Sn) microparticles with both poor size distribution and spat
292               The controllable production of microparticles with complex geometries is useful for a v
293 entatively demonstrated for a set of polymer microparticles with different aldehyde labeling densitie
294                                              Microparticles with higher loads of roasted coffee oil w
295 loss due to the transmission of electrons in microparticles with irregular shapes, a method was devel
296                                          The microparticles with maltodextrin (1:9)-100 degrees C had
297                                 Here, porous microparticles with such a structure are produced in a s
298 shold mediated by optically trapped graphene microparticles with the use of a laser beam of a few hun
299 tion of the elemental composition of uranium microparticles with undefined geometry using standardles
300 in largely uniform poly L-lactic acid (PLLA) microparticles, with the efficiency of 91.4% and yield o

 
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