ライフサイエンスコーパス: dendrimer

1 dendron, which is equivalent to generation 5 dendrimer.

2 he compactness of the periphery of the G8-OH dendrimer.

3 he hybrid hydrogenated-fluorinated RHF Janus dendrimer.

4 ase of the number of sulfamoyl groups in the dendrimer.

5 p to 27 leaving groups in a third-generation dendrimer.

6 a concept of an information-coded 2D digital dendrimer.

7 of the azide groups at the periphery of the dendrimer.

8 eased liver and spleen uptake compared to G4 dendrimers.

9 high affinity for DNA possessed by cationic dendrimers.

10 were also coassembled with hybrid RHF Janus dendrimers.

11 ent attachment of Cy5-Trolox conjugates onto dendrimers.

12 of a wide range of novel, dense, and chiral dendrimers.

13 accomplish sequence-controlled heterolayered dendrimers.

14 even vary depending on the generation of the dendrimers.

15 nd silver), various other nanomaterials, and dendrimers.

16 nsional order analogous to that of molecular dendrimers.

17 on 4, hydroxyl-functionalized polyamidoamine dendrimers.

18 Lewis X antibodies (aSlex)-conjugated PAMAM dendrimers.

19 oated with polypyrrole (PPy) and redox PAMAM dendrimers.

20 ngements of the 0- and 1-bits in the uniform dendrimers.

21 s into the potential clinical translation of dendrimers.

22 However, the corresponding dendrimers 1a and 1b containing the -NH(CH2)2NH- and the

23 ations and thus successfully converts non-LC dendrimers (1a and 1b) into LC dendrimers (2a and 2b).

24 These newly prepared dendrimers 2a and 2b containing the -NMe(CH2)2NMe- and t

25 nverts non-LC dendrimers (1a and 1b) into LC dendrimers (2a and 2b).

26 Our findings indicate that dendrimer 3 is a promising analog with higher potency fo

27 Dendrimer 3 showed similar luteinizing hormone (LH)-rele

28 In gonadotropin-release experiments, dendrimer 3 was shown to be the most potent construct.

29 A lead dendrimer, 5A2-SC8, provided a broad therapeutic window:

30 predict the intravenous pharmacokinetics of dendrimers, a commonly explored drug vector, based on ph

31 Attachment of two polycarboxylate dendrimers, a method we call "cloaking", to a bisstyrylt

32 bed new types of carriers termed amphiphilic dendrimers (ADs), which are based on polyamidoamine dend

33 Conjugation of RNA triple helices to dendrimers allows the formation of stable triplex nanopa

34 ummarizes the stepwise evolution of peptidic dendrimers along with their multifaceted applications in

35 G6 dendrimers also showed decreased renal clearance rate, s

36 es that are very similar to those of perfect dendrimer analogues.

37 The generation/size of dendrimer and surface group also affected the reaction r

38 the high data storage capacity of a uniform dendrimer and uncovers good opportunities for the digita

39 lutions from inorganic molecular clusters to dendrimers and biomacromolecules.

40 meric libraries of self-assembling dendrons, dendrimers and dendronized polymers.

41 rgent iterative methods for the synthesis of dendrimers and dendrons containing ethylenediamine (EDA)

42 hetic methods were used for the synthesis of dendrimers and dendrons.

43 ontaining sequence-defined amphiphilic Janus dendrimers and either linear or branched oligosaccharide

44 ion of naphthalene by polyamidoamine (PAMAM) dendrimers and graphene oxide (GrO).

45 investigate 3rd-6th generation (G3-G6) PAMAM dendrimers and GrO with different levels of oxidation.

46 t role in enhancing their association to the dendrimers and GrO.

47 ticles (Pd, Pt, Rh) stabilized by G4OH PAMAM dendrimers and supported in SBA-15 (MNPs/SBA-15 with M =

48 liposomes, virosomes, virus-like particles, dendrimers and the like, plus macromolecular drugs, anti

49 itic effect can be observed with any type of dendrimer, and for any type of property, even if it has

50 to the density of functional groups on each dendrimer, and insensitive to factors that promote or in

51 rticles as well as nonbiodegradable NPs like dendrimers, and carbon- or metal-based NPs for AIT.

52 systems, such as conjugated polymers (CPs), dendrimers, and J-aggregates.

53 ion of various materials including polymers, dendrimers, and other macromolecules.

54 ydrogels, polymer-drug conjugates, micelles, dendrimers, and polymersomes.

55 This DNA dendrimer architecture has the potential to overcome cur

56 phenylphosphonium ion, and G0 polyamidoamine dendrimer are tested for their ability to inhibit the he

57 nylmethane-ethynylene-based shape-persistent dendrimers are a new class of nanoobjects with an intrig

58 These results demonstrate that dendrimers are a promising targeted delivery platform to

59 Dendrimers are branched, multivalent nanoparticles with

60 Some dendrimers are considered as inorganic, as they possess

61 erminal functionality, where the majority of dendrimers are directed to the endo-lysosomal compartmen

62 These self-terminated polyamide dendrimers are enzymatically and hydrolytically stable a

63 f many examples obtained with other types of dendrimers are given.

64 Dendrimers are hyperbranched polymers having a perfectly

65 hemically-controlled branched architectures, dendrimers are ideally suited for these initial steps, s

66 cell membranes, their components, and Janus dendrimers are stable for at least 1 y.

67 chnique was achieved by employing Fe3O4@SiO2-dendrimer as immunosensing platform and PAMAM as the car

68 ymers are a suitable alternative for perfect dendrimers as building blocks for dendritic nanocarrier

69 tention to critically evaluate the status of dendrimers as drug carriers and find answers as to why t

70 one-pot approach toward these heterolayered dendrimers as proof-of-concept.

71 ent aldehyde substrates were used with PAMAM dendrimers as the common platform.

72 4/IL-4Ralpha-targeting peptide with G5 PAMAM dendrimers as the loading surface and can convey therape

73 In particular, we focus on dendrimers as well as fullerene C60-with a unique symmet

74 de here a protocol for the synthesis of this dendrimer, as well as siRNA delivery to immune cells suc

75 D-aptamer) used as detection probe and PAMAM-Dendrimers/AuNPs was used for covalent attachment of CA1

76 endrimers (PPDs) represent a unique class of dendrimers based on their rigid, shape persistent chemic

77 diagnosis based on the combination of novel dendrimer-based conjugates and a recently developed nano

78 re, we report the development of theranostic dendrimer-based lipid nanoparticle (DLNP) system contain

79 Dendrimer-based nanomedicines have shown great potential

80 response in mice immunized with our modified dendrimer-based RNA nanoparticle vaccine.

81 a novel compact nanoplasmonic platform and a dendrimer-based strategy provides a highly sensitive lab

82 In pre-clinical models, dendrimer-based therapies are viable in postnatal period

83 have used neutral high-generation phosphorus dendrimers bearing 48 (G3) or 96 (G4) bisphosphonate gro

84 ings can potentially alter the perception of dendrimers being limited to carriers to being prodrugs f

85 This analysis shows that for the dendrimers being studied, the line width for ETPA is ord

86 self-organize from supramolecular spheres of dendrimers, block copolymers, surfactants and other self

87 HCR, forming a chain-branching growth of DNA dendrimer by self-assembly.

88 ee-dimensional crystals of protein cages and dendrimers, by adsorbing proteins to the surface of mate

89 sicles self-assembled from amphiphilic Janus dendrimers, called dendrimersomes, encapsulate high conc

90 Here we show that the surface-functionalized dendrimers can be sequentially coated with two antibodie

91 Covalently attached peptide dendrimers can enhance binding affinity and functional a

92 Exposure to low dosages of polyamidoamine dendrimer carbon nanotubes (PAMAM-CNTs) did not affect T

93 ne day to five days after injury, a shift in dendrimer co-localization occurred.

94 The hybrid RHF Janus dendrimer coassembled with both RF and RH.

95 In this study, the use of dendrimer-coated carbon nanotubes (CNTs) as a delivery v

96 ed using atomic force microscopy reveal that dendrimer-coated surfaces exhibit an order of magnitude

97 Administration of the 21h release dendrimer conjugate did not produce a high initial Cmax

98 In conclusion, the aSlex-coated dendrimer conjugate displayed the great potential in cap

99 nd regulating HT29 cells by the aSlex-coated dendrimer conjugate were analyzed by microscopy and flow

100 m is ultimately expected to be used to guide dendrimer construct design and refinement prior to embar

101 The iterative synthetic protocols used for dendrimer construction were developed based on the desir

102 Two Janus dendrimers contain either chiral-racemic fluorinated den

103 endrons (RH), while one denoted hybrid Janus dendrimer, contains a combination of chiral-racemic fluo

104 Our dendrimer core-labelling approach could provide a new co

105 ms extending from a poly(amidoamine) (PAMAM) dendrimer core.

106 ion (measured by drug CSF/serum level) of G6 dendrimers correlated with the severity of neuroinflamma

107 tra-amniotically administered hydroxyl PAMAM dendrimers could be an effective drug delivery vehicle f

108 Such dendrimers could find application as an indicator, a dru

109 ed poly(amidoamine) dendrimer nanoparticles (Dendrimer-Cy5).

110 luorescence quantification of cell-extracted dendrimer-Cy5.

111 g systemic administration of the Cy5-labeled dendrimer (D-Cy5), we demonstrate dendrimer uptake in ce

112 ed to hydroxyl terminated generation-4 PAMAM dendrimer (D-Sino) as a potential therapy for attenuatin

113 cluding decacyclene- and perylene-containing dendrimer D6, in which two types of polyimide dyes are p

114 Four generations of poly(amidoamine) (PAMAM) dendrimers decorated with benzenesulfonamide moieties we

115 tribution of scFv7F9Cys after conjugation to dendrimers decreased 45 and 1.6-fold respectively, and t

116 Acid-mediated dendrimer deprotection was successful, and the resulting

117 w of the most recent synthetic strategies in dendrimer design will be presented for the purpose of co

118 iphenylphosphonium ion and G0 polyamidoamine dendrimer, despite being positively charged, interact pr

119 Herein, as a proof-of-concept, a family of dendrimers displaying internally queued disulfide bridge

120 rease with the increased generation of siRNA dendrimers due to a high charge density and structural f

121 The dendritic (or dendrimer) effect is observed when a functional group be

122 , combined with prolonged circulation of the dendrimer, enabled administration of an efficacious dose

123 For improve the sensitivity, polyamidoamine dendrimer-encapsulated gold nanoparticles (AuNPs-PAMAM)

124 in layer of ALD Al2O3 and an overlayer of Pt dendrimer-encapsulated nanoparticles (DENs) have been in

125 , however, be reactivated by immobilizing Pt dendrimer-encapsulated nanoparticles (DENs), containing

126 iated endocytotic mechanism, irrespective of dendrimer end-terminal functionality, where the majority

127 effects observed with polyphosphorhydrazone dendrimers, even if many examples obtained with other ty

128 The dual antibody-coated dendrimers exhibit a significantly enhanced specificity

129 The labelled dendrimers exhibited high fluorescent quantum yields whe

130 and G2-13C) and lower generation (G0 and G1) dendrimers failed as transfection carriers.

131 d G3) of ferrocene (Fc) cored polyamidiamine dendrimers (Fc-PAMAM) gold (Au) electrode.

132 disease, the chronic administration of such dendrimers for 5 days led to a much more efficient drop

133 Similarly, using dendrimers for physical drug entrapment is an approach w

134 Dendrimers functionalized with photoreactive cross-linke

135 n the injured brain compared to generation 4 dendrimers (G4, 4.3nm), which were undetectable in the b

136 ation, hydroxyl-terminated, poly(amidoamine) dendrimers (G6-OH DENs) having diameters of approximatel

137 ting ligands conjugated to amphiphilic Janus dendrimers generates dendrimersomes that selectively dis

138 The effect of the dendrimer generation on the binding constant and the sto

139 PEG-PAMAM with dendrimer generations of 5 (G5-PEG) or 7 (G7-PEG) were i

140 al growth (DP=2(n) -1) or double exponential dendrimer growth approaches (DP=22n -1) with significant

141 tive electrophysiology showed that alpha-ImI dendrimers had approximately 100-fold enhanced potency a

142 confirmed that each alpha-ImI moiety in the dendrimers had the same 3D structure as native alpha-ImI

143 ontaining a new, click-synthesized porphyrin dendrimer has been used to map oxygenation across an ex

144 mbly phenomenon of this class of amphiphilic dendrimers has not been molecularly explored using molec

145 Dendrimers have attracted immense interest in science an

146 The photophysical properties of the dendrimers have been studied by absorption, steady-state

147 numerous examples, two families of inorganic dendrimers have emerged as particularly promising: silic

148 Self-assembling dendrimers have facilitated the discovery of periodic an

149 e data suggest that neutral G3-G4 phosphorus dendrimers have strong potential applications in the the

150 Peptide dendrimers, unlike other classes of dendrimers, have immense applications in biomedical rese

151 A minor fraction of dendrimers, however, localize to endoplasmic reticulum a

152 e groups are deemed one of the advantages of dendrimers; however, only small amounts of drugs can be

153 These lipid/dendrimer hybrids consist of a low-generation, hydrophil

154 d that attachment of a fifth-generation (G5) dendrimer (i.e., cloaking) to the widely used 4-methoxy-

155 ocol requires simple mixing of the siRNA and dendrimer in buffer, with subsequent application to the

156 h 1,3,5-triethynylbenzene, forming two novel dendrimers in a convergent manner.

157 mental results indicate that GrO outperforms dendrimers in removing naphthalene from water.

158 play the main properties of both families of dendrimers in the fields of catalysis, materials and bio

159 A library of amphiphilic Janus dendrimers including two that are fluorescent and one gl

160 -yielding synthesis of a series of polyimide dendrimers, including decacyclene- and perylene-containi

161 Physical characteristics of the dendrimers, including their globular shapes, excellent s

162 Homogenous di- and tetravalent dendrimers incorporating the alpha7-nicotinic receptor b

163 The prepared dendrimer indeed released up to 27 leaving groups upon p

164 een used to investigate both dye-dye and dye-dendrimer interaction.

165 f Nanomaterials) to reveal real-time protein-dendrimer interactions using a systems biology approach.

166 y TITAN in a detailed temporal manner during dendrimer internalization, traceable to at least two maj

167 the stoichiometry of the fluorophore to the dendrimer is 1:1, we were able to directly compare uptak

168 torage capacity of non-linear binary digital dendrimer is established based on data matrix barcode, g

169 errin-bearing generation 3 polypropylenimine dendrimer is therefore a highly promising delivery syste

170 Synthesis of giant unimolecular dendrimers is challenging due, in part, to difficulties

171 ning seven self-assembling amphiphilic Janus dendrimers is reported.

172 differently when it is alone or linked to a dendrimer; its properties can even vary depending on the

173 Amphiphilic Janus dendrimers (JDs) and glycodendrimers (JGDs) represent th

174 sicles self-assembled from amphiphilic Janus dendrimers, known as dendrimersomes, are comparable.

175 d that the conjugation of lactoferrin to the dendrimer led to an enhanced DNA uptake by 2.1-fold in b

176 well as complex branched, hyperbranched, and dendrimer like polyethers.

177 fect of chemically modified phytoglycogen, a dendrimer-like alpha-d-glucan nanoparticle, on dendritic

178 (6)-10(7) were determined between nanometric dendrimer-like ligands and the rod-shaped micrometric ba

179 ms, e.g., polymers, nanoparticles, micelles, dendrimers, liposomes, polyplexes, and virus-like-partic

180 ed to detect RCC-CTCs through integration of dendrimer-mediated multivalent binding, a mixture of ant

181 This dendrimer-mediated siRNA delivery largely outperforms th

182 ding on the tissue source and cell type; the dendrimer-mediated siRNA delivery; and subsequent functi

183 Notably, the triggered release mechanism of dendrimer-mediated triptolide delivery significantly red

184 ked microgels as well as block copolymer and dendrimer micelles.

185 rticles, polymer-coated metal nanoparticles, dendrimers, micelles and star polymers to impart nitric

186 40-atom rhodium (Rh) NPs, encapsulated by dendrimer molecules and supported in mesoporous silica,

187 systemic administration of a single dose of dendrimer-N-acetyl cysteine conjugate (D-NAC) at either

188 Cy3-labeled folic acid (FA)-derivatized DNA dendrimer nanocarrier (3DNA).

189 gold nanoparticles-poly(amidoamine) (PAMAM) dendrimer nanocomposite (3D-Au-PAMAM) covalently immobil

190 ultichromophoric probes based on fluorescent dendrimer nanoconjugates (FDNs) was developed for single

191 ts the glyco-conjugate: organic macrocycles, dendrimers, nanomaterials, and polymers are considered.

192 ivered using a targeted, systemic, maternal, dendrimer nanoparticle (DNAC), in a mouse model of intra

193 the presence of pentobarbital increased the dendrimer nanoparticle uptake significantly ( 2-fold bot

194 fully synthetic, single-dose, adjuvant-free dendrimer nanoparticle vaccine platform wherein antigens

195 ed, hydroxyl-functionalized poly(amidoamine) dendrimer nanoparticles (Dendrimer-Cy5).

196 activate microglia, the increased uptake of dendrimer nanoparticles in their presence can be exploit

197 Anti-METH scFv7F9Cys was conjugated to dendrimer nanoparticles via a polyethylene glycol (PEG)

198 e by conjugating multiple anti-METH scFvs to dendrimer nanoparticles, extending the scFv half-life fr

199 Although the G8-OH dendrimer nearly eliminates AuNP growth, the surface of

200 he mode of uptake, trafficking and safety of dendrimers of different end-terminal functionality (carb

201 ic self-assembly of cationic polyelectrolyte dendrimers of different generations and oppositely charg

202 The MWCNTs-PPy layer was modified with PAMAM dendrimers of fourth generation (PAMAM G4) with covalent

203 The second-generation dendrimers of siRNA can be effectively complexed with a

204 ion energy for Rh NPs encapsulated in either dendrimer or poly(vinylpyrrolidone).

205 ) (ABP)-conjugated poly (amidoamine) (PAMAM) dendrimer (PAM-ABP) in hMSCs.

206 on with a fourth-generation poly(amidoamine) dendrimer (PAMAM(G4)) on gold surface for the immobilisa

207 ers (ADs), which are based on polyamidoamine dendrimers (PAMAM).

208 s particularly promising: silicon-containing dendrimers, particularly carbosilanes, and phosphorus-co

209 arly carbosilanes, and phosphorus-containing dendrimers, particularly phosphorhydrazones.

210 carrier (NLC) and PEGylated poly(amidoamine) dendrimer (PEG-PAMAM).

211 nceptual basis for improved understanding of dendrimer performance within biological settings.

212 y curated the largest relational database of dendrimer pharmacokinetic parameters and their structura

213 dendPoint successfully predicts dendrimer pharmacokinetic properties, achieving correlat

214 cribe a "double-punch" strategy by combining dendrimer platform and injectable hydrogel encapsulation

215 ddress this, we used a GnRH peptide-modified dendrimer platform with and without lipidation strategy.

216 Organic small-molecule, dendrimer, polymer, and exciplex emitters are all discus

217 and polymer-small-molecule drug conjugates, dendrimers, polymer nanoparticles and multifunctional sy

218 monium, chemically diverse cations including dendrimers, polyvalent metals, metal complexes, amphiphi

219 Polyphenylene dendrimers (PPDs) represent a unique class of dendrimers

220 Initially, dendrimer predominantly co-localized with astrocytes, wi

221 rich ssDNA(S1) immobilized on the Fe3O4@SiO2/dendrimers/QDs and AuNPs modified with complementary apt

222 ergy transfer (ECL-RET) approach, Fe3O4@SiO2/dendrimers/QDs exhibited amplified ECL emissions (switch

223 er antigen 125 (CA 125) using polyamidoamine dendrimer-quantum dots (PAMAM-QDs) and PAMAM-sulfanilic

224 zed with either citrate or by low-generation dendrimers rapidly grow during electrocatalytic reductio

225 In vitro, these dendrimers reduced the secretion of proinflammatory cyto

226 ll mice bearing MYC-driven tumors (>75 mg/kg dendrimer repeated dosing).

227 Conformational degeneracy in the dendrimers resulted in effective preorganization despite

228 geting ligand to the surface of pre-existing dendrimers results in poorly-defined compound mixtures t

229 d from a combination of a small RNA with the dendrimer's own negligible toxicity, therefore illuminat

230 njugated to the surface without altering the dendrimer's performance, for example its solubility.

231 The peptide dendrimer SB105-A10, which binds HS, reduced binding and

232 ylcholine-detecting nanosensors based on DNA dendrimer scaffolds that incorporate butyrylcholinestera

233 bilization of ferrocene cored polyamidiamine dendrimers second generation (Fc-PAMAM (G2)), after whic

234 These RF, RH, and RHF Janus dendrimers self-assembled into unilamellar or onion-like

235 eres from short helical stacks of crown-like dendrimers self-organize a Pm3 n cubic (Frank-Kasper A15

236 bilized redox center (ferrocene) cored PAMAM dendrimers served as a layer for the further binding of

237 sent data indicating that neutral phosphorus dendrimers show impressive antiinflammatory activities b

238 These dendrimers show no toxicity and have good solubility and

239 Generation 6 (G6, 6.7nm) dendrimers showed extended blood circulation times and i

240 approach also circumvents the nonideality of dendrimers, since the heteroleptic, one-step, spontaneou

241 The observed dendrimer size is in excellent correlation with the expe

242 We investigated the effect of dendrimer size on brain uptake and explored the pharmaco

243 ea is relatively underexplored, make peptide dendrimers sought-after candidates for various applicati

244 arried out at -1.20 V, the higher-generation dendrimer stabilizes encapsulated AuNPs.

245 perties to polyvalent engagement between the dendrimer surface groups, and a potential "rolling" effe

246 The dendrimer synthesis entails straightforward click coupli

247 ssed and challenged are the current state of dendrimer synthesis, for example the importance for surf

248 The whole protocol encompasses the dendrimer synthesis, which takes 10 days; the primary im

249 gence of a diversity of functions in complex dendrimer systems via first principles.

250 Hydroxyl polyamidoamine (PAMAM) dendrimers target activated microglia and damaged neuron

251 describe the use of a generation 5 l-lysine dendrimer that has been part-modified with a polyoxazoli

252 We have recently developed an amphiphilic dendrimer that is able to deliver siRNA to a variety of

253 r SN-38 conjugated to polyoxazoline-modified dendrimer that maximised efficacy and minimised adverse

254 s this issue by reporting modular degradable dendrimers that achieve the required combination of high

255 reak the hydrophobic stereotype, and provide dendrimers that can be synthetically tuned to be used in

256 treatment of relatively large polythiophene dendrimers that serve as two-photon absorbers.

257 In contrast to the G6-OH dendrimer, the higher generation G8-OH analogue stabiliz

258 rapid and facile synthesis of oxygen-sensing dendrimers through azide-alkyne click chemistry.

259 xylic acid- and pyrrolidone-terminated PAMAM dendrimers through determination of cell membrane integr

260 oolbox generated highly complex monodisperse dendrimers through simplified protocols.

261 By conjugation of a large, neutral dendrimer to a caged GABA probe we introduce a "cloaking

262 ols in all living cells, the collapse of the dendrimers to a multitude of smaller thiols was intracel

263 The binding of the alpha-ImI dendrimers to binding protein Ac-AChBP was measured by s

264 lation of the dendritic central linker leads dendrimers to possess more isomeric conformations and th

265 s of the utilitarian macromolecules known as dendrimers today, our first examples employed predesigne

266 In an orthotopic model of glioblastoma, dendrimer-triptolide achieved significantly improved ame

267 Here we present a novel dendrimer-triptolide conjugate that specifically targets

268 In this study, dendrimer type bio-reducible polymer (PAM-ABP) which was

269 Peptide dendrimers, unlike other classes of dendrimers, have imm

270 shed by the inhibitory effect of dynasore on dendrimer uptake and changes in temporal profiles of key

271 y5-labeled dendrimer (D-Cy5), we demonstrate dendrimer uptake in cells involved in ischemic injury, a

272 By conjugating SN-38 to the dendrimer via different linker technologies we sought to

273 Subsequently, the dendrimer was removed from the Pt DENs using a UV/O3 tre

274 In contrast to amino-terminated PAMAM dendrimers, we confirm safety of carboxylic acid- and py

275 re are only a handful of examples of protein dendrimers; we believe that these limited examples will

276 ed 'anionic' (D-COOH) Polyamidoamine (PAMAM) dendrimers were absorbed by fetuses and demonstrated bi-

277 The amino terminal dendrimers were analyzed by diffusion-ordered spectrosco

278 essful, and the resulting carboxy-terminated dendrimers were analyzed by NMR and DOSY experiments.

279 , 809 interacting proteins cross-linked with dendrimers were determined by TITAN in a detailed tempor

280 High levels of G6 dendrimers were found in cerebrospinal fluid (CSF) of in

281 al poly(amido amine) and poly(propylenimine) dendrimers were substituted with alkyl chains of increas

282 Two triazine-based dendrimers were successfully prepared in 60-75% yields.

283 Dendrimers were synthesized on a polylysine core and bor

284 More than 1,500 dendrimers were synthesized using sequential, orthogonal

285 PSA (anti-PSA) was covalently immobilized on dendrimers which were attached onto the modified Au surf

286 on, a dodecaiodo-terminated first generation dendrimer, which was transformed by another Sonogashira

287 owth is now demonstrated as a route to metal dendrimers, which are hierarchically branched nanocrysta

288 Unexpectedly, these oligoMan-containing dendrimers, which have their hydrophobic linker connecte

289 ff-rate kinetics compared to surface without dendrimers, which translated into cell capture improveme

290 ared by derivatizing the amino groups of the dendrimer with 4-carboxy-benzenesulfonamide functionalit

291 nthesis was observed at generation 4 for the dendrimer with an EDA core and at generation 5 for the o

292 into a methoxy-terminated second generation dendrimer with persistent globular shape and well-define

293 is of generation-4 poly-(amidoamine) (PAMAM) dendrimers with a precisely core positioned single sulfo

294 excited-state dynamics in organic conjugated dendrimers with atomistic resolution, a phenomenon expec

295 cient and controlled convergent synthesis of dendrimers with different sizes and shapes and multivale

296 Coassembly of amphiphilic Janus dendrimers with metal-chelating ligands conjugated to am

297 argeting of intra-amniotically administrated dendrimers with neutral/anionic surface functionality.

298 to an intermediate layer of a polyamidoamine dendrimer, with an ethylenediamine core from the fourth

299 development of flawless structures, such as dendrimers, with unprecedented structure-to-property cap

300 ion 3-diaminobutyric polypropylenimine (DAB) dendrimer would allow the transport of plasmid DNA to th