ライフサイエンスコーパス: dendrimer

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

2 i-PSA antibody and thionine onto AuNPs-PAMAM dendrimer.

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

4 dendron, which is equivalent to generation 5 dendrimer.

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

6 he hybrid hydrogenated-fluorinated RHF Janus dendrimer.

7 high affinity for DNA possessed by cationic dendrimers.

8 were also coassembled with hybrid RHF Janus dendrimers.

9 ent attachment of Cy5-Trolox conjugates onto dendrimers.

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

11 even vary depending on the generation of the dendrimers.

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

13 nsional order analogous to that of molecular dendrimers.

14 on 4, hydroxyl-functionalized polyamidoamine dendrimers.

15 s into the potential clinical translation of dendrimers.

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

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

18 jugates with drug moieties buried inside the dendrimers.

19 eased liver and spleen uptake compared to G4 dendrimers.

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

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

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

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

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

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

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

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

28 that loads smaller poly(amidoamine) (PAMAM) dendrimers (~5nm in diameter) into larger poly(ethylene

29 nsor based on polyprrole modified with redox dendrimers, able to detect human cellular prions PrP(C)

30 ybrid NPs encapsulating folate (FA)-targeted dendrimers achieved longer plasma circulation than free

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

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

33 G6 dendrimers also showed decreased renal clearance rate, s

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

35 yer (LbL) nanofilm of polyamidoamine (PAMAM) dendrimer and carbon nanotubes (CNTs) on capacitive elec

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

37 chain-branching growth of the assembled DNA dendrimers and an exponential increase in the fluorescen

38 ted by ferrocenyl group incorporated between dendrimers and aptamers layers.

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 olecular logic and materials, e.g. polymers, dendrimers and gels.

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 achieved longer plasma circulation than free dendrimers and higher tumor concentrations than both fre

48 The multicomponent nature of the dendrimers and of the corresponding host-guest supramole

49 ccessfully combine the in vivo advantages of dendrimers and polymeric NPs, demonstrating their potent

50 layer was probed using ferrocenyl-terminated dendrimers and scanning electrochemical microscopy.

51 nitric oxide (NO)-releasing scaffolds (i.e., dendrimers and silica particles) as anti-periodontopatho

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

53 d higher tumor concentrations than both free dendrimers and the empty PEG-PLA NPs.

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

55 t the hybrid NPs circulated longer than free dendrimers and were mostly cleared by macrophages in the

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

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

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

59 e use of polymeric nanoparticles, liposomes, dendrimers, and inorganic nanoparticles for vaginal drug

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

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

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

63 es, such as polyethylenimine, polyamidoamine dendrimers, and polymyxin B, although they attenuate thr

64 e from commercially available dyes and PAMAM dendrimers, and sensing is based on an indicator displac

65 Both dendrimer- and silica-based NO release exhibited substan

66 This DNA dendrimer architecture has the potential to overcome cur

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

68 Dendrimers are branched, multivalent nanoparticles with

69 Some dendrimers are considered as inorganic, as they possess

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

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

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

73 Dendrimers are hyperbranched polymers having a perfectly

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

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

76 AuNPs-PAMAM dendrimer as platform not only increased the amount of t

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

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

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

80 4/IL-4Ralpha-targeting peptide with G5 PAMAM dendrimers as the loading surface and can convey therape

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

82 imine) second (G2) and third (G3) generation dendrimers as well as polyethyleneimine (PEI) were devel

83 ld nanoparticles-incorporated polyamidoamine dendrimer (AuNPs-PAMAM) and multiwalled carbon nanotubes

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

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

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

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

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

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

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

91 with pyrenyl-functionalized poly(arylester) dendrimers bearing cyanobiphenyl end-groups is reported.

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

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

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

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

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

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

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

99 Uncharged dendrimers collapse by forming intramolecular hydrogen b

100 terminal exciton delivery efficiency within dendrimers compared with the first linear constructs.

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

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

103 Using estradiol (E2) and an E2-dendrimer conjugate that is excluded from the nucleus, w

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

105 f endothelial repair in response to estrogen-dendrimer conjugate, which is a membrane-selective ER li

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

107 Two Janus dendrimers contain either chiral-racemic fluorinated den

108 and substrate encapsulation, an amphiphilic dendrimer containing 27 triethylene glycol termini and 9

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

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

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

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

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

114 luorescence quantification of cell-extracted dendrimer-Cy5.

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

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

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

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

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

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

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

122 Current dendrimer-drug conjugates are synthesized by anchoring d

123 oblems, we herein report molecularly precise dendrimer-drug conjugates with drug moieties buried insi

124 livery carriers, particularly in the form of dendrimer-drug conjugates.

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

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

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

128 ent immobilization of polyamidoamine (PAMAM) dendrimer-encapsulated gold nanoparticles (Au-PAMAM) sen

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

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

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

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

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

134 The pyrenyl dendrimers exhibit a multilayered smectic A-like phase,

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

136 The labelled dendrimers exhibited high fluorescent quantum yields whe

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

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

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

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

141 Dendrimers functionalized with photoreactive cross-linke

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

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

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

145 s of these conjugates were tailorable by the dendrimer generation, surface chemistry, and acidity.

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

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

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

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

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

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

152 As a result, the negatively charged dendrimers have a significant percentage of tertiary ami

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

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

155 PAMAM dendrimers have recently been investigated as efficient

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

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

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

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

160 d by simple injection of a solution of Janus dendrimer in a water-miscible solvent into water or buff

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

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

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

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

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

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

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

168 tion of transferrin to the polypropylenimine dendrimer increased the DNA uptake by bEnd.3 murine brai

169 ht globally to the surface by the ferrocenyl dendrimer instead of a single ferrocene molecule.

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

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

172 ifts the pKa of tertiary amines of the PAMAM dendrimer interior.

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

174 ifurcated, Holliday junction, 8-arm star and dendrimers involving up to five different dyes engaging

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

176 t that transferrin-bearing polypropylenimine dendrimer is a highly promising gene delivery system to

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

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

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

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

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

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

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

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

185 (6)-10(7) were determined between nanometric dendrimer-like ligands and the rod-shaped micrometric ba

186 ture design tests, including the creation of dendrimer-like structures and scaffolds for small molecu

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

188 The structural preciseness of dendrimers makes them perfect drug delivery carriers, pa

189 ent the proof-of-concept, demonstrating that dendrimer-mediated Akt siRNA delivery, in combination wi

190 ed cell rolling and poly(amidoamine) (PAMAM) dendrimer-mediated strong multivalent binding.

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

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

193 40-atom rhodium (Rh) NPs, encapsulated by dendrimer molecules and supported in mesoporous silica,

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

195 A "cluster-bomb"-like lipid-dendrimer nanoassembly synergizes the functions of its c

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

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

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

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

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

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

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

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

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

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

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

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

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

209 e polypyrrole film coupled to polyamidoamine dendrimers of fourth generation (PAMAM G4) and ferroceny

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

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

212 present work highlights the robust nature of dendrimer oil dispersion and also illuminates potentiall

213 the immobilization of polyamidoamine (PAMAM) dendrimers on the surface, thus increasing the immobiliz

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

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

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

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

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

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

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

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

222 horing drug and functional moieties onto the dendrimer peripheral surface.

223 y hydrophobic drug molecules anchored on the dendrimer periphery can interact with blood components a

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

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

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

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

228 been used to discover six amphiphilic Janus dendrimer primary structures, which self-assemble into u

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

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

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

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

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

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

235 Conformational degeneracy in the dendrimers resulted in effective preorganization despite

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

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

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

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

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

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

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

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

244 n of transverse relaxation times (T2) within dendrimers (shorter values at the core than the peripher

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

246 These dendrimers show no toxicity and have good solubility and

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

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

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

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

251 intended or unanticipated effects of varying dendrimer surface chemistry on their encapsulation or ho

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

253 al groups and drug molecules anchored to the dendrimer surface.

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

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

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

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

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

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

260 Once in the tumor, it releases small dendrimers that act like "bomblets", enabling tumor pene

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

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

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

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

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

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

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

268 g terminal surface charge on the capacity of dendrimers to disperse model liner, polycyclic aromatic,

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

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

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

272 unctionalized high-molecular weight triazine dendrimers up to generation 9, demonstrating that even v

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

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

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

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

277 A library of dendrimers was synthesized and optimized for targeted sm

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

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

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

281 , 809 interacting proteins cross-linked with dendrimers were determined by TITAN in a detailed tempor

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

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

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

285 Dendrimers were synthesized on a polylysine core and bor

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

287 analysis, and the morphologies of the grown dendrimers were verified by AFM imaging.

288 ribe a triethanolamine-core poly(amidoamine) dendrimer which forms stable nanoparticles with the Akt

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

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

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

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

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

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

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

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

297 The association of redox dendrimers with conducting polypyrrole leads to high sen

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

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

300 errin-bearing generation 3-polypropylenimine dendrimer would allow the transport of plasmid DNA to th