ライフサイエンスコーパス: polyethylenimine

1 rom mixing polydextran aldehyde and branched polyethylenimine.

2 , ShH3, and ShH4, were complexed with linear polyethylenimine.

3 ts via tail vein injection using the carrier polyethylenimine.

4 vivo using a nonviral gene-transfer vector, polyethylenimine.

5 On Postnatal Day 2, polyethylenimine-(5) myristic acid/polyethylene glycol-o

6 Polyethylenimine affinity and sequence-specific serial i

7 e microbicidal polycation N,N-dodecyl,methyl-polyethylenimine and coating (painting) of glass slides

8 , fabricated with layer-by-layer assembly of polyethylenimine and graphene oxide, exhibit significant

9 ency of the commercial transfection reagents Polyethylenimine and Lipofectamine 2000.

10 y used as adhesive factors for cells growth: Polyethylenimine and Poly-D-Lysine.

11 uction of layer-by-layer (LbL) assemblies of polyethylenimine and urease onto reduced-graphene-oxide

12 we show that synthetic polycations, such as polyethylenimines and poly(l-lysine)s, prevent vemurafen

13 In contrast, polycations (polylysine and polyethylenimine) and low-molecular-weight anions (inosi

14 ning DNA complexed with the cationic polymer polyethylenimine are efficient vehicles to transduce DNA

15 nvironmentally relevant concentrations using polyethylenimine as a CO2 binding material.

16 fined pore size and (2) the incorporation of polyethylenimine as a gutter layer between the selective

17 By incorporating polyethylenimine as an additional monomer to piperazine

18 validate the approach using DNA delivery by polyethylenimine as an example.

19 into dendritic cells as a plasmid DNA using polyethylenimine as the gene delivery system, thereby ci

20 Here we demonstrated that linear polyethylenimine-based (PEI-based) nanoparticles encapsu

21 nated polyamines such as branched and linear polyethylenimine (BPEI and LPEI) and polyallylamine (PAL

22 but less cytotoxicity compared with branched polyethylenimine (bPEI) and Lipofectamine-2000.

23 en compared to naked siRNA, and 25k-branched-polyethylenimine (bPEI) representing the current standar

24 liposome label ruptured to release branched polyethylenimine (BPEI) to trigger the aggregation of GN

25 d (TA), polyvinylpyrrolidone (PVP), branched polyethylenimine (BPEI), polyethylene glycol (PEG)).

26 sfection efficiency comparable to commercial polyethylenimine but with lower cytotoxicity.

27 sion, with levels equal to those mediated by polyethylenimine, but with little to no cytotoxicity.

28 A clinically tested, untargeted, polyethylenimine carrier was selected to aid rapid trans

29 The blade-coated polyethylenimine cathode interlayer and active layer, an

30 osit LPS onto either freshly cleaved mica or polyethylenimine-coated mica substrates.

31 Using a cross-linked polyethylenimine coating, column efficiencies between 35

32 resonance energy transfer based sensor with polyethylenimine-coating provides high colloidal stabili

33 N,N-dodecyl,methyl-polyethylenimine coatings applied to solid surfaces have

34 PIO complexes based on dendrimer, lipid, and polyethylenimine compounds were used as test standards,

35 n in serum relative to conventional branched polyethylenimine control.

36 fects of miR-124 in vivo when complexed with polyethylenimine-derived nanoparticles.

37 re's most efficient DNA viruses and nonviral polyethylenimine/DNA nanocomplexes were revealed to incl

38 coenzyme mimics in the presence of modified-polyethylenimine enzyme mimics catalyze the benzoin cond

39 lymeric condensing agents, poly-l-lysine and polyethylenimine, form condensates with nicked- and gapp

40 We have developed a polyethylenimine-functionalized covalent organic framewo

41 High molecular weight polyethylenimine (HMW PEI; branched 25 kDa PEI) has been

42 ine-enrichment modification by hyperbranched polyethylenimine (HPEI), has been proposed to design sta

43 ed of a core of high molecular weight linear polyethylenimine (LPEI) complexed with DNA and surrounde

44 nalized with synthetic polycationic branched polyethylenimine macromolecules.

45 Silica-attaching polyethylenimine make the Dopa transforms into an active

46 a spinal nerve injection strategy to deliver polyethylenimine mixed with plasmid (PEI/DNA polyplexes)

47 DNA/polyethylenimine nanoparticles (DNPs) also elicit rapid

48 Nanoparticles coated with polyethylenimine (NP-PD1) exhibited significant retentio

49 thesized from various-amine rich precursors (polyethylenimine or chitosan) to yield cationic CDs and

50 ic oligonucleotide was either complexed with polyethylenimine or encapsulated in anionic liposomes, a

51 similar or superior levels when compared to polyethylenimine or lipofectamine complexes.

52 mple probe surface modified by a polycation (polyethylenimine or poly(acrylic acid) complexed with Fe

53 ride (PVDF) membrane and a thin polydopamine/polyethylenimine (PDA/PEI) layer grafted by sodium-funct

54 to 50-nM CdSe/CdZnS QDs coated with cationic polyethylenimine (PEI) (35.3 +/- 6.6 nm) or poly(ethylen

55 The method is demonstrated with aqueous polyethylenimine (PEI) adsorbed onto mica substrates, wh

56 acid (cmRNA) (encoding BMP-2) complexed with polyethylenimine (PEI) and made comparisons with PEI com

57 ciation and transport properties of branched polyethylenimine (PEI) and PEI-grafted silica nanopartic

58 mbrane was fabricated by assembling multiple polyethylenimine (PEI) and poly(acrylic acid) (PAA) bila

59 Poly(acrylic acid-ethylene glycol) (PAA-EG), polyethylenimine (PEI) and poly(maleic anhydride-alt-1-o

60 tages of membrane formation from assembly of polyethylenimine (PEI) and poly(sodium 4-styrenesulfonat

61 Gold tungsten wires (O: 50 mum) coated with polyethylenimine (PEI) and SWCNTs were aligned to form a

62 n eligible siRNA delivery system composed of polyethylenimine (PEI) as polycationic carrier, transfer

63 mid to donor lung using the cationic polymer polyethylenimine (PEI) as transfection reagent.

64 We show that branched polyethylenimine (PEI) beads obtained from an inverse su

65 Branched polyethylenimine (PEI) chains with an average molecular

66 elivery system employing graphene oxide (GO)-polyethylenimine (PEI) complexes for the efficient gener

67 coding either BMP-2 or FGF-2 formulated into polyethylenimine (PEI) complexes.

68 Efficiency of polyethylenimine (PEI) for nucleic acid delivery is affe

69 Polyethylenimine (PEI) functions as a co-catalyst by sig

70 Condensing RepRNA with polyethylenimine (PEI) gave positive in vitro readouts,

71 llated cellulose (NFC) and a high molar mass polyethylenimine (PEI) have been prepared via a freeze-d

72 e due to incorporated sulfonate groups, with polyethylenimine (PEI) improved recovery by 1.2- to 80-f

73 amework layer (Q-PEI@ZIF) is constructed via polyethylenimine (PEI) in situ confinement conversion an

74 Polyethylenimine (PEI) is an effective vehicle for in vi

75 roparticles are functionalized with branched polyethylenimine (PEI) molecules for efficient interpart

76 hrough the use of poly(ethyleneglycol) (PEG)/polyethylenimine (PEI) nanocomplex gene carriers and adj

77 orporation of oleate-coated iron oxide and a polyethylenimine (PEI) oleate ion-pair surface modificat

78 s of EBOV (ZEBOV) were either complexed with polyethylenimine (PEI) or formulated in stable nucleic a

79 yamine, or the strongly buffering polyamines polyethylenimine (PEI) or polyamidoamine (PAM).

80 achieved nucleic acid delivery by the 1.8kDa polyethylenimine (PEI) particles.

81 Polyethylenimine (PEI) was conjugated to antioxidative d

82 rials based on fumed silica impregnated with polyethylenimine (PEI) were found to be superior adsorbe

83 ere, quantum dots (QDs) coated with cationic polyethylenimine (PEI) were more toxic to pure cultures

84 s to transfer into the cells, especially the polyethylenimine (PEI) which has been used as a golden s

85 ly synthesized through conjugation of linear polyethylenimine (PEI) with dicyandiamide.

86 grates amine (-NH(x)) function from branched polyethylenimine (PEI) with sulfonate (-SO(3)(-)) and am

87 uminally (15 min) with one of the following: polyethylenimine (PEI)+TSP-2 siRNA, saline, PEI only, or

88 These dExo were further combined with polyethylenimine (PEI), and DNH to create polyplex hydro

89 ocarriers tested [polyethylene glycol (PEG), polyethylenimine (PEI), and PEG-PEI copolymer], MD simul

90 systems, such as the commercially available polyethylenimine (PEI), have the ability to deliver gene

91 ed to a large excess of the cationic polymer polyethylenimine (PEI), the single saRNA molecules in so

92 icles (MNPs) coated with a cationic polymer, polyethylenimine (PEI), toward the separation of Scenede

93 rize microelectrodes with CNT fibers made in polyethylenimine (PEI), which have much higher conductiv

94 spray-capillary platform, we incorporated a polyethylenimine (PEI)-coated capillary and optimized th

95 ively charged CAR-NPs and positively charged polyethylenimine (PEI)-coated CAR-(PEI)NPs were formulat

96 ium iodide (PI)-intercalated DNA (PI/DNA) to polyethylenimine (PEI)-coated monodisperse iron oxide ma

97 oylphosphatidylcholine (DMPC) bilayer onto a polyethylenimine (PEI)-coated quartz substrate were exam

98 ed intracerebroventricularly, using a linear polyethylenimine (PEI)-containing in vivo gene delivery

99 protein did not depend on the addition of a polyethylenimine (PEI)-derived transfection agent.

100 CHO, and NIH 3T3 cells were transfected with polyethylenimine (PEI)-DNA in both 384- and 1536-well pl

101 mojunction of indium oxide (In(2) O(3) ) and polyethylenimine (PEI)-doped In(2) O(3) (In(2) O(3) :x%

102 ecognition element, which was immobilized on polyethylenimine (PEI)-functionalized carbon nanotube tr

103 ibes how to prepare, construct, and optimize polyethylenimine (PEI)-functionalized SWNTs and perform

104 toylphosphatidylcholine (DMPC) vesicles onto polyethylenimine (PEI)-supported Langmuir-Blodgett lipid

105 riple-transfected for rAAV9 production using polyethylenimine (PEI).

106 magadiite and organo-magadiite modified with polyethylenimine (PEI).

107 omplexes, we demonstrate that disposition of polyethylenimine (PEI)/DNA polyplexes that were microinj

108 that lipoplexes, but not polyplexes based on polyethylenimine (PEI, 25 and 22 kDa), poly(L-lysine) (P

109 on of Ada-MOC with B-cyclodextrin-conjugated polyethylenimine (PEI-BCD) afford supramolecular nanopar

110 yocardium by using deoxycholic acid-modified polyethylenimine (PEI-DA) as a non-viral gene carrier.

111 ds such as polyethylene glycol (PEG) grafted polyethylenimine (PEI-g-PEG) are found to encapsulate an

112 d glutaraldehyde-cross-linked double-layered polyethylenimine (PEI-GA-PEI)-modified nanoporous anodic

113 Branched polyethylenimine (PEI; 25 kDa) was modified with polyeth

114 t the Beclin1 gene using the cationic linear polyethylenimines (PEI) as a gene carrier was investigat

115 e with branched or linear N,N-dodecyl methyl-polyethylenimines (PEIs) and certain other hydrophobic P

116 High-molecular-mass polyethylenimines (PEIs) are widely used vectors for nuc

117 tions of nitrogen atoms on the efficiency of polyethylenimines (PEIs) as synthetic vectors for the de

118 Crosslinked polyethylenimines (PEIs) have been frequently examined o

119 eport a new multivalent molecular motif, the polyethylenimine-perphenazine (PEI-P) conjugate which ha

120 copolymer, poly (lactide-co-glycolide)-graft-polyethylenimine (PgP) and its ability to efficiently tr

121 peutic activity of a formulation of pIC with polyethylenimine ([pIC](PEI)) in PDAC and investigated i

122 rs based on polycationic substances, such as polyethylenimine, polyamidoamine dendrimers, and polymyx

123 Peptides were conjugated to branched polyethylenimine-polyethylene glycol polymer to generate

124 viral vector, PEI-PEG-DUPA (PPD), comprising polyethylenimine-polyethyleneglycol (PEI-PEG) tethered t

125 tion of 2.5 wt% oxidized dextran and 6.9 wt% polyethylenimine sets within seconds forming a mechanica

126 this method in HeLa cells, we have observed polyethylenimine/siRNA polyplexes initially appearing in

127 monary delivery system of siRNA, transferrin-polyethylenimine (Tf-PEI), to selectively deliver siRNA

128 uble-stranded RNA (poly I:C) nanoplexed with polyethylenimine that when administered intratumorally h

129 fer, a CART transgene was delivered by using polyethylenimine to the arcuate nucleus of adult rats.

130 el predicts that even for optimally designed polyethylenimine vectors, only approximately 1% of total

131 t-off property from adsorbed linear branched polyethylenimine was successfully introduced for long te

132 Polyethylenimine was used to electrostatically stabilize

133 rbon nanotubes via noncovalent adsorption of polyethylenimine which converts p-type semiconducting na

134 structures of complexes formed from DNA with polyethylenimine, which is considered one of the most pr