Tuning the Molar Composition of “Charge-Shifting” Cationic Copolymers Based on 2-(N,N-Dimethylamino)Ethyl Acrylate and 2-(tert-Boc-Amino)Ethyl Acrylate

2017 ◽  
Vol 38 (5) ◽  
pp. 1600641 ◽  
Author(s):  
Hien The Ho ◽  
Maël Le Bohec ◽  
Julien Frémaux ◽  
Sandie Piogé ◽  
Nathalie Casse ◽  
...  
Keyword(s):  
Ethyl Acrylate ◽  
Molar Composition ◽  
Cationic Copolymers

STUDYING REACTIVITY RATIOS AND PHYSICAL PROPERTIES OF METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER

2015 ◽  
Vol 53 (2) ◽  
Author(s):  
Tran Vu Thang ◽  
Pham Thi Thu Ha ◽  
Nguyen Van Khoi ◽  
Nguyen Van Manh ◽  
Pham Thi Thu Trang
Keyword(s):  
Physical Properties ◽  
Methacrylic Acid ◽  
Ethyl Acrylate ◽  
Reactivity Ratios ◽  
Acrylate Copolymer

Comparison of the viscoelastic penetration and tensile behaviour of poly(methyl acrylate) and poly(ethyl acrylate)

1979 ◽  
Vol 44 (6) ◽  
pp. 1942-1948 ◽  
Author(s):  
Jaroslav Hrouz ◽  
Michal Ilavský ◽  
Ivan Havlíček ◽  
Karel Dušek
Keyword(s):  
Methyl Acrylate ◽  
Poisson Ratio ◽  
Young Modulus ◽  
Ethyl Acrylate ◽  
Sample Volume ◽  
Viscoelastic Behaviour ◽  
Tensile Behaviour ◽  
Temperature Superposition ◽  
Main Transition

The viscoelastic penetration and tensile behaviour of poly(methyl acrylate) and poly(ethyl acrylate) in the main transition region have been investigated. It was found that the time-temperature superposition could be carried out in the case of the penetration viscoelastic behaviour; the temperature dependence of the penetration and tensile shift factors was the same. The superimposed curves of the penetration and Young modulus allowed us to calculate the dependence of the Poisson ratio and thus to characterize the change in sample volume with deformation. It was demonstrated that the penetration method of determination of the viscoelastic behaviour is equivalent to the tensile method.

scholarly journals Natural steroid-based cationic copolymers cholesterol/diosgenin-r-PDMAEMAs and their pDNA nanoplexes: impact of steroid structures and hydrophobic/hydrophilic ratios on pDNA delivery

RSC Advances ◽  
2021 ◽  
Vol 11 (32) ◽  
pp. 19450-19460
Author(s):  
Zhao Wang ◽  
Jingjing Sun ◽  
Mingrui Li ◽  
Ting Luo ◽  
Yulin Shen ◽  
...  
Keyword(s):  
Structure Function ◽  
Cationic Copolymers

Using natural-based lipids to construct biocompatible, controllable and efficient nanocarriers and elucidating their structure–function relationships, was regarded as an important area for creating sustainable biomaterials.

Preparation and Characterization of Novel Low‐Temperature/pH Dual‐Responsive Poly( N ‐isopropylacrylamide‐ co ‐1 H ‐benzimidazolyl‐ethyl acrylate) Copolymers

2019 ◽  
Vol 220 (11) ◽  
pp. 1900123
Author(s):  
Shu‐Gui Zhang ◽  
Xiao‐Jie Ju ◽  
Xing‐Long Zhou ◽  
Xing‐Qun Pu ◽  
Han‐Yu Peng ◽  
...  
Keyword(s):  
Low Temperature ◽  
Ethyl Acrylate ◽  
Dual Responsive

Study on Relationship between Structure and Properties of Polycarboxylate Superplasticizer

2012 ◽  
Vol 487 ◽  
pp. 43-47
Author(s):  
Sheng Hua Lv ◽  
Di Li ◽  
Qiang Cao
Keyword(s):  
Acrylic Acid ◽  
Zeta Potential ◽  
Ethyl Ester ◽  
Functional Groups ◽  
Cement Paste ◽  
Ethyl Acrylate ◽  
Structure And Properties ◽  
Polycarboxylate Superplasticizer ◽  
Carboxylic Groups

A polycarboxylate superplasticizer (PCs) was synthesized by copolymerization of allyl polyoxyethylene ethers (APE), acrylic acid (AA), sodium methylallyl Sulfonate (SMAS) and ethyl acrylate (EA). The effect of functional groups and branch chain on PCs properties was investigated by the test of fluidity of cement paste, retardation performance and Zeta potential of cement particles. The results showed that carboxylic groups and ethyl ester groups can improve water reducing ratio and fluidity of cement paste, and the sulfonic groups has an important contributiion to retardation performance of PCs.

scholarly journals Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Pan He ◽  
Kyoji Hagiwara ◽  
Hui Chong ◽  
Hsiao-hua Yu ◽  
Yoshihiro Ito
Keyword(s):  
Molecular Weight ◽  
Sirna Delivery ◽  
Fluorescent Microscopy ◽  
Molar Ratio ◽  
Low Molecular Weight ◽  
Label Free ◽  
Endosomal Membrane ◽  
Cationic Copolymers ◽  
Interfering Rna

Owing to its hydrophilicity, negative charge, small size, and labile degradation by endogenous nucleases, small interfering RNA (siRNA) delivery must be achieved by a carrier system. In this study, cationic copolymers composed of low-molecular-weight polyethylenimine and polythiophenes were synthesized and evaluated as novel self-tracking siRNA delivery vectors. The concept underlying the design of these copolymers is that hydrophobicity and rigidity of polythiophenes should enhance the transport of siRNA across the cell membrane and endosomal membrane. A gel retardation assay showed that the nanosized complexes formed between the copolymers and siRNA were stable even at a molar ratio of 1 : 2. The high cellular uptake (>80%) and localization of the copolymer vectors inside the cells were easily analyzed by tracking the fluorescence of polythiophene using fluorescent microscopy and cytometry. Anin vitroluciferase knockdown (KD) assay in A549-luc cells demonstrated that the siRNA complexes with more hydrophobic copolymers achieved a higher KD efficiency of 52.8% without notable cytotoxicity, indicating protein-specific KD activity rather than solely the cytotoxicity of the materials. Our polythiophene copolymers should serve as novel, efficient, low cell toxicity, and label-free siRNA delivery systems.

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