scholarly journals Degradable PEGylated protein conjugates utilizing RAFT polymerization

2015 ◽  
Vol 65 ◽  
pp. 305-312 ◽  
Author(s):  
Caitlin G. Decker ◽  
Heather D. Maynard
2011 ◽  
Vol 32 (4) ◽  
pp. 354-359 ◽  
Author(s):  
Ming Li ◽  
Hongmei Li ◽  
Priyadarsi De ◽  
Brent S. Sumerlin

The Analyst ◽  
2019 ◽  
Vol 144 (18) ◽  
pp. 5439-5448 ◽  
Author(s):  
Xue Yang ◽  
Yan Sun ◽  
Yang Xiang ◽  
Fengtao Qiu ◽  
Guoqi Fu

Controlled synthesis of PEGylated protein-imprinted nanoparticles with enhanced recognition selectivity via surface-initiated RAFT polymerization.


Acta Naturae ◽  
2012 ◽  
Vol 4 (3) ◽  
pp. 72-81 ◽  
Author(s):  
A. V. Maksimenko

The results of the clinical use of thrombolytic and antithrombotic preparations developed on the basis of protein conjugates obtained within the framework of the conception of drug targeting delivery in the organism are considered. A decrease has been noted in the number of biomedical projects focused on these derivatives as a result of various factors: the significant depletion of financial and organizational funds, the saturation of the pharmaceutical market with preparations of this kind, and the appearance of original means for interventional procedures. Factors that actively facilitate the conspicuous potentiation of the efficacy of bioconjugates were revealed: the biomedical testing of protein domains and their selected combinations, the optimization of molecular sizes for the bioconjugates obtained, the density of target localization, the application of cell adhesion molecules as targets, and the application of connected enzyme activities. Enzyme antioxidants and the opportunity for further elaboration of the drug delivery conception via the elucidation and formation of therapeutic targets for effective drug reactions by means of pharmacological pre- and postconditioning of myocardium arouse significant interest.


1972 ◽  
Vol 68 (3_Suppl) ◽  
pp. S32
Author(s):  
W. Vetter ◽  
E. Freedlender ◽  
E. Haber
Keyword(s):  

1981 ◽  
Vol 46 (4) ◽  
pp. 933-940 ◽  
Author(s):  
Helmut Pischel ◽  
Antonín Holý ◽  
Günther Wagner

Reaction of 5'-O-p-toluenesulfonyl-2',3'-O-isopropylideneuridine (I) with sodium 4-cyanophenoxide afforded 2',3'-O-isopropylidene-5'-O-(4-cyanophenyl)uridine (II) which was converted by acid hydrolysis into 5'-O-(4-cyanophenyl)uridine (IIIa). Acid-catalyzed addition of ethanol to compound IIIa gave the imido ester hydrochloride IIIb which on reaction with ammonia or ethylamine was transformed into the amidine derivatives IIIc and IIId. Compound IIIb reacted with human serum albumine or bovine gamma-globuline at pH 9.2 to give protein conjugates with uridine, bound covalently by an amidine bond (IIIe,f).


2021 ◽  
Vol 44 (3) ◽  
Author(s):  
Ümİt Yİldİko ◽  
Ahmet Çağri Ata ◽  
Aslihan Aycan Tanriverdİ ◽  
İsmaİl Çakmak

2021 ◽  
Vol 162 ◽  
pp. 104875
Author(s):  
Vladimir Sincari ◽  
Svetlana Lukáš Petrova ◽  
Rafał Konefał ◽  
Martin Hruby ◽  
Eliézer Jäger

2021 ◽  
Vol 23 (3) ◽  
pp. 1248-1258
Author(s):  
Shannon M. North ◽  
Steven P. Armes

An atom-efficient, wholly aqueous one-pot synthesis of zwitterionic diblock copolymers has been devised. Such copolymers can serve as highly effective aqueous dispersants for nano-sized transparent yellow iron oxide particles.


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