scholarly journals Nanopatterned Protein Films Directed by Ionic Complexation with Water-Soluble Diblock Copolymers

2012 ◽  
Vol 45 (11) ◽  
pp. 4572-4580 ◽  
Author(s):  
Bokyung Kim ◽  
Christopher N. Lam ◽  
Bradley D. Olsen
2008 ◽  
Vol 67 (9-10) ◽  
pp. 741-747 ◽  
Author(s):  
Demet Topaloğlu Yazıcı ◽  
Ayşegül Aşkın ◽  
Vural Bütün

Polymer ◽  
2004 ◽  
Vol 45 (2) ◽  
pp. 367-378 ◽  
Author(s):  
Dmitry V. Pergushov ◽  
Ekaterina V. Remizova ◽  
Michael Gradzielski ◽  
Peter Lindner ◽  
Jesper Feldthusen ◽  
...  

2015 ◽  
Vol 22 (3) ◽  
pp. 844-852 ◽  
Author(s):  
Jochen Bürck ◽  
Siegmar Roth ◽  
Dirk Windisch ◽  
Parvesh Wadhwani ◽  
David Moss ◽  
...  

Synchrotron radiation circular dichroism (SRCD) is a rapidly growing technique for structure analysis of proteins and other chiral biomaterials. UV-CD12 is a high-flux SRCD beamline installed at the ANKA synchrotron, to which it had been transferred after the closure of the SRS Daresbury. The beamline covers an extended vacuum-UV to near-UV spectral range and has been open for users since October 2011. The current end-station allows for temperature-controlled steady-state SRCD spectroscopy, including routine automated thermal scans of microlitre volumes of water-soluble proteins down to 170 nm. It offers an excellent signal-to-noise ratio over the whole accessible spectral range. The technique of oriented circular dichroism (OCD) was recently implemented for determining the membrane alignment of α-helical peptides and proteins in macroscopically oriented lipid bilayers as mimics of cellular membranes. It offers improved spectral quality <200 nm compared with an OCD setup adapted to a bench-top instrument, and accelerated data collection by a factor of ∼3. In addition, it permits investigations of low hydrated protein films down to 130 nm using a rotatable sample cell that avoids linear dichroism artifacts.


2008 ◽  
Vol 55-57 ◽  
pp. 717-720 ◽  
Author(s):  
N. Niamsa ◽  
M. Srisa-ard ◽  
Y. Srisuwan ◽  
N. Kotsaeng ◽  
Y. Baimark ◽  
...  

Nanocomposite chitosan-based films incorporated with drug-loaded methoxy poly(ethylene glycol)-b-poly(D,L-lactide-co-glycolide) diblock copolymers (MPEG-b-PDLLG) nanoparticles were prepared by forming drug-loaded nanoparticles in chitosan solution before suspension-solution film casting. Salicylic acid was used as a poorly-water soluble model drug. The nanocomposite films with DLL/G ratios of 100/0 and 85/15 mol% and chitosan/diblock copolymer/drug ratios of 80/1/1, 80/2/2 and 80/4/4 (w/w) were prepared and investigated. The sizes of drug-loaded nanoparticles into the chitosan films were approximate or less than 100 nm. Nanopores were observed in the resulted chitosan films incorporated with drug-loaded nanoparticles when the diblock copolymer ratio was increased up to 2. Number and size of the nanopores increased as increasing the diblock copolymer ratio. Only the nanocomposite films with chitosan/diblock copolymer/drug ratio of 80/1/1 (w/w) showed slower drug release than the chitosan film.


2016 ◽  
Vol 18 (24) ◽  
pp. 16137-16151 ◽  
Author(s):  
Karel Šindelka ◽  
Zuzana Limpouchová ◽  
Martin Lísal ◽  
Karel Procházka

The electrostatic co-assembly in non-stoichiometric aqueous mixtures of diblock copolymers.


Polymer ◽  
2005 ◽  
Vol 46 (1) ◽  
pp. 137-146 ◽  
Author(s):  
P. Ravi ◽  
S.L. Sin ◽  
L.H. Gan ◽  
Y.Y. Gan ◽  
K.C. Tam ◽  
...  

2005 ◽  
Vol 38 (12) ◽  
pp. 4977-4982 ◽  
Author(s):  
V. Bütün ◽  
I. Bannister ◽  
N. C. Billingham ◽  
D. C. Sherrington ◽  
S. P. Armes

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