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p. 31-39
Received: 15 January 2010; in revised form: 15 April 2010 / Accepted: 22 April 2010 / Published: 26 April 2010
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| Download PDF Full-text (1644 KB) Abstract: Shape memory nanocomposites of polyurethane (PU)-clay were fabricated by melt mixing of PU and nano-clay. Based on nano-indentation and microhardness tests, the strength of the nanocomposites increased dramatically as a function of clay content, which is attributed to the enhanced nanoclay–polymer interactions. Thermal mechanical experiments demonstrated good mechanical and shape memory effects of the nanocomposites. Full shape memory recovery was displayed by both the pure PU and PU-clay nanocomposites.
p. 40-56
Received: 4 January 2010; in revised form: 11 March 2010 / Accepted: 27 April 2010 / Published: 12 May 2010
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| Download PDF Full-text (1053 KB) Abstract: Environmentally responsive poly(N -isopropylacrylamide) brushes were grafted from the surface of polymer particles or flat surfaces in order to generate reversible hydrophilic and hydrophobic surfaces. The use of atom transfer radical polymerization was demonstrated for the grafting of polymer brushes as it allows efficient control on the amount of grafted polymer. The polymer particles were generated with or without surfactant in the emulsion polymerization and their surface could be modified with the atom transfer radical polymerization (ATRP) initiator. The uniform functionalization of the surface with ATRP initiator was responsible for the uniform grafting of polymer brushes. The grafted brushes responded reversibly with changes in temperature indicating that the reversible responsive behavior could be translated to the particle surfaces. The particles were observed to adsorb and desorb protein and virus molecules by changing the temperatures below or higher than 32 °C. The initiator functionalized particles could also be adsorbed on the flat surfaces. The adsorption process also required optimization of the heat treatment conditions to form a uniform layer of the particles on the substrate. The grafted polymer brushes also responded to the changes in temperatures similar to the spherical particles studied through water droplets placed on the flat substrates.
p. 57-70
Received: 6 May 2010; in revised form: 19 May 2010 / Accepted: 23 May 2010 / Published: 26 May 2010
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| Download PDF Full-text (191 KB) Abstract: Some new phenomena involved in the physical properties of comb polyelectrolyte solutions are reviewed. Special emphasis is given to synthetic biomimetic materials, and the structures formed by these molecules are compared with those of naturally occurring glycoprotein and proteoglycan solutions. Developments in the determination of the structure and dynamics (viscoelasticity) of comb polymers in solution are also covered. Specifically the appearance of multi-globular structures, helical instabilities, liquid crystalline phases, and the self-assembly of the materials to produce hierarchical comb morphologies is examined. Comb polyelectrolytes are surface active and a short review is made of some recent experiments in this area that relate to their morphology when suspended in solution. We hope to emphasize the wide variety of phenomena demonstrated by the vast range of naturally occurring comb polyelectrolytes and the challenges presented to synthetic chemists designing biomimetic materials.
p. 71-85
Received: 27 April 2010; in revised form: 28 May 2010 / Accepted: 28 May 2010 / Published: 8 June 2010
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| Download PDF Full-text (880 KB) | Abstract: A series of segmented multiblock copolymers containing aramid hard segments and extended polycaprolactone soft segments (with an Mn of 4,200 or 8,200 g mol–1 ) was prepared and tested for their shape-memory properties. Chain extenders were essential to raise the hard segment concentration so that an extended rubbery plateau could be observed. Dynamic mechanical thermal analysis provided a useful guide in identifying (i) the presence of a rubbery plateau, (ii) the flow temperature, and (iii) the temperature when samples started to deform irreversibly.
p. 86-101
Received: 28 April 2010; in revised form: 2 June 2010 / Accepted: 18 June 2010 / Published: 22 June 2010
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| Download PDF Full-text (664 KB) Abstract: The physicochemical properties of stimuli-responsive polymers change with physical or biological signals, such as pH, enzyme concentrations, and temperature. These polymers have attracted considerable attention in the field of drug delivery. The drug carrier system, which was revolutionized by the introduction of these polymers, has recently provided a new paradigm of maximizing the therapeutic activity of drugs. This review highlights recent studies regarding stimuli-responsive drug carriers tailor-made for effective cytosolic drug delivery, with particular emphasis on tumor treatment.
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