Synthesis and blood compatibilities of novel segmented polyurethanes containing phosphatidylcholine analogous moieties in the main chains and long-chain alkyl groups in the side chains

1999 ◽  
Vol 14 (9) ◽  
pp. 3789-3798 ◽  
Author(s):  
Arata Korematsu ◽  
Yu-Jun Li ◽  
Takayuki Murakami ◽  
Tadao Nakaya

New segmented polyurethanes containing phospholipid moieties in the main chains and long-chain alkyl groups in the side chains were synthesized. The soft segments used in this study were poly(butadiene), poly(isoprene), hydrogenated poly(isoprene), and poly(1,6-hexyl-1,2-ethylcarbonate) diol. The hard segments of these polyurethanes were 4,4′-methylenediphenyl diisocyanate, bis[2-(2-hydroxyethyldimethylammonio)ethyl]2-cetyl- 1,3-propanediphosphate, and 1,4-butanediol. The blood compatibilities of the new polymers were evaluated by platelet-rich plasma contact studies and viewed by scanning electron microscopy using medical grade BioSpan® and nonphospholipid polyurethane as references. These new materials have good surfaces in terms of platelet adhesion, and the morphology of adhered platelets undergoes a relatively low degree of variation.

2009 ◽  
Vol 62 (8) ◽  
pp. 794 ◽  
Author(s):  
Taeyi Choi ◽  
Jadwiga Weksler ◽  
Ajay Padsalgikar ◽  
Rebeca Hernéndez ◽  
James Runt

Three series of segmented polyurethane block copolymers were synthesized using 4,4′-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BDO) or 1,3-bis(4-hydroxybutyl)tetramethyl disiloxane (BHTD) as the hard segments, and soft segments composed of poly(dimethyl siloxane) (PDMS)-based and poly(hexamethylene oxide) (PHMO) macrodiols. Copolymers synthesized with the PDMS macrodiol and PDMS and PHMO macrodiol mixtures consist of three microphases: a PDMS phase, hard domains, and a mixed phase of PHMO (when present), PDMS ether end-group segments and some dissolved hard segments. Degrees of phase separation were characterized using small-angle X-ray scattering by applying a pseudo two-phase model, and the morphology resulting from unlike segment demixing was found to be closely related to the in vitro oxidative biostability of these segmented polyurethanes.


Author(s):  
Chang Dae Han

Thermoplastic polyurethane (TPU) has received considerable attention from both the scientific and industrial communities (Hepburn 1982; Oertel 1985; Saunders and Frish 1962). Applications for TPUs include automotive exterior body panels, medical implants such as the artificial heart, membranes, ski boots, and flexible tubing. Figure 10.1 gives a schematic that shows the architecture of TPU, consisting of hard and soft segments. Hard segments, which form a crystalline phase at service temperature, are composed of diisocyanate and short-chain diols as a chain extender, while soft segments, which control low-temperature properties, are composed of difunctional long-chain polydiols with molecular weights ranging from 500 to 5000. The soft segments form a flexible matrix between the hard domains. TPUs are synthesized by reacting difunctional long-chain diol with diisocyanate to form a prepolymer, which is then extended by a chain extender via one of two routes: (1) by a dihydric glycol chain extender or (2) by a diamine chain extender. The most commonly used diisocyanate is 4,4’-diphenylmethane diisocyanate (MDI), which reacts with a difunctional polyol forming soft segments, such as poly(tetramethylene adipate) (PTMA) or poly(oxytetramethylene) (POTM), to produce TPU, in which 1,4-butanediol (BDO) is used as a chain extender. There are two methods widely used to produce TPU: (1) one-shot reaction sequence and (2) two-stage reaction sequence. The reaction sequences for both methods are well documented in the literature (Hepburn 1982). It should be mentioned that MDI/BDO/PTMA produces ester-based TPU. One can also produce ether-based TPU when MDI reacts with POTM using BDO as a chain extender. TPUs are often referred to as “multiblock copolymers.” In order to have a better understanding of the rheological behavior of TPUs, one must first understand the relationships between the chemical structure and the morphology; thus, a complete characterization of the materials must be conducted. The rheological behavior of TPU depends, among many factors, on (1) the composition of the soft and hard segments, (2) the lengths of the soft and hard segments and the sequence length distribution, (3) anomalous linkages (branching, cross-linking), and (4) molecular weight.


1998 ◽  
Vol 68 (7) ◽  
pp. 508-514 ◽  
Author(s):  
Chie Sawatari ◽  
Yuka Sekiguchi ◽  
Tatsuhiko Yagi

1993 ◽  
Vol 328 ◽  
Author(s):  
Ken D. Zemach ◽  
M. F. Rubner

ABSTRACTSeveral diacetylene containing polyesters with thermochromic transitions at or around room temperature have been synthesized. Some of these polymers have been shown to be highly sensitive to body temperature, giving rise to either reversible or irreversible thermochromic changes, depending upon both the molecular structure and the processing conditions. By changing the structure and processing conditions, the thermochromic transition can be moved over a wide range of temperatures. Segmented polyurethanes using these diacetylene functionalized polyesters as soft segments and containing diacetylene groups in the hard segments have also been produced. Through a selective polymerization process, it is possible to selectively cross-polymerize the hard segment diacetylene groups or cross-polymerize both the hard and soft segments thereby making it possible to examine the effects of hard and soft segment crosslinking on mechanical properties.


1996 ◽  
Vol 17 (10) ◽  
pp. 737-744 ◽  
Author(s):  
Yu-Jun Li ◽  
Naotoshi Nakamura ◽  
Tian-Ming Chen ◽  
Yan-Feng Wang ◽  
Masaya Kitamura ◽  
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