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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 2151-2159 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new model of molecular scale microcapsule named “super microcapsule” (SMC) obtained from a star copolymer consisting of hydrophilic and hydrophobic blocks was presented. As a first stage, 3 and 4-arm star polyethylene oxide-polylactide copolymers (s-PEO-PLA) were synthesized by the use of triethanolamine and pentaerythritol and initiating agent, respectively. The block length of PLA and PEO for the copolymers can be controlled by feed and reaction conditions. The molecular weight distributions found to be in the range of 1.3-1.7. The DTA data indicated that the phase separation behavior of s-PEO—PLA copolymers is different from that of linear PEO—PLA copolymers with comparable block length. As a evidence of SMC, the shell-core structure of s-PEO—PLA copolymers in solid state was observed by TEM. The SMC dimensions were estimated to be about 400-1000 Å
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 331-337 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 1965-1972 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(N-vinyl-2-pyrrolidone) (PVP) was blended with poly[styrene-co-(4-hydroxytyrene)] (PSH) which was obtained from the random copolymer poly[styrene-co-(4-acetoxystyrene)] (PSA). The miscibility of PVP/PSH blends in a composition 1 : 1 by weight was evaluated by differential scanning calorimetry (DSC), non-radiative energy transfer (NET) and Fourier transform infrared (FTIR) spectroscopy. It was found that the blends become miscible when the hydroxystyrene units (HS) in PSH exceed 11 mol-%. The driving force of miscibility may be attributed to hydrogen bonding between —OH in PSH and in PVP. The experimental results of miscibility were compared with that estimated from a “miscibility parameter” (MP) concept, and we found that the general trend of MP values is in agreement with the experimental results.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 369-375 
    ISSN: 0959-8103
    Keywords: poly(1,3-trimethylene carbonate-co-glycolide) ; polymer surface biodegradation ; protein-controlled release matrix ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Poly(1,3-trimethylene carbonate-co-glycolide) (PGCA) has been synthesized by ring-opening polymerization of 1,3-trimethylene carbonate (CA) and glycolide (GA) with stannous octoate as catalyst. The copolymers were characterized by 1H nuclear magnetic resonance (NMR), 13C NMR and differential scanning calorimetry. Water content and static contact angle of distilled water on the polymer surface were used to evaluate the hydrophobicity of the copolymers. There was no apparent difference in hydrophobicities of copolymers containing up to 30 mol% GA. The biodegradation of PGCA was conducted in phosphate buffer solution at 37°C and in rats. The results indicated that the degradation rates of PGCA were higher than that of PCA and depended on the GA fraction in the copolymers. Furthermore, degradation occurred in the bulk when the GA content exceeded 20 mol%. With less GA units the degradation became a surface reaction both in vitro and in vivo. These properties of PGCA may be useful in protein delivery systems.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 1-9 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polylactide (PLA)-poly(ethylene glycol) (PEG) copolymers were synthesized from polyethylene glycol and D,L-lactide using low toxic stannous octoate as catalyst at 180°C by bulk polymerization. The copolymers were characterized by GPC, IR, and 13C-NMR. A full assignment NMR spectrum is presented. The physical, drug release, and biodegradable properties in vitro of PLA-PEG copolymers were investigated. The result indicates that the rates of drug release and biodegradation could be tailored by adjusting polymer composition. This amorphous material might be used as a drug carrier in medical applications.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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