• Title/Summary/Keyword: poly(p-dioxanone)(PPDO)

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Interfacial Evaluation of Plasma-Treated Biodegradable Poly(p-dioxanone) Fiber/Poly(L-lactide) Composites Using Micromechanical Technique and Dynamic Contact Angle Measurement (Micromechanical 시험법과 동적접촉각 측정을 이용한 플라즈마 처리된 생분해성 Poly(p-dioxanone) 섬유강화 Poly(L-lactide) 복합재료의 계면물성 평가)

  • Park, Joung-Man;Kim, Dae-Sik;Kim, Sung-Ryong
    • Journal of Adhesion and Interface
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    • v.4 no.1
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    • pp.18-27
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    • 2003
  • Interfacial properties and microfailure degradation mechanisms of the oxygen-plasma treated biodegradable poly(p-dioxanone) (PPDO) fiber/poly(L-lactide) (PLLA)composites were investigated for the orthopedic applications as implant materials using micromechanical technique and surface wettability measurement. PPDO fiber reinforced PLLA composite can provide good mechanical performance for long hydrolysis time. The degree of degradation for PPDO fiber and PLLA matrix was measured by thermal analysis and optical observation. IFSS and work of adhesion, $W_a$ between PPDO fiber and PLLA matrix showed the maximum at the plasma treatment time, at 60 seconds. Work of adhesion was lineally proportional to the IFSS. PPDO fiber showed ductile microfailure modes at We initial state, whereas brittle microfailure modes appeared with elapsing hydrolysis time. Interfacial properties and microfailure degradation mechanisms can be important factors to control bioabsorbable composites performance because IFSS changes with hydrolytic degradation.

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Synthesis and characterization of ABA types tri-block copolymers derived from p-dioxanone, ${\varepsilon}-caprolactone$ and poly(ethylene glycol)

  • Remant Bahadur K.C.;Bhattarai Shanta Raj;Aryal Santosh;Khil, Myung-Seob;Kim, Hak-Yong;Lee, Douk-Rae
    • Proceedings of the Polymer Society of Korea Conference
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    • 2006.10a
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    • pp.255-255
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    • 2006
  • Polymeric nanoparticles are recognized as promising drug carriers [1]. Here, novel tri-block copolymers based on poly PPDO, PCL and PEG were synthesized and employed for the formulation of reproducible polymeric nanoparticles [2]. To estimate the feasibility of the polymer to form polymeric nanoparticles, nanoparticles were prepared by co-solvent evaporation technique. Polymerization and structural features of the polymer were analyzed by different physico-chemical techniques. Existence of hydrophobic domains as a core of nanoparticles was characterized by $^{1}H-NMR$ spectroscopy, and further confirmed by fluorescence technique using pyrene as probe.

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