期刊
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
卷 22, 期 4-6, 页码 489-504出版社
TAYLOR & FRANCIS LTD
DOI: 10.1163/092050610X487765
关键词
Polypropylene fumarate; polycaprolactone; injectable biomaterials; in situ polymerizable
资金
- National Institutes of Health [AR056212-01, 1T32AR056950]
- NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [T32AR056950, R01AR056212] Funding Source: NIH RePORTER
In this work, a series of co-polymers of polypropylene fumarate-co-polycaprolactone (PPF-co-PCL) were synthesized via a three-step polycondensation reaction of oligomeric polypropylene fumarate (PPF) with polycaprolactone (PCL). The effects of PPF precursor molecular weight, PCL precursor molecular weight and PCL fraction in the co-polymer (PCL feed ratio) on the maximum cross-linking temperature, gelation time and mechanical properties of the cross-linked co-polymers were investigated. The maximum cross-linking temperature fell between 38.2 +/- 0.3 and 47.2 +/- 0.4 degrees C, which increased with increasing PCL precursor molecular weight. The gelation time was between 4.2 +/- 0.2 and 8.5 +/- 0.7 min, and decreased with increasing PCL precursor molecular weight. The compressive moduli ranged from 44 +/- 1.8 to 142 +/- 7.4 MPa, with enhanced moduli at higher PPF precursor molecular weight and lower PCL feed ratio. The compressive toughness was in the range of 4.1 +/- 0.3 and 17.1 +/- 1.3 kJ/m(3). Our data suggest that the cross-linking and mechanical properties of PPF-co-PCL can be modulated by varying the composition. Therefore, the PPF-co-PCL co-polymers may offer increased versatility as an injectable, in situ polymerizable biomaterial than the individual polymers of PPF and PCL. (C) Koninklijke Brill NV, Leiden, 2011
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