PHB;
PHBHHx;
in vivo biodegradation;
tissue response;
in vivo biocompatibility;
D O I:
10.1016/j.biomaterials.2006.02.015
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
The in vivo tissue reactions and biodegraclations of poly(3-hydroxybtityrate-co-3-hydroxyhexanoate) (PHBHHx), poly(lactide) (PLA), poly(3-hydroxybutyrate) (PHB), blends of PHBHHx (X) and poly(ethylene glycol) (PEG) (E) with ratios of 1: 1 (E1X1) and 1:5 (E1X5), respectively, were evaluated by Subcutaneous implantation in rabbits. Results revealed that the degradation rate increased in the order of PHB < PHBHHx < PLA. During the implantation period, crystallinity of PHBHHx increased from 19% to 22% and then dropped to 14%. Gel permeation chromatography (GPC) displayed increasing polydispersity and typical bimodal distribution from 3 to 6 months. The above results suggested that rapid PHBHHx degradation occurred in amorphous region rather than in crystalline region. While the in vivo hydrolysis of PHB was found to start from a random chain scission both in amorphous and crystalline regions of the polymer matrix, as demonstrated by its hydrolysis process accompanied by a decrease in molecular weight with unimodal distribution and relatively narrow polydispersity. Compared to pure PHBHHx, PHBHHx-PEG blends showed accelerated weight loss of PHBHHx with weak molecular weight reduction. In general, PHBHHx elicited a very mild tissue response during implantation lasting 6 months compared with relative acute immunological reactions observed among PHB and PLA objects, respectively. Pronounced tissue responses were observed in the capsule surrounding E1X1 and EIX5 as characterized by the presence of lymphocytes, eosinophils and vascularization, which might be resulted from the continuous leaching of PEG. (c) 2006 Elsevier Ltd. All rights reserved.
机构:Hong Kong Polytech Univ, Inst Mol Technol Drug Discovery & Synth, Dept Appl Biol & Chem Technol, Open Lab Chirotechnol, Hong Kong, Hong Kong, Peoples R China
Chen, C
Cheung, MK
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机构:
Hong Kong Polytech Univ, Inst Mol Technol Drug Discovery & Synth, Dept Appl Biol & Chem Technol, Open Lab Chirotechnol, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Inst Mol Technol Drug Discovery & Synth, Dept Appl Biol & Chem Technol, Open Lab Chirotechnol, Hong Kong, Hong Kong, Peoples R China
Cheung, MK
Yu, PHF
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机构:Hong Kong Polytech Univ, Inst Mol Technol Drug Discovery & Synth, Dept Appl Biol & Chem Technol, Open Lab Chirotechnol, Hong Kong, Hong Kong, Peoples R China
机构:
Univ Sains Malaysia, Sch Biol Sci, Ecobiomat Res Lab, Minden, Malaysia
Univ Malaya, Nanotechnol & Catalysis Res Ctr, Kuala Lumpur, MalaysiaNatl Def Univ Malaysia, Fac Def Sci & Technol, Dept Maritime Sci & Technol, Kuala Lumpur, Malaysia
Sudesh, Kumar
Sagadevan, Suresh
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机构:Natl Def Univ Malaysia, Fac Def Sci & Technol, Dept Maritime Sci & Technol, Kuala Lumpur, Malaysia
Sagadevan, Suresh
Mukheem, Abdul
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Natl Def Univ Malaysia, Fac Def Sci & Technol, Dept Maritime Sci & Technol, Kuala Lumpur, MalaysiaNatl Def Univ Malaysia, Fac Def Sci & Technol, Dept Maritime Sci & Technol, Kuala Lumpur, Malaysia
机构:
Univ Massachusetts Dartmouth, Dept Bioengn, 285 Old Westport Rd, N Dartmouth, MA 02747 USAUniv Massachusetts Dartmouth, Dept Bioengn, 285 Old Westport Rd, N Dartmouth, MA 02747 USA
Kehail, Abdulrahman A.
Foshey, Michael
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Univ Massachusetts Dartmouth, Dept Mech Engn, 285 Old Westport Rd, N Dartmouth, MA 02747 USAUniv Massachusetts Dartmouth, Dept Bioengn, 285 Old Westport Rd, N Dartmouth, MA 02747 USA
Foshey, Michael
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机构:
Chalivendra, Vijaya
Brigham, Christopher J.
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机构:
Univ Massachusetts Dartmouth, Dept Bioengn, 285 Old Westport Rd, N Dartmouth, MA 02747 USAUniv Massachusetts Dartmouth, Dept Bioengn, 285 Old Westport Rd, N Dartmouth, MA 02747 USA