Biocompatibility and Inflammation Profile of B2A-Coated Granules Used in Arthrodesis

被引:2
作者
Zamora, Paul O. [1 ]
Liu, Yi [1 ]
Guo, Henry [1 ]
Lin, Xinhua [1 ]
机构
[1] BioSurface Engn Technol Inc, Rockville, MD 20850 USA
关键词
B2A; coated granules; biocompatible; inflammation models; BONE MORPHOGENETIC PROTEIN-2; B2A PEPTIDE; E-SELECTIN; AIR POUCH; FUSION; MODEL; SPINE; RESPONSES;
D O I
10.1177/1091581813476960
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The biocompatibility/inflammation profile of B2A-coated ceramic granules was evaluated using a panel of standard biocompatibility protocols (International Organization for Standardization-10993) including skin irritation and delayed-type hypersensitivity (Kligman maximization test), as well as acute, subacute, and chronic toxicity. Additionally, the potential of B2A-coated granules to elicit inflammatory reactions was also assessed using in vivo air pouch models, and B2A was evaluated using in vitro models of leukocyte recruitment and endothelial cell activation. Overall, the findings demonstrate that B2A-coated ceramic granules exhibit good biocompatibility profiles in the murine air pouch model and in standard subcutaneous implant models, and B2A did not demonstrate evidence of leukocyte recruitment or endothelial cell activation. These findings suggest that B2A and B2A-coated granules have little, if any, propensity to initiate inflammation reactions based on leukocyte recruitment. Thus, traditional biocompatibility and specially designed inflammation models indicate a high degree of biocompatibility and a low possibility of toxicity, inflammation, or edema following the implant of B2A-coated granules.
引用
收藏
页码:154 / 161
页数:8
相关论文
共 29 条
[1]   Targeting selectins and selectin ligands in inflammation and cancer [J].
Barthel, Steven R. ;
Gavino, Jacyln D. ;
Descheny, Leyla ;
Dimitroff, Charles J. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2007, 11 (11) :1473-1491
[2]   Bone morphogenetic protein-2 induces proinflammatory endothelial phenotype [J].
Csiszar, A ;
Ahmad, M ;
Smith, KE ;
Labinskyy, N ;
Gao, O ;
Kaley, G ;
Edwards, JG ;
Wolin, MS ;
Ungvari, Z .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 168 (02) :629-638
[3]   Ceramic granules enhanced with B2A peptide for lumbar interbody spine fusion: an experimental study using an instrumented model in sheep Laboratory investigation [J].
Cunningham, Bryan W. ;
Atkinson, Brent L. ;
Hu, Nianbin ;
Kikkawa, Jun ;
Jenis, Louis ;
Bryant, Joseph ;
Zamora, Paul O. ;
McAfee, Paul C. .
JOURNAL OF NEUROSURGERY-SPINE, 2009, 10 (04) :300-307
[4]  
Duarte D.B., 2012, Curr Protoc Pharmacol
[5]  
GALLAGHER R, 1979, BLOOD, V54, P713
[6]   Formation of Painful Seroma and Edema After the Use of Recombinant Human Bone Morphogenetic Protein-2 in Posterolateral Lumbar Spine Fusions [J].
Garrett, Mark P. ;
Kakarla, Udaya K. ;
Porter, Randall W. ;
Sonntag, Volker K. H. .
NEUROSURGERY, 2010, 66 (06) :1044-1049
[7]  
GlazebrookM Younger A, PROSPECTIVE PI UNPUB
[8]   Commentary: Important considerations on bone morphogenetic protein-2 and neuroinflammation [J].
Heggeness, Michael H. .
SPINE JOURNAL, 2011, 11 (06) :506-506
[9]   Is It Safe to Use Recombinant Human Bone Morphogenetic Protein in Posterior Cervical Fusion? [J].
Hiremath, Girish K. ;
Steinmetz, Michael P. ;
Krishnaney, Ajit A. .
SPINE, 2009, 34 (09) :885-889
[10]   Bone morphogenetic protein-binding peptide reduces the inflammatory response to recombinant human bone morphogenetic protein-2 and recombinant human bone morphogenetic protein-7 in a rodent model of soft-tissue inflammation [J].
Lee, Kwang-Bok ;
Murray, Samuel S. ;
Taghavi, Cyrus E. ;
Song, Kyung-Jin ;
Brochmann, Elsa J. ;
Johnson, Jared S. ;
Keorochana, Gun ;
Liao, Jen-Chung ;
Wang, Jeffrey C. .
SPINE JOURNAL, 2011, 11 (06) :568-576