The influence of functional groups of self-assembled monolayers on fibrous capsule formation and cell recruitment

被引:44
作者
Barbosa, JN
Madureira, P
Barbosa, MA
Aguas, AP
机构
[1] INEB, Lab Biomat, P-4150180 Oporto, Portugal
[2] Univ Porto, IBMC, Fac Engn, Dept Engn Met & Mat, Oporto, Portugal
[3] Univ Porto, Inst Ciencias Biomed Abel Salazar, Dept Imunofisiol & Farmacol, Oporto, Portugal
[4] Univ Porto, ICBAS, Dept Anat, Oporto, Portugal
[5] Univ Porto, UMIB, Oporto, Portugal
关键词
self-assembled monolayers; inflammation; tissue responses; flow cytometry; histology;
D O I
10.1002/jbm.a.30602
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The contribution of the Surface chemistry of an implant to the thickness of the fibrous capsule formed after implantation was herein investigated. For that, self-assembled monolayers (SAMs) of alkanethiols oil gold with different terminal functional groups (COOH, OH, and CH.) were used. These surfaces were implanted ill Subcutaneous air pouches of BALB/c mice and the ensuing fibrous capsules were evaluated and compared with the initial inflammatory response caused by the implant. The thickness of the fibrous capsules that are under organization around the implant was measured I week after implantation by histology. Inflammatory exudates were collected from the air Pouches 24 h after the implantation of SAMs and were analyzed by flow cytometry. A significant increase in the thickness of fibrous capsules was seen around implanted CH3-terminated SAMs, and also in gold surfaces, in comparison with the air pouch wall of sham-operated mice and of COOH- and OH-covered SAMs. The CH3-coated implants also recruited higher numbers of inflammatory cells; this enhancement involved a significant number of Mac-1(+) cells. Our data indicate that implant surfaces coated with CH, induce thick fibrous capsules and this may be the result of the stronger inflammatory effect of CH, in comparison with COOH or OH chemical groups. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:737 / 743
页数:7
相关论文
共 28 条
[1]   LEUKOCYTE ADHESION DEFICIENCY - AN INHERITED DEFECT IN THE MAC-1, LFA-1, AND P150,95 GLYCOPROTEINS [J].
ANDERSON, DC ;
SPRINGER, TA .
ANNUAL REVIEW OF MEDICINE, 1987, 38 :175-194
[2]   Biological responses to materials [J].
Anderson, JM .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :81-110
[3]  
ANDERSON JM, 1994, EUR J PHARM BIOPHARM, V40, P1
[4]   Host response to tissue engineered devices [J].
Babensee, JE ;
Anderson, JM ;
McIntire, LV ;
Mikos, AG .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 33 (1-2) :111-139
[5]   The attraction of Mac-1+ phagocytes during acute inflammation by methyl-coated self-assembled monolayers [J].
Barbosa, JN ;
Madureira, P ;
Barbosa, MA ;
Aguas, AP .
BIOMATERIALS, 2005, 26 (16) :3021-3027
[6]  
Barbosa JN, 2004, BIOMATERIALS, V25, P2557, DOI 10.1016/j .biomaterials.2003.09.047
[7]   LIVE BUT NOT HEAT-KILLED MYCOBACTERIA CAUSE RAPID CHEMOTAXIS OF LARGE NUMBERS OF EOSINOPHILS INVIVO AND ARE INGESTED BY THE ATTRACTED GRANULOCYTES [J].
CASTRO, AG ;
ESAGUY, N ;
MACEDO, PM ;
AGUAS, AP ;
SILVA, MT .
INFECTION AND IMMUNITY, 1991, 59 (09) :3009-3014
[8]  
ISAJI M, 1989, BRIT J EXP PATHOL, V70, P705
[9]  
Lin JC, 2000, J BIOMED MATER RES, V51, P413, DOI 10.1002/1097-4636(20000905)51:3<413::AID-JBM16>3.0.CO
[10]  
2-L