Immuno-targeting of nonionic surfactant vesicles to inflammation

被引:21
|
作者
Hood, Elizabeth
Gonzalez, Monica
Plaas, Anna
Strom, Joel
VanAuker, Michael [1 ]
机构
[1] Univ S Florida, Dept Chem Engn, Biomed Engn Program, Tampa, FL 33620 USA
[2] Univ S Florida, Coll Med, Dept Med, Tampa, FL 33612 USA
[3] Univ S Florida, Coll Med, Div Rheumatol, Tampa, FL USA
关键词
niosomes; drug targeting; surfactants; antibodies;
D O I
10.1016/j.ijpharm.2006.12.048
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Niosomes composed of sorbitan monostearate (Span 60), polyoxyethylene sorbitan monostearate (Tween 6 1), cholesterol, and dicetyl phosphate were conjugated with a purified monoclonal antibody to CD44 (IM7) through a cyanuric chloride (CC) linkage on the polyoxyethylene group of the Tween 61 molecule. Inclusion of small amounts of Tween 61 within the surfactant component of niosomes formed using thin film hydration techniques and sonication did not hamper vesicle stability as compared to Span 60 niosomes. Conjugation was verified by UV absorbance of fluorescently tagged IM7 in non-fluorescing niosomes and fluorescent micrographs. The immuno-niosomes were incubated with synovial lining cells expressing CD44. Attachment of niosomes was evident and showed selectivity and specificity compared to controls. These findings suggest that the resulting immuno-niosomes may provide an effective method for targeted drug delivery. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:222 / 230
页数:9
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