The anti-inflammatory properties of halloysite

被引:31
作者
Cornejo-Garrido, Hilda
Nieto-Camacho, Antonio [4 ]
Gomez-Vidales, Virginia [4 ]
Teresa Ramirez-Apan, Maria [4 ]
del Angel, Paz
Ascencion Montoya, Jose
Dominguez-Lopez, Mariana [5 ]
Kibanova, Dania [1 ]
Cervini-Silva, Javiera [1 ,2 ,3 ]
机构
[1] Univ Autonoma Metropolitana, Dept Proc & Tecnol, Unidad Cuajimalpa, Mexico City 01120, DF, Mexico
[2] NASA, Astrobiol Inst, Washington, DC USA
[3] Lawrence Berkeley Natl Lab, Div Earth Sci, Berkeley, CA USA
[4] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico
[5] Univ Nacl Autonoma Mexico, Inst Fisiol Celular, Mexico City 04510, DF, Mexico
关键词
Vehicle-delivery drugs; lndomethacin; Naturally-occurring; Clays; Inexpensive; LIPID-PEROXIDATION; OXIDATIVE STRESS; NITRIC-OXIDE; MOUSE EAR; CHEMISTRY; MACROPHAGES; SUSPENSIONS; PARTICLES; TISSUES; AGENTS;
D O I
10.1016/j.clay.2011.12.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Halloysite can serve as an alternative agent for drug delivery because its production is not tedious, hazardous, or expensive. In this study we show that halloysite presented anti-inflammatory properties comparable to indomethacin as evidenced by determination of the mieloperoxidase (MPO) enzymatic activity, a specific marker for migration and cellular infiltration. Edema reached maximum levels after 4 h. Cellular migration was noted to be low. After 24 h, however, cellular migration was noted to increase. Experiments conducted with mice primary peritoneal macrophages showed that halloysite (vs aminoguanidine) inhibited the production of nitric oxide. Halloysite inhibited oxidative stress via lipid peroxidation (ca. IC50 = 2023 ppm). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:10 / 16
页数:7
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