胰弹性蛋白酶
弹性蛋白酶
腹主动脉瘤
强力霉素
抑制性突触后电位
主动脉瘤
药理学
医学
内科学
动脉瘤
化学
主动脉
外科
生物化学
酶
抗生素
作者
Maomao Yu,Anjie Dong,Cong Chen,Shuxin Xu,Yini Cao,Shu Liu,Qiang Zhang,Rong Qi
标识
DOI:10.1002/adhm.201700671
摘要
Doxycycline (DOX) is reported to exert therapeutic effects against abdominal aortic aneurysm (AAA), a severe degenerative disease. In this study, a DOX hydrogel formulation of DOX/PECTgel is studied, and its phase transition behavior and in vitro release profiles are explored. In addition, the anti-AAA effects and bioavailability of DOX/PECTgel are evaluated in an elastase induced AAA mouse model. The results show that the phase transition temperature of 30% poly(e-caprolactone-co-1,4,8-trioxa[4.6]spiro-9-undecanone) (PECT) solution is above 34 °C. In vitro release profiles of DOX/PECTgel indicate a fast release of DOX at the first two days, followed by a slow and sustained release for 14 d. In vivo single-dose single subcutaneous injection of DOX/PECTgel containing 8.4 or 4.2 mg mL-1 DOX presents comparatively preventive effects on AAA, compared to intraperitoneal injections of DOX alone at a dose of 15 mg kg-1 for seven injections, while DOX bioavailability of the DOX/PECTgel treated groups is 1.39 times or 1.19 times of the DOX alone treated group, respectively.
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