Thermosensitive Hydrogel Containing Doxycycline Exerts Inhibitory Effects on Abdominal Aortic Aneurysm Induced By Pancreatic Elastase in Mice

被引:11
作者
Yu, Maomao [1 ]
Dong, Anjie [2 ]
Chen, Cong [1 ]
Xu, Shuxin [2 ]
Cao, Yini [1 ]
Liu, Shu [1 ,3 ]
Zhang, Qiang [4 ]
Qi, Rong [1 ]
机构
[1] Peking Univ, Inst Cardiovasc Sci,Hlth Sci Ctr, Key Lab Mol Cardiovasc Sci,Minist Educ, Beijing Key Lab Mol Pharmaceut & New Drug Deliver, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[2] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[3] Shihezi Univ, Coll Pharm, Key Lab Xinjiang Endem Phytomed Resources, Minist Educ, Xinjiang 832003, Peoples R China
[4] Peking Univ, Sch Pharmaceut Sci, Beijing Key Lab Mol Pharmaceut & New Drug Deliver, 38 Xueyuan Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
abdominal aortic aneurysm; doxycycline; PECT; thermosensitive hydrogels; SUSTAINED-RELEASE; HYALURONIC-ACID; DRUG-RELEASE; DELIVERY; DEGRADATION; MODEL;
D O I
10.1002/adhm.201700671
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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 degrees 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.
引用
收藏
页数:10
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