Poly(ester amide) blend microspheres for oral insulin delivery

被引:35
作者
He, Pan [1 ,5 ]
Liu, Huaiyu [3 ]
Tang, Zhaohui [1 ]
Deng, Mingxiao [2 ]
Yang, Yan [4 ]
Pang, Xuan [1 ]
Chen, Xuesi [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] NE Normal Univ, Dept Chem, Changchun 130021, Peoples R China
[3] Jilin Univ, Lab Anim Ctr, Changchun 130022, Peoples R China
[4] Jilin Univ, Res Ctr Drug Metab, Changchun 130022, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(ester amide); Blend microspheres; Oral insulin delivery; pH sensitivity; POLYMERIC MICROPARTICLES; INTESTINAL-ABSORPTION; NANOPARTICLES; BIOAVAILABILITY; HYDROGELS; PEPTIDES; CHITOSAN;
D O I
10.1016/j.ijpharm.2013.07.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study developed a novel oral insulin formulation centered on microspheres consisting of a blend of biodegradable poly(ester amide) (PEA). In the formulation, L-lysine-/L-leucine-based PEA with pendant COOH groups (PEA-COOH) was used as a pH-responsive material for the protection of insulin from the harsh environmental conditions of the stomach. Arginine-based PEA (Arg-PEA) was introduced to improve the intestinal absorption of the drug. The influence of both the hydrophobicity of PEA-COOH and the content of Arg-PEA was investigated in detail on microsphere surface morphology, drug loading, and the in vitro release profile of insulin. The PEA-COOH/Arg-PEA blend microspheres protected the loaded insulin in simulated gastric fluid and released insulin in a fast and sustained manner in simulated intestinal fluid. The in vivo test demonstrated that the oral administration of insulin-loaded PEA blend microspheres could effectively suppress the blood glucose level in diabetic rats for 10h, and the oral bioavailability was improved to 5.89 + 1.84% in healthy rats. These results indicate that the PEA blend microspheres are promising vehicles for the oral delivery of insulin. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:259 / 266
页数:8
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