Assessment of poly(methacrylic acid-co-N-vinyl pyrrolidone) as a carrier for the oral delivery of therapeutic proteins using Caco-2 and HT29-MTX cell lines

被引:36
作者
Carr, Daniel A. [1 ]
Peppas, Nicholas A. [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Div Pharmaceut, Coll Pharm, Austin, TX 78712 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
hydrogels; insulin; oral delivery; cytocompatibility; cell culture; COMPLEXATION HYDROGELS; INSULIN DELIVERY; MEDIATED TRANSPORT; GLYCOL); MECHANISMS; MONOLAYERS; SYSTEMS; MODEL;
D O I
10.1002/jbm.a.32395
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hydrogels of poly(methacrylic acid-co-N-vinyl pyrrolidone) were synthesized and evaluated for their use as carriers for oral protein delivery. Insulin loading efficiencies were determined to be near 90% for carriers crosslinked with ethylene glycol dimethacrylate with corresponding weight incorporation levels near 12%. Although no insulin was released in gastric conditions, as desired, near instantaneous release occurred when the pH was raised to values typical of the intestinal area. Cytocompatibility studies with Caco-2 and Caco-2/HT29-MTX cultures demonstrated that microparticles did not elicit toxic effects at concentrations up to 5.0 mg/mL. Insulin transport studies revealed that the carriers did not disrupt the cell layer and thus did not change the insulin permeability in the apical-to-basolateral direction. Therefore, microparticles of this system were best suited for oral delivery of therapeutic agents that do not require transport facilitation. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res 92A: 504-512, 2010
引用
收藏
页码:504 / 512
页数:9
相关论文
共 29 条
[1]  
[Anonymous], 2000, Pract Diab Int, DOI 10.1002/pdi.91
[2]  
[Anonymous], ADV POLYM SCI
[3]   Cell culture-based models for intestinal permeability: a critique [J].
Balimane, PV ;
Chong, S .
DRUG DISCOVERY TODAY, 2005, 10 (05) :335-343
[4]   Do cell culture conditions influence the carrier-mediated transport of peptides in Caco-2 cell monolayers? [J].
Behrens, I ;
Kissel, T .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 19 (05) :433-442
[5]  
Bell CL, 1995, ADV POLYM SCI, V122, P125
[6]   Loading and mobility of spin-labeled insulin in physiologically responsive complexation hydrogels intended for oral administration [J].
Besheer, A ;
Wood, KM ;
Peppas, NA ;
Mäder, K .
JOURNAL OF CONTROLLED RELEASE, 2006, 111 (1-2) :73-80
[7]   Cellular evaluation of oral chemotherapy carriers [J].
Blanchette, J ;
Peppas, NA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 72A (04) :381-388
[8]   Oral chemotherapeutic delivery: Design and cellular response [J].
Blanchette, J ;
Peppas, NA .
ANNALS OF BIOMEDICAL ENGINEERING, 2005, 33 (02) :142-149
[9]   Investigation of the cytotoxicity and insulin transport of acrylic-based copolymer protein delivery systems in contact with Caco-2 cultures [J].
Foss, AC ;
Peppas, NA .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (03) :447-455
[10]   Gastrointestinal transit and mucoadhesive characteristics of complexation hydrogels in rats [J].
Goto, T ;
Morishita, M ;
Kavimandan, NJ ;
Takayama, K ;
Peppas, NA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (02) :462-469