Poly(ethylene glycol)-containing hydrogels for oral protein delivery applications

被引:70
作者
Kim, B
Peppas, NA [1 ]
机构
[1] Univ Texas, Dept Chem Engn, Biomat Lab, Austin, TX 78712 USA
[2] Univ Texas, Dept Chem Engn, Drug Delivery & Mol Recognit Lab, Austin, TX 78712 USA
[3] Univ Texas, Dept Biomed Engn, Drug Delivery & Mol Recognit Lab, Austin, TX 78712 USA
[4] Univ Texas, Dept Biomed Engn, Biomat Lab, Austin, TX 78712 USA
[5] Univ Texas, Dept Pharmaceut, Biomat Lab, Austin, TX 78712 USA
[6] Univ Texas, Dept Pharmaceut, Drug Delivery & Mol Recognit Lab, Austin, TX 78712 USA
[7] Purdue Univ, Sch Chem Engn, W Lafayette, IN 47907 USA
基金
美国国家卫生研究院;
关键词
poly(ethylene glycol); macromonomers; pH-sensitive; hydrogel; insulin release; G-ETHYLENE GLYCOL); GRAFT COPOLYMER NETWORKS; ENTRAPPED INSULIN; COMPLEXATION; PEPTIDE; NANOSPHERES; CALCITONIN; ABSORPTION; BEHAVIOR; SYSTEMS;
D O I
10.1023/A:1027313931273
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Novel pH-sensitive hydrogels were developed as suitable candidates for carriers in bioMEMS devices as well as for oral delivery of therapeutic peptides and proteins due to their ability to respond to environmental pH change. Macromonomers containing various PEG molecular weights were synthesized and used to prepare P(MAA-g-EG) hydrogels were by photopolymerization. P(MAA-g-EG) hydrogels showed a drastic change of the equilibrium swelling ratio between pH 2.2 and 7.0. At pH 7.0, hydrogels with PEGMA2000 exhibited higher swelling ratio than hydrogels with PEGMA1000. For both hydrogels with PEGMA1000 and PEGMA2000, the swelling mechanism became more relaxation-controled as the environmental pH changed from 2.2 to 7.0 due to the ionization of the functional groups in polymer networks at high pH. In vitro release studies of insulin were conducted. P(MAA-g-EG) hydrogels exhibited drastic increase of insulin release as the pH of the medium was changed from acidic to basic. Insulin release from P(MAA-g-EG) hydrogels with PEGMA2000 was slower than from hydrogels with PEGMA1000 at both low and high pH. These results were used to design and improve protein release behavior from these carriers.
引用
收藏
页码:333 / 341
页数:9
相关论文
共 27 条
[1]   PARTITION OF PROTEINS IN AQUEOUS POLYMER 2-PHASE SYSTEMS AND THE EFFECT OF MOLECULAR-WEIGHT OF THE POLYMER [J].
ALBERTSSON, PA ;
CAJARVILLE, A ;
BROOKS, DE ;
TJERNELD, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 926 (01) :87-93
[2]   ORALLY-ADMINISTERED LIPOSOME-ENTRAPPED INSULIN IN DIABETIC ANIMALS - A CRITICAL-ASSESSMENT [J].
ARRIETAMOLERO, JF ;
ALECK, K ;
SINHA, MK ;
BROWNSCHEIDLE, CM ;
SHAPIRO, LJ ;
SPERLING, MA .
HORMONE RESEARCH, 1982, 16 (04) :249-256
[3]   Water, solute and protein diffusion in physiologically responsive hydrogels of poly(methacrylic acid-g-ethylene glycol) [J].
Bell, CL ;
Peppas, NA .
BIOMATERIALS, 1996, 17 (12) :1203-1218
[4]   The use of inhibitory agents to overcome the enzymatic barrier to perorally administered therapeutic peptides and proteins [J].
Bernkop-Schnurch, A .
JOURNAL OF CONTROLLED RELEASE, 1998, 52 (1-2) :1-16
[5]   NANOPARTICLES AND MICROPARTICLES FOR THE DELIVERY OF POLYPEPTIDES AND PROTEINS [J].
COUVREUR, P ;
PUISIEUX, F .
ADVANCED DRUG DELIVERY REVIEWS, 1993, 10 (2-3) :141-162
[6]   Direct measurement of interactions between tethered poly(ethylene glycol) chains and adsorbed mucin layers [J].
Efremova, NV ;
Huang, Y ;
Peppas, NA ;
Leckband, DE .
LANGMUIR, 2002, 18 (03) :836-845
[7]   EFFECT OF PARTICLE-SIZE ON MECHANISM CONTROLLING NORMAL-HEXANE SORPTION IN GLASSY POLYSTYRENE MICROSPHERES [J].
ENSCORE, DJ ;
HOPFENBERG, HB ;
STANNETT, VT .
POLYMER, 1977, 18 (08) :793-800
[8]  
GNANOU Y, 1987, MAKROMOL CHEM, V188, P2111
[9]  
Harris J.M., 1992, Polyethylene Glycol: Chemistry and Biological Applications, DOI DOI 10.1016/j.indcrop.2013.04.030
[10]   Molecular aspects of muco- and bioadhesion: Tethered structures and site-specific surfaces [J].
Huang, YB ;
Leobandung, W ;
Foss, A ;
Peppas, NA .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :63-71