Formulating the alginate-polyornithine biocapsule for prolonged stability: Evaluation of composition and manufacturing technique

被引:43
作者
Thanos, C. G. [1 ]
Calafiore, R.
Basta, G.
Bintz, B. E.
Bell, W. J.
Hudak, J.
Vasconcellos, A.
Schneider, P.
Skinner, S. J. M.
Geaney, M.
Tan, P.
Elliot, R. B.
Tatnell, M.
Escobar, L.
Qian, H.
Mathiowitz, E.
Emerich, D. F.
机构
[1] LCT BioPharma Inc, Providence, RI 02906 USA
[2] Brown Univ, Dept Mol Pharmacol Physiol & Biotechnol, Providence, RI 02912 USA
[3] Univ Perugia, Sch Med, Dept Internal Med, I-06126 Perugia, Italy
[4] Living Cell Technol Ltd, Auckland, New Zealand
关键词
alginate; microcapsule; polyornithine; degradation; intraperitoneal; delivery;
D O I
10.1002/jbm.a.31472
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Alginate encapsulation is one of the most widely used techniques for introducing cell-based therapeutics into the body. Numerous encapsulation methodologies exist, utilizing a variety of alginates, purification technologies, and unique polycationic membrane components. The stability of a conventional alginate formulation encapsulated using a commercially available technique and apparatus has been characterized extensively. The current study employs an encapsulation protocol and ultra-pure alginate pioneered at the University of Perugia. The enhanced microcapsules were produced, characterized, and implanted into the brain, peritoneal cavity, and subcutaneous space of Long-Evans rats. After 14, 28, 60, 90, 120, and 180 or 215 days, capsules were explanted and the surface was analyzed using Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Image analysis was carried out to measure changes in diameter and wall thickness. FTIR peak analysis and surface morphology from SEM indicated that the enhanced encapsulation technique and formulation produced a stable biocapsule capable of survival in all sites, including the harsh peritoneal environment, for at least 215 days. Preimplant analysis showed a marked increase in the structural integrity of the enhanced formulation with improved elasticity and burst strength compared with the baseline formulation, which remained stable for less than 60 days. The enhanced microcapsule composition showed advantages in physical strength and longevity, indicating that small changes in encapsulation methodologies and materials selection can dramatically impact the stability and longevity of alginate microcapsules and their contents. (c) 2007 Wiley Periodicals.
引用
收藏
页码:216 / 224
页数:9
相关论文
共 29 条
[1]
TRANSPLANTATION OF MICROENCAPSULATED BOVINE CHROMAFFIN CELLS REDUCES LESION-INDUCED ROTATIONAL ASYMMETRY IN RATS [J].
AEBISCHER, P ;
TRESCO, PA ;
SAGEN, J ;
WINN, SR .
BRAIN RESEARCH, 1991, 560 (1-2) :43-49
[2]
Alginate hydrogels as biomaterials [J].
Augst, Alexander D. ;
Kong, Hyun Joon ;
Mooney, David J. .
MACROMOLECULAR BIOSCIENCE, 2006, 6 (08) :623-633
[3]
Optimized parameters for microencapsulation of pancreatic islet cells: an in vitro study clueing on islet graft immunoprotection in type 1 diabetes mellitus [J].
Basta, G ;
Sarchielli, P ;
Luca, G ;
Racanicchi, L ;
Nastruzzi, C ;
Guido, L ;
Mancuso, F ;
Macchiarulo, G ;
Calabrese, G ;
Brunetti, P ;
Calafiore, R .
TRANSPLANT IMMUNOLOGY, 2004, 13 (04) :289-296
[4]
Controlling alginate gel degradation utilizing partial oxidation and bimodal molecular weight distribution [J].
Boontheekul, T ;
Kong, HJ ;
Mooney, DJ .
BIOMATERIALS, 2005, 26 (15) :2455-2465
[5]
Degradation of partially oxidized alginate and its potential application for tissue engineering [J].
Bouhadir, KH ;
Lee, KY ;
Alsberg, E ;
Damm, KL ;
Anderson, KW ;
Mooney, DJ .
BIOTECHNOLOGY PROGRESS, 2001, 17 (05) :945-950
[6]
Deletion of the tissue response against alginate-pll capsules by temporary release of co-encapsulated steroids [J].
Bünger, CM ;
Tiefenbach, B ;
Jahnke, A ;
Gerlach, C ;
Freier, T ;
Schmitz, KP ;
Hopt, UT ;
Schareck, W ;
Klar, E ;
de Vos, P .
BIOMATERIALS, 2005, 26 (15) :2353-2360
[7]
Biocompatibility and surface structure of chemically modified immunoisolating alginate-PLL capsules [J].
Bünger, CM ;
Gerlach, C ;
Freier, T ;
Schmitz, KP ;
Pilz, M ;
Werner, C ;
Jonas, L ;
Schareck, W ;
Hopt, UT ;
de Vos, P .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 67A (04) :1219-1227
[8]
Standard technical procedures for microencapsulation of human islets for graft into nonimmunosuppressed patients with type 1 diabetes mellitus [J].
Calafiore, R. ;
Basta, G. ;
Luca, G. ;
Lemmi, A. ;
Racanicchi, L. ;
Mancuso, F. ;
Montanucci, M. P. ;
Brunetti, P. .
TRANSPLANTATION PROCEEDINGS, 2006, 38 (04) :1156-1157
[9]
THE EFFECT OF CAPSULE COMPOSITION ON THE BIOCOMPATIBILITY OF ALGINATE-POLY-L-LYSINE CAPSULES [J].
CLAYTON, HA ;
LONDON, NJM ;
COLLOBY, PS ;
BELL, PRF ;
JAMES, RFL .
JOURNAL OF MICROENCAPSULATION, 1991, 8 (02) :221-233
[10]
DeVos P, 1997, DIABETOLOGIA, V40, P262