Microencapsulation: a review of polymers and technologies with a focus on bioartificial organs

被引:17
作者
Renken, A [1 ]
Hunkeler, D [1 ]
机构
[1] Swiss Fed Inst Technol, Lab Polymers & Biomat, Dept Chem, CH-1015 Lausanne, Switzerland
关键词
alginate; bioartificial organ; cytotoxicity; encapsulation; immunoisolation; membrane; microencapsulation;
D O I
10.14314/polimery.1998.530
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Various immunoisolation technologies including arteriovenous shunts, diffusion chambers and microcapsules are reviewed and various microcapsule production techniques are discussed. This encompasses syringe based droplet generation devices, various emulsion techniques and rotating discs. Polymers used for the formation of permselective microcapsules and capsular membranes are also presented. In particular, the immunoisolation of islets for the production of a bioartificial pancreas is evaluated. Screening of polyelectrolytes with respect to cell cytotoxicity is discussed along with a summary of various polymer chemistries, mechanisms of membrane formation and microencapsulation technologies. A systematic categorization is proposed and four cases are compared in detail: Sun's alginate/calcium chloride-based precast beads (Type I-B-chi), Dautzenberg's binary polyanion/polycation coacervation systems (Type II-A-alpha), Sefton's phase inversion systems based on non-ionic, elastic, hydrophobic copolymers (Type IV-F-delta), and a new multicomponent polyelectrolyte capsule with gel precasting and oligocation diffusion to control the cutoff (Type III-E-chi). In vitro and in vivo testing of xenograft functioning in the Type III-E-chi system will be reported.
引用
收藏
页码:530 / 539
页数:10
相关论文
共 54 条
[21]   ALGINATE AS IMMOBILIZATION MATERIAL .1. CORRELATION BETWEEN CHEMICAL AND PHYSICAL-PROPERTIES OF ALGINATE GEL BEADS [J].
MARTINSEN, A ;
SKJAKBRAEK, G ;
SMIDSROD, O .
BIOTECHNOLOGY AND BIOENGINEERING, 1989, 33 (01) :79-89
[22]  
MATULOVIC U, 1987, BIOTECHNOL BIOENG, V29, P370
[23]  
MCKENNA TF, 1996, 4 M WORK PART POLYM
[24]   Immunoprotection of therapeutic cell transplants by encapsulation [J].
Morris, PJ .
TRENDS IN BIOTECHNOLOGY, 1996, 14 (05) :163-167
[25]   AN APPROACH TO PREPARE MICROPARTICLES OF UNIFORM SIZE [J].
MURAMATSU, N ;
KONDO, T .
JOURNAL OF MICROENCAPSULATION, 1995, 12 (02) :129-136
[26]  
Nawab M., 1958, J COLLOID SCI, V13, P179, DOI [10.1016/0095-8522(58)90023-0, DOI 10.1016/0095-8522(58)90023-0]
[27]   PRODUCTION OF MICRO-GEL BEADS BY A ROTATING-DISK ATOMIZER [J].
OGBONNA, JC ;
MATSUMURA, M ;
YAMAGATA, T ;
SAKUMA, H ;
KATAOKA, H .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1989, 68 (01) :40-48
[28]   SYNTHESIS OF UNIFORM PMMA MICROSPHERES EMPLOYING MODIFIED SPG (SHIRASU POROUS-GLASS) EMULSIFICATION TECHNIQUE [J].
OMI, S ;
KATAMI, KI ;
TAGUCHI, T ;
KANEKO, K ;
ISO, M .
JOURNAL OF APPLIED POLYMER SCIENCE, 1995, 57 (08) :1013-1024
[29]   Preparation of monodisperse microspheres using the Shirasu porous glass emulsification technique [J].
Omi, S .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1996, 109 :97-107
[30]   PROLONGED SURVIVAL OF TRANSPLANTED ISLETS OF LANGERHANS ENCAPSULATED IN A BIOCOMPATIBLE MEMBRANE [J].
OSHEA, GM ;
GOOSEN, MFA ;
SUN, AM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 804 (01) :133-136