Effect of matrix composition and process conditions on casein-gelatin beads floating properties

被引:28
作者
Bulgarelli, E [1 ]
Forni, F [1 ]
Bernabei, MT [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Pharmaceut Sci, I-41100 Modena, Italy
关键词
oral drug delivery systems; casein; gelatin; floating beads;
D O I
10.1016/S0378-5173(00)00327-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Casein-gelatin beads have been prepared by emulsification extraction method and cross-linked with D,L-glyceraldehyde in an acetone water mixture 3:1 (v/v). Casein emulsifying properties cause air bubble incorporation and the formation of large holes in the beads. The high porosity of the matrix influences the bead properties such as drug loading, drug release and floatation. These effects have been stressed by comparison with low porous beads, artificially prepared without cavities. The percentage of casein in the matrix increases the drug loading of both low and high porous matrices, although the loading of high porous matrices is lower than that of low porous matrices. As a matter of fact, the drug should be more easily removed during washing and recovery because of the higher superficial pore area of the beads. This can explain the drug release rate increase, observed in high porous matrix, in comparison with beads without cavities. This is due to the rapid diffusion of the drug through water filled ports. The study shows that cavities act as an air reservoir and enable beads to float. Therefore, casein seems to be a material suitable to the inexpensive formation of an air reservoir for floating systems. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 165
页数:9
相关论文
共 19 条
[1]   FOAMING PROPERTIES OF PROTEINS AS AFFECTED BY CONCENTRATION [J].
BRITTEN, M ;
LAVOIE, L .
JOURNAL OF FOOD SCIENCE, 1992, 57 (05) :1219-&
[2]   Casein/gelatin beads: I. Cross-linker solution composition effect on cross-linking degree [J].
Bulgarelli, E ;
Forni, F ;
Bernabei, MT .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 190 (02) :175-182
[3]  
Buri P., 1985, FORMES PHARM NOUVELL, P175
[4]  
Chein YW, 1992, NOVEL DRUG DELIVERY, V2, P139
[5]   COMPARISON OF ALBUMIN AND CASEIN MICROSPHERES AS A CARRIER FOR DOXORUBICIN [J].
CHEN, Y ;
WILLMOTT, N ;
ANDERSON, J ;
FLORENCE, AT .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1987, 39 (12) :978-985
[6]  
Daumesnil R, 1994, MULTIPARTICULATE ORA, P457
[7]  
DOELKER E, 1985, FORMES PHARM NOUVELL, P5
[8]   KINETICS OF LIQUID DRAINAGE FROM PROTEIN-STABILIZED FOAMS [J].
ELIZALDE, BE ;
GIACCAGLIA, D ;
PILOSOF, AMR ;
BARTHOLOMAI, GB .
JOURNAL OF FOOD SCIENCE, 1991, 56 (01) :24-&
[9]   CONCEPTION AND INVIVO INVESTIGATION OF PERORAL SUSTAINED-RELEASE FLOATING DOSAGE FORMS WITH ENHANCED GASTROINTESTINAL TRANSIT [J].
INGANI, HM ;
TIMMERMANS, J ;
MOES, AJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 35 (1-2) :157-164
[10]   SURFACE-ACTIVITY OF FOOD PROTEINS - RELATIONSHIPS BETWEEN SURFACE PRESSURE DEVELOPMENT, VISCOELASTICITY OF INTERFACIAL FILMS AND FOAM STABILITY OF BOVINE SERUM-ALBUMIN [J].
KIM, SH ;
KINSELLA, JE .
JOURNAL OF FOOD SCIENCE, 1985, 50 (06) :1526-1530