Enzyme loaded biodegradable microspheres in vitro ex vivo evaluation

被引:34
作者
Genta, I
Perugini, P
Pavanetto, F
Maculotti, K
Modena, T
Casado, B
Lupi, A
Iadarola, P
Conti, B
机构
[1] Univ Pavia, Dept Pharmaceut Chem A Castellani, I-27100 Pavia, Italy
[2] Univ Pavia, Dept Biochem A Castellani, I-27100 Pavia, Italy
关键词
biodegradable microspheres; enzyme delivery; prolidase; ex vivo evaluation; sustained release;
D O I
10.1016/S0168-3659(01)00511-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prolidase is a naturally occurring enzyme involved in the final stage of protein catabolism. Deficient enzyme activity causes prolidase deficiency (PD), a rare autosomal recessive inherited disorder whose main manifestations are chronic, intractable ulcerations of the skin, particularly of lower limbs. Although several attempts have been made towards the treatment of this pathology, a cure for this disease has yet to be found. The purpose of this work is to evaluate the possibility of enzyme replacement therapy through prolidase microencapsulation in biodegradable microspheres. The poly(D,L-lactide-co-glycolide) (PLGA) prolidase loaded microparticulate systems have been prepared utilizing the w-o-w double emulsion solvent evaporation method. They have been characterized "in vitro" by morphological analysis, total protein content and an in vitro dissolution test of active protein. "Ex vivo" evaluation of prolidase activity from the microspheres has been performed on cellular extracts of cultured skin fibroblasts from healthy subjects (controls) and from patients affected by PD. The results reported in this work on prolidase from pig kidney (available on the market) demonstrate the positive role of microencapsulation as a process of enzymatic activity stabilization inside PLGA microspheres achieving both in vitro and ex vivo active enzyme release. This formulation can be proposed as a parenteral depot drug delivery system. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
相关论文
共 20 条
[1]   PROLIDASE DEFICIENCY - A MULTISYSTEMIC HEREDITARY DISORDER [J].
BISSONNETTE, R ;
FRIEDMANN, D ;
GIROUX, JM ;
DOLENGA, M ;
HECHTMAN, P ;
DERKALOUSTIAN, VM ;
DUBUC, R .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1993, 29 (05) :818-821
[2]  
BORIGHT AP, 1989, AM J HUM GENET, V44, P731
[3]  
CHINARD FP, 1952, J BIOL CHEM, V199, P91
[4]  
DELUCA PP, 1997, P 16 PHARM TECHN C A, P14
[5]   BIOCHEMICAL BASIS OF PROLIDASE DEFICIENCY - POLYPEPTIDE AND RNA PHENOTYPES AND THE RELATION TO CLINICAL PHENOTYPES [J].
ENDO, F ;
TANOUE, A ;
KITANO, A ;
ARATA, J ;
DANKS, DM ;
LAPIERE, CM ;
SEI, Y ;
WADMAN, SK ;
MATSUDA, I .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (01) :162-169
[6]  
Gaspar MM, 1998, J CONTROL RELEASE, V52, P53
[7]  
GREGOR PE, 1996, PEDIAT DERMATOL, V13, P58
[8]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC PROCEDURE FOR THE DETERMINATION OF SERUM PROLIDASE ACTIVITY [J].
HARADA, M ;
FUKASAWA, KM ;
HIRAOKA, BY ;
FUKASAWA, K ;
MOGI, M .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1990, 530 (01) :116-121
[9]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[10]  
LEDOUX P, 1994, AM J HUM GENET, V54, P1014