Polyester nanocapsules as new topical ocular delivery systems for cyclosporin A

被引:102
作者
Calvo, P
Sanchez, A
Martinez, J
Lopez, MI
Calonge, M
Pastor, JC
Alonso, MJ
机构
[1] UNIV SANTIAGO DE COMPOSTELA,SCH PHARM,DEPT PHARM & PHARMACEUT TECHNOL,SANTIAGO,SPAIN
[2] UNIV VALLADOLID,INST APPL OPTHALMOBIOL,VALLADOLID,SPAIN
关键词
nanocapsules; polyepsiloncaprolactone; cyclosporin A; ophthalmic administration; corneal penetration;
D O I
10.1023/A:1016015803611
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose, Nanocapsules composed of an oily core (Migliol 840) (MG) surrounded by a poly-epsilon-caprolactone (PECL) coat were evaluated as potential vehicles for the topical ocular administration of cyclosporin A (CyA). Methods. A 2(3) experimental factorial design was applied to optimize the coating of the oily nanodroplets by a solvent displacement tecnique and to encapsulate a high dose of CyA. The variables investigated were: volume of oil (RIG), amount of polymer (PECL), and volume of the organic solvent (acetone) used to dissolve the polymer. Results, Nanocapsules had a mean size in the range of 210-270 nm, a negative zeta potential (between -55 and -60 mV) and a maximum loading capacity of 50% (CyA/PECL ratio). These highly loaded nanocapsules displayed a thick spongeous polymer coating around the oily nanodroplets. The corneal levels of CyA were up to 5 times higher for the encapsulated CyA than for the oily solution of CyA. In addition, these levels remained significantly higher than those of the control group (oily solution) for up to 3 days. Furthermore, the area-under-the-curve (AUG) values were significantly increased for the encapsulated CyA (319.98) with respect to the oily control (74.34). Conclusions. The CyA-loaded nanocapsules are shown to be interesting vehicles for the improvement of the ocular penetration of CyA.
引用
收藏
页码:311 / 315
页数:5
相关论文
共 14 条
[1]  
[Anonymous], 1992, STP PHARMA SCI
[2]  
BELIN MW, 1990, CORNEA, V9, P184
[3]  
BONDUELLE S, 1992, J MICROENCAPSUL, V9, P173
[4]   STUDY OF THE MECHANISM OF INTERACTION OF POLY(EPSILON-CAPROLACTONE) NANOCAPSULES WITH THE CORNEA BY CONFOCAL LASER-SCANNING MICROSCOPY [J].
CALVO, P ;
THOMAS, C ;
ALONSO, MJ ;
VILAJATO, JL ;
ROBINSON, JR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 103 (03) :283-291
[5]   NANOCAPSULE FORMATION BY INTERFACIAL POLYMER DEPOSITION FOLLOWING SOLVENT DISPLACEMENT [J].
FESSI, H ;
PUISIEUX, F ;
DEVISSAGUET, JP ;
AMMOURY, N ;
BENITA, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 55 (01) :R1-R4
[6]   TOPICAL CYCLOSPORINE-A IN THE TREATMENT OF ANTERIOR SEGMENT INFLAMMATORY DISEASE [J].
HOLLAND, EJ ;
OLSEN, TW ;
KETCHAM, JM ;
FLORINE, C ;
KRACHMER, JH ;
PURCELL, JJ ;
LAM, S ;
TESSLER, HH ;
SUGAR, J .
CORNEA, 1993, 12 (05) :413-419
[7]   IMPROVEMENT OF OCULAR PENETRATION OF AMIKACIN SULFATE BY ASSOCIATION TO POLY(BUTYLCYANOACRYLATE) NANOPARTICLES [J].
LOSA, C ;
CALVO, P ;
CASTRO, E ;
VILAJATO, JL ;
ALONSO, MJ .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1991, 43 (08) :548-552
[8]   DESIGN OF NEW FORMULATIONS FOR TOPICAL OCULAR ADMINISTRATION - POLYMERIC NANOCAPSULES CONTAINING METIPRANOLOL [J].
LOSA, C ;
MARCHALHEUSSLER, L ;
ORALLO, F ;
JATO, JLV ;
ALONSO, MJ .
PHARMACEUTICAL RESEARCH, 1993, 10 (01) :80-87
[9]   SIDE-EFFECTS OF SYSTEMIC CYCLOSPORINE IN PATIENTS NOT UNDERGOING TRANSPLANTATION [J].
PALESTINE, AG ;
NUSSENBLATT, RB ;
CHAN, CC .
AMERICAN JOURNAL OF MEDICINE, 1984, 77 (04) :652-656
[10]   OCULAR ABSORPTION OF CYCLOSPORINE-A FROM LIPOSOMES INCORPORATED INTO COLLAGEN SHIELDS [J].
PLEYER, U ;
ELKINS, B ;
RUCKERT, D ;
LUTZ, S ;
GRAMMER, J ;
CHOU, J ;
SCHMIDT, KH ;
MONDINO, BJ .
CURRENT EYE RESEARCH, 1994, 13 (03) :177-181