RETRACTED: In situ.-forming hydrogels for sustained ophthalmic drug delivery (Retracted article. See vol. 167, pg. 219, 2013)

被引:160
作者
Nanjawade, Basavaraj K. [1 ]
Manvi, F. V. [1 ]
Manjappa, A. S. [1 ]
机构
[1] KLESs Coll Pharm, Dept Pharmaceut, Belgaum 590010, Karnataka, India
关键词
in situ; gelation; ophthalmic drug delivery; hydrogels; nasolachrymal drainage; PLURONIC F-127 GELS; SYSTEMIC ABSORPTION; OCULAR DELIVERY; RABBIT EYES; GELLAN GUM; VISCOUS PHENYLEPHRINE; TOPICAL DELIVERY; HYALURONIC-ACID; ALBINO RABBITS; CORNEAL;
D O I
10.1016/j.jconrel.2007.07.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ophthalmic drug delivery is one of the most interesting and challenging endeavors facing the pharmaceutical scientist. The conventional ocular drug delivery systems like solutions, suspensions, and ointments show drawbacks such as increased precorneal elimination, high variability in efficiency, and blurred vision respectively. in situ-forming hydrogels are liquid upon instillation and undergo phase transition in the ocular cul-de-sac to form visco-elastic gel and this provides a response to environmental changes. In the past few years, an impressive number of novel temperature, pH, and ion induced in situ-forming systems have been reported for sustain ophthalmic drug delivery. Each system has its own advantages and drawbacks. The choice of a particular hydrogel depends on its intrinsic properties and envisaged therapeutic use. This review includes various temperature, pH, and ion induced in situ-forming polymeric systems used to achieve prolonged contact time of drugs with the cornea and increase their bioavailability. (C) 2007 Elsevier B.V All rights reserved.
引用
收藏
页码:119 / 134
页数:16
相关论文
共 123 条
[1]  
AHMED I, 1985, INVEST OPHTH VIS SCI, V26, P584
[2]   DISPOSITION OF TIMOLOL AND INULIN IN THE RABBIT EYE FOLLOWING CORNEAL VERSUS NON-CORNEAL ABSORPTION [J].
AHMED, I ;
PATTON, TF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 38 (1-3) :9-21
[3]  
[Anonymous], FOOD POLYM GELS COLL
[4]  
BHASKARAN S, 2005, INDIAN J PHARM SCI, V67, P404
[5]   Characterization of a new ocular delivery system based on a dispersion of liposomes in a thermosensitive gel [J].
Bochot, A ;
Fattal, E ;
Grossiord, JL ;
Puisieux, F ;
Couvreur, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 162 (1-2) :119-127
[6]   ASSESSMENT OF TRANSPORT BARRIERS USING CELL AND TISSUE-CULTURE SYSTEMS [J].
BORCHARDT, RT .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (18) :2595-2612
[7]   RHEOLOGICAL CHARACTERIZATION OF TEAR SUBSTITUTES [J].
BOTHNER, H ;
WAALER, T ;
WIK, O .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (05) :755-768
[8]   THE OCULAR SURFACE IN KERATOCONJUNCTIVITIS SICCA [J].
BRON, AJ ;
MENGHER, LS .
EYE, 1989, 3 :428-437
[9]   Study of the gelation process of polyethylene oxide(a) polypropylene oxide(b) polyethylene oxide(a) copolymer (Poloxamer 407) aqueous solutions [J].
Cabana, A ;
AitKadi, A ;
Juhasz, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 190 (02) :307-312
[10]   INTERACTION BETWEEN ETHYL(HYDROXYETHYL)CELLULOSE AND SODIUM DODECYL-SULFATE IN AQUEOUS-SOLUTION [J].
CARLSSON, A ;
KARLSTROM, G ;
LINDMAN, B ;
STENBERG, O .
COLLOID AND POLYMER SCIENCE, 1988, 266 (11) :1031-1036