In situ gel systems as 'smart' carriers for sustained ocular drug delivery

被引:158
作者
Agrawal, Ashish Kumar [1 ]
Das, Manasmita [1 ]
Jain, Sanyog [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Ctr Pharmaceut Nanotechnol, Dept Pharmaceut, Sas Nagar 160062, Punjab, India
关键词
in situ gel systems; ocular drug delivery; polymers; sol-gel interconversion; stimuli-responsive; OPHTHALMIC DELIVERY; CIPROFLOXACIN HYDROCHLORIDE; CONTROLLED-RELEASE; GELLING SYSTEMS; RHEOLOGICAL EVALUATION; SENSITIVE HYDROGELS; FORMING HYDROGELS; GLAUCOMA THERAPY; ACID) COPOLYMERS; VITRO RELEASE;
D O I
10.1517/17425247.2012.665367
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In situ gel systems refer to a class of novel delivery vehicles, composed of natural, semisynthetic or synthetic polymers, which present the unique property of sol-gel conversion on receipt of biological stimulus. Areas covered: The present review summarizes the latest developments in in situ gel technology, with regard to ophthalmic drug delivery. Starting with the mechanism of ocular absorption, the review expands on the fabrication of various polymeric in situ gel systems, made up of two or more polymers presenting multi-stimuli sensitivity, coupled with other interesting features, such as bio-adhesion, enhanced penetration or sustained release. Various key issues and challenges in this area have been addressed and critically analyzed. Expert opinion: The advent of in situ gel systems has inaugurated a new transom for 'smart' ocular delivery. By virtue of possessing stimuli-responsive phase transition properties, these systems can easily be administered into the eye, similar to normal eye drops. Their unique gelling properties endow them with special features, such as prolonged retention at the site of administration, followed by sustained drug release. Despite the superiority of these systems as compared with conventional ophthalmic formulations, further investigations are necessary to address the toxicity issues, so as to minimize regulatory hurdles during commercialization.
引用
收藏
页码:383 / 402
页数:20
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