Supercritical fluid impregnation of a biocompatible polymer for ophthalmic drug delivery

被引:75
作者
Duarte, Ana Rita C.
Simplicio, Ana Luisa
Vega-Gonzalez, Arlette
Subra-Paternault, Pascale
Coimbra, Patricia
Gil, M. H.
de Sousa, Herminio C.
Duarte, Catarina M. M.
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, IBET, Nutraceut & Delivery Lab, P-2780 Oeiras, Portugal
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol, IBET, Anal Lab, P-2780 Oeiras, Portugal
[3] Univ Paris 13, Lab Ingn Mat & Hautes Press, CNRS, Inst Galilee, F-93430 Villetaneuse, France
[4] Univ Coimbra, Dept Engn Quim, FCT, P-3030790 Coimbra, Portugal
关键词
supercritical fluids; impregnation; biocompatible polymers; ophthalmic drug delivery;
D O I
10.1016/j.supflu.2007.01.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
Supercritical fluid impregnation was tested to prepare a new ophthalmic drug delivery device. Poly(methylmethaerylate-co-ethylhexylacrylate-co-ethyleneglycoldimethacrylate), P(MMA-EHA-EGDMA) has been proposed by Mariz [M. Mariz, Preparacao de uma lente intra-ocular dotada de um sistema de libertacao controlada de farmaco, Master Thesis, Universidade de Coimbra, 1999] as a promising matrix to be used for intraocular delivery of anti-inflammatory drugs used in eye surgery. This matrix was successfully impregnated with flurbiprofen, a non-steroidal anti -inflammatorv agent. The success of the impregnation was evaluated by scanning electron microscopy (SEM) analysis and also by in vitro drug release studies. The effect of some operating parameters was evaluated, namely, pressure and contact time. The operating pressure will influence both the solubility of the drug in the supercritical fluid but also the sorption degree of the polymeric matrix in the presence of carbon dioxide. The solubility of the drug in carbon dioxide and the sorption degree are reported in previous studies. A comparison between the batch and the semi-continuous impregnation process is also presented. The supercritical fluid impregnation proved to be feasible for the preparation of a new ophthalmic drug delivery system. The drug release profiles suggest that the drug can be released up to three months, which is a major advantage for the prevention of the inflammatory response after ophthalmic surgery. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:373 / 377
页数:5
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