酮洛芬
透皮
材料科学
药物输送
膜
药品
药理学
生物医学工程
医学
化学
纳米技术
生物化学
作者
Juliana Ferreira Floriano,Natan Roberto de Barros,José Luiz Ferreira Cinman,Rosângela Gonçalves da Silva,Augusto Villela Loffredo,Felipe Azevedo Borges,Ana Maria Q. Norberto,Ana Laura Destro Chagas,Bruna Cambraia Garms,Carlos F. O. Graeff,Rondinelli Donizetti Herculano
标识
DOI:10.1007/s10924-017-1127-x
摘要
Ketoprofen is an analgesic with potent anti-inflammatory activity against acute inflammation, subacute inflammation, for the acute and long-term treatment of various inflammatory pathologies, as rheumatoid arthritis and colonic adenocarcinoma. In order to minimize the incidence of systemic events related to ketoprofen, the transdermal drug delivery system development has been most important. The advantages of using natural rubber latex membranes include not only the reduction of adverse systemic events, but also the suitability of the low cost of the material together with its physicochemical properties such as flexibility, mechanical stability, surface porosity and water vapor permeability, and besides being a biocompatible material also presents biological activity to stimulate the angiogenesis, being able to be used in tissue repair. This study demonstrated that ketoprofen was successfully incorporated into natural latex membranes for drug delivery. FTIR indicated that the drug did not interact chemically with the membrane. Moreover, the natural latex membranes released 60% of the ketoprofen incorporated in 50 h. SEM images indicated that a portion of the drug was present on the membrane surface, being this portion responsible for the burst release. The tensile tests showed that the addition of the drug into the natural latex membrane did not influence on the polymer mechanical behavior. In addition, drug-natural latex membranes presented no red blood cell damaging effects. Our data shows that the ketoprofen loaded natural latex membranes is a promising system for sustained drug delivery which can be used to minimize the adverse side effects of high dose systemic drug delivery.
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