Li Fengfu, Hurley Bernard, Liu Yun, Leonard Brian, Griffith May
Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, Ontario K1H8L6, Canada.
Open Ophthalmol J. 2012;6:54-8. doi: 10.2174/1874364101206010054. Epub 2012 Jun 25.
Bevacizumab (Avastin(®)) has been used by ophthalmologists in many countries as an off-label drug for the treatment of wet age-related macular degeneration (AMD). Due to its short half-life necessitating frequent intravitreal injection, a method for sustained delivery is in need. We demonstrated that bevacizumab could be released in a sustained fashion over 90 days from nano- and microspheres fabricated from poly(DL-lactide-co-glycolide) and poly(ethylene glycol)-b-poly(D,L-lactic acid), respectively. The drug release rate could be adjusted by alteration of the drug/polymer ratio. The use of such nano- and microspheres as bevacizumab delivery vehicles may improve the treatment of wet AMD.
在许多国家,眼科医生已将贝伐单抗(阿瓦斯汀®)作为治疗湿性年龄相关性黄斑变性(AMD)的非标签药物使用。由于其半衰期短,需要频繁进行玻璃体内注射,因此需要一种持续给药的方法。我们证明,贝伐单抗可以分别从由聚(DL-丙交酯-共-乙交酯)和聚(乙二醇)-b-聚(D,L-乳酸)制成的纳米球和微球中以持续的方式释放90天以上。药物释放速率可通过改变药物/聚合物比例来调节。使用此类纳米球和微球作为贝伐单抗的给药载体可能会改善湿性AMD的治疗效果。