Punch P I, Costa N D, Edwards M E, Wilcox G E
J Vet Pharmacol Ther. 1987 Mar;10(1):37-42. doi: 10.1111/j.1365-2885.1987.tb00074.x.
The release rate of procaine penicillin, erythromycin and erythromycin estolate from soluble and insoluble collagen films was investigated in vitro to develop an ocular insert for the treatment of infectious bovine keratoconjunctivitis. The release rate and duration of release varied according to the selection of antibiotic and vehicle. The combination of erythromycin estolate and soluble collagen produced the most sustained drug-delivery system. However, due to the inappropriate physical properties of collagen and poor retention of ocular inserts, it was considered that the development of an antibiotic-impregnated collagen ocular insert requires further investigation.
研究了普鲁卡因青霉素、红霉素和无味红霉素从可溶性和不溶性胶原膜中的体外释放速率,以开发一种用于治疗牛传染性角膜结膜炎的眼用插入物。释放速率和释放持续时间因抗生素和载体的选择而异。无味红霉素与可溶性胶原的组合产生了最持久的给药系统。然而,由于胶原的物理性质不合适以及眼用插入物的保留性差,认为含抗生素的胶原眼用插入物的开发需要进一步研究。