Ding S, Chen C C, Salome-Kesslak R, Tang-Liu D D, Himmelstein K J
Allergan, Inc. Irvine, California.
J Ocul Pharmacol. 1992 Summer;8(2):151-9. doi: 10.1089/jop.1992.8.151.
Drug-cornea contact time is a critical issue in ocular drug delivery. Existing methods for its experimental determination are developed mainly for eye drops and ointments, and have not been reported for ophthalmic gels. The present study evaluated two tear film sampling techniques (capillary tubes and Schirmer strips) and one recovery technique (cotton swab) for their suitability for the determination of precorneal drug concentration as a function of time for ophthalmic gels. The study was conducted using the rabbit eye model, and the gel studied was a commercial polyacrylate-based gel containing pilocarpine HCl. The three techniques explored yield similar results with respect to drug-cornea contact time, about one hour for the gel studied. The strip method suffers from a gel-carry-over problem at the early time points; therefore it is not recommended for tear sampling until most of the gel is cleared from the cul-de-sac. Successful tear sampling was accomplished using capillary tubes. Drug concentration in the tear film as a function of time determined using this technique reveals not only the duration of contact between the drug and the cornea, but also demonstrates a nonuniform drug distribution in the tear film at the early time points (10 and 30 minutes). Finally the cotton swab technique is gentle, easy, and nondestructive. It recovers total drug remaining in the cul-de-sac but does not yield information for the tear film.
药物与角膜的接触时间是眼部药物递送中的一个关键问题。现有的实验测定方法主要是针对滴眼液和眼膏开发的,尚未见有关眼用凝胶的报道。本研究评估了两种泪膜采样技术(毛细管和泪液试纸)和一种回收技术(棉签),以确定它们是否适用于测定眼用凝胶角膜前药物浓度随时间的变化。该研究使用兔眼模型进行,所研究的凝胶是一种含有盐酸毛果芸香碱的市售聚丙烯酸酯基凝胶。就药物与角膜的接触时间而言,所探索的三种技术得出了相似的结果,所研究的凝胶约为一小时。试纸法在早期时间点存在凝胶残留问题;因此,在大部分凝胶从结膜囊清除之前,不建议用于泪液采样。使用毛细管成功完成了泪液采样。使用该技术测定的泪膜中药物浓度随时间的变化不仅揭示了药物与角膜的接触持续时间,还表明在早期时间点(10分钟和30分钟)泪膜中药物分布不均匀。最后,棉签技术操作轻柔、简便且无损。它能回收结膜囊中残留的全部药物,但无法提供泪膜的相关信息。