Lawrenson J G, Edgar D F, Gudgeon A C, Burns J M, Geraint M, Barnard N A
Department of Optometry and Visual Science, City University, London.
Br J Ophthalmol. 1993 Nov;77(11):713-5. doi: 10.1136/bjo.77.11.713.
A novel ophthalmic drug delivery system (NODS) has been developed to give precise and controlled delivery of a drug to the eye. The drug is incorporated into a polyvinyl alcohol flag attached to a carrier. When applied to the eye the flag detaches and gradually dissolves, releasing the drug. We investigated corneal anaesthesia produced by different concentrations of proxymetacaine NODS, and conventional eye drops. Subjects consisted of 28 normal males (mean age 25.3 (SD 3.9) years). Corneal touch sensitivity was measured with a biomicroscope mounted Cochet-Bonnet aesthesiometer. Each subject attended for two visits separated by 7 days. On each visit each eye randomly received one of four proxymetacaine preparations: 44 micrograms, 74 micrograms, 124 micrograms NODS, or 35 microliters of 0.5% proxymetacaine drops (175 micrograms). Corneal touch sensitivity was measured before, and at 1, 2, 5, 10, 15, 20, 30, 45, and 60 minutes following instillation. Complete anesthesia was achieved in the majority of subjects within 1 minute of instillation. The lowest NODS dose (44 micrograms) produced longer lasting anaesthesia than the 35 microliters drop (175 micrograms) (p < 0.05). Higher NODS doses produced a correspondingly greater increase in the duration of anaesthesia. The greater bioavailability achieved by this vehicle allows much lower drug concentrations to be used, reducing the likelihood of systemic adverse reactions.
一种新型眼科药物递送系统(NODS)已被开发出来,用于将药物精确且可控地递送至眼部。药物被掺入附着在载体上的聚乙烯醇旗中。当应用于眼部时,旗会分离并逐渐溶解,释放出药物。我们研究了不同浓度的丙美卡因NODS和传统眼药水产生的角膜麻醉效果。受试者包括28名正常男性(平均年龄25.3(标准差3.9)岁)。使用安装了科谢 - 博内眼压计的生物显微镜测量角膜触觉敏感性。每位受试者分两次就诊,间隔7天。每次就诊时,每只眼睛随机接受四种丙美卡因制剂中的一种:44微克、74微克、124微克NODS,或35微升0.5%丙美卡因滴眼液(175微克)。在滴入前以及滴入后1、2、5、10、15、20、30、45和60分钟测量角膜触觉敏感性。大多数受试者在滴入后1分钟内实现了完全麻醉。最低剂量的NODS(44微克)产生的麻醉持续时间比35微升滴眼液(175微克)更长(p < 0.05)。更高剂量的NODS相应地使麻醉持续时间增加更多。这种载体实现的更高生物利用度允许使用低得多的药物浓度,降低了全身不良反应的可能性。