首页> 美国卫生研究院文献>The British Journal of Ophthalmology >A comparison of the efficacy and duration of action of topically applied proxymetacaine using a novel ophthalmic delivery system versus eye drops in healthy young volunteers.
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A comparison of the efficacy and duration of action of topically applied proxymetacaine using a novel ophthalmic delivery system versus eye drops in healthy young volunteers.

机译:在健康的年轻志愿者中使用新型眼科给药系统与滴眼剂对局部应用替米卡因的疗效和作用持续时间的比较。

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摘要

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.
机译:已经开发了新颖的眼科药物递送系统(NODS)以将药物精确地和受控地递送至眼睛。将该药物掺入附在载体上的聚乙烯醇标记中。当应用于眼睛时,标志分离并逐渐溶解,从而释放药物。我们调查了由不同浓度的代孕酮NODS和常规滴眼剂产生的角膜麻醉。受试者包括28名正常男性(平均年龄25.3(SD 3.9)岁)。角膜接触灵敏度是用装有生物显微镜的Cochet-Bonnet麻醉仪测量的。每个主题参加两次访问,相隔7天。每次探视时,每只眼睛随机接受四种替卡他卡因制剂中的一种:44微克,74微克,124微克NODS或35微升0.5%代卡因他卡因滴剂(175微克)。在滴注之前和之后1、2、5、10、15、20、30、45和60分钟测量角膜触摸灵敏度。滴注后1分钟内,大多数受试者已完全麻醉。最低的NODS剂量(44微克)产生的持续麻醉时间长于35微升的液滴(175微克)(p <0.05)。较高的NODS剂量会使麻醉持续时间相应增加。通过这种载体获得的更高的生物利用度允许使用更低的药物浓度,从而降低了全身性不良反应的可能性。

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