匹罗卡品掺入亚微米乳剂载体中,在家兔中引起出乎意料的长时间的眼部降压作用。

N Naveh, S Muchtar, S Benita
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引用次数: 64

摘要

将广泛应用的抗青光眼药物匹洛卡平掺入新研制的适合眼部局部给药的亚微米乳剂(匹洛卡平乳剂)中。研究了匹罗卡品乳剂单次给药对正常血压家兔眼压的影响。发现膜过滤(蒸汽高压灭菌)对匹罗卡品乳液制备的粒径分布、zeta电位和pH没有影响。单次给药1.7%(相当于2%盐酸匹洛卡平)的皮洛卡平乳剂,在正常血压的家兔体内引起长期的渐进式IOP下降,从给药后11小时开始,在29小时达到最大值6.0 +/- 0.2 mmHg。匹洛卡品乳剂治疗的降压效果与通用匹洛卡品(盐酸匹洛卡品2%滴眼液)不同;在后一组中,IOP下降(开始于2小时)在滴注后的最初5小时内持续,而在前一组中,降压作用在较晚阶段开始,并在29小时的随访中保持,导致IOP下降幅度大于普通组(% δ IOP分别为28.5%和18%)。在匹罗卡品乳剂处理的兔的对侧眼中,在应用后(注射后11小时至29小时)发现了眼部降压作用,而在水溶液处理的兔中,这种作用可以忽略不计。我们的研究结果表明,新的制剂纳入亚微米乳剂可能作为一种长效形式的匹罗卡品,这可能需要一个单一的每日应用。需要进一步的研究来阐明该制剂的作用机制和作用。
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Pilocarpine incorporated into a submicron emulsion vehicle causes an unexpectedly prolonged ocular hypotensive effect in rabbits.

Pilocarpine, a widely used antiglaucoma drug, was incorporated into a newly developed submicron emulsion (pilocarpine emulsion) suitable for local ocular administration. Pilocarpine-Emulsion effect on the intraocular pressure (IOP) was studied following a single dose application in normotensive rabbits. Membrane filtration (steam autoclaving) was found not to affect particle size distribution, zeta potential or pH of the pilocarpine emulsion preparation. A single dose application of pilocarpine emulsion 1.7% (equivalent to 2% pilocarpine hydrochloride) induced a prolonged progressive decrease in IOP in normotensive rabbits, which started at eleven hours post instillation and reached its maximal value of 6.0 +/- 0.2 mmHg at 29 hours. The pressure decreasing effect induced by pilocarpine emulsion treatment followed a pattern different from that generated by generic pilocarpine (Pilocarpine Hydrochloride 2% eye drops); In the latter group, IOP reduction (starting at two hours) persisted during the initial five hours post-instillation, while in the former, the hypotensive effect started at a later stage, and was maintained during a twenty nine hour follow-up causing a greater IOP decrease than in the generic group (% delta IOP of 28.5% and 18%, respectively). In the contralateral eyes of Pilocarpine Emulsion treated rabbits, an ocular hypotensive effect was noted late after application (11 hours through 29 hours post-instillation), while this effect was negligible in rabbits-treated with aqueous pilocarpine. Our findings point to the possibility that the novel preparation of pilocarpine incorporated into submicron emulsion might serve as a long-acting form of pilocarpine which might require a single daily application. Further studies are required to elucidate the mechanism and action of this preparation.

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