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Exploratory ocular surface distribution studies of Azithromycin formulations based on semifluorinated alkanes

阿奇霉素 医学 药理学 房水 眼科 抗生素 化学 生物化学
作者
Kirsten Fischer,Ralf Grillenberger,Thierry Amar,Sonja Krösser
出处
期刊:Acta Ophthalmologica [Wiley]
卷期号:95 (S259) 被引量:1
标识
DOI:10.1111/j.1755-3768.2017.0s029
摘要

Purpose Azithromycin is an antimicrobial agent with broad spectrum activity and anti‐inflammatory properties. The aim of this study was to investigate the ocular distribution of azithromycin after a single topical instillation of a new semifluorinated alkane ( SFA ) based formulation in rabbits. Methods Rabbits were treated with either a single administration of 1.5% or 3% SFA ‐azithromycin suspensions. Due to the low surface and interface tension of the SFA , and its excellent spreading properties, droplet size is smaller compared to other ophthalmic formulations which lead to a low instillation volume of ~11 μ L. Tears (T), aqueous humor ( AH ), cornea (C), bulbar conjunctiva ( BCJ ), and eyelids ( EL ) from individual eyes were collected up to 144 h post dosing and drug concentrations were measured using a validated LC ‐ MS / MS method. Results Following a single topical instillation of SFA ‐azithromycin in rabbit eyes, both formulations were macroscopically well tolerated. The highest exposure was found in the general order of EL > T > C > BCJ > AH . The obtained values were compared with data from a similar experiment of a marketed 1.5% azithromycin formulation in medium‐chain triglycerides1, with a single instillation of 25 μ L. The comparison showed that azithromycin exposure after administration of 1.5% SFA ‐azithromycin formulation was similar to the marketed formulation despite the lower absolute dose. Amar et al, Current Eye Research, 33: 149‐158, 2008 Conclusions The preservative‐free, multi‐dose SFA ‐azithromycin formulation was well tolerated. Both concentrations resulted in adequate and long‐lasting azithromycin levels in T and EL , C and BCJ . Based on these results this azithromycin formulation may lead to a new therapeutic well‐tolerated option in treating ocular surface bacterial infections.

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