Asano Nagayoshi, Wiseman Justin Michael, Tsuji Fumio, Kawazu Kouichi
Nara Research and Development Center, Santen Pharmaceutical Co., Ltd.
Prosolia, Inc.
Biol Pharm Bull. 2017;40(9):1586-1589. doi: 10.1248/bpb.b17-00288.
Meibomian gland dysfunction (MGD) is the leading cause of dry eye, and although it affects approximately 4% of the population, treatment options remain limited. Topical azithromycin is one of the most promising pharmacological agents because of its multiple mechanisms of action and long sustainability. Azithromycin is frequently used as an off-label medication in the U.S. However, although azithromycin is presumed to act directly on meibomian gland cells, the mechanisms of action that contribute to its clinical efficacy remain unclear because no studies using a pharmacokinetic approach have been performed. Therefore, we aimed to clarify whether topical azithromycin reaches the meibomian glands sufficiently to generate a biological effect. We measured azithromycin concentrations in rabbit meibomian glands collected using a recently developed method. Moreover, we also visualized the azithromycin micro-distribution using desorption electrospray ionization (DESI) imaging. Azithromycin concentration in the meibomian glands reached only 0.8 µg/g tissue following a single application of a 1% azithromycin ophthalmic solution and was 1000-fold lower than the concentration in conjunctival epithelium. Similarly, no signal was observed in the meibomian glands on DESI images. Our results clearly demonstrated that topical azithromycin had limited access to the meibomian glands and was predominantly distributed in ocular surface tissues such as the palpebral conjunctiva and lid margins. These findings provide new insight into the clinical responses to topical azithromycin therapy and will aid in the further development of effective drugs with more suitable pharmacokinetic properties.
睑板腺功能障碍(MGD)是干眼的主要原因,尽管它影响着约4%的人口,但治疗选择仍然有限。局部用阿奇霉素是最有前景的药物之一,因为它有多种作用机制且可持续时间长。在美国,阿奇霉素经常被用作非标签药物。然而,尽管推测阿奇霉素直接作用于睑板腺细胞,但由于尚未进行使用药代动力学方法的研究,其临床疗效的作用机制仍不清楚。因此,我们旨在阐明局部用阿奇霉素是否能充分到达睑板腺以产生生物学效应。我们使用最近开发的方法测量了兔睑板腺中的阿奇霉素浓度。此外,我们还使用解吸电喷雾电离(DESI)成像观察了阿奇霉素的微观分布。单次应用1%阿奇霉素眼药水后,睑板腺中的阿奇霉素浓度仅达到0.8μg/g组织,比结膜上皮中的浓度低1000倍。同样,在DESI图像上睑板腺中未观察到信号。我们的结果清楚地表明,局部用阿奇霉素进入睑板腺的机会有限,主要分布在睑结膜和睑缘等眼表组织中。这些发现为局部用阿奇霉素治疗的临床反应提供了新的见解,并将有助于进一步开发具有更合适药代动力学特性的有效药物。