Early-Stage Development of an Anti-Evaporative Liposomal Formulation for the Potential Treatment of Dry Eyes

被引:2
作者
Jantti, Janika [1 ]
Viitaja, Tuomo [2 ,3 ,4 ]
Sevon, Julia [2 ]
Lajunen, Tatu [1 ,5 ]
Raitanen, Jan-Erik [2 ]
Schlegel, Cordula [2 ]
Viljanen, Mira [2 ]
Paananen, Riku O. [2 ,3 ]
Moilanen, Jukka [3 ]
Ruponen, Marika [1 ,2 ]
Ekholm, Filip. S. [2 ]
机构
[1] Univ Eastern Finland, Sch Pharm, FI-70211 Kuopio, Finland
[2] Univ Helsinki, Dept Chem, FI-00014 Helsinki, Finland
[3] Univ Helsinki, Ophthalmol, FI-00290 Helsinki, Finland
[4] Helsinki Univ Hosp, FI-00290 Helsinki, Finland
[5] Univ Helsinki, Fac Pharm, FI-00790 Helsinki, Finland
基金
芬兰科学院;
关键词
anti-evaporative; biophysical characterization; dry eye disease; liposomal formulation; tear filmlipids; preclinical screening; RISK-FACTORS; MEIBOMIAN GLAND; PREVALENCE; DISEASE; MANAGEMENT; THERAPY; HEALTH; MEIBUM; MODEL;
D O I
10.1021/acsptsci.3c00147
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dry eye disease (DED), the most common ocular disorder, reduces the quality of life for hundreds of millions of people annually. In healthy eyes, the tear film lipid layer (TFLL) stabilizes the tear film and moderates the evaporation rate of tear fluid. In >80% of DED cases, these central features are compromised leading to tear film instability and excessive evaporation of tear fluid. Herein we assess the potential of liposomal formulations featuring phosphatidylcholines and tailored lipid species from the wax ester and O-acyl-?-hydroxy fatty acid categories in targeting this defect. The developed lead formulation displays good evaporation-resistant properties and respreadability over compression-expansion cycles in our Langmuir model system and a promising safety and efficacy profile in vitro. Preclinical in vivo studies will in the future be required to further assess and validate the potential of this concept in the treatment of DED.
引用
收藏
页码:1518 / 1530
页数:13
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