Krawczyk-Santos Anna Paula, Marreto Ricardo Neves, Concheiro Angel, Alvarez-Lorenzo Carmen, Taveira Stephânia Fleury
Laboratory of Nanosystems and Drug Delivery Devices (NanoSYS), School of Pharmacy, Universidade Federal de Goiás (UFG), Rua 240, Setor Leste Universitário, 74, 605-170 Goiânia, GO, Brazil.
Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+DFarma Group (GI-1645), Facultad de Farmacia, iMATUS and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Int J Pharm X. 2022 May 10;4:100118. doi: 10.1016/j.ijpx.2022.100118. eCollection 2022 Dec.
This work aimed to develop water-based formulations for onychomycosis topical treatment using micelles of small pegylated surfactants associated with α-cyclodextrin (αCD) to deliver terbinafine to the nail. Kolliphor® RH40 (RH40) and Gelucire® 48/16 (GEL) single and mixed micelles (RH40:GEL 1:1) were prepared. αCD was added to the surfactants dispersions to form poly(pseudo)rotaxanes (PPR). Formulations were characterized in terms of drug solubilization (3 to 34-fold increase), particle size (9-11 nm) and -potential (+0.3 - +1.96 mV), blood compatibility (non-hemolytic), rheological behavior (solid-like viscoelastic properties after 5-10% αCD addition), drug release and interaction with the nail plate. GEL micelles and surfactant-10% αCD PPRs notably hydrated the nail plate. The high viscosity of PPR led to a slower drug release, except for RH40:GEL +10% αCD that surprisingly released terbinafine faster. The RH40:GEL +10% αCD formulation delivered twice more amount of terbinafine to deeper regions of nail plate compared to other formulations. The results evidenced the potential of PPR formed by small pegylated surfactants as a water-based formulation for nail drug delivery.
这项工作旨在开发用于甲癣局部治疗的水性制剂,该制剂使用与α-环糊精(αCD)相关联的小聚乙二醇化表面活性剂的胶束将特比萘芬递送至指甲。制备了聚氧乙烯蓖麻油RH40(RH40)和Gelucire®48/16(GEL)单胶束和混合胶束(RH40:GEL 1:1)。将αCD添加到表面活性剂分散体中以形成聚(准)轮烷(PPR)。对制剂进行了药物增溶(增加3至34倍)、粒径(9 - 11纳米)和ζ电位(+0.3 - +1.96毫伏)、血液相容性(非溶血)、流变行为(添加5 - 10%αCD后呈类固体粘弹性)、药物释放以及与指甲板相互作用等方面的表征。GEL胶束和含10%αCD的表面活性剂PPR显著使指甲板水合。PPR的高粘度导致药物释放较慢,除了RH40:GEL +10%αCD令人惊讶地更快释放特比萘芬。与其他制剂相比,RH40:GEL +10%αCD制剂向指甲板深层区域递送的特比萘芬量多两倍。结果证明了由小聚乙二醇化表面活性剂形成的PPR作为用于指甲药物递送的水性制剂的潜力。