Nair Anroop B, Aldhubiab Bandar, Shah Jigar, Jacob Shery, Attimarad Mahesh, Sreeharsha Nagaraja, Venugopala Katharigatta N, Joseph Alex, Morsy Mohamed A
Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Department of Pharmaceutics, Institute of Pharmacy, Nirma University, Ahmedabad 382481, India.
Pharmaceutics. 2023 May 6;15(5):1422. doi: 10.3390/pharmaceutics15051422.
The efficacy of topical antifungal therapy in onychomycosis has been hindered by the failure of the antimycotic to permeate the nail plate. This research aims to design and develop a transungual system for the effective delivery of efinaconazole utilizing constant voltage iontophoresis. Seven prototype drug-loaded hydrogel formulations (E1-E7) were prepared to assess the influence of solvent (ethanol) and cosolvent (Labrasol) on transungual delivery. Optimization was performed to evaluate the effect of three independent variables; voltage, solvent-to-cosolvent ratio, and penetration enhancer (PEG 400) concentration on critical quality attributes (CQAs), such as drug permeation and loading into the nail. The selected hydrogel product was characterized for pharmaceutical properties, efinaconazole release from the nail, and antifungal activity. Preliminary data indicates ethanol, Labrasol, and voltage influence the transungual delivery of efinaconazole. Optimization design indicates a significant impact by applied voltage (-0.0001) and enhancer concentration (-0.0004) on the CQAs. Excellent correlation between selected independent variables and CQAs was confirmed by the high desirability value (0.9427). A significant ( < 0.0001) enhancement in the permeation (~78.59 µg/cm) and drug loading (3.24 µg/mg) was noticed in the optimized transungual delivery with 10.5 V. FTIR spectral data indicates no interaction between the drug and excipients, while the DSC thermograms confirmed the amorphous state of the drug in the formulation. Iontophoresis produces a drug depot in the nail that releases above the minimum inhibitory concentration level for an extended period, potentially reducing the need for frequent topical treatment. Antifungal studies further substantiate the release data and have shown remarkable inhibition of . Overall, the promising results obtained here demonstrate the prospective of this non-invasive method for the effective transungual delivery of efinaconazole, which could improve the treatment of onychomycosis.
局部抗真菌疗法治疗甲真菌病的疗效一直受到抗真菌药物无法穿透甲板的阻碍。本研究旨在设计并开发一种利用恒压离子电渗疗法有效递送艾氟康唑的经甲给药系统。制备了七种载药凝胶原型制剂(E1 - E7),以评估溶剂(乙醇)和助溶剂(Labrasol)对经甲给药的影响。进行优化以评估三个独立变量;电压、溶剂与助溶剂比例以及渗透促进剂(PEG 400)浓度对关键质量属性(CQA)的影响,如药物渗透和在指甲中的载药量。对所选水凝胶产品进行了药学性质、艾氟康唑从指甲中的释放以及抗真菌活性表征。初步数据表明乙醇、Labrasol和电压会影响艾氟康唑的经甲给药。优化设计表明施加电压(-0.0001)和促进剂浓度(-0.0004)对CQA有显著影响。通过高可取性值(0.9427)证实了所选独立变量与CQA之间具有良好的相关性。在10.5 V的优化经甲给药中,观察到渗透(~78.59 µg/cm)和载药量(3.24 µg/mg)有显著提高(<0.0001)。傅里叶变换红外光谱(FTIR)数据表明药物与辅料之间无相互作用,而差示扫描量热法(DSC)热谱图证实制剂中药物为无定形状态。离子电渗疗法在指甲中产生一个药物储库,可在较长时间内释放高于最低抑菌浓度水平的药物,这可能减少频繁局部治疗的需求。抗真菌研究进一步证实了释放数据,并显示出对……有显著抑制作用。总体而言,此处获得的有前景的结果证明了这种非侵入性方法在有效经甲递送艾氟康唑方面的前景,这可能改善甲真菌病的治疗。