Verboni Michele, Perinelli Diego Romano, Qiu Carol Yingshan, Tiboni Mattia, Aluigi Annalisa, Lucarini Simone, Lam Jenny K W, Duranti Andrea
Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento 6, 61029 Urbino, PU, Italy.
School of Pharmacy, University of Camerino, Via Gentile III da Varano, 62032 Camerino, MC, Italy.
Pharmaceuticals (Basel). 2023 Feb 1;16(2):223. doi: 10.3390/ph16020223.
The delivery of therapeutics across biological membranes (e.g., mucosal barriers) by avoiding invasive routes (e.g., injection) remains a challenge in the pharmaceutical field. As such, there is the need to discover new compounds that act as drug permeability enhancers with a favorable toxicological profile. A valid alternative is represented by the class of sugar-based ester surfactants. In this study, sucrose and lactose alkyl aromatic and aromatic ester derivatives have been synthesized with the aim to characterize them in terms of their physicochemical properties, structure-property relationship, and cytotoxicity, and to test their ability as permeability enhancer agents across Calu-3 cells. All of the tested surfactants showed no remarkable cytotoxic effect on Calu-3 cells when applied both below and above their critical micelle concentration. Among the explored molecules, lactose -biphenyl benzoate (URB1420) and sucrose -phenyl benzoate (URB1481) cause a reversible ~30% decrease in transepithelial electrical resistance (TEER) with the respect to the basal value. The obtained result matches with the increased in vitro permeability coefficients (P) calculated for FTIC-dextran across Calu-3 cells in the presence of 4 mM solutions of these surfactants. Overall, this study proposes sucrose- and lactose-based alkyl aromatic and aromatic ester surfactants as novel potential and safe permeation enhancers for pharmaceutical applications.
通过避免侵入性途径(如注射)实现治疗药物跨生物膜(如黏膜屏障)递送,在制药领域仍是一项挑战。因此,需要发现具有良好毒理学特征且能作为药物渗透增强剂的新化合物。基于糖的酯类表面活性剂是一种有效的替代物。在本研究中,已合成了蔗糖和乳糖的烷基芳基及芳基酯衍生物,旨在对其理化性质、结构-性质关系和细胞毒性进行表征,并测试它们作为跨Calu-3细胞渗透增强剂的能力。当在临界胶束浓度以下和以上应用时,所有测试的表面活性剂对Calu-3细胞均未显示出显著的细胞毒性作用。在所研究的分子中,乳糖-联苯苯甲酸酯(URB1420)和蔗糖-苯基苯甲酸酯(URB1481)使跨上皮电阻(TEER)相对于基础值出现约30%的可逆下降。所得结果与在这些表面活性剂4 mM溶液存在下,计算得出的FTIC-葡聚糖跨Calu-3细胞的体外渗透系数(P)增加相匹配。总体而言,本研究提出基于蔗糖和乳糖的烷基芳基及芳基酯表面活性剂作为制药应用中新型潜在且安全的渗透增强剂。