Clinical Unit of Occupational Medicine, University of Trieste, Italy; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Italy.
DermoLAB, Department of Surgical, Medical, Dental and Morphological Science, University of Modena and Reggio Emilia, Modena, Italy.
Int J Pharm. 2024 Jan 5;649:123612. doi: 10.1016/j.ijpharm.2023.123612. Epub 2023 Nov 21.
Sildenafil citrate is an approved drug used for the treatment of erectile dysfunction and premature ejaculation. Despite a widespread application, sildenafil citrate shows numerous adverse cardiovascular effects in high-risk patients. Local transdermal drug delivery of this drug is therefore being explored as an interesting and noninvasive alternative administration method that avoids adverse effects arised from peak plasma drug concentrations. Although human and animal skin represents the most reliable models to perform penetration studies, they involve a series of ethical issues and restrictions. For these reasons new in vitro approaches based on artificially reconstructed human skin or "human skin equivalents" are being developed as possible alternatives for transdermal testing. There is little information, however, on the efficiency of such new in vitro methods on cutaneous penetration of active ingredients. The objective of the current study was to investigate the sildenafil citrate loaded in three commercial transdermal vehicles using 3D full-thickness skin equivalent and compare the results with the permeability experiments using porcine skin. Our results demonstrated that, while the formulation plays an imperative role in an appropriate dermal uptake of sildenafil citrate, the D coefficient results obtained by using the 3D skin equivalent are comparable to those obtained by using the porcine skin when a simple drug suspension is applied (1.17 × 10 ± 0.92 × 10 cm/s vs 3.5 × 10 ± 3.3 × 10 cm/s), suggesting that in such case, this 3D skin model can be a valid alternative for ex-vivo skin absorption experiments.
枸橼酸西地那非是一种已被批准用于治疗勃起功能障碍和早泄的药物。尽管广泛应用,但枸橼酸西地那非在高危患者中显示出许多不良心血管作用。因此,正在探索将该药物的局部透皮给药作为一种有趣且非侵入性的替代给药方法,以避免因血浆药物浓度峰值引起的不良反应。虽然人体和动物皮肤是进行渗透研究的最可靠模型,但它们涉及一系列伦理问题和限制。出于这些原因,基于人工重建的人体皮肤或“人体皮肤等效物”的新的体外方法正在被开发为透皮测试的可能替代方法。然而,关于这些新的体外方法对活性成分经皮渗透的效率的信息很少。本研究的目的是使用 3D 全厚度皮肤等效物研究三种商业透皮制剂中的枸橼酸西地那非,并将结果与使用猪皮进行的渗透实验进行比较。我们的结果表明,虽然制剂在适当的皮肤摄取枸橼酸西地那非中起着重要作用,但当应用简单的药物混悬液时,通过使用 3D 皮肤等效物获得的 D 系数结果与通过使用猪皮获得的结果相当(1.17×10±0.92×10 cm/s 对 3.5×10±3.3×10 cm/s),表明在这种情况下,该 3D 皮肤模型可以作为离体皮肤吸收实验的有效替代方法。