Ioele Giuseppina, Muzzalupo Rita, Gündüz Miyase Gözde, De Luca Michele, Mazzotta Elisabetta, Grande Fedora, Occhiuzzi Maria Antonietta, Garofalo Antonio, Ragno Gaetano
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Hacettepe University, 06100 Ankara, Turkey.
Pharmaceutics. 2021 Apr 10;13(4):527. doi: 10.3390/pharmaceutics13040527.
1,4-Dihydropyridines (DHPs) are the most important class of L-type calcium channel blockers that are employed for the treatment of cardiovascular diseases, particularly hypertension. Various modifications on this scaffold lead to the discovery of new DHPs blocking different types of calcium channels. Among them, the T-type calcium channel has recently attracted great interest due to its role in chronic pain conditions. In this study, we selected three newly synthesized DHPs (HM8, HM10 and MD20) with different selectivity profiles to the T-type calcium channel and formulated them in micellar solutions and micellar-in-gel matrices to be tested for potential topical use in the treatment of neuropathic pain. To prevent the well-known sensitivity to light of the DHPs, the studied compounds were entrapped in colloidal aggregates obtained by using edible Pluronic surfactants and adding α-tocopherol as an antioxidant. All the prepared formulations were exposed to stressing light, according to international rules. Along with the degradation experiments, the concentrations of the parent compounds and by-products were calculated by multivariate curve resolution-alternating least squares (MCR-ALS) applied to the spectral data. The defined formulations proved suitable as light-stable matrices for the DHP compounds, showing an increase in stability for HM8 and MD20 and an almost complete photoprotection for HM10, compared to ethanol solutions and standard gel formulations.
1,4-二氢吡啶(DHPs)是最重要的一类L型钙通道阻滞剂,用于治疗心血管疾病,尤其是高血压。对该骨架进行的各种修饰导致了新型DHPs的发现,这些DHPs可阻断不同类型的钙通道。其中,T型钙通道因其在慢性疼痛状态中的作用,最近引起了极大的关注。在本研究中,我们选择了三种对T型钙通道具有不同选择性的新合成DHPs(HM8、HM10和MD20),并将它们制成胶束溶液和胶束-凝胶基质,以测试其在治疗神经性疼痛方面的潜在局部应用。为了防止DHPs众所周知的光敏感性,所研究的化合物被包裹在通过使用可食用的普朗尼克表面活性剂并添加α-生育酚作为抗氧化剂而获得的胶体聚集体中。根据国际规则,所有制备的制剂都要接受强光照射。除了降解实验外,还通过应用于光谱数据的多元曲线分辨-交替最小二乘法(MCR-ALS)计算母体化合物和副产物的浓度。与乙醇溶液和标准凝胶制剂相比,所定义的制剂被证明适合作为DHPs化合物的光稳定基质,HM8和MD20的稳定性有所提高,HM10几乎完全受到光保护。