Coelho Maria Miguel, Lima Rita, Almeida Ana Sofia, Fernandes Pedro Alexandrino, Remião Fernando, Fernandes Carla, Tiritan Maria Elizabeth
Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy of the University of Porto, 4050-313, Porto, Portugal.
CIIMAR-Interdisciplinary Center for Marine and Environmental Research University of Porto, Porto de Leixões Cruise Terminal, 4450-208, Matosinhos, Portugal.
Anal Bioanal Chem. 2024 Aug;416(20):4605-4618. doi: 10.1007/s00216-024-05409-3. Epub 2024 Jul 4.
"Purple Drank", a soft drink containing promethazine (PMZ) and codeine (COD), has gained global popularity for its hallucinogenic effects. Consuming large amounts of this combination can lead to potentially fatal events. The binding of these drugs to plasma proteins can exacerbate the issue by increasing the risk of drug interactions, side effects, and/or toxicity. Herein, the binding affinity to human serum albumin (HSA) of PMZ and its primary metabolites [N-desmethyl promethazine (DMPMZ) and promethazine sulphoxide (PMZSO)], along with COD, was investigated by high-performance affinity chromatography (HPAC) though zonal approach. PMZ and its metabolites exhibited a notable binding affinity for HSA (%b values higher than 80%), while COD exhibited a %b value of 65%. To discern the specific sites of HSA to which these compounds were bound, displacement experiments were performed using warfarin and (S)-ibuprofen as probes for sites I and II, respectively, which revealed that all analytes were bound to both sites. Molecular docking studies corroborated the experimental results, reinforcing the insights gained from the empirical data. The in silico data also suggested that competition between PMZ and its metabolites with COD can occur in both sites of HSA, but mainly in site II. As the target compounds are chiral, the enantioselectivity for HSA binding was also explored, showing that the binding for these compounds was not enantioselective.
“紫色饮料”是一种含有异丙嗪(PMZ)和可待因(COD)的软饮料,因其致幻作用而在全球流行。大量饮用这种混合物可能导致潜在的致命事件。这些药物与血浆蛋白的结合会增加药物相互作用、副作用和/或毒性的风险,从而加剧问题的严重性。在此,通过高效亲和色谱法(HPAC)的区域法研究了PMZ及其主要代谢物[N-去甲基异丙嗪(DMPMZ)和异丙嗪亚砜(PMZSO)]以及COD与人血清白蛋白(HSA)的结合亲和力。PMZ及其代谢物对HSA表现出显著的结合亲和力(%b值高于80%),而COD的%b值为65%。为了识别这些化合物在HSA上的具体结合位点,分别使用华法林和(S)-布洛芬作为位点I和位点II的探针进行了置换实验,结果表明所有分析物都与这两个位点结合。分子对接研究证实了实验结果,强化了从实验数据中获得的见解。计算机模拟数据还表明,PMZ及其代谢物与COD之间的竞争可能在HSA的两个位点发生,但主要发生在位点II。由于目标化合物是手性的,还探索了它们对HSA结合的对映选择性,结果表明这些化合物的结合没有对映选择性。