Endo Pharmaceuticals, Chadds Ford, PA, USA.
J Cardiovasc Pharmacol. 2010 Apr;55(4):368-76. doi: 10.1097/FJC.0b013e3181d2ce39.
In vitro hERG blocking potency is measured in drug discovery as part of an integrated cardiovascular risk assessment. Typically, the concentrations producing 50% inhibition are measured in protein-free saline solutions and compared with calculated free therapeutic in vivo Cmax values to estimate a hERG safety multiple. The free/unbound fraction is believed responsible for activity. We tested the validity of this approach with 12 compounds by determining potencies in voltage clamp studies conducted in the absence and presence of 100% dialyzed fetal bovine serum (FBS). Bath drug concentrations in saline solutions were measured to account for loss of compounds due to solubility, stability, and/or adsorption. Protein binding in dialyzed FBS was measured to enable predictions of serum IC50s based on the unbound fraction and the saline IC50. For 11 of 12 compounds, the measured potency in the presence of dialyzed FBS was within 2-fold of the predicted potency. The predicted IC50 in dialyzed FBS for one highly bound compound, amiodarone, was 9-fold higher than the measured serum IC50. These data suggest that for highly bound compounds, direct measurement of IC50s in the presence of 100% serum may provide a more accurate estimate of in vivo potencies than the approach based on calculated serum shifts.
在药物发现过程中,体外 hERG 阻断效力作为综合心血管风险评估的一部分进行测量。通常,在无蛋白盐溶液中测量产生 50%抑制的浓度,并与计算的体内游离治疗 Cmax 值进行比较,以估计 hERG 安全性倍数。游离/未结合分数被认为与活性有关。我们通过在不存在和存在 100%透析胎牛血清 (FBS) 的情况下进行电压钳研究来测试 12 种化合物的这种方法的有效性。测量盐溶液中的浴药物浓度,以补偿由于溶解度、稳定性和/或吸附导致的化合物损失。测量透析 FBS 中的蛋白结合,以便根据游离分数和盐水 IC50 预测血清 IC50。对于 12 种化合物中的 11 种,在存在透析 FBS 的情况下测量的效力与预测的效力相差 2 倍以内。一种高度结合的化合物胺碘酮在透析 FBS 中的预测 IC50 比测量的血清 IC50 高 9 倍。这些数据表明,对于高度结合的化合物,直接在 100%血清中测量 IC50 可能比基于计算的血清转移的方法更能准确估计体内效力。