Perucca E, Richens A
Ciba Found Symp. 1979(74):51-68. doi: 10.1002/9780470720578.ch4.
Many centrally acting drugs bind extensively to plasma proteins, particularly albumin. It is generally the free concentration rather than the total concentration which determines the intensity of pharmacological action and the distribution and rate of elimination of a drug. Measurement of the total plasma concentration may therefore give a false idea of the amount of active drug available. Furthermore, variation in the degree of binding from one subject to another, and displacement of drug molecules by a second drug, may complicate the interpretation of serum levels when both bound and free drug are measured together. The strict use of therapeutic ranges of serum levels may therefore be harmful when a larger than normal proportion of the drug is free. In theory, monitoring the free concentration would have advantages, but on a routine basis this is not practical at present for technical reasons. Cerebrospinal fluid is an ultrafiltrate of plasma but lumbar puncture for routine monitoring purposes cannot be justified. Monitoring salivary concentrations is a practical alternative but for some drugs variation in the degree of ionization of the compound may make salivary levels unreliable.
许多中枢作用药物与血浆蛋白,尤其是白蛋白广泛结合。通常是游离浓度而非总浓度决定药物的药理作用强度、分布及消除速率。因此,测定血浆总浓度可能会对可用活性药物量产生错误认识。此外,个体之间结合程度的差异,以及第二种药物对药物分子的置换,可能会使同时测量结合型和游离型药物时血清水平的解读变得复杂。因此,当游离药物比例高于正常时,严格使用血清水平治疗范围可能有害。理论上,监测游离浓度会有优势,但目前由于技术原因,在常规情况下这并不实际。脑脊液是血浆的超滤液,但进行腰椎穿刺用于常规监测并无正当理由。监测唾液浓度是一种切实可行的替代方法,但对于某些药物,化合物电离程度的变化可能会使唾液水平不可靠。