Nozaki K, Suzuki S, Maeda F, Takagaki S, Suzuki A, Hata T
Department of Pharmaceutical, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
J Pharm Biomed Anal. 1998 Sep;17(8):1381-92. doi: 10.1016/s0731-7085(98)00026-0.
A sensitive and specific enzyme immunoassay for FK480, a novel cholecystokinin type-A (CCK-A) receptor antagonist, was developed to study the pharmacokinetics of the drug at low-dose administration using a specific monoclonal antibody. The high performance liquid chromatography (HPLC) method had been used for studying toxicokinetics, but its determination limit (2.5 ng ml-1) was too high for use in clinical studies. Subsequently we developed an enzyme immunoassay (EIA) using rabbit anti-FK480 serum (polyclonal antibody). It had higher sensitivity (0.1 ng ml-1) when 0.5 ml of plasma was used but its specificity was low because of the cross-reactivity of the metabolites of FK480. Therefore we produced several monoclonal antibodies for FK480 by cell fusion, and selected the antibody which was least cross-reactive for the isolated metabolites of FK480. Finally we developed a sensitive and specific EIA using this monoclonal antibody. The lower limit of quantification of this method was 0.2 ng ml-1 when 0.2 ml of human plasma was used. The coefficient of variation over the calibration range (0.2-10 ng ml-1) was less than 15%. We used this method for clinical studies, and it showed a good correlation to the HPLC method when plasma concentration was 2.5 ng ml-1 or more.
一种用于新型胆囊收缩素A(CCK-A)受体拮抗剂FK480的灵敏且特异的酶免疫分析法被开发出来,该方法使用一种特异性单克隆抗体来研究低剂量给药时该药物的药代动力学。高效液相色谱(HPLC)法曾被用于研究毒代动力学,但其检测限(2.5 ng/ml)对于临床研究来说过高。随后我们使用兔抗FK480血清(多克隆抗体)开发了一种酶免疫分析法(EIA)。当使用0.5 ml血浆时,它具有更高的灵敏度(0.1 ng/ml),但由于FK480代谢产物的交叉反应,其特异性较低。因此,我们通过细胞融合制备了几种针对FK480的单克隆抗体,并选择了对分离出的FK480代谢产物交叉反应最小的抗体。最后,我们使用这种单克隆抗体开发了一种灵敏且特异的EIA。当使用0.2 ml人血浆时,该方法的定量下限为0.2 ng/ml。在校准范围(0.2 - 10 ng/ml)内的变异系数小于15%。我们将该方法用于临床研究,当血浆浓度为2.5 ng/ml或更高时,它与HPLC法显示出良好的相关性。