Conversion from Sandimmune to Neoral in Organ Transplant Recipients

M. Bartucci, L. Bayer, B. Brooks, L. Chandler, V. Himes, D. Meiergerd, B. Newby, N. T. Satmary, V. Shieck
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Abstract

Journal of Transplant Coordination, Vol. 8, Number 4, December 1998 Pharmacokinetic parameters that are particularly important for cyclosporine include Cmax, tmax, Cmin, and area under the curve (AUC). Cmax represents the peak or maximum concentration of a drug, and tmax is the time needed to reach the maximum concentration. Conversely, Cmin is the minimum drug concentration or trough. Area under the curve is the area under the concentration-versus-time curve, reflecting the total drug exposure (bioavailability) over the dosing interval or duration of therapy. An important clinical mandate is that drugs must be delivered to target tissues in concentrations high enough to be therapeutic but low enough to avoid toxicity.2 The term “therapeutic range” refers to the range of drug concentrations in the blood in which the likelihood of the desired clinical response is relatively high and the risk of unacceptable toxicity is relatively low.1 It is typically a population mean, and there may be great individual differences in patient response within this range. Cyclosporine, like other immunosuppressants, has a relatively narrow therapeutic range.3 Conversion from Sandimmune to Neoral in organ transplant recipients
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器官移植受者从Sandimmune到Neoral的转化
对环孢素特别重要的药代动力学参数包括Cmax、tmax、Cmin和曲线下面积(AUC)。Cmax表示药物的峰值或最大浓度,tmax是达到最大浓度所需的时间。相反,Cmin是最低药物浓度或波谷。曲线下面积是浓度-时间曲线下的面积,反映了在给药间隔或治疗持续时间内的总药物暴露(生物利用度)。一项重要的临床任务是,药物必须以足够高的浓度递送到目标组织,以达到治疗效果,但又足够低以避免毒性术语“治疗范围”是指血液中药物浓度的范围,在这个范围内,期望的临床反应的可能性相对较高,而不可接受的毒性风险相对较低它通常是一个总体平均值,在这个范围内,患者的反应可能存在很大的个体差异。环孢素和其他免疫抑制剂一样,具有相对狭窄的治疗范围器官移植受者从Sandimmune到Neoral的转化
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