Robinson P J, Rapoport S I
Pediatrics. 1987 Apr;79(4):553-8.
A mathematical model is presented to describe quantitatively the uptake of bilirubin into the brain from blood, under conditions of extensive binding to plasma proteins. The model relates bilirubin uptake to the rate constants for dissociation and association of the albumin/bilirubin complex and to the transit time of blood through brain capillaries. A rational basis is given for deciding between the total or the free bilirubin concentration as an appropriate indicator of brain exposure to the toxic effects of bilirubin. The effect of competition for binding sites by drugs such as sulfonamides on the brain uptake of bilirubin is also described quantitatively.
提出了一个数学模型,用于定量描述在胆红素与血浆蛋白广泛结合的情况下,胆红素从血液进入大脑的摄取过程。该模型将胆红素摄取与白蛋白/胆红素复合物的解离和缔合速率常数以及血液通过脑毛细血管的转运时间联系起来。为确定总胆红素浓度或游离胆红素浓度作为大脑暴露于胆红素毒性作用的合适指标提供了合理依据。还定量描述了磺胺类等药物对结合位点的竞争对胆红素脑摄取的影响。