Wasan Kishor M, Ramaswamy Manisha, Kwong Mona, Boulanger Kathy D
Division of Pharmaceutics and Biopharmaceutics, Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3.
AAPS PharmSci. 2002;4(4):E30. doi: 10.1208/ps040430.
Lipoproteins are a heterogeneous population of macromolecular aggregates of lipids and proteins that are responsible for the transport of lipids through the vascular and extravascular fluids from their site of synthesis or absorption to peripheral tissues. Lipoproteins are involved in other biological processes as well, including coagulation and tissue repair, and serve as carriers of a number of hydrophobic compounds within the systemic circulation. It has been well documented that disease states (eg, AIDS, diabetes, cancer) significantly influence circulating lipoprotein content and composition. Therefore, it appears possible that changes in the lipoprotein profile would affect not only the ability of a compound to associate with lipoproteins but also the distribution of the compound within the lipoprotein subclasses. Such an effect could alter the pharmacokinetics and pharmacological action of the drug. This paper reviews the factors that influence the interaction of one model hydrophobic compound, cyclosporine A, with lipoproteins and the implications of altered plasma lipoprotein concentrations on the pharmacological behavior of this compound.
脂蛋白是脂质和蛋白质的大分子聚集体的异质群体,负责脂质通过血管和血管外液从其合成或吸收部位运输到外周组织。脂蛋白也参与其他生物学过程,包括凝血和组织修复,并在体循环中作为多种疏水化合物的载体。已有充分的文献证明,疾病状态(如艾滋病、糖尿病、癌症)会显著影响循环脂蛋白的含量和组成。因此,脂蛋白谱的变化似乎不仅会影响化合物与脂蛋白结合的能力,还会影响该化合物在脂蛋白亚类中的分布。这种效应可能会改变药物的药代动力学和药理作用。本文综述了影响一种模型疏水化合物环孢素A与脂蛋白相互作用的因素,以及血浆脂蛋白浓度改变对该化合物药理行为的影响。