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Low density lipoprotein bionanoparticles: From cholesterol transport to delivery of anti-cancer drugs

机译:低密度脂蛋白生物纳米颗粒:从胆固醇转运到抗癌药物的转运

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In this review article, we highlight the importance of low-density lipoprotein (LDL) and its implications in the field of drug delivery to cancer cells. LDL is naturally occurring bionanoparticles (BNP) with a size of 18-25nm. These BNPs specifically transport cholesterol to cells expressing the LDL receptors (LDLRs). Several tumors overexpress LDLRs, presumably to provide cholesterol for sustaining a high rate of membrane synthesis. LDL BNPs are biocompatible and biodegradable, favorably bind hydrophobic and amphiphilic drugs, are taken up by a receptor-mediated mechanism, have a half-life of 2-4days, and can be rerouted. Drugs can be loaded onto LDL BNPs by surface loading, core loading, and apoprotein interaction. LDL may be used as a drug carrier for treatment of atherosclerosis, cancer, and in photodynamic therapies.
机译:在这篇综述文章中,我们强调了低密度脂蛋白(LDL)的重要性及其在药物向癌细胞递送领域的意义。 LDL是天然存在的生物纳米粒子(BNP),尺寸为18-25nm。这些BNP特异性地将胆固醇转运至表达LDL受体(LDLR)的细胞。几种肿瘤过表达LDLR,大概是为了提供胆固醇以维持高的膜合成速率。 LDL BNP具有生物相容性和生物可降解性,可以很好地结合疏水性和两亲性药物,并通过受体介导的机制吸收,半衰期为2-4天,并且可以重新布线。可以通过表面加载,核心加载和载脂蛋白相互作用将药物加载到LDL BNP上。 LDL可用作治疗动脉粥样硬化,癌症和进行光动力疗法的药物载体。

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