KAIST Institute for the BioCentury, Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Daejeon, 34141, Republic of Korea.
Angew Chem Int Ed Engl. 2016 Aug 26;55(36):10676-80. doi: 10.1002/anie.201604858. Epub 2016 Aug 3.
Although stimuli-responsive materials hold potential for use as drug-delivery carriers for treating cancers, their clinical translation has been limited. Ideally, materials used for the purpose should be biocompatible and nontoxic, provide "on-demand" drug release in response to internal or external stimuli, allow large-scale manufacturing, and exhibit intrinsic anticancer efficacy. We present multistimuli-responsive nanoparticles formed from bilirubin, a potent endogenous antioxidant that possesses intrinsic anticancer and anti-inflammatory activity. Exposure of the bilirubin nanoparticles (BRNPs) to either reactive oxygen species (ROS) or external laser light causes rapid disruption of the BRNP nanostructure as a result of a switch in bilirubin solubility, thereby releasing encapsulated drugs. In a xenograft tumor model, BRNPs loaded with the anticancer drug doxorubicin (DOX@BRNPs), when combined with laser irradiation of 650 nm, significantly inhibited tumor growth. This study suggests that BRNPs may be used as a drug-delivery carrier as well as a companion medicine for effectively treating cancers.
虽然刺激响应材料在作为治疗癌症的药物输送载体方面具有潜力,但它们的临床转化受到了限制。理想情况下,用于该目的的材料应该是生物相容的和无毒的,能够在内部或外部刺激下“按需”释放药物,允许大规模制造,并具有内在的抗癌功效。我们提出了由胆红素形成的多刺激响应纳米粒子,胆红素是一种有效的内源性抗氧化剂,具有内在的抗癌和抗炎活性。胆红素纳米粒子(BRNP)暴露于活性氧(ROS)或外部激光光会导致 BRNP 纳米结构的快速破坏,这是由于胆红素溶解度的转变,从而释放封装的药物。在异种移植肿瘤模型中,负载抗癌药物阿霉素(DOX@BRNPs)的 BRNPs 与 650nm 的激光照射相结合,显著抑制了肿瘤生长。这项研究表明,BRNPs 可用作药物输送载体以及伴随药物,以有效治疗癌症。