Ismail Maytham, Kanapathipillai Mathumai
Department of Mechanical Engineering, University of Michigan-Dearborn, Dearborn, MI 48128, USA.
Pharmaceuticals (Basel). 2024 Jun 13;17(6):777. doi: 10.3390/ph17060777.
Amyloid aggregates have attracted significant interest in regard to diverse biomedical applications, particularly in the field of drug delivery. Here, we report novel amyloid aggregates based on a 12-amino-acid peptide from the amyloidogenic region of the receptor-interacting kinase 3 (RIP3) protein and a thermoresponsive triblock copolymer, namely, Pluronic F127 (RIP3/F127). Physicochemical characterization was performed to determine the aggregation size, morphology, and stimuli-responsive properties. The potential of the aggregates as a drug depot was assessed in lung cancer cells, using Doxorubicin (Dox) as a model drug. The results show that RIP3 and RIP3/F127 exhibit amyloidogenic properties. Further, the RIP3/F127 amyloids exhibited significant ultrasound-responsive properties compared to amyloid aggregates without Pluronic F127. Moreover, the RIP3/F127/Dox amyloid formulations that were subjected to ultrasound treatment exhibited greater toxicity to lung cancer cells compared to that of Dox alone at equal concentrations. Overall, the results from this proof-of-concept study show that amyloidogenic peptide aggregates with stimuli-responsive properties can be utilized as efficient drug delivery depots.
淀粉样聚集体在多种生物医学应用方面引起了广泛关注,尤其是在药物递送领域。在此,我们报道了基于受体相互作用激酶3(RIP3)蛋白淀粉样生成区域的一种12个氨基酸的肽和一种热响应性三嵌段共聚物,即普朗尼克F127(RIP3/F127)形成的新型淀粉样聚集体。进行了物理化学表征以确定聚集体的大小、形态和刺激响应特性。以阿霉素(Dox)作为模型药物,在肺癌细胞中评估了聚集体作为药物储存库的潜力。结果表明,RIP3和RIP3/F127具有淀粉样生成特性。此外,与不含普朗尼克F127的淀粉样聚集体相比,RIP3/F127淀粉样聚集体表现出显著的超声响应特性。而且,在相同浓度下,经过超声处理的RIP3/F127/Dox淀粉样制剂对肺癌细胞的毒性比单独使用Dox更大。总体而言,这项概念验证研究的结果表明,具有刺激响应特性的淀粉样生成肽聚集体可作为高效的药物递送储存库。