College of Economics and Management, Qingdao University of Science and Technology, Qingdao, China.
College of Economics and Management, Qingdao University of Science and Technology, Qingdao, China.
Colloids Surf B Biointerfaces. 2024 Jul;239:113954. doi: 10.1016/j.colsurfb.2024.113954. Epub 2024 May 7.
The efficacy of chemotherapeutic drugs in tumor treatment is limited by their toxicity and side effects due to their inability to selectively accumulate in tumor tissue. In addition, chemotherapeutic agents are easily pumped out of tumor cells, resulting in their inadequate accumulation. To overcome these challenges, a drug delivery system utilizing the amphiphilic peptide Pep1 was designed. Pep1 can self-assemble into spherical nanoparticles (PL/Pep1) and encapsulate paclitaxel (PTX) and lapatinib (LAP). PL/Pep1 transformed into nanofibers in an acidic environment, resulting in longer drug retention and higher drug concentrations within tumor cells. Ultimately, PL/Pep1 inhibited tumor angiogenesis and enhanced tumor cell apoptosis. The use of shape-changing peptides as drug carriers to enhance cancer cell apoptosis is promising.
化疗药物在肿瘤治疗中的疗效受到其毒性和副作用的限制,因为它们不能选择性地在肿瘤组织中积累。此外,化疗药物很容易从肿瘤细胞中泵出,导致其积累不足。为了克服这些挑战,设计了一种利用两亲肽 Pep1 的药物递送系统。Pep1 可以自组装成球形纳米颗粒 (PL/Pep1),并包载紫杉醇 (PTX) 和拉帕替尼 (LAP)。PL/Pep1 在酸性环境中转化为纳米纤维,导致药物滞留时间延长,肿瘤细胞内药物浓度升高。最终,PL/Pep1 抑制了肿瘤血管生成并增强了肿瘤细胞凋亡。使用形状变化肽作为药物载体来增强癌细胞凋亡具有广阔的前景。