材料科学
乳腺癌
肽
三阴性乳腺癌
化疗
共价键
癌症
癌症研究
纳米技术
肿瘤科
核磁共振
内科学
医学
有机化学
化学
物理
作者
Farah Benyettou,Mostafa Khair,Thirumurugan Prakasam,Sabu Varghese,Zineb Matouk,Maryam Al-Kaabi,Pilar Pena-Sánchez,Maylis Boitet,Rasha G. AbdulHalim,Sudhir Kumar Sharma,Rose Ghemrawi,Sneha Thomas,Jamie Whelan,Renu Pasricha,Ramesh Jagannathan,Felipe Gándara,Ali Trabolsi
标识
DOI:10.1021/acsami.4c10812
摘要
This study presents the use of nanoscale covalent organic frameworks (nCOFs) conjugated with tumor-targeting peptides for the targeted therapy of triple-negative breast cancer (TNBC). While peptides have previously been used for targeted delivery, their conjugation with COFs represents an innovative approach in this field. In particular, we have developed alkyne-functionalized nCOFs chemically modified with cyclic RGD peptides (Alkyn-nCOF-cRGD). This configuration is designed to specifically target αvβ3 integrins that are overexpressed in TNBC cells. These nCOFs exhibit excellent biocompatibility and are engineered to selectively disintegrate under acidic conditions, allowing for precise and localized drug release in tumor environment. Doxorubicin, a chemotherapeutic agent, has been encapsulated in these nCOFs with high loading efficiency. The therapeutic potential of Alkyn-nCOF-cRGD has been demonstrated in vitro and in vivo models. It shows significantly improved drug uptake and targeted cell death in TNBC, highlighting the efficacy of receptor-mediated endocytosis and pH-controlled drug release. This strategy leverages the unique properties of nCOFs with targeted drug delivery to achieve significant advances in personalized cancer therapy and set a new standard for precision chemotherapeutic delivery.
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