药品
适体
药物输送
靶向给药
结合
抗药性
药理学
癌症治疗
联合疗法
医学
癌症
纳米技术
材料科学
生物
内科学
分子生物学
数学分析
微生物学
数学
作者
Fang Zhou,Peng Wang,Yongbo Peng,Pengge Zhang,Qin Huang,Weidi Sun,Nongyue He,Ting Fu,Zilong Zhao,Xiaohong Fang,Weihong Tan
标识
DOI:10.1002/anie.201903807
摘要
Polytherapy (or drug combination cancer therapy (DCCT)), targeting multiple mechanisms associated with tumor proliferation, can efficiently maximize therapeutic efficacy, decrease drug dosage, and reduce drug resistance. However, most DCCT strategies cannot coordinate the specific delivery of a drug combination in an accurately tuned ratio into cancer cells. To address these limitations, the present work reports the engineering of circular bivalent aptamer-drug conjugates (cb-ApDCs). The cb-ApDCs exhibit high stability, specific recognition, excellent cellular uptake, and esterase-triggered release. Furthermore, the drug ratios in cb-ApDCs can be tuned for an enhanced synergistic effect without the need for complex chemistry. Therefore, cb-ApDCs provide a promising platform for the development of DCCT strategies for different drug combinations and ratios.
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