| Literature DB >> 31125154 |
Fang Zhou1, Peng Wang1, Yongbo Peng1, Pengge Zhang1, Qin Huang1, Weidi Sun1, Nongyue He2, Ting Fu1, Zilong Zhao1, Xiaohong Fang3, Weihong Tan1,4.
Abstract
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.Entities:
Keywords: aptamer-drug conjugates; aptamers; drug combination cancer therapy; drug delivery; molecular engineering
Year: 2019 PMID: 31125154 DOI: 10.1002/anie.201903807
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336