Peptide-Drug Conjugates with Different Linkers for Cancer Therapy

被引:172
作者
Alas, Mona [1 ]
Saghaeidehkordi, Azam [1 ]
Kaur, Kamaljit [1 ]
机构
[1] Chapman Univ, Sch Pharm CUSP, Harry & Diane Rinker Hlth Sci Campus, Irvine, CA 92618 USA
基金
美国国家卫生研究院;
关键词
BREAST-CANCER; TUMOR-GROWTH; DOXORUBICIN; DELIVERY; ALDOXORUBICIN; HYDROLYSIS; PACLITAXEL; EPHA2; RADIOPHARMACEUTICALS; METASTASIS;
D O I
10.1021/acs.jmedchem.0c01530
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Drug conjugates are chemotherapeutic or cytotoxic agents covalently linked to targeting ligands such as an antibody or a peptide via a linker. While antibody-drug conjugates (ADCs) are now clinically established for cancer therapy, peptide-drug conjugates (PDCs) are gaining recognition as a new modality for targeted drug delivery with improved efficacy and reduced side effects for cancer treatment. The linker in a drug conjugate plays a key role in the circulation time of the conjugate and release of the drug for full activity at the target site. Herein, we highlight the main linker chemistries utilized in the design of PDCs and discuss representative examples of PDCs with different linker chemistries with the related outcome in cell and animal studies.
引用
收藏
页码:216 / 232
页数:17
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