Heterocyclic Drug-polymer Conjugates for Cancer Targeted Drug Delivery

被引:3
作者
Kaur, Harmeet [1 ]
Desai, Sapna D. [2 ]
Kumar, Virender [3 ]
Rathi, Pooja [3 ]
Singh, Jasbir [3 ]
机构
[1] Maharshi Dayanand Univ, Dept Pharmaceut Sci, Rohtak 124001, Haryana, India
[2] Pioneer Pharm Degree Coll, Vadodara, Gujarat, India
[3] Univ Hlth Sci, Coll Pharm, Rohtak 124001, Haryana, India
关键词
Cancer; targeting; endocytosis; angiogenesis; apoptosis; ligand; dendrimer; micelles; block copolymers; COPOLYMER-BOUND DOXORUBICIN; HPMA COPOLYMER; BREAST-CANCER; IN-VITRO; PHASE-I; MULTIDRUG-RESISTANCE; PRECLINICAL EFFICACY; TUMOR ACCUMULATION; SENSITIVE MICELLES; ANTITUMOR-ACTIVITY;
D O I
10.2174/1871520615666160504094044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New polymer therapeutics like polymer-drug conjugates (PDCs) are developing day by day. Heterocyclic drugs with excellent cytotoxic properties are available, but lack of their specificity makes them available to the normal cells also, which is the main cause of their toxicity. Drugs in the form of PDCs make delivery possible to the specific sites. Most of the PDCs are designed with the aim to either target and/or to get activated in specific cancer microenvironments. Therefore, the most exploited targets for cancer drug delivery are; cancer cell enzymes, heat shock protein 90 (HSP90), multi-drug resistance (MDR) proteins, angiogenesis, apoptosis and cell membrane receptors (e.g., folates, transferrin, etc.). In this review, we will summarize PDCs of heterocyclic drugs, like doxorubicin (DOX), daunorubicin, paclitaxel (PTX), docetaxel (DTX), cisplatin, camptothecin (CPT), geldanamycin (GDM), etc., and some of their analogs for efficient delivery of drugs to cancer cells.
引用
收藏
页码:1355 / 1377
页数:23
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