Polymer-Based Prodrugs: Improving Tumor Targeting and the Solubility of Small Molecule Drugs in Cancer Therapy

被引:83
作者
Dragojevic, Sonja [1 ]
Ryu, Jung Su [1 ]
Raucher, Drazen [1 ]
机构
[1] Univ Mississippi, Med Ctr, Dept Biochem, Jackson, MS 39216 USA
来源
MOLECULES | 2015年 / 20卷 / 12期
关键词
polymer based prodrugs; anticancer drugs; macromolecules; drug delivery; cancer therapy; genetically engineered biopolymers; synthetic and natural polymers; ELASTIN-LIKE POLYPEPTIDE; IN-VITRO; HPMA COPOLYMER; OVARIAN-CANCER; DOXORUBICIN CONJUGATE; METHACRYLAMIDE COPOLYMER; COMBINATION THERAPY; ANTICANCER ACTIVITY; ANTITUMOR-ACTIVITY; DELIVERY;
D O I
10.3390/molecules201219804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The majority of anticancer drugs have poor aqueous solubility, produce adverse effects in healthy tissue, and thus impose major limitations on both clinical efficacy and therapeutic safety of cancer chemotherapy. To help circumvent problems associated with solubility, most cancer drugs are now formulated with co-solubilizers. However, these agents often also introduce severe side effects, thereby restricting effective treatment and patient quality of life. A promising approach to addressing problems in anticancer drug solubility and selectivity is their conjugation with polymeric carriers to form polymer-based prodrugs. These polymer-based prodrugs are macromolecular carriers, designed to increase the aqueous solubility of antitumor drugs, can enhance bioavailability. Additionally, polymer-based prodrugs approach exploits unique features of tumor physiology to passively facilitate intratumoral accumulation, and so improve chemodrug pharmacokinetics and pharmacological properties. This review introduces basic concepts of polymer-based prodrugs, provides an overview of currently emerging synthetic, natural, and genetically engineered polymers that now deliver anticancer drugs in preclinical or clinical trials, and highlights their major anticipated applications in anticancer therapies.
引用
收藏
页码:21750 / 21769
页数:20
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