Self-assembled phenylisoxazole-peptide hybrid assemblies and their interactions with breast and ovarian tumor cells

被引:1
|
作者
Hurley, Sara K. [1 ]
Cutrone, Nicole M. [1 ]
Fath, Karl R. [2 ]
Pajovich, Harrison T. [1 ]
Garcia, Jeremy [2 ]
Smith, Andrew M. [1 ]
Banerjee, Ipsita A. [1 ]
机构
[1] Fordham Univ, Dept Chem, Bronx, NY 10458 USA
[2] CUNY Queens Coll, Dept Biol, New York, NY USA
基金
美国国家科学基金会;
关键词
Bio-organic; conjugates; drug release; nanoscale; peptide; self-assembly; targeting; TARGETED DRUG-DELIVERY; IN-VITRO; BIOLOGICAL EVALUATION; CIRCULAR-DICHROISM; POLYMERIC MICELLES; TOPOTECAN; MIGRATION; ISOXAZOLE; APOPTOSIS; VIVO;
D O I
10.1080/00914037.2018.1525542
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A new self-assembled microscale biomaterial was developed by conjugating carboxyl functionalized phenylisoxazole with spermidine and attachment of the peptide sequence WSGPGVWGASVK (WSG). The chemotherapeutic drug topotecan was then entrapped into the assemblies. Release studies showed an initial burst release followed by a steady release. Furthermore the drug entrapped assemblies were potent against cell proliferation, mitigated cell migration and induced the loss of lamellopodia in breast MDA-MB-231 tumor cells and ovarian SK-OV-3. Higher efficacy was observed for MDA-MB-231 cells. Thus, a new phenylisoxazole-sperimidyl amide-WSG nanovehicle was developed for targeting MDA-MB-231 and SK-OV-3 cancer cells. [GRAPHICS] .
引用
收藏
页码:978 / 992
页数:15
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