标题:Redox-Sensitive Prodrug Molecules Meet Graphene Oxide: An Efficient Graphene Oxide-Based Nanovehicle toward Cancer Therapy
作者:Ma, Naxin; Song, Aixin; Li, Zhonghao; Luan, Yuxia
作者机构:[Ma, Naxin; Luan, Yuxia] Shandong Univ, Minist Educ, Key Lab Chem Biol, Sch Pharmaceut Sci, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China 更多
通讯作者:Luan, YX
通讯作者地址:[Luan, YX]Shandong Univ, Minist Educ, Key Lab Chem Biol, Sch Pharmaceut Sci, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China.
来源:ACS BIOMATERIALS SCIENCE & ENGINEERING
出版年:2019
卷:5
期:3
页码:1384-1391
DOI:10.1021/acsbiomaterials.9b00114
关键词:graphene oxide; redox-sensitive; prodrug; cancer therapy
摘要:The stability and slow and incomplete drug release are the key problems for graphene oxide nanocarrier systems. To solve the above problems, we constructed a new drug delivery system from the graphene oxide (GO) decorated with the redoxsensitive prodrug molecules for cancer therapy. PEG-PCL-SS-DOX (prodrug) was synthesized by linking the anticancer drug doxorubicin (DOX) to the biodegradable and biocompatible amphiphilic copolymers PEG-PCL via redox-sensitive disulfide bond. The GO/prodrug nanohybrids (GOPN) was prepared via the hydrophobic and rc rc interaction between the hydrophobic block of PCL-SS-DOX and the aromatic ring of GO. The redox-sensitive PEG-PCL-SS-DOX molecules integrate the anticancer drug and dispersant/stabilizing agent together into GO. In other words, prodrug molecules act as the dispersant/stabilizing agent and simultaneously provide the redox-sensitive property which ensures the effective release of the anticancer drug in tumor site demonstrated by the in vitro release results. The in vitro cell cytotoxicity showed that the GOPN could significantly enhance DOX accumulation in A549 and B16 cells and effectively enhance the anticancer activity. In vivo antitumor and histological examination results suggested that GOPN could reduce the DOX systemic toxicity with remarkable inhibition of tumor growth. The prepared GOPN could solve the incomplete and slow release problem of the previously reported GO-based drug delivery system, and resulting in the desirable anticancer effect of DOX. Therefore, the present constructed GOPN bring a new opportunity for effective cancer therapy.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061910963&doi=10.1021%2facsbiomaterials.9b00114&partnerID=40&md5=416cc924e991d81bcae41373d7a4715b
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