| Literature DB >> 27845234 |
Xin Jin1, Mengying Li2, Lifang Yin2, Jianping Zhou2, Zhenhai Zhang3, Huixia Lv4.
Abstract
Tyroservatide (YSV) is a tripeptide that has been approved for clinical testing, as a new anticancer drug. In the current study, YSV-stearic acid (YSV-SA) was inserted into the surface of d-alpha-tocopheryl polyethylene glycol 1000 succinate monoester (TPGS)-modified paclitaxel (PTX) liposomes (TP-Lip) to form YSV-conjugated TP-Lip (TYP-Lip). Both in vivo imaging and in vitro cell uptake analysis indicated that these modifications could increase tumor-targeting and cell uptake of the liposomes. Optimal antitumor effects were achieved via tail vein injections of TYP-Lip in MB-231 tumor-bearing nude mice. Overall, the formed TYP-Lip not only achieved a synergistic anticancer effect through YSV and PTX, but also improved tumor-targeting and exhibited further antitumor capabilities. These results indicated that combining biological (YSV) and chemotherapeutic (PTX) agents is an efficient combinatorial delivery strategy for enhanced tumor targeting and synergistic antitumor effects.Entities:
Keywords: Co-delivery; Paclitaxel; Synergy effect; Tumor targeting; Tyroservatide
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Year: 2016 PMID: 27845234 DOI: 10.1016/j.nano.2016.10.017
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307