Abstract：
:Arginine-glycine-aspartate (RGD) has been shown to be essential for the recognition of integrins overexpressed in tumor cells, especially during tumor invasion, angiogenesis, and metasis. In this study, a novel tetrapeptide, RGD-valine (RGDV), was designed and attached to the N position of 1-β-D-arabinofuranosylcytosine (Ara-C) at the valine end, as a homing device for the delivery of Ara-C to tumor cells. Furthermore, fatty acids of various chain lengths (C(n)H(2n+1)COOH, n = 7, 9, 11, 13, and 15) were attached to the arginine end of RGDV to form a series of C(n)H(2n+1)CO-RGDV-Ara-C compounds. The structures of C(n)H(2n+1)CO-RGDV-Ara-C compounds were confirmed using mass spectrometry and nuclear magnetic resonance. The liposomal preparations of the synthesized C(n)H(2n+1)CO-RGDV-Ara-C compounds were obtained using the film dispersion method in the presence of phospholipids. The particle size, zeta potential, and dispersity index of the liposomes formed were found to be approximately 215 nm (diameter), approximately -30 mV, and <0.3, respectively. The antitumor activity of the liposomal preparations containing the respective C(n)H(2n+1)CO-RGDV-Ara-C compounds was evaluated in mice inoculated with sarcoma S(180). Liposomal Ara-C preparation, liposomal C(11)H(23)CO-V-Ara-C preparation, Ara-C, and C(11)H(23)CO-V-Ara-C sodium carboxymethyl cellulose (CMC-Na) suspensions were used as controls. C(n)H(2n+1)CO-RGDV-Ara-C containing liposomal preparations were shown with an enhanced antitumor activity, likely because of the targeting effect of RGDV.
journal_name
J Pharm Scijournal_title
Journal of pharmaceutical sciencesauthors
Wang F,Cui C,Ren Z,Wang L,Liu H,Cui Gdoi
10.1002/jps.23326subject
Has Abstractpub_date
2012-12-01 00:00:00pages
4559-68issue
12eissn
0022-3549issn
1520-6017pii
S0022-3549(15)31313-7journal_volume
101pub_type
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