TY - JOUR
T1 - Enhancement of in vivo anticancer effects of cisplatin by incorporation inside single-wall carbon nanohorns
AU - Ajima, Kumiko
AU - Murakami, Tatsuya
AU - Mizoguchi, Yoshikazu
AU - Tsuchida, Kunihiro
AU - Ichihashi, Toshinari
AU - Iijima, Sumio
AU - Yudasaka, Masako
PY - 2008/10
Y1 - 2008/10
N2 - Cisplatin (CDDP) was incorporated inside single-wall carbon nanohoms with holes opened (SWNHox) by a nanoprecipitation method that involved dispersion of CDDP and SWNHox in a solvent followed by the solvent evaporation. The incorporated CDDP quantity increased from the previously reported value of 15 to 46%, and the total released quantity of CDDP also increased from 60 to 100% by changing the solvent from dimethylformamide to water. Concurrently, in vitro anticancer efficiency of CDDPΣWNHox increased to 4-6 times greater than that of the intact CDDP. In vivo, CDDPΣWNHox intratumorally injected to transplanted tumors of mice suppressed the tumor growth more than the intact CDDP. We observed that CDDPΣWRHox adhered to the cell surfaces in vitro and stayed within the tumor tissues in vivo. Therefore, we think that the CDDP released from SWNHox realized high concentrations locally at the cells in vitro and in the tissues in vivo and could efficiently attack the tumor cells. We also found that SWNHox itself had an in vivo anticancer effect, which might increase the anticancer activities of CDDPΣWNHox.
AB - Cisplatin (CDDP) was incorporated inside single-wall carbon nanohoms with holes opened (SWNHox) by a nanoprecipitation method that involved dispersion of CDDP and SWNHox in a solvent followed by the solvent evaporation. The incorporated CDDP quantity increased from the previously reported value of 15 to 46%, and the total released quantity of CDDP also increased from 60 to 100% by changing the solvent from dimethylformamide to water. Concurrently, in vitro anticancer efficiency of CDDPΣWNHox increased to 4-6 times greater than that of the intact CDDP. In vivo, CDDPΣWNHox intratumorally injected to transplanted tumors of mice suppressed the tumor growth more than the intact CDDP. We observed that CDDPΣWRHox adhered to the cell surfaces in vitro and stayed within the tumor tissues in vivo. Therefore, we think that the CDDP released from SWNHox realized high concentrations locally at the cells in vitro and in the tissues in vivo and could efficiently attack the tumor cells. We also found that SWNHox itself had an in vivo anticancer effect, which might increase the anticancer activities of CDDPΣWNHox.
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U2 - 10.1021/nn800395t
DO - 10.1021/nn800395t
M3 - Article
C2 - 19206452
AN - SCOPUS:56849132060
SN - 1936-0851
VL - 2
SP - 2057
EP - 2064
JO - ACS Nano
JF - ACS Nano
IS - 10
ER -