TY - JOUR
T1 - Tumor delivery of Photofrin® by PLL-g-PEG for photodynamic therapy
AU - Kano, Arihiro
AU - Taniwaki, Yuki
AU - Nakamura, Izumi
AU - Shimada, Naohiko
AU - Moriyama, Kenji
AU - Maruyama, Atsushi
N1 - Funding Information:
We would like to gratefully acknowledge the Grant-in-Aid for Scientific Research (nos. 20500410 , 24510300 , and 23240074 ) from the Japan Society for the Promotion of Science (JSPS) , and Project of Integrated Research on Chemical Synthesis , and Innovative area “Nanomedicine Molecular Science (No. 2306)” from the Ministry of Education, Culture, Science, Sports and Technology of Japan (MEXT) for support of this research.
PY - 2013/5/10
Y1 - 2013/5/10
N2 - Photofrin® (porfimer sodium) is a photosensitive reagent used for photodynamic therapy (PDT) of tumors and dysplasias. Because only photo-irradiated sites are damaged, PDT is less invasive than systemic treatments. However, a photosensitive reaction is a major side effect of systemically delivered Photofrin. To enhance localization of Photofrin to tumors, we have formulated Photofrin with the tumor-localizing graft copolymer poly(ethylene glycol)-grafted poly(l-lysine), PLL-g-PEG. We demonstrate that Photofrin preferentially interacts with PLL-g-PEG through both ionic and hydrophobic interactions. The serum competitive study showed that the highly PEG-grafted PLL is better for preventing serum binding to the Photofrin/PLL-g-PEG complex. In tumor-bearing mice, formulation of Photofrin with PLL-g-PEG enhanced tumor localization of Photofrin as twice as Photofrin alone and concomitantly suppressed the photosensitivity reaction drastically.
AB - Photofrin® (porfimer sodium) is a photosensitive reagent used for photodynamic therapy (PDT) of tumors and dysplasias. Because only photo-irradiated sites are damaged, PDT is less invasive than systemic treatments. However, a photosensitive reaction is a major side effect of systemically delivered Photofrin. To enhance localization of Photofrin to tumors, we have formulated Photofrin with the tumor-localizing graft copolymer poly(ethylene glycol)-grafted poly(l-lysine), PLL-g-PEG. We demonstrate that Photofrin preferentially interacts with PLL-g-PEG through both ionic and hydrophobic interactions. The serum competitive study showed that the highly PEG-grafted PLL is better for preventing serum binding to the Photofrin/PLL-g-PEG complex. In tumor-bearing mice, formulation of Photofrin with PLL-g-PEG enhanced tumor localization of Photofrin as twice as Photofrin alone and concomitantly suppressed the photosensitivity reaction drastically.
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U2 - 10.1016/j.jconrel.2013.02.016
DO - 10.1016/j.jconrel.2013.02.016
M3 - Article
C2 - 23454112
AN - SCOPUS:84875043582
SN - 0168-3659
VL - 167
SP - 315
EP - 321
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 3
ER -