TY - JOUR
T1 - Stable paclitaxel formulations in oily contrast medium
AU - Lee, In Hyun
AU - Park, Yeong Taek
AU - Roh, Kyungho
AU - Chung, Hesson
AU - Kwon, Ick Chan
AU - Jeong, Seo Young
N1 - Funding Information:
This study was supported by a grant 02-PJ10-PG4-PT02-0044 of the Korea Health 21 R&D Project, Ministry of Health and Welfare, Republic of Korea.
Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2005/2/2
Y1 - 2005/2/2
N2 - Stable paclitaxel/Lipiodol solutions as well as emulsions were developed for the treatment of solid tumors including hepatocellular carcinoma. Paclitaxel could be dissolved in Lipiodol, an oily contrast medium, but precipitated out and formed aggregates with time. Paclitaxel precipitation was due to the inter- and intra-molecular hydrogen bonding of paclitaxel molecules. Time-dependent paclitaxel aggregation was completely prevented by adding small amounts of additional solvents, which are miscible with Lipiodol. It was also notable that paclitaxel helped in stabilizing the water-in-oil (w/o) type emulsion of Lipiodol and Iopamiro. The stability, physical properties and in vitro drug release profiles of the stable paclitaxel solutions and emulsions were characterized. When the stable oily paclitaxel solution was used for the treatment of B16F10 melanoma in C57BL/6 mice, the malignant cells were eradicated completely in 2 weeks, whereas the solid tumor grew rapidly and metastasized to the thigh and to other organs in the control group. Also, the mice survived for more than 1 year after the paclitaxel treatment, whereas all of those in the control group died in 40 days.
AB - Stable paclitaxel/Lipiodol solutions as well as emulsions were developed for the treatment of solid tumors including hepatocellular carcinoma. Paclitaxel could be dissolved in Lipiodol, an oily contrast medium, but precipitated out and formed aggregates with time. Paclitaxel precipitation was due to the inter- and intra-molecular hydrogen bonding of paclitaxel molecules. Time-dependent paclitaxel aggregation was completely prevented by adding small amounts of additional solvents, which are miscible with Lipiodol. It was also notable that paclitaxel helped in stabilizing the water-in-oil (w/o) type emulsion of Lipiodol and Iopamiro. The stability, physical properties and in vitro drug release profiles of the stable paclitaxel solutions and emulsions were characterized. When the stable oily paclitaxel solution was used for the treatment of B16F10 melanoma in C57BL/6 mice, the malignant cells were eradicated completely in 2 weeks, whereas the solid tumor grew rapidly and metastasized to the thigh and to other organs in the control group. Also, the mice survived for more than 1 year after the paclitaxel treatment, whereas all of those in the control group died in 40 days.
KW - Cancer
KW - Emulsion
KW - Lipiodol
KW - Oily contrast medium
KW - Paclitaxel
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U2 - 10.1016/j.jconrel.2004.10.023
DO - 10.1016/j.jconrel.2004.10.023
M3 - Article
C2 - 15653161
AN - SCOPUS:11844255661
SN - 0168-3659
VL - 102
SP - 415
EP - 425
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 2
ER -