TY - JOUR
T1 - Transcatheter hepatic arterial chemoembolization using epirubicin-lipiodol
T2 - experimental and pharmacological evaluation
AU - Kobayashi, Seiji
AU - Narimatsu, Yoshiaki
AU - Ogawa, Kenji
AU - Hashimoto, Subaru
AU - Nakatsuka, Seishi
AU - Miura, Hiroshi
AU - Ohzono, Hirokuni
AU - Ka, Wei Jei
AU - Ido, Kunio
AU - Hiramatsu, Kyoichi
AU - Tsuzuki, Toshiharu
AU - Tsuchiya, Masaharu
PY - 1992/1
Y1 - 1992/1
N2 - The experimental and pharmacological characteristics of various formulations of an anticancer agent (epirubicin, EPI) and lipiodol were evaluated in vitro and in vivo. Three forms of EPI-lipiodol, i.e., an oil-in-water type of emulsion (O/W type), a water-in-oil type of emulsion (W/O type), and a suspension (S type), were prepared and investigated for their stability. An O/W-type emulsion using a stock solution of Iopamidol as the solvent for EPI was the most stable form in the stationary state in vitro. In 16 patients with malignant liver tumors (14 hepatocellular carcinomas and 2 liver metastases), the three forms of EPI-lipiodol were injected into the proper hepatic artery. The plasma EPI level was monitored periodically and analyzed pharmacokinetically. No significant difference in the pharmacokinetics of EPI was detected among the O/W, W/O, and S types.
AB - The experimental and pharmacological characteristics of various formulations of an anticancer agent (epirubicin, EPI) and lipiodol were evaluated in vitro and in vivo. Three forms of EPI-lipiodol, i.e., an oil-in-water type of emulsion (O/W type), a water-in-oil type of emulsion (W/O type), and a suspension (S type), were prepared and investigated for their stability. An O/W-type emulsion using a stock solution of Iopamidol as the solvent for EPI was the most stable form in the stationary state in vitro. In 16 patients with malignant liver tumors (14 hepatocellular carcinomas and 2 liver metastases), the three forms of EPI-lipiodol were injected into the proper hepatic artery. The plasma EPI level was monitored periodically and analyzed pharmacokinetically. No significant difference in the pharmacokinetics of EPI was detected among the O/W, W/O, and S types.
UR - http://www.scopus.com/inward/record.url?scp=0026564495&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026564495&partnerID=8YFLogxK
U2 - 10.1007/BF00687104
DO - 10.1007/BF00687104
M3 - Article
C2 - 1333908
AN - SCOPUS:0026564495
SN - 0344-5704
VL - 31
SP - S45-S50
JO - Cancer Chemotherapy and Pharmacology
JF - Cancer Chemotherapy and Pharmacology
IS - 1 Supplement
ER -