Pharmacodynamics of Co-Administration of Uracil and 1-(2-Tetrahydrofuryl)-5-Fluorouracil (FT-207) for Malignant Brain Tumors

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Title ( eng )
Pharmacodynamics of Co-Administration of Uracil and 1-(2-Tetrahydrofuryl)-5-Fluorouracil (FT-207) for Malignant Brain Tumors
Title ( jpn )
悪性脳腫瘍における UFT の pharmacodynamics
Creator
Harada Kiyoshi
Okamoto Hirofumi
Fujioka Yoshimi
Kiya Katsuzo
Uozumi Tohru
Source Title
Hiroshima Journal of Medical Sciences
Volume 32
Issue 4
Start Page 443
End Page 449
Journal Identifire
[PISSN] 0018-2052
[EISSN] 2433-7668
[NCID] AA00664312
Abstract
UFT, a mixture of FT-207 and uracil in a molar ratio 1 : 4, has been noticed to have the higher antitumor activity to various tumors other than FT-207. We studied the pharmacodynamics of UFT (900 mg for FT-207) after oral administration on 3 cases of malignant glioma and 4 cases of metastatic brain tumor by using high performance liquid chromatography, and the following results obtained;

1. Most of unchanged FT-207, 5-FU and uracil were excreted in the urine within 24 hours.

2. The t1/2 of α-phase of FT-207 was 4.59 hours and that of β-phase was 9.99 hours. The t1/2 ofα-phase of 5-FT was 0.75 hours, and that ofβ-phase was 11.04 hours. The AUC of 5-FU was 12.434 µg· hrs/ml. This drug was found to stay in the plasma over a long period, followed by a slow elimination. In CSF, the higher concentration of 5-FU stayed over a longer period.

3. The concentration of FT-207 in the brain tumor tissues was 17.11 µg/g on the average in malignant glioma and 17.61 µg/g on the average in metastatic brain tumor. The concentration of 5-FU was 0.02 µg/g on the average in the former, and 0.47 µg/g on the average in the latter, which indicating an efficient transfer to the tissues of metastatic brain tumor. The concentration of FT-207 and 5-FU in the brain tissues adjacent to the tumor was approximately the same as that in the brain tumor tissues, indicating an effective transfer to the brain tissues adjacent to the tumor.

4. On the basis of the results of this study, uracil seems to inhibit the degradation of 5-FU in the liver and/or in the tumor tissues themselves, and to enhance the concentration of 5-FU in the brain tumor tissues and the brain tissues adjacent to the tumor. UFT would be useful as a chemotherapeutic agent agent for malignant brain tumors.
Keywords
Pharmacodynamics
Futrafur
Uracil
UFT
Brain tumor
NDC
Medical sciences [ 490 ]
Language
eng
Resource Type departmental bulletin paper
Publisher
Hiroshima University School of Medicine
Date of Issued 1983-12
Publish Type Version of Record
Access Rights open access
Source Identifier
[ISSN] 0018-2052
[NCID] AA00664312
[PMID] 6432742