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Evaluation of the Key Advantages Between Two Modalities of Boronophenylalanine Administration for Clinical Boron Neutron Capture Therapy Using an Animal Model

Overview
Journal Cells
Publisher MDPI
Date 2022 Sep 9
PMID 36078143
Authors
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Abstract

In clinical boron neutron capture therapy (BNCT), boronophenylalanine (BPA) administrations through one-step infusion (OSI) and two-step infusion (TSI) are the most widely used. This study compared the advantages of OSI and TSI using a human oral squamous cell carcinoma-bearing animal model. OSI was administered at a high-dose rate of 20 mg/kg/min for 20 min (total dose: 400 mg/kg) as the first step infusion. TSI was a prolonged infusion at a low-dose rate of 1.67 mg/kg/min for 15, 30, 45, and 60 min (total dose: 25, 50, 75, and 100 mg/kg) following the first step infusion. The sigmoid model was used to evaluate the boron accumulation effect in the tumor. The advantages of TSI were observed to be greater than those of OSI. The observed advantages of TSI were as follows: a stable level of boron concentration in blood; tumor to blood boron ratio (T/B); tumor to muscle boron ratio (T/M); and skin to blood boron ratio (S/B). The boron accumulation effect in tumors increased to 68.98%. Thus, effective boron concentration in these tumor cells was achieved to enhance the lethal damage in BNCT treatment. Boron concentration in the blood was equal to that in the skin. Therefore, the equivalent dose was accurately estimated for the skin.

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PMID: 37759639 PMC: 10525593. DOI: 10.3390/biology12091240.


Boron Delivery to Brain Cells via Cerebrospinal Fluid (CSF) Circulation in BNCT of Brain-Tumor-Model Rats-Ex Vivo Imaging of BPA Using MALDI Mass Spectrometry Imaging.

Kusaka S, Miyake Y, Tokumaru Y, Morizane Y, Tamaki S, Akiyama Y Life (Basel). 2022; 12(11).

PMID: 36362940 PMC: 9695333. DOI: 10.3390/life12111786.

References
1.
Detta A, Cruickshank G . L-amino acid transporter-1 and boronophenylalanine-based boron neutron capture therapy of human brain tumors. Cancer Res. 2009; 69(5):2126-32. DOI: 10.1158/0008-5472.CAN-08-2345. View

2.
Wada Y, Hirose K, Harada T, Sato M, Watanabe T, Anbai A . Impact of oxygen status on 10B-BPA uptake into human glioblastoma cells, referring to significance in boron neutron capture therapy. J Radiat Res. 2018; 59(2):122-128. PMC: 5950927. DOI: 10.1093/jrr/rrx080. View

3.
Mager D, Wyska E, Jusko W . Diversity of mechanism-based pharmacodynamic models. Drug Metab Dispos. 2003; 31(5):510-8. DOI: 10.1124/dmd.31.5.510. View

4.
Ryynanen P, Kortesniemi M, Coderre J, Diaz A, Hiismaki P, Savolainen S . Models for estimation of the (10)B concentration after BPA-fructose complex infusion in patients during epithermal neutron irradiation in BNCT. Int J Radiat Oncol Biol Phys. 2000; 48(4):1145-54. DOI: 10.1016/s0360-3016(00)00766-5. View

5.
Levy G . Kinetics of pharmacologic effects. Clin Pharmacol Ther. 1966; 7(3):362-72. DOI: 10.1002/cpt196673362. View