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Treatment efficacy of low-dose 5-fluorouracil with ultrasound in mediating 5-fluorouracil-loaded microbubble cavitation in head and neck cancer.

Authors :
Liao, Ai-Ho
Lee, Yu-An
Lin, Dao-Lung
Chuang, Ho-Chiao
Wang, Jehng-Kang
Chang, Ching-En
Li, Hsiang-Tzu
Wu, Ting-Yi
Shih, Cheng-Ping
Wang, Chih-Hung
Chu, Yueng-Hsiang
Source :
Drug Delivery; Dec2023, Vol. 30 Issue 1, p1-13, 13p
Publication Year :
2023

Abstract

Over the past 50 years, 5-fluorouracil (5-FU) has played a critical role in the systemic chemotherapy of cancer patients. Bolus intravenous (IV) 5-FU infusion has been used due to the limitation of its extremely short half-life (10–15 min). This study used ultrasound (US) mediating 5-FU-loaded microbubbles (MBs) cavitation as a tool to increase local intratumoral 5-FU levels with a reduced dose of 5-FU (a single IV injection of 2.5 mg/kg instead of a single intraperitoneal injection of 25–200 mg/kg as used in previous studies in mice). The 5-FU-MBs were prepared with a 132 mg/mL albumin solution and a 0.30 mg/mL 5-FU solution. The diameters of the MBs and 5-FU-MBs were 1.24 ± 0.85 and 2.00 ± 0.53 µm (mean ± SEM), respectively, and the maximum loading efficiency of 5-FU on MBs was 19.04 ± 0.25%. In the in vitro study, the cell viabilities of 5-FU and 5-FU-MBs did not differ significantly, but compared with the 5-FU-MBs treatment-alone group, cell toxicity increased to 31% in the 5-FU-MBs + US group (p < 0.001). The biodistribution results indicated that the 5-FU levels of the tumors in small animals were significant higher for the 5-FU-MBs + US treatment than for either the 5-FU-MBs or 5-FU treatment with low 5-FU systemic treatment doses (2.5 mg/kg 5-FU IV). In small-animal treatment, 2.5 mg/kg 5-FU therapeutic IV doses injected into mice caused a more-significant reduction in tumor growth in the 5-FU-MBs + US group (65.9%) than in the control group after 34 days of treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10717544
Volume :
30
Issue :
1
Database :
Complementary Index
Journal :
Drug Delivery
Publication Type :
Academic Journal
Accession number :
174236344
Full Text :
https://doi.org/10.1080/10717544.2022.2154410