肿瘤微环境
化学
药理学
阿霉素
碳酸氢钠
全身给药
癌症研究
口服
碳酸氢盐
血管生成
弱碱
盐酸阿霉素
医学
体内
化疗
肿瘤细胞
内科学
生物
有机化学
生物技术
物理化学
作者
Hidenori Ando,Ai Ikeda,Maho Tagami,Nana Cristina Amorim Matsuo,Taro Shimizu,Yu Ishima,Kiyoshi Eshima,Tatsuhiro Ishida
标识
DOI:10.1016/j.jconrel.2022.08.031
摘要
The pH of the tumor microenvironment in solid tumors is reported to be more acidic than that of normal tissues. The pH is controlled by over-expression of several transporters that are associated with the progression, angiogenesis, and metastasis of solid tumors. Antitumor effects of weak-base anticancer agents, such as doxorubicin (DXR), could be reduced in an acidic environment because of increases in the ionized form of the drug under these conditions, reducing its membrane penetrability. In our previous studies, we demonstrated that oral administration of sodium bicarbonate (NaHCO3) can neutralize the acidic tumor microenvironment and enhance the effects of small molecule anticancer drugs. However, it is not known whether or not increasing the tumor pH by oral administration of NaHCO3 leads to enhanced antitumor effects of lipidic nanoparticle formulations of weak-base anticancer drugs, such as Doxil®. In this study, we investigated the antitumor efficacy of Doxil® in combination with oral administration of NaHCO3 in a Colon26 tumor-bearing mouse model. NaHCO3 clearly enhanced the tumor-growth inhibitory effect of Doxil® without exacerbating any systemic side effects. In vitro studies indicated that high levels of DXR were internalized into cells at neutral pH. These studies demonstrate that the neutralization of acidic tumor microenvironment by an oral administration of NaHCO3 could be a promising approach to enhance the therapeutic outcomes of Doxil®.
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