Guangxi Key Laboratory of Bioactive Molecules Research and Evaluation, Pharmaceutical College, Guangxi Medical University, 22 Shuangyong Road, Nanning 530021, P. R. China.
Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Guangxi Medical University, 22 Shuangyong Road, Nanning 530021, P. R. China.
ACS Appl Mater Interfaces. 2024 Oct 30;16(43):58489-58505. doi: 10.1021/acsami.4c15320. Epub 2024 Oct 16.
Berberine (BB) has demonstrated significant inhibitory effects on tumorigenesis and progression. However, its clinical application is hindered by challenges such as low bioavailability due to limited cell membrane permeability, nontargeted accumulation away from solid tumors, and increased toxicity associated with intravenous administration. To overcome these challenges, a lipophilic salt-forming strategy was employed to enhance lipophilicity, thereby promoting membrane permeability and targetability for tumor accumulation while simultaneously mitigating the toxicity associated with intravenous injection. findings revealed an almost 10-fold increase in fluorescence intensity with BB-GA NDs compared to BB alone. Furthermore, selective cytotoxicity against tumor cells exhibited a 4-fold elevation compared to normal cells. results underscored the remarkable tumor-selective accumulation of BB-GA NDs, effectively mitigating the intravenous injection toxicity associated with pure BB. The self-assembly of binary cooperative nanodrugs utilizing berberine glycyrrhetinic acid salts opens up innovative possibilities for drug delivery systems in traditional Chinese medicine.
小檗碱 (BB) 已被证明对肿瘤发生和进展具有显著的抑制作用。然而,由于细胞膜通透性有限,导致其生物利用度低,非靶向性地远离实体瘤积累,以及静脉给药相关的毒性增加,其临床应用受到阻碍。为了克服这些挑战,采用亲脂性盐形成策略来提高亲脂性,从而促进膜通透性和靶向性以实现肿瘤积累,同时减轻与静脉注射相关的毒性。研究结果显示,与单独使用 BB 相比,BB-GA NDs 的荧光强度几乎增加了 10 倍。此外,与正常细胞相比,对肿瘤细胞的选择性细胞毒性提高了 4 倍。这些结果强调了 BB-GA NDs 的显著肿瘤选择性积累,有效减轻了与纯 BB 相关的静脉注射毒性。利用小檗碱甘草次酸盐的二元协同纳米药物自组装为中药给药系统开辟了新的可能性。