Tyagi Tushar, Solanki Raghu, Patel Sunita, Maity Prasenjit
School of Engineering and Technology, National Forensic Sciences University, Gandhinagar, 382007, India.
School of Life Sciences, Central University of Gujarat, Gandhinagar, 382030, India.
Med Oncol. 2025 Jun 13;42(7):258. doi: 10.1007/s12032-025-02810-5.
The development of effective drug delivery strategy by employing novel nano-careers are advantageous for targeted and controlled drug release. The present work describes about such a strategy in the form of a protein stabilized ultrasmall gold nanocluster as nano-career for the delivery of anticancer drug Gemcitabine (Gem). Gold nanocluster (AuNCs) stabilized by bovine serum albumin (BSA) was synthesized and characterized in detail including its stability, size distribution, toxicity, and photo-physical properties. It was revealed that monodispersed gold particles (~ 1.5 nm) dispersible in aqueous phase with unique optical absorption and emission characteristics (λabs = 450 nm, λemi = 650 nm), high stability and minimum toxicity was obtained. Afterward, an anticancer drug (Gem) was conjugated with the gold cluster through simple chemical mixing resulting in the formation of 55% drug load Au nanocluster (Gem-AuNCs-BSA). The resultant Gem-AuNCs-BSA showed enhanced delivery of drug and therapeutic effects for the treatment of breast cancer and lung cancer with better efficacy than free Gemcitabine.
通过采用新型纳米载体开发有效的药物递送策略,有利于实现靶向和可控药物释放。本研究以蛋白质稳定的超小金纳米簇作为纳米载体,描述了一种用于递送抗癌药物吉西他滨(Gem)的策略。合成了由牛血清白蛋白(BSA)稳定的金纳米簇(AuNCs),并对其稳定性、尺寸分布、毒性和光物理性质进行了详细表征。结果表明,获得了可分散在水相中的单分散金颗粒(约1.5纳米),具有独特的光吸收和发射特性(λabs = 450纳米,λemi = 650纳米)、高稳定性和最低毒性。随后,通过简单的化学混合将抗癌药物(Gem)与金簇偶联,形成了载药量为55%的金纳米簇(Gem-AuNCs-BSA)。所得的Gem-AuNCs-BSA在治疗乳腺癌和肺癌方面显示出增强的药物递送和治疗效果,疗效优于游离吉西他滨。