Bio/Nano Technology Laboratory, Institute for Nanoscience & Engineering, University of Arkansas, Fayetteville, AR, USA.
Nanoscale. 2016 Jul 7;8(25):12658-67. doi: 10.1039/c5nr08686h. Epub 2016 Mar 3.
Cancer nanomedicines are opening new paradigms in cancer management and recent research points to how they can vastly improve imaging and therapy through multimodality and multifunctionality. However, challenges to achieving optimal efficacy are manifold starting from processing materials and evaluating their intended effectiveness on biological tissue, to developing new strategies aimed at improving transport of these materials through the biological milieu to the target tissue. Here, we report a fluorescent derivative of a beta-lactam antibiotic, ampicillin (termed iAmp) and its multifunctional physicobiochemical characteristics and potential as a biocompatible shielding agent and an effective dispersant. Carbon nanotubes (CNTs) were chosen to demonstrate the efficacy of iAmp. CNTs are known for their versatility and have been used extensively for cancer theranostics as photothermal and photoacoustic agents, but have limited solubility in water and biocompatibility. Traditional dispersants are associated with imaging artifacts and are not fully biocompatible. The chemical structure of iAmp is consistent with a deamination product of ampicillin. Although the four-membered lactam ring is intact, it does not retain the antibiotic properties. The iAmp is an effective dispersant and simultaneously serves as a fluorescent label for single-walled CNTs (SWNTs) with minimal photobleaching. The iAmp also enables bioconjugation of SWNTs to bio-ligands such as antibodies through functional carboxyl groups. Viability tests show that iAmp-coated SWNTs have minimal toxicity. Bio-stability tests under physiological conditions reveal that iAmp coating not only remains stable in a biologically relevant environment with high protein and salt concentrations, but also renders SWNTs transparent against nonspecific protein adsorption, also known as protein corona. Mammalian tissue culture studies with macrophages and opsonins validate that iAmp coating affords immunological resistance to SWNTs. Furthermore, iAmp coating offers protection to SWNTs against their nonspecific adsorption across disparate cell types, which has precluded a targeted strategy, and enables selective molecular targeting. The iAmp can therefore be used as an efficient dispersant, a photostable fluorescent agent, and a biocompatible disguising agent, alleviating CNTs' drawbacks and rendering them suitable for nanotheranostic and drug delivery applications.
癌症纳米医学在癌症治疗方面开辟了新的范例,最近的研究表明,通过多模态和多功能性,它们可以极大地改善成像和治疗效果。然而,从处理材料和评估其对生物组织的预期效果开始,到开发旨在改善这些材料通过生物环境向靶组织运输的新策略,实现最佳疗效存在多种挑战。在这里,我们报告了一种β-内酰胺抗生素氨苄西林的荧光衍生物(称为 iAmp)及其多功能物理化学特性和作为生物相容的屏蔽剂和有效分散剂的潜力。选择碳纳米管 (CNT) 来证明 iAmp 的功效。碳纳米管以其多功能性而闻名,并已被广泛用于癌症治疗学,作为光热和光声剂,但在水中的溶解度有限,生物相容性有限。传统的分散剂与成像伪影有关,并且不完全生物相容。iAmp 的化学结构与氨苄西林的脱氨产物一致。尽管四元内酰胺环完整,但它不保留抗生素特性。iAmp 是一种有效的分散剂,同时也是单壁碳纳米管 (SWNTs) 的荧光标记物,几乎没有光漂白。iAmp 还使 SWNTs 能够通过功能羧基与生物配体(如抗体)进行生物偶联。细胞活力测试表明,iAmp 涂层的 SWNTs 毒性最小。生理条件下的生物稳定性测试表明,iAmp 涂层不仅在高蛋白质和盐浓度的生物相关环境中保持稳定,而且还使 SWNTs 对非特异性蛋白质吸附(也称为蛋白质冠)透明。巨噬细胞和调理素的哺乳动物组织培养研究验证了 iAmp 涂层使 SWNTs 具有免疫抗性。此外,iAmp 涂层可以保护 SWNTs 免受其在不同细胞类型中的非特异性吸附,这阻止了靶向策略的实施,并实现了选择性分子靶向。因此,iAmp 可用作高效分散剂、光稳定荧光剂和生物相容的伪装剂,减轻 CNT 的缺点,使其适用于纳米治疗和药物输送应用。