Francisco Telmo N, Malafaia Daniela, Melo Lúcia, Silva Artur M S, Albuquerque Hélio M T
LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal.
ACS Omega. 2024 Mar 11;9(12):13556-13591. doi: 10.1021/acsomega.3c10417. eCollection 2024 Mar 26.
Alzheimer's disease (AD) is the most common form of neurodegenerative dementia that is rapidly becoming a major health problem, especially in developed countries because of their increasing life expectancy. Two main problems are often associated with the disease: (i) the absence of a widely accessible "gold-standard" for early diagnosis and (ii) lack of effective therapies with disease-modifying effects. The recent success of the monoclonal antibody lecanemab played an important role not only in clarifying a possible druggable pathway but also in spelling the revival of small molecule drug discovery. Unlike bulky biologics, small molecules are structurally less complex, generally cheaper, and compatible with at-home oral consumption, making it feasible for people to start their drug regimen early and stay on it longer. In this sense, small-molecule near-infrared fluorescent theranostics have been gaining more and more attention from the scientific community, as they have the potential to simultaneously provide diagnostic outputs and deliver therapeutic action, paving the way toward personalized medicine in AD patients. They also have the potential to shift the diagnostic "status-quo" from expensive and limited-access PET radiotracers toward inexpensive and handy imaging tools widely available for primary patient screening and preclinical animal studies. Herein, we review the most recent advances in the field of fluorescent theranostics for Alzheimer's disease, detailing their design strategies, synthetic approaches and imaging and therapeutic properties and . With this Review, we intend to provide a milestone in the acquired knowledge in the field of AD theranostics, encouraging the future development of properly designed theranostic compounds with improved chances to reach clinical applications.
阿尔茨海默病(AD)是神经退行性痴呆最常见的形式,由于发达国家预期寿命的增加,它正迅速成为一个主要的健康问题。该疾病通常与两个主要问题相关:(i)缺乏广泛可用的早期诊断“金标准”;(ii)缺乏具有疾病修饰作用的有效疗法。单克隆抗体lecanemab最近的成功不仅在阐明一条可能的可药物化途径方面发挥了重要作用,而且在预示小分子药物发现的复兴方面也发挥了重要作用。与庞大的生物制剂不同,小分子结构上不太复杂,通常更便宜,并且适合在家口服,这使得人们能够尽早开始药物治疗并坚持更长时间。从这个意义上说,小分子近红外荧光诊疗试剂越来越受到科学界的关注,因为它们有可能同时提供诊断结果并发挥治疗作用,为AD患者的个性化医疗铺平道路。它们还有可能将诊断的“现状”从昂贵且获取受限的PET放射性示踪剂转变为广泛用于初级患者筛查和临床前动物研究的廉价且便捷的成像工具。在此,我们综述了阿尔茨海默病荧光诊疗领域的最新进展,详细介绍了它们的设计策略、合成方法以及成像和治疗特性。通过本综述,我们旨在为AD诊疗领域已获得的知识提供一个里程碑,鼓励未来开发设计合理的诊疗化合物,提高其进入临床应用的机会。