荧光
分子成像
荧光寿命成像显微镜
纳米技术
生命科学中的荧光
化学
材料科学
激光诱导荧光
生物
物理
光学
生物技术
体内
作者
Nkune Williams Nkune,Kave Moloudi,Blassan P. George,Heidi Abrahamse
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:15 (28): 22267-22284
被引量:17
摘要
Fluorescence molecular imaging (FMI) is a powerful imaging technique used primarily in biomedical research and clinical applications to visualize molecular and cellular processes of tumors and other diseases. FMI involves the use of fluorescent molecules (fluorophores) that absorb light at one wavelength and emit it at a longer wavelength. These fluorophores can be attached to specific molecules and markers (such as proteins, nucleic acids, or small molecules) in a biological sample. FMI typically offers non-radioactive and safe, real-time and higher spatial resolution compared to positron emission tomography (PET) for superficial tumors. Additionally, sensitivity and specificity of FMI for superficial tumors in better than PET is some cases. However, FMI and the materials used in molecular imaging (MI) have revolutionized biomedical research, diagnostics, and therapeutic monitoring. In contrast, despite their significant contributions, several challenges remain to be solved to improve the effective application of fluorescence-based techniques. These challenges are related to poor tissue penetration depth, background autofluorescence, photobleaching of fluorophores, low signal-to-noise ratio in deep tissues and the necessity for biocompatible and photostable probes. Hence, ongoing improvements in probe development, imaging technologies and analytical methods are required to overcome current challenges. Future advancements in fluorescence materials and imaging techniques hold promise for making MI more accurate, efficient and applicable for clinical and research scenarios. This review gives an overview of recent advances in the materials used in MI and findings of FMI. Finally, limitations of FMI are highlighted and recommendations for future research directions are proposed.
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