Chronological development of functional fluorophores for bio-imaging
文献情報
Subrata Munan, Young-Tae Chang, Animesh Samanta
Functional fluorophores represent an emerging research field, distinguished by their diverse applications, especially in sensing and cellular imaging. After the discovery of quinine sulfate and subsequent elucidation of the fluorescence mechanism by Sir George Stokes, research in the field of fluorescence gained momentum. Over the past few decades, advancements in sophisticated instruments, including super-resolution microscopy, have further promoted cellular imaging using traditional fluorophores. These advancements include deciphering sensing mechanisms via photochemical reactions and scrutinizing the applications of fluorescent probes that specifically target organelles. This approach elucidates molecular interactions with biomolecules. Despite the abundance of literature illustrating different classes of probe development, a concise summary of newly developed fluorophores remains inadequate. In this review, we systematically summarize the chronological discovery of traditional fluorophores along with new fluorophores. We briefly discuss traditional fluorophores ranging from visible to near-infrared (NIR) in the context of cellular imaging and in vivo imaging. Furthermore, we explore ten new core fluorophores developed between 2007 and 2022, which exhibit advanced optical properties, providing new insights into bioimaging. We illustrate the utilization of new fluorophores in cellular imaging of biomolecules, such as reactive oxygen species (ROS), reactive nitrogen species (RNS), and proteins and microenvironments, especially pH and viscosity. Few of the fluorescent probes provided new insights into disease progression. Furthermore, we speculate on the potential prospects and significant challenges of existing fluorophores and their potential biomedical research applications. By addressing these aspects, we intend to illuminate the compelling advancements in fluorescent probe development and their potential influence across various fields.
関連文献
Viscoelastic and thermoreversible networks crosslinked by non-covalent interactions between “clickable” nucleic acid oligomers and DNA
Alex J. Anderson, Heidi R. Culver
DOI: 10.1039/D0PY00165A
Controlling the crystal structure of precisely spaced polyethylene-like polyphosphoesters
Tobias Haider, Oksana Suraeva, Miriam L. O'Duill, Julian Mars, Markus Mezger, Ingo Lieberwirth, Frederik R. Wurm
DOI: 10.1039/D0PY00272K
Aromatic thioketone-mediated radical polymerization of methacrylates and the preparation of amphiphilic quasi-block copolymers
DOI: 10.1039/D0PY00322K
Silicone dielectric elastomers optimized by crosslinking pattern – a simple approach to high-performance actuators
Codrin Tugui, George T. Stiubianu, Maria Cazacu
DOI: 10.1039/D0PY00223B
Assembly of miscible supramolecular network blends using DDA·AAD hydrogen-bonding interactions of pendent side-chains
Heather M. Coubrough, Matthew Reynolds, James A. Goodchild, Simon D. A. Connell, Johan Mattsson
DOI: 10.1039/C9PY01913H
Fluorescent chemosensors based on conjugated polymers with N-heterocyclic moieties: two decades of progress
Wei Bai, Yinyin Bao
DOI: 10.1039/D0PY00336K
Metal-free polycycloaddition of aldehyde-activated internal diynes and diazides toward post-functionalizable poly(formyl-1,2,3-triazole)s
Baixue Li, Anjun Qin
DOI: 10.1039/D0PY00193G
Morphological evolution and mechanical properties of an “anchor chain” nanodomain structure of a reactive amphiphilic triblock copolymer in epoxy resin
Quan Zhou, Qi Liu, Yueru Yu, Yuxiao Zhuang, Yizhe Lv, Hanliang Xiao, Ning Song, Lizhong Ni
DOI: 10.1039/D0PY00365D
Photo-controlled RAFT polymerization mediated by organic/inorganic hybrid photoredox catalysts: enhanced catalytic efficiency
Wulong Wang, Sheng Zhong, Guicheng Wang, Hongliang Cao, Yun Gao, Weian Zhang
DOI: 10.1039/D0PY00171F
こちらもおすすめ
カルボニル基が付いた5-氰基-1-{[(2-メチル-2-プロpanyl)オキシ]カーボンイル}1H-吲哚-2-イリド-2-ボリン酸はどのように保存すればよいですか?
カルボニル基が付いた5-氰基-1-{[(2-メチル-2-プロpanyl)オキシ]カーボンイル}1H-吲哚-2-イリド-2-ボリン酸は、直射日光を避けて室温(15...
tert-ブチル2-クロロメチルピリジン-3-基炭酸エステルの市場動向や研究トレンドはどうですか?
この化合物は合成化学分野において、特にピリジン化合物の合成や改良に用いられます。最近の研究では、ピリジン化合物の新規合成法や特性の改良が注目されています。市場動...
聚二季戊四醇六丙烯酸酯はどの業界で使用されていますか?
聚二季戊四醇六丙烯酸酯は、医薬品、ポリマー、センサー、半導体などの業界で広く使用されています。特にポリマー業界では硬化剤として、医薬分野では医療機器の製造に使用...
1-氯-5-硝基异喹啉の市場動向や研究トレンドはどうですか?
1-氯-5-硝基异喹啉は、薬理学や合成化学の研究分野で注目されています。市場動向としては、その生物学的な活性や合成可能性を評価する研究が増えています。また、代替...
2-チロール-5-メチルスルフェニル-3-trifルオルメチルベンゼンはどのように合成されますか?
2-チロール-5-メチルスルフェニル-3-trifルオルメチルベンゼンは、トリフルオロメチル化反応と硫化反応を経て合成されます。通常、トリフルオロメチル化剤と硫...
p-トールイルマグネシウムブロミドの物理化学的性質は何ですか?
p-トールイルマグネシウムブロミドのCAS番号は4294-57-9です。この化合物は白色の結晶性粉末で、分子量は204.32です。溶剤中で良好に溶解しますが、水...
1-(5-甲基-2-硫化素基)プロパン-1-酮の市場動向や研究トレンドはどうですか?
1-(5-甲基-2-硫化素基)プロパン-1-酮の市場動向は、化学産業全体の需要に影響を受けますが、最近では pharmaceutical 分野での応用が注目され...
十一碳烯酰甘氨酸を取り扱う際の実験室安全事項は何ですか?
十一碳烯酰甘氨酸は吸入や皮膚から吸収されることがあり、取り扱う際には防塵マスクと手袋を使用してください。ドラフトチャンバーを用いて漏洩を処理し、適切なSDS(S...
1H,1H-全氟-3,6-二氧杂葵-1-醇を取り扱う際の実験室安全事項は何ですか?
この化合物は吸入や皮膚吸収による毒性があるため、防塵マスク、ゴーグル、防護手袋を使用する必要があります。ドラフトチャンバーでの操作が必要です。漏洩時には即座に換...
3-(4-(フルオロメチルオキシ)フェニル)-1,2,4-オキサジアゾール-5-カルボハイドライドは安全ですか?
安全性は化合物の使用方法によります。直接的な毒性は報告されていませんが、吸入や皮膚接触には注意が必要です。適切な防護服を着用し、換気を図ることを推奨します。
掲載誌
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry










![2-Methyl-2-propanyl [2-(2-oxa-6-azaspiro[3.3]hept-6-yl)ethyl]carbamate structure 2-Methyl-2-propanyl [2-(2-oxa-6-azaspiro[3.3]hept-6-yl)ethyl]carbamate structure](https://static.chemtradehub.com/structs/141/1415562-38-7-c0a4.webp)
-1,2-cyclohexanediamine structure N,N'-Bis[3-(2-methoxyphenyl)-2-hydroxybenzyl](1R,2R)-1,2-cyclohexanediamine structure](https://static.chemtradehub.com/structs/928/928769-12-4-a4f0.webp)
![1-(2-Chlorophenyl)-6-[(2S)-3,3,3-trifluoro-2-methylpropyl]-1,7-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one structure 1-(2-Chlorophenyl)-6-[(2S)-3,3,3-trifluoro-2-methylpropyl]-1,7-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one structure](https://static.chemtradehub.com/structs/794/794568-91-5-0c34.webp)

![2-morpholino-2-[2-(trifluoromethyl)pyrimidin-5-yl]ethanamine structure 2-morpholino-2-[2-(trifluoromethyl)pyrimidin-5-yl]ethanamine structure](https://static.chemtradehub.com/structs/119/1192570-20-9-2810.webp)