Water-soluble BODIPY-nido-carborane nanoparticles applied to biocompatibility tumor cell imaging
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[1] Hao Chen,et al. A multiple acetal chalcone-BODIPY-based fluorescence: synthesis, physical property, and biological studies , 2021, Analytical and Bioanalytical Chemistry.
[2] D. Trifiletti,et al. Boron Neutron Capture Therapy: A Review of Clinical Applications , 2021, Frontiers in Oncology.
[3] F. Khan,et al. Correlation between microstructure parameters and anti-cancer activity of the [Mn0.5Zn0.5](EuxNdxFe2-2x)O4 nanoferrites produced by modified sol-gel and ultrasonic methods , 2020 .
[4] Fuyan Xiao,et al. Acetonitrilated Unsymmetric BODIPYs having glycine fluorescence responsive quenching: Design, synthesis and spectroscopic properties. , 2020, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
[5] Tianyan You,et al. Enzyme-triggered inner filter effect on the fluorescence of gold nanoclusters for ratiometric detection of mercury(II) ions via a dual-signal responsive logic , 2020 .
[6] Lei Liu,et al. A water-soluble colorimetric and fluorescent probe for rapidly sensing of ClO− in organisms , 2020 .
[7] A. Kozlovskiy,et al. Electrochemical Behaviour of Ti/Al2O3/Ni Nanocomposite Material in Artificial Physiological Solution: Prospects for Biomedical Application , 2020, Nanomaterials.
[8] Zhi Zhu,et al. Developed a novel quinazolinone based turn-on fluorescence probe for highly selective monitoring hypochlorite and its bioimaging applications. , 2019, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
[9] A. Kozlovskiy,et al. Immobilization of boron-rich compound on Fe3O4 nanoparticles: Stability and cytotoxicity , 2019, Journal of Alloys and Compounds.
[10] Yi-Wei Chen,et al. Nuclear Theranostics in Taiwan , 2019, Nuclear Medicine and Molecular Imaging.
[11] C. Chiang,et al. Engineering Novel Targeted Boron‐10‐Enriched Theranostic Nanomedicine to Combat against Murine Brain Tumors via MR Imaging‐Guided Boron Neutron Capture Therapy , 2017, Advanced materials.
[12] P. Hobza,et al. The properties of substituted 3D-aromatic neutral carboranes: the potential for σ-hole bonding. , 2015, Physical chemistry chemical physics : PCCP.
[13] F. Teixidor,et al. π aromaticity and three-dimensional aromaticity: two sides of the same coin? , 2014, Angewandte Chemie.
[14] L. Andrade,et al. Chemoenzymatic synthesis of boron-containing chiral amines and amides , 2010 .
[15] K. Tsuboi,et al. [Particle radiotherapy for malignant gliomas]. , 2009, Brain and nerve = Shinkei kenkyu no shinpo.
[16] S. Kang,et al. New types of potential BNCT agents, o-carboranyl aminoalcohols , 2009 .
[17] Andrea F Armstrong,et al. The bioinorganic and medicinal chemistry of carboranes: from new drug discovery to molecular imaging and therapy. , 2007, Dalton Transactions.
[18] P. Jacobsen,et al. Structure-activity relationship for aryl and heteroaryl boronic acid inhibitors of hormone-sensitive lipase. , 2005, Bioorganic & medicinal chemistry.
[19] M. Hawthorne,et al. A critical assessment of boron target compounds for boron neutron capture therapy , 2003, Journal of Neuro-Oncology.
[20] M. Berns,et al. Fluorescence detection of cervical intraepithelial neoplasia for photodynamic therapy with the topical agents 5-aminolevulinic acid and benzoporphyrin-derivative monoacid ring. , 2001, American journal of obstetrics and gynecology.
[21] N. Gupta,et al. Boron neutron capture therapy of brain tumors: an emerging therapeutic modality. , 1999, Neurosurgery.
[22] J. Carlsson,et al. Uptake of a boronated epidermal growth factor-dextran conjugate in CHO xenografts with and without human EGF-receptor expression. , 1998, Anti-cancer drug design.
[23] M. Hawthorne,et al. Novel carboranyl amino acids and peptides: reagents for antibody modification and subsequent neutron-capture studies. , 1991, Bioconjugate chemistry.
[24] M. A. Davis,et al. Penetration of brain and brain tumor. VII. Tumor-binding sulfhydryl boron compounds. , 1967, Journal of medicinal chemistry.
[25] Fuyan Xiao,et al. Strategies of porous network quinolone polymers: A comprehensive evaluation of their biological activity , 2021 .
[26] Fuyan Xiao,et al. Well Defined Rich Electronic Structure: Facile Approach for Nido-Carborane Fused Azaspirodecaniums in Water Solution , 2020 .
[27] E. Barbu,et al. Towards carborane-functionalised structures for the treatment of brain cancer. , 2018, Drug discovery today.
[28] Ji-Ho Yoon,et al. Synthesis and characterization of polar functional group substituted mono- and bis-(o-carboranyl)-1,3,5-triazine derivatives , 2008 .