Abstract:The aim of the investigation was to study the biodistribution of amino-amide chlorin e 6 derivative conjugate with cobalt bis-dicarbollide as a potential boron transporter for the tasks of boron neutron-capture therapy.Materials and Methods. The experiments were carried out on Balb/c mice with induced murine colon carcinoma CT-26. Amino-amide chlorin e 6 derivative conjugate with cobalt bis-dicarbollide was administered intravenously, the dose being 5 and 10 mg/kg body mass. The sampling for microscopic study … Show more
“…As for synthesized or commercialized 0D boron nanomaterials, suitable modications via surface ligand coupling with other molecules are oen adopted to improve various properties, structures, functions and application performances of products. 77,[129][130][131][132] Guo et al prepared BQDs via rst grinding with a mortar, followed by solvothermal treatment of ground boron powder, NaOH and N-methyl-2-pyrrolidone. 77 The dispersion of BQDs was mixed with PEG-NH 2 .…”
Section: Surface Ligand Coupling With Moleculesmentioning
confidence: 99%
“…Volovetsky et al reported the chemical conjugation action of amine-amide chlorin e6 derivative with a boron nanoparticle. 130 The photosensitizer (chlorin e6) conjugated with boron particles via the amine-amide coupling of chlorin e6 with cobalt bis-dicarbollide (Fig. 10a and b).…”
Section: Surface Ligand Coupling With Moleculesmentioning
confidence: 99%
“…Previous experimental studies have reported luminescence, photoacoustic and photothermal properties of 0D boron nanomaterials, displaying great prospects toward biological imaging applications. 70,76,77,80,81,96,130,131,162 Fluorescence and phosphorescence emission properties of 0D boron nanomaterials have been reported, but very few reports refer to luminescence imaging applications. Rickard et al explored a method for quantifying the oxygen consumption rate of tumor cell lines through using oxygen-sensitive dual-emission BNPs.…”
Section: Biological Imagingmentioning
confidence: 99%
“…Volovetskiy et al prepared the conjugates of BNPs with amino-amide derivatives of chlorin e 6 containing the linker length (n ¼ 6, 8). 130,131 Under excitation at 514 nm, uorescence signals of the coupled derivatives (not BNPs) were recorded in the range of 560-710 nm. There are observable uorescence distributions (collected in 650-693 nm) in tumor tissues (or muscles, vessels, skin, liver, kidneys, spleen, wall of the small intestine, etc.)…”
The past decade has witnessed a rapid growth in scientific studies on zero-dimensional (0D) boron nanomaterials, mainly involving boron nanoparticles, boron quantum dots, boron nanodots, boron nanoclusters and functionalized 0D...
“…As for synthesized or commercialized 0D boron nanomaterials, suitable modications via surface ligand coupling with other molecules are oen adopted to improve various properties, structures, functions and application performances of products. 77,[129][130][131][132] Guo et al prepared BQDs via rst grinding with a mortar, followed by solvothermal treatment of ground boron powder, NaOH and N-methyl-2-pyrrolidone. 77 The dispersion of BQDs was mixed with PEG-NH 2 .…”
Section: Surface Ligand Coupling With Moleculesmentioning
confidence: 99%
“…Volovetsky et al reported the chemical conjugation action of amine-amide chlorin e6 derivative with a boron nanoparticle. 130 The photosensitizer (chlorin e6) conjugated with boron particles via the amine-amide coupling of chlorin e6 with cobalt bis-dicarbollide (Fig. 10a and b).…”
Section: Surface Ligand Coupling With Moleculesmentioning
confidence: 99%
“…Previous experimental studies have reported luminescence, photoacoustic and photothermal properties of 0D boron nanomaterials, displaying great prospects toward biological imaging applications. 70,76,77,80,81,96,130,131,162 Fluorescence and phosphorescence emission properties of 0D boron nanomaterials have been reported, but very few reports refer to luminescence imaging applications. Rickard et al explored a method for quantifying the oxygen consumption rate of tumor cell lines through using oxygen-sensitive dual-emission BNPs.…”
Section: Biological Imagingmentioning
confidence: 99%
“…Volovetskiy et al prepared the conjugates of BNPs with amino-amide derivatives of chlorin e 6 containing the linker length (n ¼ 6, 8). 130,131 Under excitation at 514 nm, uorescence signals of the coupled derivatives (not BNPs) were recorded in the range of 560-710 nm. There are observable uorescence distributions (collected in 650-693 nm) in tumor tissues (or muscles, vessels, skin, liver, kidneys, spleen, wall of the small intestine, etc.)…”
The past decade has witnessed a rapid growth in scientific studies on zero-dimensional (0D) boron nanomaterials, mainly involving boron nanoparticles, boron quantum dots, boron nanodots, boron nanoclusters and functionalized 0D...
Icosahedral boron clusters have unique properties useful in medicinal chemistry: rigidity, chemical stability, and three-dimensional aromaticity. Furthermore, these abiotic compounds have low toxicity and are stable in the biological environment. All these features ultimately give them the ability to interact with biological molecules in a different mode than organic compounds. Areas covered: In the present article, we aim to introduce boron clusters as a class of entities suitable for modifications of biomolecules to obtain a specific biological effect. We will focus on icosahedral boron clusters, as well as metallacarboranes, and their biological activity and interaction with the biological environment. Expert opinion: Boron clusters are suitable for altering structural and functional features of biomolecules and can be used in the development of new drugs and drug delivery systems. The high affinity of boron clusters, especially metallacarboranes, to albumin creates a new possibility to use them to optimize the pharmacokinetics of biologically active peptides. Boron clusters have high potential in biological and medicinal applications. Due to their peculiar properties, they can be used to optimize parameters critical for the biological activity of therapeutic substances and their affinity toward biological targets.
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