# US 12,181,414 B2 · Method and probe for monitoring oxygen status in live mammalian cells > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 12,181,414 B2 - Document ID: US12181414B2 - Status: Granted - Kind: B2 - Application number: 16/704,587 - Filed: 2019-12-05 - Published: 2020-06-04 - Granted: 2024-12-31 - Earliest claimed: 2019-12-05 - Assignees: University College Cork, National University of Ireland, Cork - Applicants: University College Cork, National University of Ireland, Cork - Inventors: Dmitri Papkovsky; Andreas Fercher; Ingo Klimant; Sergey Borisov; Alexander Zhdanov - Web page: https://patentgrep.com/patent/US12181414B2 ## CPC - G01N 21/6486: {Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence)} - B82Y 30/00: Nanotechnology for materials or surface science, e.g. nanocomposites - G01N 33/5005: {involving human or animal cells (immunoassay G01N33/56966; immunoassays of protozoa G01N33/56905; protozoa in screening assays C12Q1/025)} - G01N 33/5008: {for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics} - G01N 33/582: {with fluorescent label} - G01N 33/587: {Nanoparticles} - G01N 33/84: involving inorganic compounds or pH - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) - B82Y: SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES ## Abstract A method of determining oxygen concentration, metabolic activity, and/or the effects of a test substance on the metabolic activity of a live cell sample by photoluminescence quenching technique employing a photoluminescent probe that self-loads sans any loading reagent into the cells of the cell sample. The probe comprises a plurality of polymeric particles each comprising an amphiphilic cationic polymer matrix having a hydrophobic core and a hydrophilic positively charged surface provided by quaternary amino groups, and a hydrophobic oxygen-sensitive photoluminescent dye embedded in the hydrophobic core. ## Claims ### Claim 1 A method of determining oxygen concentration in a live mammalian cell sample by photoluminescence quenching technique, which method employs a photoluminescent probe, the method comprising: incubating the live mammalian cell sample in a suitable growth medium with the photoluminescent probe capable of self-loading sans any loading reagent into the cells of the mammalian cell sample; detecting a photoluminescent signal of the photoluminescent probe from the probe-loaded cell sample; and correlating the detected photoluminescent signal to local oxygen concentration within the live mammalian cell sample, wherein the photoluminescent probe is a plurality of polymeric particles each comprising an amphiphilic cationic polymer matrix having a hydrophobic core and a hydrophilic positively charged surface provided by quaternary amino groups, and a hydrophobic oxygen-sensitive photoluminescent dye embedded in the hydrophobic core, wherein the photoluminescent probe is a Pt-tetrakis (pentafluorophenyl) porphine (PtPFPP)-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe, and wherein the PtPFPP-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe comprises the PtPFPP as a hydrophobic oxygen sensitive photoluminescent dye and the Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) as an amphiphilic cationic polymer. ### Claim 2 (depends on 1) The method of claim 1, wherein the photoluminescent probe is in the form of an aqueous suspension of nanoparticles at a working concentration of 0.1 to 100 μg/ml. ### Claim 3 (depends on 1) The method of claim 1, wherein the photoluminescent probe has low intrinsic toxicity on the cells. ### Claim 4 (depends on 1) The method of claim 1, wherein the photoluminescent probe is capable of 1.5 to 15 fold quenching at ambient oxygen concentration of 21 kPa or 250 μM O2. ### Claim 5 (depends on 1) The method of claim 1, wherein the cell sample is washed prior to measurement of the photoluminescent signal to remove extracellular probe. ### Claim 6 (depends on 1) The method of claim 1, wherein the photoluminescent signal is detected by time-resolved fluorometry in the microsecond domain. ### Claim 7 (depends on 1) The method of claim 1, wherein the photoluminescent signal is detected by fluorescence microscopy imaging technique. ### Claim 8 (depends on 1) The method of claim 1, wherein detecting the photoluminescent signal includes measuring the photoluminescence lifetime of the photoluminescent signal or a parameter related to it. ### Claim 9 (depends on 1) The method of claim 1, wherein the photoluminescent signal is detected using ratiometric intensity based oxygen sensing or imaging and the photoluminescent probe further contains an oxygen-insensitive dye which is used as a reference or as part of a FRET pair. ### Claim 10 A method of determining the metabolic activity of a cell or a cell population, wherein the method comprises monitoring oxygen concentration of the cell or cell population by: incubating the cell or cell population in a suitable growth medium with a photoluminescent probe capable of self-loading sans any loading reagent into the cell or cells of the cell population; detecting a photoluminescent signal of the photoluminescent probe from the probe-loaded cell or cell population; correlating the detected photoluminescent signal to local oxygen concentration within the cell or cell population, and correlating the measured oxygen concentration, or changes in the oxygen concentration, of the cell or cell population to metabolic activity of the cell or cell population, wherein the photoluminescent probe is a plurality of polymeric particles each comprising an amphiphilic cationic polymer matrix having a hydrophobic core and a hydrophilic positively charged surface provided by quaternary amino groups, and a hydrophobic oxygen-sensitive photoluminescent dye embedded in the hydrophobic core, wherein the photoluminescent probe is a Pt-tetrakis (pentafluorophenyl) porphine (PtPFPP)-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe, and wherein the PtPFPP-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe comprises the PtPFPP as a hydrophobic oxygen sensitive photoluminescent dye and the Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) as an amphiphilic cationic polymer. ### Claim 11 A method of determining the effects of a test substance on the metabolic activity of a cell or cell population, the method comprising stimulating the cell or cell population with the test substance and determining the metabolic activity of the cell or cell population by: incubating the cell or cell population in a suitable growth medium with a photoluminescent probe capable of self-loading sans any loading reagent into the cell or cells of the cell population; detecting a photoluminescent signal of the photoluminescent probe from the probe-loaded cell or cell population using ratiometric intensity based oxygen sensing or imaging; correlating the detected photoluminescent signal to local oxygen concentration within the cell or cell population, and correlating the measured oxygen concentration, or changes in the oxygen concentration, of the cell or cell population to metabolic activity of the cell or cell population, wherein the photoluminescent probe contains an oxygen-insensitive dye which is used as a reference or as part of a FRET pair, the photoluminescent probe being a plurality of polymeric particles each comprising an amphiphilic cationic polymer matrix having a hydrophobic core and a hydrophilic positively charged surface provided by quaternary amino groups, and a hydrophobic oxygen-sensitive photoluminescent dye embedded in the hydrophobic core, wherein the photoluminescent probe is a Pt-tetrakis (pentafluorophenyl) porphine (PtPFPP)-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe, and wherein the PtPFPP-Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) probe comprises the PtPFPP as a hydrophobic oxygen sensitive photoluminescent dye and the Poly (ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) as an amphiphilic cationic polymer.