JP2011501190A - 細胞分析の進歩した方法および装置 - Google Patents
細胞分析の進歩した方法および装置 Download PDFInfo
- Publication number
- JP2011501190A JP2011501190A JP2010531056A JP2010531056A JP2011501190A JP 2011501190 A JP2011501190 A JP 2011501190A JP 2010531056 A JP2010531056 A JP 2010531056A JP 2010531056 A JP2010531056 A JP 2010531056A JP 2011501190 A JP2011501190 A JP 2011501190A
- Authority
- JP
- Japan
- Prior art keywords
- cells
- cell
- cartridge
- sample
- analysis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 172
- 238000004458 analytical method Methods 0.000 title claims abstract description 83
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 92
- 238000012545 processing Methods 0.000 claims abstract description 49
- 238000012360 testing method Methods 0.000 claims description 85
- 238000002955 isolation Methods 0.000 claims description 63
- 239000003153 chemical reaction reagent Substances 0.000 claims description 57
- 238000011282 treatment Methods 0.000 claims description 57
- 201000011510 cancer Diseases 0.000 claims description 45
- 238000001574 biopsy Methods 0.000 claims description 44
- 230000000694 effects Effects 0.000 claims description 35
- 230000014509 gene expression Effects 0.000 claims description 35
- 108090000623 proteins and genes Proteins 0.000 claims description 33
- 239000000090 biomarker Substances 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims description 21
- 239000012530 fluid Substances 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 239000003814 drug Substances 0.000 claims description 19
- 230000036961 partial effect Effects 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 18
- 229940079593 drug Drugs 0.000 claims description 16
- 230000037361 pathway Effects 0.000 claims description 15
- 238000011160 research Methods 0.000 claims description 15
- 238000000338 in vitro Methods 0.000 claims description 14
- 230000006698 induction Effects 0.000 claims description 13
- 230000035899 viability Effects 0.000 claims description 12
- 102000001301 EGF receptor Human genes 0.000 claims description 10
- 108060006698 EGF receptor Proteins 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 238000007689 inspection Methods 0.000 claims description 10
- 238000007479 molecular analysis Methods 0.000 claims description 9
- 230000000087 stabilizing effect Effects 0.000 claims description 9
- 108010089430 Phosphoproteins Proteins 0.000 claims description 8
- 102000007982 Phosphoproteins Human genes 0.000 claims description 8
- 230000020411 cell activation Effects 0.000 claims description 8
- 230000007246 mechanism Effects 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 230000001413 cellular effect Effects 0.000 claims description 7
- 238000007789 sealing Methods 0.000 claims description 7
- 230000003042 antagnostic effect Effects 0.000 claims description 6
- 102000004190 Enzymes Human genes 0.000 claims description 5
- 108090000790 Enzymes Proteins 0.000 claims description 5
- 230000004913 activation Effects 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 4
- 230000007274 generation of a signal involved in cell-cell signaling Effects 0.000 claims description 4
- 241000124008 Mammalia Species 0.000 claims description 3
- 230000003111 delayed effect Effects 0.000 claims description 3
- 108091005626 post-translationally modified proteins Proteins 0.000 claims description 3
- 102000035123 post-translationally modified proteins Human genes 0.000 claims description 3
- 102000027426 receptor tyrosine kinases Human genes 0.000 claims description 3
- 108091008598 receptor tyrosine kinases Proteins 0.000 claims description 3
- 230000010076 replication Effects 0.000 claims description 3
- 102000003688 G-Protein-Coupled Receptors Human genes 0.000 claims description 2
- 108090000045 G-Protein-Coupled Receptors Proteins 0.000 claims description 2
- 108020004459 Small interfering RNA Proteins 0.000 claims description 2
- 230000001270 agonistic effect Effects 0.000 claims description 2
- 230000033115 angiogenesis Effects 0.000 claims description 2
- 230000005775 apoptotic pathway Effects 0.000 claims description 2
- 150000002500 ions Chemical group 0.000 claims description 2
- 230000002934 lysing effect Effects 0.000 claims description 2
- 230000037353 metabolic pathway Effects 0.000 claims description 2
- 229910021645 metal ion Inorganic materials 0.000 claims description 2
- 230000005298 paramagnetic effect Effects 0.000 claims description 2
- 102000040430 polynucleotide Human genes 0.000 claims description 2
- 108091033319 polynucleotide Proteins 0.000 claims description 2
- 239000002157 polynucleotide Substances 0.000 claims description 2
- 229920001184 polypeptide Polymers 0.000 claims description 2
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 2
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 2
- 230000002285 radioactive effect Effects 0.000 claims description 2
- 239000012857 radioactive material Substances 0.000 claims description 2
- 230000001629 suppression Effects 0.000 claims description 2
- 238000003325 tomography Methods 0.000 claims description 2
- 230000004640 cellular pathway Effects 0.000 claims 1
- 150000002632 lipids Chemical class 0.000 claims 1
- 231100000590 oncogenic Toxicity 0.000 claims 1
- 230000002246 oncogenic effect Effects 0.000 claims 1
- 230000007170 pathology Effects 0.000 abstract description 3
- 210000004027 cell Anatomy 0.000 description 424
- 239000000523 sample Substances 0.000 description 149
- 210000001519 tissue Anatomy 0.000 description 39
- 230000035882 stress Effects 0.000 description 38
- 230000008569 process Effects 0.000 description 30
- 239000000758 substrate Substances 0.000 description 30
- 238000010494 dissociation reaction Methods 0.000 description 29
- 230000005593 dissociations Effects 0.000 description 29
- 210000004881 tumor cell Anatomy 0.000 description 24
- 239000000975 dye Substances 0.000 description 21
- 230000006870 function Effects 0.000 description 21
- 239000000243 solution Substances 0.000 description 21
- 239000006185 dispersion Substances 0.000 description 18
- 206010006187 Breast cancer Diseases 0.000 description 17
- 208000026310 Breast neoplasm Diseases 0.000 description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- 102000004169 proteins and genes Human genes 0.000 description 16
- 239000002609 medium Substances 0.000 description 14
- 235000018102 proteins Nutrition 0.000 description 14
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 238000010586 diagram Methods 0.000 description 12
- 238000003384 imaging method Methods 0.000 description 12
- 102000039446 nucleic acids Human genes 0.000 description 12
- 108020004707 nucleic acids Proteins 0.000 description 12
- 150000007523 nucleic acids Chemical class 0.000 description 12
- 230000000638 stimulation Effects 0.000 description 12
- 238000003860 storage Methods 0.000 description 12
- 108020004414 DNA Proteins 0.000 description 11
- 210000003855 cell nucleus Anatomy 0.000 description 11
- 239000000356 contaminant Substances 0.000 description 11
- 238000009826 distribution Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 230000035945 sensitivity Effects 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 238000011156 evaluation Methods 0.000 description 10
- 239000012508 resin bead Substances 0.000 description 10
- 230000004044 response Effects 0.000 description 10
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 9
- 230000003833 cell viability Effects 0.000 description 9
- 239000003550 marker Substances 0.000 description 9
- 108020004999 messenger RNA Proteins 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000005411 L01XE02 - Gefitinib Substances 0.000 description 8
- 239000002202 Polyethylene glycol Substances 0.000 description 8
- 239000000872 buffer Substances 0.000 description 8
- 239000006285 cell suspension Substances 0.000 description 8
- 229940116977 epidermal growth factor Drugs 0.000 description 8
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical compound C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 description 8
- 229920001223 polyethylene glycol Polymers 0.000 description 8
- 239000002356 single layer Substances 0.000 description 8
- 230000007704 transition Effects 0.000 description 8
- VBEQCZHXXJYVRD-GACYYNSASA-N uroanthelone Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)CNC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C1=CC=C(O)C=C1 VBEQCZHXXJYVRD-GACYYNSASA-N 0.000 description 8
- 239000005551 L01XE03 - Erlotinib Substances 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 230000006907 apoptotic process Effects 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 230000008901 benefit Effects 0.000 description 7
- 210000000170 cell membrane Anatomy 0.000 description 7
- 239000002299 complementary DNA Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 238000005192 partition Methods 0.000 description 7
- 238000003672 processing method Methods 0.000 description 7
- 102400001368 Epidermal growth factor Human genes 0.000 description 6
- 101800003838 Epidermal growth factor Proteins 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 230000002776 aggregation Effects 0.000 description 6
- 230000001419 dependent effect Effects 0.000 description 6
- 229960002584 gefitinib Drugs 0.000 description 6
- 239000003446 ligand Substances 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 235000002639 sodium chloride Nutrition 0.000 description 6
- 238000010186 staining Methods 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 102000003952 Caspase 3 Human genes 0.000 description 5
- 108090000397 Caspase 3 Proteins 0.000 description 5
- 206010009944 Colon cancer Diseases 0.000 description 5
- 238000003556 assay Methods 0.000 description 5
- 239000011324 bead Substances 0.000 description 5
- 239000002738 chelating agent Substances 0.000 description 5
- 229960001433 erlotinib Drugs 0.000 description 5
- 102000015694 estrogen receptors Human genes 0.000 description 5
- 108010038795 estrogen receptors Proteins 0.000 description 5
- HQPMKSGTIOYHJT-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.CC(O)CO HQPMKSGTIOYHJT-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000000834 fixative Substances 0.000 description 5
- 238000003364 immunohistochemistry Methods 0.000 description 5
- 230000033001 locomotion Effects 0.000 description 5
- 238000007726 management method Methods 0.000 description 5
- 210000004940 nucleus Anatomy 0.000 description 5
- 210000000056 organ Anatomy 0.000 description 5
- 230000001575 pathological effect Effects 0.000 description 5
- 239000002953 phosphate buffered saline Substances 0.000 description 5
- 229920001993 poloxamer 188 Polymers 0.000 description 5
- 102000005962 receptors Human genes 0.000 description 5
- 108020003175 receptors Proteins 0.000 description 5
- 238000007790 scraping Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000006641 stabilisation Effects 0.000 description 5
- 238000011105 stabilization Methods 0.000 description 5
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000012981 Hank's balanced salt solution Substances 0.000 description 4
- 101001081172 Homo sapiens Humanin-like 11 Proteins 0.000 description 4
- 102100027736 Humanin-like 11 Human genes 0.000 description 4
- NKANXQFJJICGDU-QPLCGJKRSA-N Tamoxifen Chemical compound C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 NKANXQFJJICGDU-QPLCGJKRSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 230000001120 cytoprotective effect Effects 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- GTSMOYLSFUBTMV-UHFFFAOYSA-N ethidium homodimer Chemical compound [H+].[H+].[Cl-].[Cl-].[Cl-].[Cl-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2C(C)=[N+]1CCCNCCNCCC[N+](C1=CC(N)=CC=C1C1=CC=C(N)C=C11)=C1C1=CC=CC=C1 GTSMOYLSFUBTMV-UHFFFAOYSA-N 0.000 description 4
- 230000005284 excitation Effects 0.000 description 4
- 239000012634 fragment Substances 0.000 description 4
- 230000002068 genetic effect Effects 0.000 description 4
- 229940022353 herceptin Drugs 0.000 description 4
- 238000001727 in vivo Methods 0.000 description 4
- 238000001802 infusion Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 210000004379 membrane Anatomy 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000013615 primer Substances 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 238000010008 shearing Methods 0.000 description 4
- 150000003384 small molecules Chemical class 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000002699 waste material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229920000936 Agarose Polymers 0.000 description 3
- 108020001019 DNA Primers Proteins 0.000 description 3
- 239000003155 DNA primer Substances 0.000 description 3
- 102100034343 Integrase Human genes 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 description 3
- 239000013504 Triton X-100 Substances 0.000 description 3
- 229920004890 Triton X-100 Polymers 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 239000012472 biological sample Substances 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 239000007975 buffered saline Substances 0.000 description 3
- 238000004113 cell culture Methods 0.000 description 3
- 208000029742 colonic neoplasm Diseases 0.000 description 3
- 238000012258 culturing Methods 0.000 description 3
- 230000001186 cumulative effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000003745 diagnosis Methods 0.000 description 3
- 238000002405 diagnostic procedure Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000001861 endoscopic biopsy Methods 0.000 description 3
- 210000002889 endothelial cell Anatomy 0.000 description 3
- 238000013467 fragmentation Methods 0.000 description 3
- 238000006062 fragmentation reaction Methods 0.000 description 3
- 239000001963 growth medium Substances 0.000 description 3
- 229940088597 hormone Drugs 0.000 description 3
- 239000005556 hormone Substances 0.000 description 3
- 238000011534 incubation Methods 0.000 description 3
- 230000002147 killing effect Effects 0.000 description 3
- 230000005291 magnetic effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 238000007431 microscopic evaluation Methods 0.000 description 3
- 238000013188 needle biopsy Methods 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 229920000729 poly(L-lysine) polymer Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 230000003938 response to stress Effects 0.000 description 3
- 229960004641 rituximab Drugs 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 238000003211 trypan blue cell staining Methods 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 238000012800 visualization Methods 0.000 description 3
- ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 2
- 206010052358 Colorectal cancer metastatic Diseases 0.000 description 2
- 229920002307 Dextran Polymers 0.000 description 2
- 239000012591 Dulbecco’s Phosphate Buffered Saline Substances 0.000 description 2
- 101150029707 ERBB2 gene Proteins 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 102000009465 Growth Factor Receptors Human genes 0.000 description 2
- 108010009202 Growth Factor Receptors Proteins 0.000 description 2
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- 102000035195 Peptidases Human genes 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- GLNADSQYFUSGOU-GPTZEZBUSA-J Trypan blue Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(/N=N/C3=CC=C(C=C3C)C=3C=C(C(=CC=3)\N=N\C=3C(=CC4=CC(=CC(N)=C4C=3O)S([O-])(=O)=O)S([O-])(=O)=O)C)=C(O)C2=C1N GLNADSQYFUSGOU-GPTZEZBUSA-J 0.000 description 2
- 102000004142 Trypsin Human genes 0.000 description 2
- 108090000631 Trypsin Proteins 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000001833 anti-estrogenic effect Effects 0.000 description 2
- 230000000259 anti-tumor effect Effects 0.000 description 2
- 239000002246 antineoplastic agent Substances 0.000 description 2
- 229940120638 avastin Drugs 0.000 description 2
- 239000003855 balanced salt solution Substances 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 229940098773 bovine serum albumin Drugs 0.000 description 2
- 239000006172 buffering agent Substances 0.000 description 2
- BQRGNLJZBFXNCZ-UHFFFAOYSA-N calcein am Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(CN(CC(=O)OCOC(C)=O)CC(=O)OCOC(C)=O)=C(OC(C)=O)C=C1OC1=C2C=C(CN(CC(=O)OCOC(C)=O)CC(=O)OCOC(=O)C)C(OC(C)=O)=C1 BQRGNLJZBFXNCZ-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 230000005754 cellular signaling Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 229940044683 chemotherapy drug Drugs 0.000 description 2
- 210000000349 chromosome Anatomy 0.000 description 2
- 238000003759 clinical diagnosis Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000002338 cryopreservative effect Effects 0.000 description 2
- 230000002380 cytological effect Effects 0.000 description 2
- 230000009089 cytolysis Effects 0.000 description 2
- 231100000433 cytotoxic Toxicity 0.000 description 2
- 230000001472 cytotoxic effect Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 229940126534 drug product Drugs 0.000 description 2
- 230000002900 effect on cell Effects 0.000 description 2
- 229940082789 erbitux Drugs 0.000 description 2
- 229940011871 estrogen Drugs 0.000 description 2
- 239000000262 estrogen Substances 0.000 description 2
- 239000000328 estrogen antagonist Substances 0.000 description 2
- 238000010195 expression analysis Methods 0.000 description 2
- 239000012091 fetal bovine serum Substances 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000003318 immunodepletion Methods 0.000 description 2
- 238000002991 immunohistochemical analysis Methods 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 229940084651 iressa Drugs 0.000 description 2
- FZWBNHMXJMCXLU-BLAUPYHCSA-N isomaltotriose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)O1 FZWBNHMXJMCXLU-BLAUPYHCSA-N 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 230000004807 localization Effects 0.000 description 2
- 210000001165 lymph node Anatomy 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002679 microRNA Substances 0.000 description 2
- 238000002493 microarray Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 210000003470 mitochondria Anatomy 0.000 description 2
- 230000000877 morphologic effect Effects 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229940049954 penicillin Drugs 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 239000008177 pharmaceutical agent Substances 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000001507 sample dispersion Methods 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 230000004936 stimulating effect Effects 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 230000009221 stress response pathway Effects 0.000 description 2
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 229960001603 tamoxifen Drugs 0.000 description 2
- 229940120982 tarceva Drugs 0.000 description 2
- 229940063683 taxotere Drugs 0.000 description 2
- 238000011269 treatment regimen Methods 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- 239000012588 trypsin Substances 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- AOUOVFRSCMDPFA-QSDJMHMYSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-amino-3-carboxypropanoyl]amino]-4-carboxybutanoyl]amino]-3-methylbutanoyl]amino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O AOUOVFRSCMDPFA-QSDJMHMYSA-N 0.000 description 1
- PRDFBSVERLRRMY-UHFFFAOYSA-N 2'-(4-ethoxyphenyl)-5-(4-methylpiperazin-1-yl)-2,5'-bibenzimidazole Chemical compound C1=CC(OCC)=CC=C1C1=NC2=CC=C(C=3NC4=CC(=CC=C4N=3)N3CCN(C)CC3)C=C2N1 PRDFBSVERLRRMY-UHFFFAOYSA-N 0.000 description 1
- BHNQPLPANNDEGL-UHFFFAOYSA-N 2-(4-octylphenoxy)ethanol Chemical compound CCCCCCCCC1=CC=C(OCCO)C=C1 BHNQPLPANNDEGL-UHFFFAOYSA-N 0.000 description 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- FWBHETKCLVMNFS-UHFFFAOYSA-N 4',6-Diamino-2-phenylindol Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 206010005003 Bladder cancer Diseases 0.000 description 1
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- 206010055113 Breast cancer metastatic Diseases 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 208000005623 Carcinogenesis Diseases 0.000 description 1
- 206010008342 Cervix carcinoma Diseases 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 108020004705 Codon Proteins 0.000 description 1
- 206010052360 Colorectal adenocarcinoma Diseases 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 230000003682 DNA packaging effect Effects 0.000 description 1
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 1
- 229940122558 EGFR antagonist Drugs 0.000 description 1
- 239000006145 Eagle's minimal essential medium Substances 0.000 description 1
- 241000283074 Equus asinus Species 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 description 1
- VWUXBMIQPBEWFH-WCCTWKNTSA-N Fulvestrant Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3[C@H](CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F)CC2=C1 VWUXBMIQPBEWFH-WCCTWKNTSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 108010033040 Histones Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 102000004310 Ion Channels Human genes 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 206010025323 Lymphomas Diseases 0.000 description 1
- 102000018697 Membrane Proteins Human genes 0.000 description 1
- 108010052285 Membrane Proteins Proteins 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 108700011259 MicroRNAs Proteins 0.000 description 1
- 238000000342 Monte Carlo simulation Methods 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 108091005461 Nucleic proteins Proteins 0.000 description 1
- 206010033128 Ovarian cancer Diseases 0.000 description 1
- 206010061535 Ovarian neoplasm Diseases 0.000 description 1
- 206010061902 Pancreatic neoplasm Diseases 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 102000013566 Plasminogen Human genes 0.000 description 1
- 108010051456 Plasminogen Proteins 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 206010060862 Prostate cancer Diseases 0.000 description 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 1
- 108700020978 Proto-Oncogene Proteins 0.000 description 1
- 102000052575 Proto-Oncogene Human genes 0.000 description 1
- 238000002123 RNA extraction Methods 0.000 description 1
- 239000013614 RNA sample Substances 0.000 description 1
- 239000012979 RPMI medium Substances 0.000 description 1
- 206010039491 Sarcoma Diseases 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- 206010041067 Small cell lung cancer Diseases 0.000 description 1
- QTENRWWVYAAPBI-YZTFXSNBSA-N Streptomycin sulfate Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@H]1[C@H](N=C(N)N)[C@@H](O)[C@H](N=C(N)N)[C@@H](O)[C@@H]1O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@H]1[C@H](N=C(N)N)[C@@H](O)[C@H](N=C(N)N)[C@@H](O)[C@@H]1O QTENRWWVYAAPBI-YZTFXSNBSA-N 0.000 description 1
- 208000002847 Surgical Wound Diseases 0.000 description 1
- 229940123237 Taxane Drugs 0.000 description 1
- 102000003978 Tissue Plasminogen Activator Human genes 0.000 description 1
- 108090000373 Tissue Plasminogen Activator Proteins 0.000 description 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 description 1
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 description 1
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 description 1
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 description 1
- DFPAKSUCGFBDDF-ZQBYOMGUSA-N [14c]-nicotinamide Chemical compound N[14C](=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-ZQBYOMGUSA-N 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 238000002679 ablation Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000000516 activation analysis Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 229940045799 anthracyclines and related substance Drugs 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 229940046836 anti-estrogen Drugs 0.000 description 1
- 230000000340 anti-metabolite Effects 0.000 description 1
- 229940100197 antimetabolite Drugs 0.000 description 1
- 239000002256 antimetabolite Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229960000397 bevacizumab Drugs 0.000 description 1
- 239000013060 biological fluid Substances 0.000 description 1
- 238000009534 blood test Methods 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 239000012888 bovine serum Substances 0.000 description 1
- 210000000621 bronchi Anatomy 0.000 description 1
- 238000013276 bronchoscopy Methods 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 239000012830 cancer therapeutic Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 238000000423 cell based assay Methods 0.000 description 1
- 239000006143 cell culture medium Substances 0.000 description 1
- 230000006037 cell lysis Effects 0.000 description 1
- 239000013553 cell monolayer Substances 0.000 description 1
- 238000003693 cell processing method Methods 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 238000003570 cell viability assay Methods 0.000 description 1
- 108091092356 cellular DNA Proteins 0.000 description 1
- 108091092328 cellular RNA Proteins 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 201000010881 cervical cancer Diseases 0.000 description 1
- 229960005395 cetuximab Drugs 0.000 description 1
- 230000009920 chelation Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 210000000038 chest Anatomy 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000002591 computed tomography Methods 0.000 description 1
- 238000013170 computed tomography imaging Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005138 cryopreservation Methods 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 238000002574 cystoscopy Methods 0.000 description 1
- 230000001461 cytolytic effect Effects 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000007405 data analysis Methods 0.000 description 1
- 238000013500 data storage Methods 0.000 description 1
- 238000012631 diagnostic technique Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 1
- 238000009509 drug development Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000003708 edge detection Methods 0.000 description 1
- 229940121647 egfr inhibitor Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001839 endoscopy Methods 0.000 description 1
- 230000006353 environmental stress Effects 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 description 1
- 229960001123 epoprostenol Drugs 0.000 description 1
- 210000003238 esophagus Anatomy 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 229940106582 estrogenic substances Drugs 0.000 description 1
- 239000003172 expectorant agent Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 238000000799 fluorescence microscopy Methods 0.000 description 1
- 229960002949 fluorouracil Drugs 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 229960002258 fulvestrant Drugs 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 230000009422 growth inhibiting effect Effects 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- 238000001794 hormone therapy Methods 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001969 hypertrophic effect Effects 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 238000011532 immunohistochemical staining Methods 0.000 description 1
- 238000011273 incision biopsy Methods 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 102000006495 integrins Human genes 0.000 description 1
- 108010044426 integrins Proteins 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 239000000644 isotonic solution Substances 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000002357 laparoscopic surgery Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 201000007270 liver cancer Diseases 0.000 description 1
- 208000014018 liver neoplasm Diseases 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 description 1
- 238000009607 mammography Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 210000005015 mediastinal lymph node Anatomy 0.000 description 1
- 230000004066 metabolic change Effects 0.000 description 1
- 230000006609 metabolic stress Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 206010061289 metastatic neoplasm Diseases 0.000 description 1
- 108091070501 miRNA Proteins 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 239000007758 minimum essential medium Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003068 molecular probe Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 229940066491 mucolytics Drugs 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229960002378 oftasceine Drugs 0.000 description 1
- 238000011275 oncology therapy Methods 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 201000002528 pancreatic cancer Diseases 0.000 description 1
- 208000008443 pancreatic carcinoma Diseases 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000013610 patient sample Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004393 prognosis Methods 0.000 description 1
- 239000000092 prognostic biomarker Substances 0.000 description 1
- 230000026447 protein localization Effects 0.000 description 1
- 238000007388 punch biopsy Methods 0.000 description 1
- 238000012113 quantitative test Methods 0.000 description 1
- 230000008261 resistance mechanism Effects 0.000 description 1
- 238000003757 reverse transcription PCR Methods 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 239000003161 ribonuclease inhibitor Substances 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 238000005464 sample preparation method Methods 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 108010085082 sigma receptors Proteins 0.000 description 1
- 230000008054 signal transmission Effects 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 208000000587 small cell lung carcinoma Diseases 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 206010041823 squamous cell carcinoma Diseases 0.000 description 1
- 208000017572 squamous cell neoplasm Diseases 0.000 description 1
- 238000007447 staining method Methods 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 230000009211 stress pathway Effects 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 239000003104 tissue culture media Substances 0.000 description 1
- 229960000187 tissue plasminogen activator Drugs 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 229960000575 trastuzumab Drugs 0.000 description 1
- 239000003656 tris buffered saline Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 238000001262 western blot Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Optical investigation techniques, e.g. flow cytometry
- G01N15/1429—Signal processing
- G01N15/1433—Signal processing using image recognition
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/42—Integrated assemblies, e.g. cassettes or cartridges
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/02—Form or structure of the vessel
- C12M23/12—Well or multiwell plates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M37/00—Means for sterilizing, maintaining sterile conditions or avoiding chemical or biological contamination
- C12M37/04—Seals
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N2035/1027—General features of the devices
- G01N2035/1032—Dilution or aliquotting
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Sustainable Development (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Clinical Laboratory Science (AREA)
- Analytical Chemistry (AREA)
- Pathology (AREA)
- Dispersion Chemistry (AREA)
- Physics & Mathematics (AREA)
- Signal Processing (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Computer Vision & Pattern Recognition (AREA)
- Sampling And Sample Adjustment (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98227907P | 2007-10-24 | 2007-10-24 | |
| US9905908P | 2008-09-22 | 2008-09-22 | |
| PCT/US2008/012148 WO2009055052A2 (en) | 2007-10-24 | 2008-10-24 | Improved methods and devices for cellular analysis |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015151362A Division JP6177841B2 (ja) | 2007-10-24 | 2015-07-30 | 細胞分析の進歩した方法および装置 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011501190A true JP2011501190A (ja) | 2011-01-06 |
| JP2011501190A5 JP2011501190A5 (https=) | 2015-09-17 |
Family
ID=40340698
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010531056A Pending JP2011501190A (ja) | 2007-10-24 | 2008-10-24 | 細胞分析の進歩した方法および装置 |
| JP2015151362A Expired - Fee Related JP6177841B2 (ja) | 2007-10-24 | 2015-07-30 | 細胞分析の進歩した方法および装置 |
| JP2017136044A Expired - Fee Related JP6675355B2 (ja) | 2007-10-24 | 2017-07-12 | 細胞分析の進歩した方法および装置 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015151362A Expired - Fee Related JP6177841B2 (ja) | 2007-10-24 | 2015-07-30 | 細胞分析の進歩した方法および装置 |
| JP2017136044A Expired - Fee Related JP6675355B2 (ja) | 2007-10-24 | 2017-07-12 | 細胞分析の進歩した方法および装置 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US9121801B2 (https=) |
| EP (2) | EP2210080B1 (https=) |
| JP (3) | JP2011501190A (https=) |
| KR (1) | KR101658245B1 (https=) |
| AU (1) | AU2008317329B2 (https=) |
| CA (2) | CA2971968C (https=) |
| ES (1) | ES2535631T3 (https=) |
| PL (1) | PL2210080T3 (https=) |
| WO (1) | WO2009055052A2 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023504585A (ja) * | 2019-11-27 | 2023-02-03 | サーモ フィッシャー サイエンティフィック （ブレーメン） ゲーエムベーハー | サンプルを画像化およびアブレーションするためのシステムおよび方法 |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007224386B2 (en) | 2006-03-06 | 2013-12-19 | Zetiq Technologies Ltd. | Methods and compositions for identifying a cell phenotype |
| NZ573187A (en) * | 2006-06-02 | 2011-11-25 | Pfizer Prod Inc | Circulating tumor cell assay for predicting efficacy of 1gf-1r antagonist therapy |
| CA3138078C (en) | 2007-10-02 | 2024-02-13 | Labrador Diagnostics Llc | Modular point-of-care devices and uses thereof |
| US20090226059A1 (en) * | 2008-02-12 | 2009-09-10 | Richard Levenson | Tissue Processing And Assessment |
| WO2010134073A1 (en) | 2009-05-19 | 2010-11-25 | Zetiq Technologies Ltd. | Kits for and methods of differential staining of cervical cancer cells and/or tissues |
| EP2453005B1 (en) * | 2009-07-08 | 2019-09-04 | Nikon Corporation | Cell picking-assisting device |
| CN102947706B (zh) | 2010-04-19 | 2018-04-13 | 生物标志物策略公司 | 预测药物敏感性、抗性和疾病进展的组合物和方法 |
| US9228785B2 (en) | 2010-05-04 | 2016-01-05 | Alexander Poltorak | Fractal heat transfer device |
| JP5629939B2 (ja) * | 2010-09-09 | 2014-11-26 | 株式会社パソロジー研究所 | パイルアップ組織アレイ |
| MX349288B (es) | 2011-01-21 | 2017-07-21 | Theranos Inc | Sistemas y metodos para maximizacion de uso de muestras. |
| CN103998394B (zh) | 2011-08-01 | 2016-08-17 | 德诺弗科学公司 | 细胞捕获系统和使用方法 |
| US10466160B2 (en) | 2011-08-01 | 2019-11-05 | Celsee Diagnostics, Inc. | System and method for retrieving and analyzing particles |
| US9404864B2 (en) | 2013-03-13 | 2016-08-02 | Denovo Sciences, Inc. | System for imaging captured cells |
| US9664702B2 (en) | 2011-09-25 | 2017-05-30 | Theranos, Inc. | Fluid handling apparatus and configurations |
| US9619627B2 (en) | 2011-09-25 | 2017-04-11 | Theranos, Inc. | Systems and methods for collecting and transmitting assay results |
| US8475739B2 (en) | 2011-09-25 | 2013-07-02 | Theranos, Inc. | Systems and methods for fluid handling |
| US20140170735A1 (en) | 2011-09-25 | 2014-06-19 | Elizabeth A. Holmes | Systems and methods for multi-analysis |
| US9632102B2 (en) | 2011-09-25 | 2017-04-25 | Theranos, Inc. | Systems and methods for multi-purpose analysis |
| US10012664B2 (en) | 2011-09-25 | 2018-07-03 | Theranos Ip Company, Llc | Systems and methods for fluid and component handling |
| US9810704B2 (en) | 2013-02-18 | 2017-11-07 | Theranos, Inc. | Systems and methods for multi-analysis |
| JP2013185920A (ja) * | 2012-03-07 | 2013-09-19 | Pathology Institute | 組織アレイシートの製造方法およびその製造装置 |
| WO2013142393A1 (en) * | 2012-03-19 | 2013-09-26 | Hudson River Biolabs | Method and apparatus for collecting, transporting and maintaining live tumor specimens ex vivo |
| US9707562B2 (en) | 2013-03-13 | 2017-07-18 | Denovo Sciences, Inc. | System for capturing and analyzing cells |
| US10391490B2 (en) | 2013-05-31 | 2019-08-27 | Celsee Diagnostics, Inc. | System and method for isolating and analyzing cells |
| FR3009622B1 (fr) * | 2013-08-09 | 2015-08-07 | Novacyt | Procede et dispositif de lavage d'un dispositif de pipetage-distribution |
| JP2017527288A (ja) | 2014-09-04 | 2017-09-21 | セラノス， インコーポレイテッドＴｈｅｒａｎｏｓ， Ｉｎｃ． | 病原体及び抗菌薬耐性試験 |
| KR102328995B1 (ko) * | 2014-11-26 | 2021-11-23 | 나노리소스 주식회사 | 폭발형 나노다이아몬드의 분리 방법 |
| US10852291B2 (en) | 2015-02-03 | 2020-12-01 | University Of Washington | Fluidic device and methods of use for processing tissue for pathology |
| US10542961B2 (en) | 2015-06-15 | 2020-01-28 | The Research Foundation For The State University Of New York | System and method for infrasonic cardiac monitoring |
| WO2017079674A1 (en) * | 2015-11-04 | 2017-05-11 | Northeastern University | Systems for producing cellular immunotherapeutics and methods of use thereof |
| US10830545B2 (en) | 2016-07-12 | 2020-11-10 | Fractal Heatsink Technologies, LLC | System and method for maintaining efficiency of a heat sink |
| US12072333B2 (en) * | 2016-11-02 | 2024-08-27 | University Of Iowa Research Foundation | Method and apparatus for selective removal of cells from a cell suspension by mechanical lysis |
| US10391492B2 (en) | 2017-08-29 | 2019-08-27 | Celsee Diagnostics, Inc. | System and method for isolating and analyzing cells |
| DE102018206454A1 (de) * | 2018-04-26 | 2019-10-31 | Robert Bosch Gmbh | System und Verfahren zum Einbringen von Probenmaterial |
| US10647954B1 (en) | 2018-11-15 | 2020-05-12 | Flaskworks, Llc | Dendritic cell generating apparatus and method |
| US12560590B2 (en) * | 2019-01-23 | 2026-02-24 | Massachusetts Institute Of Technology | Rapid analysis of live cells |
| US10633693B1 (en) | 2019-04-16 | 2020-04-28 | Celsee Diagnostics, Inc. | System and method for leakage control in a particle capture system |
| AU2020267743B2 (en) | 2019-05-07 | 2023-04-06 | Bio-Rad Laboratories, Inc. | System and method for automated single cell processing |
| US11273439B2 (en) | 2019-05-07 | 2022-03-15 | Bio-Rad Laboratories, Inc. | System and method for target material retrieval from microwells |
| WO2020251802A1 (en) | 2019-06-14 | 2020-12-17 | Bio-Rad Laboratories, Inc. | System and method for automated single cell processing and analyses |
| US11566217B2 (en) | 2019-08-13 | 2023-01-31 | Flaskworks, Llc | Duty cycle for cell culture systems |
| CN114901799A (zh) | 2019-10-21 | 2022-08-12 | 弗拉斯沃克斯有限责任公司 | 用于细胞培养的系统和方法 |
| JP7363390B2 (ja) * | 2019-11-08 | 2023-10-18 | Jsr株式会社 | 細胞凝集塊分散装置および細胞凝集塊分散方法 |
| WO2021188562A1 (en) * | 2020-03-17 | 2021-09-23 | Detect, Inc. | Seal component for a rapid diagnostic test |
| KR102639140B1 (ko) * | 2020-08-14 | 2024-02-20 | 연세대학교 산학협력단 | 조직 검사 방법 및 조직 검사 장치 |
| JP2022071963A (ja) * | 2020-10-29 | 2022-05-17 | シスメックス株式会社 | 試料調製方法、細胞分析方法、試料調製装置および細胞分析装置 |
| CN215727578U (zh) * | 2021-05-28 | 2022-02-01 | 上海睿钰生物科技有限公司 | 一种计数组件及计数装置 |
| CN118369438A (zh) | 2021-12-10 | 2024-07-19 | 伯乐实验室有限公司 | 用形态可调节功能化颗粒进行样品处理的组合物、方法和系统 |
| KR20240140095A (ko) * | 2022-01-14 | 2024-09-24 | 디풀 다이어그노스틱스 에스.엘. | 병원체 식별을 위한 시스템들, 방법들, 및 디바이스들 |
| CN114518425B (zh) * | 2022-02-11 | 2023-03-10 | 中国科学技术大学 | 同时检测单个免疫细胞胞浆和细胞膜的代谢物的分析方法 |
| KR20230121326A (ko) | 2022-02-11 | 2023-08-18 | 연세대학교 산학협력단 | 세포 검사 방법 및 장치 |
| US20230365911A1 (en) * | 2022-04-25 | 2023-11-16 | Multiply Labs Inc. | System, method, and apparatus for manufacture of engineered cells |
| WO2025171036A1 (en) * | 2024-02-06 | 2025-08-14 | Effani Agriculture, Inc. | Automation of biopsy analysis systems and methods |
Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4350768A (en) * | 1980-09-19 | 1982-09-21 | Bristol Myers Company | Method for preparing single cell suspension |
| JPS63502929A (ja) * | 1986-03-20 | 1988-10-27 | ベックマン インスツルメンツ インコーポレーテッド | モジュール式貯蔵機構 |
| JPH06213788A (ja) * | 1992-09-29 | 1994-08-05 | F Hoffmann La Roche Ag | 細胞学的物質の分解デバイス |
| JPH0751559A (ja) * | 1993-08-20 | 1995-02-28 | Rigoushiya:Kk | 液体試料の分配秤量装置 |
| JPH08502401A (ja) * | 1992-05-25 | 1996-03-19 | ガンブロ アクチーボラグ | 細胞毒性試験の実施方法およびそのための系およびこの系に包含されるキット |
| JPH0894634A (ja) * | 1994-09-22 | 1996-04-12 | Suzuki Motor Corp | 酵素免疫反応測定装置 |
| JPH09196917A (ja) * | 1996-01-12 | 1997-07-31 | Suzuki Motor Corp | テストプレート用自動判定装置 |
| JPH1062436A (ja) * | 1996-08-21 | 1998-03-06 | Fujirebio Inc | 液体の分注方法とその装置 |
| JP2005512023A (ja) * | 2001-09-21 | 2005-04-28 | アクセス ジェネティックス エルエルシー | 遠隔遺伝子分析及び診察用のシステム、方法及びキット |
| US20050233309A1 (en) * | 2004-04-19 | 2005-10-20 | Hankins William D | Kinetic process for the detection, diagnosis, processing, and monitoring of clonal cell populations |
| JP2006158203A (ja) * | 2004-12-02 | 2006-06-22 | Univ Nagoya | リガンド親和性複合タンパク質の取得方法、抗体スクリーニング方法、抗体スクリーニング用キット、医療方法、抗体医薬、非免疫反応性抗体医薬、投薬方法 |
| JP2006526390A (ja) * | 2003-01-13 | 2006-11-24 | エモリー ユニバーシティ | 正常細胞およびがん細胞における遺伝子発現を検出する方法 |
| JP2008039551A (ja) * | 2006-08-04 | 2008-02-21 | Hitachi High-Technologies Corp | 検体処理システム |
| JP2008532539A (ja) * | 2005-03-16 | 2008-08-21 | ロビオ システムズ リミテッド | 細胞の実体の成熟および輸送システム |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3941317A (en) * | 1973-10-26 | 1976-03-02 | Lnih, Inc. | Method and apparatus for tissue disaggregation |
| CA2175893C (en) * | 1993-11-23 | 2010-06-22 | Paul J. Godowski | Protein tyrosine kinases named rse |
| US6025145A (en) * | 1993-11-23 | 2000-02-15 | Genentech, Inc. | Kinase receptor activation assay |
| EP2275821A1 (en) * | 1995-07-31 | 2011-01-19 | Precision System Science Co., Ltd | Container |
| JP3923968B2 (ja) * | 1995-07-31 | 2007-06-06 | プレシジョン・システム・サイエンス株式会社 | 容器使用方法 |
| US5854009A (en) * | 1995-09-19 | 1998-12-29 | Immuna Care Corporation | Method of detecting estrogen-sensitive pathologies |
| US6077684A (en) * | 1996-11-14 | 2000-06-20 | Vanderbilt University | Automated assay for measuring apoptosis in cell culture |
| JP2003144149A (ja) * | 1997-03-31 | 2003-05-20 | Takara Holdings Inc | 分離装置及びその使用方法 |
| DE19729028C1 (de) * | 1997-07-08 | 1999-05-06 | Fraunhofer Ges Forschung | Vorrichtung sowie Verfahren zur Isolierung von Zellmaterial aus einem Gewebeverband und/oder einer Flüssigkeit |
| DE19804372A1 (de) * | 1998-02-04 | 1999-08-05 | Michael W Dr Dr Dahm | Verfahren zur quantitativen Bestimmung von Tumorzellen in einer Körperflüssigkeit und dazu geeignete Testkits |
| JP3142521B2 (ja) * | 1998-11-04 | 2001-03-07 | 大成プラス株式会社 | 針刺し止栓とその製造方法 |
| JP2001000178A (ja) * | 1999-06-23 | 2001-01-09 | Asahi Medical Co Ltd | 細胞分離方法及び細胞分離装置 |
| ATE335196T1 (de) * | 2000-03-08 | 2006-08-15 | Cytyc Corp | Verfahren und vorrichtung zur vorbereitung von zellproben |
| HRP20031022A2 (en) * | 2001-05-09 | 2005-10-31 | Axis Shield Asa | Assay system |
| US7133543B2 (en) * | 2001-06-12 | 2006-11-07 | Applied Imaging Corporation | Automated scanning method for pathology samples |
| JP2003294765A (ja) * | 2002-03-29 | 2003-10-15 | Nippon Soda Co Ltd | セプタム装着治具 |
| US20040014097A1 (en) | 2002-05-06 | 2004-01-22 | Mcglennen Ronald C. | Genetic test apparatus and method |
| US20040157336A1 (en) * | 2002-11-14 | 2004-08-12 | Affymetrix, Inc. | Automated fluid control system and process |
| US7648678B2 (en) * | 2002-12-20 | 2010-01-19 | Dako Denmark A/S | Method and system for pretreatment of tissue slides |
| JP5795699B2 (ja) * | 2004-04-28 | 2015-10-14 | サノフィ パスツール ヴァックスデザイン コーポレーション | 人工免疫システム：作製および使用方法 |
| MX2007001469A (es) * | 2004-08-06 | 2007-03-26 | Genentech Inc | Ensayos y metodos que utilizan biomarcadores. |
| US20060183223A1 (en) * | 2005-01-21 | 2006-08-17 | King Michael R | Continuous flow chamber device for separation, concentration, and/or purification of cells |
| US20070031283A1 (en) * | 2005-06-23 | 2007-02-08 | Davis Charles Q | Assay cartridges and methods for point of care instruments |
| NZ569791A (en) | 2005-12-16 | 2011-10-28 | Larry Mark Weisenthal | Microaggregates including endothelial cells for microscopic observation |
-
2008
- 2008-10-24 PL PL08841971T patent/PL2210080T3/pl unknown
- 2008-10-24 EP EP08841971.8A patent/EP2210080B1/en active Active
- 2008-10-24 EP EP12197989A patent/EP2573541A1/en not_active Ceased
- 2008-10-24 WO PCT/US2008/012148 patent/WO2009055052A2/en not_active Ceased
- 2008-10-24 KR KR1020107011082A patent/KR101658245B1/ko not_active Expired - Fee Related
- 2008-10-24 ES ES08841971.8T patent/ES2535631T3/es active Active
- 2008-10-24 CA CA2971968A patent/CA2971968C/en not_active Expired - Fee Related
- 2008-10-24 US US12/258,251 patent/US9121801B2/en active Active
- 2008-10-24 CA CA2703631A patent/CA2703631C/en not_active Expired - Fee Related
- 2008-10-24 AU AU2008317329A patent/AU2008317329B2/en not_active Ceased
- 2008-10-24 JP JP2010531056A patent/JP2011501190A/ja active Pending
-
2015
- 2015-07-30 JP JP2015151362A patent/JP6177841B2/ja not_active Expired - Fee Related
- 2015-08-20 US US14/831,789 patent/US20150353880A1/en not_active Abandoned
-
2017
- 2017-07-12 JP JP2017136044A patent/JP6675355B2/ja not_active Expired - Fee Related
Patent Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4350768A (en) * | 1980-09-19 | 1982-09-21 | Bristol Myers Company | Method for preparing single cell suspension |
| JPS63502929A (ja) * | 1986-03-20 | 1988-10-27 | ベックマン インスツルメンツ インコーポレーテッド | モジュール式貯蔵機構 |
| JPH08502401A (ja) * | 1992-05-25 | 1996-03-19 | ガンブロ アクチーボラグ | 細胞毒性試験の実施方法およびそのための系およびこの系に包含されるキット |
| JPH06213788A (ja) * | 1992-09-29 | 1994-08-05 | F Hoffmann La Roche Ag | 細胞学的物質の分解デバイス |
| JPH0751559A (ja) * | 1993-08-20 | 1995-02-28 | Rigoushiya:Kk | 液体試料の分配秤量装置 |
| JPH0894634A (ja) * | 1994-09-22 | 1996-04-12 | Suzuki Motor Corp | 酵素免疫反応測定装置 |
| JPH09196917A (ja) * | 1996-01-12 | 1997-07-31 | Suzuki Motor Corp | テストプレート用自動判定装置 |
| JPH1062436A (ja) * | 1996-08-21 | 1998-03-06 | Fujirebio Inc | 液体の分注方法とその装置 |
| JP2005512023A (ja) * | 2001-09-21 | 2005-04-28 | アクセス ジェネティックス エルエルシー | 遠隔遺伝子分析及び診察用のシステム、方法及びキット |
| JP2006526390A (ja) * | 2003-01-13 | 2006-11-24 | エモリー ユニバーシティ | 正常細胞およびがん細胞における遺伝子発現を検出する方法 |
| US20050233309A1 (en) * | 2004-04-19 | 2005-10-20 | Hankins William D | Kinetic process for the detection, diagnosis, processing, and monitoring of clonal cell populations |
| JP2006158203A (ja) * | 2004-12-02 | 2006-06-22 | Univ Nagoya | リガンド親和性複合タンパク質の取得方法、抗体スクリーニング方法、抗体スクリーニング用キット、医療方法、抗体医薬、非免疫反応性抗体医薬、投薬方法 |
| JP2008532539A (ja) * | 2005-03-16 | 2008-08-21 | ロビオ システムズ リミテッド | 細胞の実体の成熟および輸送システム |
| JP2008039551A (ja) * | 2006-08-04 | 2008-02-21 | Hitachi High-Technologies Corp | 検体処理システム |
Non-Patent Citations (1)
| Title |
|---|
| JPN7013002491; Ｍａｌｕ Ｐｏｌａｎｓｋｉ ａｎｄ Ｎ． Ｌｅｉｇｈ Ａｎｄｅｒｓｏｎ: 'Ａ Ｌｉｓｔ ｏｆ Ｃａｎｄｉｄａｔｅ Ｃａｎｃｅｒ Ｂｉｏｍａｒｋｅｒｓ ｆｏｒ Ｔａｒｇｅｔｅｄ Ｐｒｏｔｅｏｍｉｃｓ' Ｂｉｏｍａｒｋｅｒ Ｉｎｓｉｇｈｔｓ Ｖｏｌ．２, 2006, ｐｐ．１-４８ * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023504585A (ja) * | 2019-11-27 | 2023-02-03 | サーモ フィッシャー サイエンティフィック （ブレーメン） ゲーエムベーハー | サンプルを画像化およびアブレーションするためのシステムおよび方法 |
| US12272538B2 (en) | 2019-11-27 | 2025-04-08 | Thermo Fisher Scientific (Bremen) Gmbh | Systems and methods for imaging and ablating a sample |
Also Published As
| Publication number | Publication date |
|---|---|
| JP6177841B2 (ja) | 2017-08-09 |
| JP2016001184A (ja) | 2016-01-07 |
| CA2703631A1 (en) | 2009-04-30 |
| JP2018004651A (ja) | 2018-01-11 |
| AU2008317329B2 (en) | 2014-10-02 |
| US20090162853A1 (en) | 2009-06-25 |
| EP2210080B1 (en) | 2015-01-28 |
| PL2210080T3 (pl) | 2015-06-30 |
| ES2535631T3 (es) | 2015-05-13 |
| EP2210080A2 (en) | 2010-07-28 |
| CA2703631C (en) | 2017-08-22 |
| WO2009055052A3 (en) | 2009-07-02 |
| CA2971968C (en) | 2019-08-13 |
| JP6675355B2 (ja) | 2020-04-01 |
| KR20100115341A (ko) | 2010-10-27 |
| US20150353880A1 (en) | 2015-12-10 |
| US9121801B2 (en) | 2015-09-01 |
| CA2971968A1 (en) | 2009-04-30 |
| WO2009055052A2 (en) | 2009-04-30 |
| KR101658245B1 (ko) | 2016-09-22 |
| EP2573541A1 (en) | 2013-03-27 |
| HK1145878A1 (en) | 2011-05-06 |
| AU2008317329A1 (en) | 2009-04-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6177841B2 (ja) | 細胞分析の進歩した方法および装置 | |
| JP2011501190A5 (https=) | ||
| Jacob et al. | Generation and biobanking of patient-derived glioblastoma organoids and their application in CAR T cell testing | |
| JP7212523B2 (ja) | スクリーニングキットおよび方法 | |
| JP2021035372A (ja) | サンプル分析のための方法、機器、及びシステム | |
| CA2557568C (en) | Pharmacodynamic assays using flow cytometry | |
| TW202235842A (zh) | 用於個人化醫療及藥物開發之微器官球體(micro-organospheres) | |
| WO2022144365A1 (en) | Predicting efficacy of or resistance to treatment of colon cancer | |
| US20050233309A1 (en) | Kinetic process for the detection, diagnosis, processing, and monitoring of clonal cell populations | |
| JP7144511B2 (ja) | 診療現場診断のための血液サンプルの収集および調製 | |
| AU2014277688B2 (en) | Improved methods and devices for cellular analysis | |
| Goliwas et al. | Preparation and analysis of in vitro three dimensional breast carcinoma surrogates | |
| JP4977325B2 (ja) | 精度管理用疑似組織及びそれを用いた精度管理方法 | |
| CN116615654A (zh) | 基于液滴类器官的免疫肿瘤学分析及其使用方法 | |
| HK1145878B (en) | Improved methods and devices for cellular analysis | |
| Gangavarapu et al. | Isolation and applications of prostate side population cells based on dye cycle violet efflux | |
| Parent | A microfluidic droplet platform for dissecting tumor behaviour in response to physical stimulation and anticancer drugs delivery | |
| JP7113132B2 (ja) | 細胞内における化合物の動態解析法 | |
| Shang et al. | A protocol for organoids from the gynecomastia patients | |
| JP2025529807A (ja) | マイクロオルガノスフェアへの成分送達方法 | |
| CN119677867A (zh) | 用于使用微有机球测试肝细胞毒性的方法和装置 | |
| WO2026060068A1 (en) | High-throughput 3d droplet microfluidics system for analyzing tumor spheroids and immune cell interaction |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20111024 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120824 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20130321 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130703 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20131001 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140604 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140904 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140904 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140911 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150330 |
|
| A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20150730 |