ES2952700T3 - Composiciones oftálmicas y métodos de uso de las mismas - Google Patents

Info

Publication number

ES2952700T3

ES2952700T3 ES16759200T ES16759200T ES2952700T3 ES 2952700 T3 ES2952700 T3 ES 2952700T3 ES 16759200 T ES16759200 T ES 16759200T ES 16759200 T ES16759200 T ES 16759200T ES 2952700 T3 ES2952700 T3 ES 2952700T3

Authority

ES

Spain

Prior art keywords

composition

corneal

tgfp3

dexamethasone

cornea

Prior art date

2015-03-05

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.)

Active

Links

• Espacenet
• Global Dossier
• Discuss

• 239000000203 mixture Substances 0.000 title claims abstract description 171
• 238000000034 method Methods 0.000 title claims abstract description 43
• 210000004087 cornea Anatomy 0.000 claims abstract description 197
• UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 claims description 102
• 229960003957 dexamethasone Drugs 0.000 claims description 92
• 238000011282 treatment Methods 0.000 claims description 79
• 102000004196 processed proteins & peptides Human genes 0.000 claims description 68
• 108090000765 processed proteins & peptides Proteins 0.000 claims description 68
• 229920001184 polypeptide Polymers 0.000 claims description 67
• 102000008186 Collagen Human genes 0.000 claims description 38
• 108010035532 Collagen Proteins 0.000 claims description 38
• 229920001436 collagen Polymers 0.000 claims description 38
• 239000003795 chemical substances by application Substances 0.000 claims description 36
• 201000002287 Keratoconus Diseases 0.000 claims description 31
• 239000007943 implant Substances 0.000 claims description 31
• 238000001727 in vivo Methods 0.000 claims description 28
• 238000004132 cross linking Methods 0.000 claims description 24
• 238000009472 formulation Methods 0.000 claims description 24
• 150000002148 esters Chemical class 0.000 claims description 22
• 150000003839 salts Chemical class 0.000 claims description 22
• 150000004678 hydrides Chemical class 0.000 claims description 21
• 208000014733 refractive error Diseases 0.000 claims description 19
• 150000001413 amino acids Chemical class 0.000 claims description 18
• 239000000243 solution Substances 0.000 claims description 18
• 208000001491 myopia Diseases 0.000 claims description 15
• 230000004379 myopia Effects 0.000 claims description 15
• 239000000499 gel Substances 0.000 claims description 12
• 238000001356 surgical procedure Methods 0.000 claims description 12
• 201000009310 astigmatism Diseases 0.000 claims description 8
• 229940121363 anti-inflammatory agent Drugs 0.000 claims description 7
• 239000002260 anti-inflammatory agent Substances 0.000 claims description 7
• 239000003193 general anesthetic agent Substances 0.000 claims description 7
• 201000010041 presbyopia Diseases 0.000 claims description 7
• 239000004599 antimicrobial Substances 0.000 claims description 5
• 239000000314 lubricant Substances 0.000 claims description 5
• 206010020675 Hypermetropia Diseases 0.000 claims description 4
• 239000000839 emulsion Substances 0.000 claims description 4
• 201000006318 hyperopia Diseases 0.000 claims description 4
• 230000004305 hyperopia Effects 0.000 claims description 4
• 239000006071 cream Substances 0.000 claims description 3
• 238000010828 elution Methods 0.000 claims description 3
• 239000000882 contact lens solution Substances 0.000 claims description 2
• 125000003275 alpha amino acid group Chemical group 0.000 claims 12
• 229960004833 dexamethasone phosphate Drugs 0.000 claims 3
• VQODGRNSFPNSQE-CXSFZGCWSA-N dexamethasone phosphate Chemical group C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COP(O)(O)=O)(O)[C@@]1(C)C[C@@H]2O VQODGRNSFPNSQE-CXSFZGCWSA-N 0.000 claims 3
• 238000013519 translation Methods 0.000 abstract description 2
• 210000001508 eye Anatomy 0.000 description 77
• 210000004027 cell Anatomy 0.000 description 64
• 102000000503 Collagen Type II Human genes 0.000 description 63
• 108010041390 Collagen Type II Proteins 0.000 description 63
• 210000001519 tissue Anatomy 0.000 description 53
• 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 33
• 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 33
• 239000002609 medium Substances 0.000 description 33
• 210000002744 extracellular matrix Anatomy 0.000 description 32
• 239000003889 eye drop Substances 0.000 description 31
• 230000008021 deposition Effects 0.000 description 30
• 229940012356 eye drops Drugs 0.000 description 27
• 230000014509 gene expression Effects 0.000 description 25
• 238000000465 moulding Methods 0.000 description 22
• 230000009816 chondrogenic differentiation Effects 0.000 description 21
• 239000003102 growth factor Substances 0.000 description 21
• 210000000845 cartilage Anatomy 0.000 description 20
• 241000700159 Rattus Species 0.000 description 19
• 108090000623 proteins and genes Proteins 0.000 description 16
• 239000000523 sample Substances 0.000 description 16
• 239000010410 layer Substances 0.000 description 15
• 230000008672 reprogramming Effects 0.000 description 15
• 238000012360 testing method Methods 0.000 description 15
• 102000012422 Collagen Type I Human genes 0.000 description 14
• 108010022452 Collagen Type I Proteins 0.000 description 14
• 238000002372 labelling Methods 0.000 description 14
• 102000004169 proteins and genes Human genes 0.000 description 14
• 241001494479 Pecora Species 0.000 description 13
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 13
• 230000000694 effects Effects 0.000 description 13
• 239000001963 growth medium Substances 0.000 description 13
• 150000003431 steroids Chemical class 0.000 description 13
• CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
• 241001465754 Metazoa Species 0.000 description 12
• 210000002950 fibroblast Anatomy 0.000 description 12
• 238000002474 experimental method Methods 0.000 description 11
• 238000005259 measurement Methods 0.000 description 11
• 230000008859 change Effects 0.000 description 10
• 210000003239 corneal fibroblast Anatomy 0.000 description 10
• 230000007423 decrease Effects 0.000 description 10
• 239000002953 phosphate buffered saline Substances 0.000 description 10
• 102000004190 Enzymes Human genes 0.000 description 9
• 108090000790 Enzymes Proteins 0.000 description 9
• 230000002648 chondrogenic effect Effects 0.000 description 9
• 150000001875 compounds Chemical class 0.000 description 9
• 210000003683 corneal stroma Anatomy 0.000 description 9
• 201000010099 disease Diseases 0.000 description 9
• 229940088598 enzyme Drugs 0.000 description 9
• -1 for example Substances 0.000 description 9
• 238000000338 in vitro Methods 0.000 description 9
• 230000001965 increasing effect Effects 0.000 description 9
• 206010023332 keratitis Diseases 0.000 description 9
• 229920002148 Gellan gum Polymers 0.000 description 8
• 239000012634 fragment Substances 0.000 description 8
• 230000002829 reductive effect Effects 0.000 description 8
• 239000000126 substance Substances 0.000 description 8
• 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 7
• 229930006000 Sucrose Natural products 0.000 description 7
• CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 7
• 210000001612 chondrocyte Anatomy 0.000 description 7
• 206010011005 corneal dystrophy Diseases 0.000 description 7
• 230000007547 defect Effects 0.000 description 7
• 239000006196 drop Substances 0.000 description 7
• 239000000216 gellan gum Substances 0.000 description 7
• 235000010492 gellan gum Nutrition 0.000 description 7
• 238000011065 in-situ storage Methods 0.000 description 7
• 230000002265 prevention Effects 0.000 description 7
• 230000035755 proliferation Effects 0.000 description 7
• 238000011069 regeneration method Methods 0.000 description 7
• 239000005720 sucrose Substances 0.000 description 7
• 208000024891 symptom Diseases 0.000 description 7
• 108091032973 (ribonucleotides)n+m Proteins 0.000 description 6
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
• 208000006069 Corneal Opacity Diseases 0.000 description 6
• 208000003923 Hereditary Corneal Dystrophies Diseases 0.000 description 6
• 241000283984 Rodentia Species 0.000 description 6
• 206010064996 Ulcerative keratitis Diseases 0.000 description 6
• 230000002776 aggregation Effects 0.000 description 6
• 238000004220 aggregation Methods 0.000 description 6
• 230000004075 alteration Effects 0.000 description 6
• 229910002092 carbon dioxide Inorganic materials 0.000 description 6
• 238000004113 cell culture Methods 0.000 description 6
• 231100000269 corneal opacity Toxicity 0.000 description 6
• 230000006378 damage Effects 0.000 description 6
• 239000003814 drug Substances 0.000 description 6
• 238000005516 engineering process Methods 0.000 description 6
• 230000008014 freezing Effects 0.000 description 6
• 238000007710 freezing Methods 0.000 description 6
• JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 6
• 238000003384 imaging method Methods 0.000 description 6
• 230000002055 immunohistochemical effect Effects 0.000 description 6
• 238000007373 indentation Methods 0.000 description 6
• 239000007788 liquid Substances 0.000 description 6
• 230000008929 regeneration Effects 0.000 description 6
• 210000000130 stem cell Anatomy 0.000 description 6
• 230000004304 visual acuity Effects 0.000 description 6
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
• 206010016654 Fibrosis Diseases 0.000 description 5
• 229930040373 Paraformaldehyde Natural products 0.000 description 5
• 238000004458 analytical method Methods 0.000 description 5
• 230000015572 biosynthetic process Effects 0.000 description 5
• 230000007850 degeneration Effects 0.000 description 5
• 230000004069 differentiation Effects 0.000 description 5
• 210000000981 epithelium Anatomy 0.000 description 5
• 238000011156 evaluation Methods 0.000 description 5
• 230000004761 fibrosis Effects 0.000 description 5
• 239000011521 glass Substances 0.000 description 5
• 238000003364 immunohistochemistry Methods 0.000 description 5
• 210000000651 myofibroblast Anatomy 0.000 description 5
• 229920002866 paraformaldehyde Polymers 0.000 description 5
• 230000037390 scarring Effects 0.000 description 5
• 239000002356 single layer Substances 0.000 description 5
• 210000002536 stromal cell Anatomy 0.000 description 5
• 230000001225 therapeutic effect Effects 0.000 description 5
• 238000002560 therapeutic procedure Methods 0.000 description 5
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
• 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 4
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
• 229940035674 anesthetics Drugs 0.000 description 4
• 238000010171 animal model Methods 0.000 description 4
• 230000004071 biological effect Effects 0.000 description 4
• 210000005252 bulbus oculi Anatomy 0.000 description 4
• 230000008668 cellular reprogramming Effects 0.000 description 4
• ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 4
• 239000002299 complementary DNA Substances 0.000 description 4
• 201000007717 corneal ulcer Diseases 0.000 description 4
• 238000012937 correction Methods 0.000 description 4
• 239000006184 cosolvent Substances 0.000 description 4
• 230000003247 decreasing effect Effects 0.000 description 4
• 238000011161 development Methods 0.000 description 4
• 230000018109 developmental process Effects 0.000 description 4
• PLCQGRYPOISRTQ-FCJDYXGNSA-L dexamethasone sodium phosphate Chemical compound [Na+].[Na+].C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COP([O-])([O-])=O)(O)[C@@]1(C)C[C@@H]2O PLCQGRYPOISRTQ-FCJDYXGNSA-L 0.000 description 4
• 230000029087 digestion Effects 0.000 description 4
• 208000035475 disorder Diseases 0.000 description 4
• 229940079593 drug Drugs 0.000 description 4
• 230000004438 eyesight Effects 0.000 description 4
• 239000000835 fiber Substances 0.000 description 4
• FAOZLTXFLGPHNG-KNAQIMQKSA-N fluorometholone Chemical compound C([C@@]12C)=CC(=O)C=C1[C@@H](C)C[C@@H]1[C@]2(F)[C@@H](O)C[C@]2(C)[C@@](O)(C(C)=O)CC[C@H]21 FAOZLTXFLGPHNG-KNAQIMQKSA-N 0.000 description 4
• 238000011534 incubation Methods 0.000 description 4
• 230000006698 induction Effects 0.000 description 4
• 208000014674 injury Diseases 0.000 description 4
• 239000000463 material Substances 0.000 description 4
• 108020004999 messenger RNA Proteins 0.000 description 4
• 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 4
• 230000003287 optical effect Effects 0.000 description 4
• 239000008188 pellet Substances 0.000 description 4
• 229920000642 polymer Polymers 0.000 description 4
• 238000011160 research Methods 0.000 description 4
• WVYADZUPLLSGPU-UHFFFAOYSA-N salsalate Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1O WVYADZUPLLSGPU-UHFFFAOYSA-N 0.000 description 4
• 210000003786 sclera Anatomy 0.000 description 4
• 238000002864 sequence alignment Methods 0.000 description 4
• 210000002966 serum Anatomy 0.000 description 4
• CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
• 241000283707 Capra Species 0.000 description 3
• 206010054760 Corneal thinning Diseases 0.000 description 3
• 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 3
• 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 3
• 241000700157 Rattus norvegicus Species 0.000 description 3
• 208000027418 Wounds and injury Diseases 0.000 description 3
• 230000006907 apoptotic process Effects 0.000 description 3
• 238000003556 assay Methods 0.000 description 3
• 239000000872 buffer Substances 0.000 description 3
• 239000006143 cell culture medium Substances 0.000 description 3
• 230000001413 cellular effect Effects 0.000 description 3
• 239000003246 corticosteroid Substances 0.000 description 3
• 238000010790 dilution Methods 0.000 description 3
• 239000012895 dilution Substances 0.000 description 3
• 238000009826 distribution Methods 0.000 description 3
• 210000003560 epithelium corneal Anatomy 0.000 description 3
• 102000013373 fibrillar collagen Human genes 0.000 description 3
• 108060002894 fibrillar collagen Proteins 0.000 description 3
• 230000003176 fibrotic effect Effects 0.000 description 3
• 239000007789 gas Substances 0.000 description 3
• 230000035876 healing Effects 0.000 description 3
• 229960000890 hydrocortisone Drugs 0.000 description 3
• 230000001939 inductive effect Effects 0.000 description 3
• 208000015181 infectious disease Diseases 0.000 description 3
• 238000003780 insertion Methods 0.000 description 3
• 230000037431 insertion Effects 0.000 description 3
• 229910052740 iodine Inorganic materials 0.000 description 3
• 230000000670 limiting effect Effects 0.000 description 3
• 238000004519 manufacturing process Methods 0.000 description 3
• 239000011159 matrix material Substances 0.000 description 3
• 230000001537 neural effect Effects 0.000 description 3
• 229910052757 nitrogen Inorganic materials 0.000 description 3
• 238000003752 polymerase chain reaction Methods 0.000 description 3
• 239000003755 preservative agent Substances 0.000 description 3
• 230000008569 process Effects 0.000 description 3
• 230000000750 progressive effect Effects 0.000 description 3
• 230000002062 proliferating effect Effects 0.000 description 3
• 238000003753 real-time PCR Methods 0.000 description 3
• 210000001525 retina Anatomy 0.000 description 3
• 229960002477 riboflavin Drugs 0.000 description 3
• 235000019192 riboflavin Nutrition 0.000 description 3
• 239000002151 riboflavin Substances 0.000 description 3
• 239000004094 surface-active agent Substances 0.000 description 3
• 239000005526 vasoconstrictor agent Substances 0.000 description 3
• MDKGKXOCJGEUJW-VIFPVBQESA-N (2s)-2-[4-(thiophene-2-carbonyl)phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1C(=O)C1=CC=CS1 MDKGKXOCJGEUJW-VIFPVBQESA-N 0.000 description 2
• CBHWNVHRXOVHJV-URWONLMNSA-N (8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-17-[2-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyacetyl]-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one Chemical compound O=C([C@]1(O)[C@@]2(C)C[C@H](O)[C@]3(F)[C@@]4(C)C=CC(=O)C=C4CC[C@H]3[C@@H]2C[C@H]1C)CO[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O CBHWNVHRXOVHJV-URWONLMNSA-N 0.000 description 2
• GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
• CNIIGCLFLJGOGP-UHFFFAOYSA-N 2-(1-naphthalenylmethyl)-4,5-dihydro-1H-imidazole Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=NCCN1 CNIIGCLFLJGOGP-UHFFFAOYSA-N 0.000 description 2
• WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
• VIBDVOOELVZGDU-UHFFFAOYSA-N 4-(1h-indol-2-yl)benzene-1,3-dicarboximidamide Chemical compound NC(=N)C1=CC(C(=N)N)=CC=C1C1=CC2=CC=CC=C2N1 VIBDVOOELVZGDU-UHFFFAOYSA-N 0.000 description 2
• GIKNHHRFLCDOEU-UHFFFAOYSA-N 4-(2-aminopropyl)phenol Chemical compound CC(N)CC1=CC=C(O)C=C1 GIKNHHRFLCDOEU-UHFFFAOYSA-N 0.000 description 2
• 238000006037 Brook Silaketone rearrangement reaction Methods 0.000 description 2
• 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
• 208000032544 Cicatrix Diseases 0.000 description 2
• 102000001187 Collagen Type III Human genes 0.000 description 2
• 108010069502 Collagen Type III Proteins 0.000 description 2
• 108060005980 Collagenase Proteins 0.000 description 2
• 102000029816 Collagenase Human genes 0.000 description 2
• 206010051559 Corneal defect Diseases 0.000 description 2
• 208000028006 Corneal injury Diseases 0.000 description 2
• 102000004127 Cytokines Human genes 0.000 description 2
• 108090000695 Cytokines Proteins 0.000 description 2
• 102000016911 Deoxyribonucleases Human genes 0.000 description 2
• 108010053770 Deoxyribonucleases Proteins 0.000 description 2
• BQTXJHAJMDGOFI-NJLPOHDGSA-N Dexamethasone 21-(4-Pyridinecarboxylate) Chemical compound O=C([C@]1(O)[C@@]2(C)C[C@H](O)[C@]3(F)[C@@]4(C)C=CC(=O)C=C4CC[C@H]3[C@@H]2C[C@H]1C)COC(=O)C1=CC=NC=C1 BQTXJHAJMDGOFI-NJLPOHDGSA-N 0.000 description 2
• 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 2
• ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 2
• 208000010412 Glaucoma Diseases 0.000 description 2
• 206010019233 Headaches Diseases 0.000 description 2
• 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
• 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
• 206010061218 Inflammation Diseases 0.000 description 2
• CMWTZPSULFXXJA-UHFFFAOYSA-N Naproxen Natural products C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 description 2
• 108010088225 Nestin Proteins 0.000 description 2
• 102000008730 Nestin Human genes 0.000 description 2
• 241000233805 Phoenix Species 0.000 description 2
• 229920001213 Polysorbate 20 Polymers 0.000 description 2
• 239000004372 Polyvinyl alcohol Substances 0.000 description 2
• KCLANYCVBBTKTO-UHFFFAOYSA-N Proparacaine Chemical compound CCCOC1=CC=C(C(=O)OCCN(CC)CC)C=C1N KCLANYCVBBTKTO-UHFFFAOYSA-N 0.000 description 2
• 102000006382 Ribonucleases Human genes 0.000 description 2
• 108010083644 Ribonucleases Proteins 0.000 description 2
• 102000056172 Transforming growth factor beta-3 Human genes 0.000 description 2
• 108090000097 Transforming growth factor beta-3 Proteins 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
• 102000013127 Vimentin Human genes 0.000 description 2
• 108010065472 Vimentin Proteins 0.000 description 2
• 206010047513 Vision blurred Diseases 0.000 description 2
• HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
• 238000005299 abrasion Methods 0.000 description 2
• 238000010521 absorption reaction Methods 0.000 description 2
• 239000002253 acid Substances 0.000 description 2
• 206010002537 anisometropia Diseases 0.000 description 2
• 229940121375 antifungal agent Drugs 0.000 description 2
• 208000003464 asthenopia Diseases 0.000 description 2
• HSWPZIDYAHLZDD-UHFFFAOYSA-N atipamezole Chemical compound C1C2=CC=CC=C2CC1(CC)C1=CN=CN1 HSWPZIDYAHLZDD-UHFFFAOYSA-N 0.000 description 2
• 230000003416 augmentation Effects 0.000 description 2
• 230000001580 bacterial effect Effects 0.000 description 2
• 230000009286 beneficial effect Effects 0.000 description 2
• 229960000686 benzalkonium chloride Drugs 0.000 description 2
• BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 2
• CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 2
• 239000000227 bioadhesive Substances 0.000 description 2
• 238000001574 biopsy Methods 0.000 description 2
• 230000004397 blinking Effects 0.000 description 2
• 230000000903 blocking effect Effects 0.000 description 2
• 238000004364 calculation method Methods 0.000 description 2
• 239000004202 carbamide Substances 0.000 description 2
• 235000013877 carbamide Nutrition 0.000 description 2
• 239000001569 carbon dioxide Substances 0.000 description 2
• 239000001768 carboxy methyl cellulose Substances 0.000 description 2
• 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
• 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
• 230000022159 cartilage development Effects 0.000 description 2
• 230000015556 catabolic process Effects 0.000 description 2
• RZEKVGVHFLEQIL-UHFFFAOYSA-N celecoxib Chemical compound C1=CC(C)=CC=C1C1=CC(C(F)(F)F)=NN1C1=CC=C(S(N)(=O)=O)C=C1 RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 description 2
• 230000005779 cell damage Effects 0.000 description 2
• 239000013553 cell monolayer Substances 0.000 description 2
• 230000033077 cellular process Effects 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• OSASVXMJTNOKOY-UHFFFAOYSA-N chlorobutanol Chemical compound CC(C)(O)C(Cl)(Cl)Cl OSASVXMJTNOKOY-UHFFFAOYSA-N 0.000 description 2
• MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 description 2
• 229960003920 cocaine Drugs 0.000 description 2
• 230000000052 comparative effect Effects 0.000 description 2
• 208000021921 corneal disease Diseases 0.000 description 2
• 238000012258 culturing Methods 0.000 description 2
• 238000005520 cutting process Methods 0.000 description 2
• GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
• 238000006731 degradation reaction Methods 0.000 description 2
• DDIWRLSEGOVQQD-BJRLRHTOSA-N dexamethasone acefurate Chemical compound O([C@]1([C@@]2(C)C[C@H](O)[C@]3(F)[C@@]4(C)C=CC(=O)C=C4CC[C@H]3[C@@H]2C[C@H]1C)C(=O)COC(C)=O)C(=O)C1=CC=CO1 DDIWRLSEGOVQQD-BJRLRHTOSA-N 0.000 description 2
• CIWBQSYVNNPZIQ-PKWREOPISA-N dexamethasone dipropionate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COC(=O)CC)(OC(=O)CC)[C@@]1(C)C[C@@H]2O CIWBQSYVNNPZIQ-PKWREOPISA-N 0.000 description 2
• 229960002344 dexamethasone sodium phosphate Drugs 0.000 description 2
• 238000003745 diagnosis Methods 0.000 description 2
• 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 2
• 238000006073 displacement reaction Methods 0.000 description 2
• 238000001035 drying Methods 0.000 description 2
• 230000002255 enzymatic effect Effects 0.000 description 2
• 238000011124 ex vivo culture Methods 0.000 description 2
• 238000010195 expression analysis Methods 0.000 description 2
• 238000000605 extraction Methods 0.000 description 2
• 239000012530 fluid Substances 0.000 description 2
• 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 2
• 238000003633 gene expression assay Methods 0.000 description 2
• 150000004676 glycans Chemical class 0.000 description 2
• 231100000869 headache Toxicity 0.000 description 2
• 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
• CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 2
• 230000004054 inflammatory process Effects 0.000 description 2
• 201000000766 irregular astigmatism Diseases 0.000 description 2
• 230000001050 lubricating effect Effects 0.000 description 2
• 239000003550 marker Substances 0.000 description 2
• 229920000609 methyl cellulose Polymers 0.000 description 2
• 239000001923 methylcellulose Substances 0.000 description 2
• 235000010981 methylcellulose Nutrition 0.000 description 2
• LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
• 238000012986 modification Methods 0.000 description 2
• 230000004048 modification Effects 0.000 description 2
• 229960002009 naproxen Drugs 0.000 description 2
• CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 2
• 210000005055 nestin Anatomy 0.000 description 2
• 235000015097 nutrients Nutrition 0.000 description 2
• 239000002674 ointment Substances 0.000 description 2
• 238000005457 optimization Methods 0.000 description 2
• 230000037361 pathway Effects 0.000 description 2
• 230000000149 penetrating effect Effects 0.000 description 2
• 230000002093 peripheral effect Effects 0.000 description 2
• 230000035479 physiological effects, processes and functions Effects 0.000 description 2
• 229920003023 plastic Polymers 0.000 description 2
• 239000004033 plastic Substances 0.000 description 2
• 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
• 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
• 229920001282 polysaccharide Polymers 0.000 description 2
• 239000005017 polysaccharide Substances 0.000 description 2
• 229920002451 polyvinyl alcohol Polymers 0.000 description 2
• 239000011148 porous material Substances 0.000 description 2
• 229960005205 prednisolone Drugs 0.000 description 2
• OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 description 2
• VJZLQIPZNBPASX-OJJGEMKLSA-L prednisolone sodium phosphate Chemical compound [Na+].[Na+].O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)COP([O-])([O-])=O)[C@@H]4[C@@H]3CCC2=C1 VJZLQIPZNBPASX-OJJGEMKLSA-L 0.000 description 2
• 238000002360 preparation method Methods 0.000 description 2
• 230000002035 prolonged effect Effects 0.000 description 2
• 229960003981 proparacaine Drugs 0.000 description 2
• QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
• 238000000746 purification Methods 0.000 description 2
• 239000011541 reaction mixture Substances 0.000 description 2
• 230000009467 reduction Effects 0.000 description 2
• 238000007634 remodeling Methods 0.000 description 2
• 230000008439 repair process Effects 0.000 description 2
• 230000004044 response Effects 0.000 description 2
• 206010039073 rheumatoid arthritis Diseases 0.000 description 2
• 229960000953 salsalate Drugs 0.000 description 2
• 229930182490 saponin Natural products 0.000 description 2
• 150000007949 saponins Chemical class 0.000 description 2
• 235000017709 saponins Nutrition 0.000 description 2
• 238000004621 scanning probe microscopy Methods 0.000 description 2
• 231100000241 scar Toxicity 0.000 description 2
• 230000037387 scars Effects 0.000 description 2
• 230000002784 sclerotic effect Effects 0.000 description 2
• 230000035807 sensation Effects 0.000 description 2
• 239000011780 sodium chloride Substances 0.000 description 2
• AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
• 235000019345 sodium thiosulphate Nutrition 0.000 description 2
• 238000010561 standard procedure Methods 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• 238000006467 substitution reaction Methods 0.000 description 2
• 235000000346 sugar Nutrition 0.000 description 2
• 229960004492 suprofen Drugs 0.000 description 2
• 239000000725 suspension Substances 0.000 description 2
• 238000003786 synthesis reaction Methods 0.000 description 2
• 230000009885 systemic effect Effects 0.000 description 2
• BYJAVTDNIXVSPW-UHFFFAOYSA-N tetryzoline Chemical compound N1CCN=C1C1C2=CC=CC=C2CCC1 BYJAVTDNIXVSPW-UHFFFAOYSA-N 0.000 description 2
• 229940124597 therapeutic agent Drugs 0.000 description 2
• 230000017423 tissue regeneration Effects 0.000 description 2
• 238000011200 topical administration Methods 0.000 description 2
• MDYZKJNTKZIUSK-UHFFFAOYSA-N tyloxapol Chemical compound O=C.C1CO1.CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 MDYZKJNTKZIUSK-UHFFFAOYSA-N 0.000 description 2
• 229920001664 tyloxapol Polymers 0.000 description 2
• 229960004224 tyloxapol Drugs 0.000 description 2
• 210000005048 vimentin Anatomy 0.000 description 2
• 229940088594 vitamin Drugs 0.000 description 2
• 229930003231 vitamin Natural products 0.000 description 2
• 235000013343 vitamin Nutrition 0.000 description 2
• 239000011782 vitamin Substances 0.000 description 2
• XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 description 1
• RDJGLLICXDHJDY-NSHDSACASA-N (2s)-2-(3-phenoxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](C)C1=CC=CC(OC=2C=CC=CC=2)=C1 RDJGLLICXDHJDY-NSHDSACASA-N 0.000 description 1
• RUDATBOHQWOJDD-UHFFFAOYSA-N (3beta,5beta,7alpha)-3,7-Dihydroxycholan-24-oic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)CC2 RUDATBOHQWOJDD-UHFFFAOYSA-N 0.000 description 1
• UCTWMZQNUQWSLP-VIFPVBQESA-N (R)-adrenaline Chemical compound CNC[C@H](O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-VIFPVBQESA-N 0.000 description 1
• 229930182837 (R)-adrenaline Natural products 0.000 description 1
• TWBNMYSKRDRHAT-RCWTXCDDSA-N (S)-timolol hemihydrate Chemical compound O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 TWBNMYSKRDRHAT-RCWTXCDDSA-N 0.000 description 1
• MXDYUONTWJFUOK-UHFFFAOYSA-N 1-(azepan-1-yl)dodecan-1-one Chemical compound CCCCCCCCCCCC(=O)N1CCCCCC1 MXDYUONTWJFUOK-UHFFFAOYSA-N 0.000 description 1
• AHPMSOZQRIEVLQ-UHFFFAOYSA-N 1-(azepan-1-yl)octan-1-one Chemical compound CCCCCCCC(=O)N1CCCCCC1 AHPMSOZQRIEVLQ-UHFFFAOYSA-N 0.000 description 1
• FAAHNQAYWKTLFD-UHFFFAOYSA-N 1-butan-2-ylpyrrolidin-2-one Chemical compound CCC(C)N1CCCC1=O FAAHNQAYWKTLFD-UHFFFAOYSA-N 0.000 description 1
• LEBVLXFERQHONN-UHFFFAOYSA-N 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide Chemical compound CCCCN1CCCCC1C(=O)NC1=C(C)C=CC=C1C LEBVLXFERQHONN-UHFFFAOYSA-N 0.000 description 1
• AXTGDCSMTYGJND-UHFFFAOYSA-N 1-dodecylazepan-2-one Chemical compound CCCCCCCCCCCCN1CCCCCC1=O AXTGDCSMTYGJND-UHFFFAOYSA-N 0.000 description 1
• CPKVUHPKYQGHMW-UHFFFAOYSA-N 1-ethenylpyrrolidin-2-one;molecular iodine Chemical compound II.C=CN1CCCC1=O CPKVUHPKYQGHMW-UHFFFAOYSA-N 0.000 description 1
• NZJXADCEESMBPW-UHFFFAOYSA-N 1-methylsulfinyldecane Chemical compound CCCCCCCCCCS(C)=O NZJXADCEESMBPW-UHFFFAOYSA-N 0.000 description 1
• LEZWWPYKPKIXLL-UHFFFAOYSA-N 1-{2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl}imidazole Chemical compound C1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 LEZWWPYKPKIXLL-UHFFFAOYSA-N 0.000 description 1
• FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
• NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 description 1
• LWNPNOFGINFGGV-UHFFFAOYSA-N 2-(diethylamino)-n-(2,6-dimethylphenyl)acetamide;2-(dimethylamino)ethyl 4-(butylamino)benzoate Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C.CCCCNC1=CC=C(C(=O)OCCN(C)C)C=C1 LWNPNOFGINFGGV-UHFFFAOYSA-N 0.000 description 1
• JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 1
• IEQAICDLOKRSRL-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO IEQAICDLOKRSRL-UHFFFAOYSA-N 0.000 description 1
• JJOFNSLZHKIJEV-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;2-[2-chloro-5-cyano-3-(oxaloamino)anilino]-2-oxoacetic acid Chemical compound OCC(N)(CO)CO.OCC(N)(CO)CO.OC(=O)C(=O)NC1=CC(C#N)=CC(NC(=O)C(O)=O)=C1Cl JJOFNSLZHKIJEV-UHFFFAOYSA-N 0.000 description 1
• WZRJTRPJURQBRM-UHFFFAOYSA-N 4-amino-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide;5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1.COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 WZRJTRPJURQBRM-UHFFFAOYSA-N 0.000 description 1
• BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 description 1
• VVIAGPKUTFNRDU-UHFFFAOYSA-N 6S-folinic acid Natural products C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-UHFFFAOYSA-N 0.000 description 1
• RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
• 102000007469 Actins Human genes 0.000 description 1
• 108010085238 Actins Proteins 0.000 description 1
• 108010067219 Aggrecans Proteins 0.000 description 1
• 102000016284 Aggrecans Human genes 0.000 description 1
• 239000012099 Alexa Fluor family Substances 0.000 description 1
• APKFDSVGJQXUKY-KKGHZKTASA-N Amphotericin-B Natural products O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1C=CC=CC=CC=CC=CC=CC=C[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-KKGHZKTASA-N 0.000 description 1
• 108010001478 Bacitracin Proteins 0.000 description 1
• 102100024506 Bone morphogenetic protein 2 Human genes 0.000 description 1
• 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
• 235000003197 Byrsonima crassifolia Nutrition 0.000 description 1
• 240000001546 Byrsonima crassifolia Species 0.000 description 1
• 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
• 241000579895 Chlorostilbon Species 0.000 description 1
• 108090000819 Chondroitin-sulfate-ABC endolyases Proteins 0.000 description 1
• 102000037716 Chondroitin-sulfate-ABC endolyases Human genes 0.000 description 1
• 101710106625 Chondroitinase-AC Proteins 0.000 description 1
• 208000017667 Chronic Disease Diseases 0.000 description 1
• 241001550206 Colla Species 0.000 description 1
• 206010010356 Congenital anomaly Diseases 0.000 description 1
• 201000004182 Congenital stromal corneal dystrophy Diseases 0.000 description 1
• 206010010741 Conjunctivitis Diseases 0.000 description 1
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
• 206010011033 Corneal oedema Diseases 0.000 description 1
• 201000009343 Cornelia de Lange syndrome Diseases 0.000 description 1
• 235000004035 Cryptotaenia japonica Nutrition 0.000 description 1
• 229920000858 Cyclodextrin Polymers 0.000 description 1
• 208000003471 De Lange Syndrome Diseases 0.000 description 1
• 206010052122 Dellen Diseases 0.000 description 1
• 229920002307 Dextran Polymers 0.000 description 1
• BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
• 208000003164 Diplopia Diseases 0.000 description 1
• 208000003556 Dry Eye Syndromes Diseases 0.000 description 1
• 206010013774 Dry eye Diseases 0.000 description 1
• 208000002197 Ehlers-Danlos syndrome Diseases 0.000 description 1
• 241000196324 Embryophyta Species 0.000 description 1
• 241001635598 Enicostema Species 0.000 description 1
• 241000588724 Escherichia coli Species 0.000 description 1
• VTUSIVBDOCDNHS-UHFFFAOYSA-N Etidocaine Chemical compound CCCN(CC)C(CC)C(=O)NC1=C(C)C=CC=C1C VTUSIVBDOCDNHS-UHFFFAOYSA-N 0.000 description 1
• 206010015548 Euthanasia Diseases 0.000 description 1
• 206010015946 Eye irritation Diseases 0.000 description 1
• 108010067306 Fibronectins Proteins 0.000 description 1
• 102000016359 Fibronectins Human genes 0.000 description 1
• 206010016845 Foetal alcohol syndrome Diseases 0.000 description 1
• MPJKWIXIYCLVCU-UHFFFAOYSA-N Folinic acid Natural products NC1=NC2=C(N(C=O)C(CNc3ccc(cc3)C(=O)NC(CCC(=O)O)CC(=O)O)CN2)C(=O)N1 MPJKWIXIYCLVCU-UHFFFAOYSA-N 0.000 description 1
• 201000001925 Fuchs' endothelial dystrophy Diseases 0.000 description 1
• 208000014260 Fungal keratitis Diseases 0.000 description 1
• IECPWNUMDGFDKC-UHFFFAOYSA-N Fusicsaeure Natural products C12C(O)CC3C(=C(CCC=C(C)C)C(O)=O)C(OC(C)=O)CC3(C)C1(C)CCC1C2(C)CCC(O)C1C IECPWNUMDGFDKC-UHFFFAOYSA-N 0.000 description 1
• 241000287828 Gallus gallus Species 0.000 description 1
• 108010026132 Gelatinases Proteins 0.000 description 1
• 102000013382 Gelatinases Human genes 0.000 description 1
• 229930182566 Gentamicin Natural products 0.000 description 1
• CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 1
• 206010072579 Granulomatosis with polyangiitis Diseases 0.000 description 1
• 239000012981 Hank's balanced salt solution Substances 0.000 description 1
• 208000005100 Herpetic Keratitis Diseases 0.000 description 1
• 241000282412 Homo Species 0.000 description 1
• 101000762366 Homo sapiens Bone morphogenetic protein 2 Proteins 0.000 description 1
• 101001013150 Homo sapiens Interstitial collagenase Proteins 0.000 description 1
• 101000712663 Homo sapiens Transforming growth factor beta-3 proprotein Proteins 0.000 description 1
• 108010003272 Hyaluronate lyase Proteins 0.000 description 1
• 102000001974 Hyaluronidases Human genes 0.000 description 1
• 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
• XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
• HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
• 238000012404 In vitro experiment Methods 0.000 description 1
• 206010060833 Infectious crystalline keratopathy Diseases 0.000 description 1
• 108010002350 Interleukin-2 Proteins 0.000 description 1
• 102000004388 Interleukin-4 Human genes 0.000 description 1
• 108090000978 Interleukin-4 Proteins 0.000 description 1
• 206010022998 Irritability Diseases 0.000 description 1
• UETNIIAIRMUTSM-UHFFFAOYSA-N Jacareubin Natural products CC1(C)OC2=CC3Oc4c(O)c(O)ccc4C(=O)C3C(=C2C=C1)O UETNIIAIRMUTSM-UHFFFAOYSA-N 0.000 description 1
• 206010023335 Keratitis interstitial Diseases 0.000 description 1
• 102100021497 Keratocan Human genes 0.000 description 1
• 101710153980 Keratocan Proteins 0.000 description 1
• YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 1
• ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
• 229930182816 L-glutamine Natural products 0.000 description 1
• 241000446313 Lamella Species 0.000 description 1
• 229930182504 Lasalocid Natural products 0.000 description 1
• NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
• 102000000380 Matrix Metalloproteinase 1 Human genes 0.000 description 1
• 102000000424 Matrix Metalloproteinase 2 Human genes 0.000 description 1
• 108010016165 Matrix Metalloproteinase 2 Proteins 0.000 description 1
• 102000000422 Matrix Metalloproteinase 3 Human genes 0.000 description 1
• SBDNJUWAMKYJOX-UHFFFAOYSA-N Meclofenamic Acid Chemical compound CC1=CC=C(Cl)C(NC=2C(=CC=CC=2)C(O)=O)=C1Cl SBDNJUWAMKYJOX-UHFFFAOYSA-N 0.000 description 1
• GZENKSODFLBBHQ-ILSZZQPISA-N Medrysone Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)[C@@H](C(C)=O)CC[C@H]21 GZENKSODFLBBHQ-ILSZZQPISA-N 0.000 description 1
• 102000005741 Metalloproteases Human genes 0.000 description 1
• 108010006035 Metalloproteases Proteins 0.000 description 1
• BYBLEWFAAKGYCD-UHFFFAOYSA-N Miconazole Chemical compound ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 BYBLEWFAAKGYCD-UHFFFAOYSA-N 0.000 description 1
• 206010057414 Microcornea Diseases 0.000 description 1
• 206010027626 Milia Diseases 0.000 description 1
• 208000024599 Mooren ulcer Diseases 0.000 description 1
• 206010028347 Muscle twitching Diseases 0.000 description 1
• HSHXDCVZWHOWCS-UHFFFAOYSA-N N'-hexadecylthiophene-2-carbohydrazide Chemical compound CCCCCCCCCCCCCCCCNNC(=O)c1cccs1 HSHXDCVZWHOWCS-UHFFFAOYSA-N 0.000 description 1
• IJHNSHDBIRRJRN-UHFFFAOYSA-N N,N-dimethyl-3-phenyl-3-(2-pyridinyl)-1-propanamine Chemical compound C=1C=CC=NC=1C(CCN(C)C)C1=CC=CC=C1 IJHNSHDBIRRJRN-UHFFFAOYSA-N 0.000 description 1
• BLXXJMDCKKHMKV-UHFFFAOYSA-N Nabumetone Chemical compound C1=C(CCC(C)=O)C=CC2=CC(OC)=CC=C21 BLXXJMDCKKHMKV-UHFFFAOYSA-N 0.000 description 1
• 206010028813 Nausea Diseases 0.000 description 1
• 241000772415 Neovison vison Species 0.000 description 1
• 241000207746 Nicotiana benthamiana Species 0.000 description 1
• 206010030113 Oedema Diseases 0.000 description 1
• 206010073938 Ophthalmic herpes simplex Diseases 0.000 description 1
• 208000002193 Pain Diseases 0.000 description 1
• 208000031816 Pathologic Dilatation Diseases 0.000 description 1
• 206010034960 Photophobia Diseases 0.000 description 1
• 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
• 229920000148 Polycarbophil calcium Polymers 0.000 description 1
• 206010065159 Polychondritis Diseases 0.000 description 1
• 108010093965 Polymyxin B Proteins 0.000 description 1
• 229920001214 Polysorbate 60 Polymers 0.000 description 1
• 239000004793 Polystyrene Substances 0.000 description 1
• 229920000153 Povidone-iodine Polymers 0.000 description 1
• LRJOMUJRLNCICJ-JZYPGELDSA-N Prednisolone acetate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)COC(=O)C)(O)[C@@]1(C)C[C@@H]2O LRJOMUJRLNCICJ-JZYPGELDSA-N 0.000 description 1
• 102100033237 Pro-epidermal growth factor Human genes 0.000 description 1
• 102000016611 Proteoglycans Human genes 0.000 description 1
• 108010067787 Proteoglycans Proteins 0.000 description 1
• 201000002154 Pterygium Diseases 0.000 description 1
• 238000002123 RNA extraction Methods 0.000 description 1
• 206010038848 Retinal detachment Diseases 0.000 description 1
• 241001303601 Rosacea Species 0.000 description 1
• 201000004224 Schnyder corneal dystrophy Diseases 0.000 description 1
• 206010039897 Sedation Diseases 0.000 description 1
• 102000054727 Serum Amyloid A Human genes 0.000 description 1
• 108700028909 Serum Amyloid A Proteins 0.000 description 1
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
• ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 1
• 229920002125 Sokalan® Polymers 0.000 description 1
• 241000790234 Sphingomonas elodea Species 0.000 description 1
• NHUHCSRWZMLRLA-UHFFFAOYSA-N Sulfisoxazole Chemical compound CC1=NOC(NS(=O)(=O)C=2C=CC(N)=CC=2)=C1C NHUHCSRWZMLRLA-UHFFFAOYSA-N 0.000 description 1
• 239000000150 Sympathomimetic Substances 0.000 description 1
• 102000043168 TGF-beta family Human genes 0.000 description 1
• 108091085018 TGF-beta family Proteins 0.000 description 1
• WBWWGRHZICKQGZ-UHFFFAOYSA-N Taurocholic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(=O)NCCS(O)(=O)=O)C)C1(C)C(O)C2 WBWWGRHZICKQGZ-UHFFFAOYSA-N 0.000 description 1
• 239000004098 Tetracycline Substances 0.000 description 1
• 102000004887 Transforming Growth Factor beta Human genes 0.000 description 1
• 108090001012 Transforming Growth Factor beta Proteins 0.000 description 1
• 102000009618 Transforming Growth Factors Human genes 0.000 description 1
• 108010009583 Transforming Growth Factors Proteins 0.000 description 1
• 102100033460 Transforming growth factor beta-3 proprotein Human genes 0.000 description 1
• 240000002913 Trifolium pratense Species 0.000 description 1
• 235000015724 Trifolium pratense Nutrition 0.000 description 1
• 108060008682 Tumor Necrosis Factor Proteins 0.000 description 1
• 208000026928 Turner syndrome Diseases 0.000 description 1
• 208000025865 Ulcer Diseases 0.000 description 1
• OIRDTQYFTABQOQ-UHTZMRCNSA-N Vidarabine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O OIRDTQYFTABQOQ-UHTZMRCNSA-N 0.000 description 1
• 206010047571 Visual impairment Diseases 0.000 description 1
• FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
• 229930003779 Vitamin B12 Natural products 0.000 description 1
• 229930003427 Vitamin E Natural products 0.000 description 1
• 229930003448 Vitamin K Natural products 0.000 description 1
• 208000026724 Waardenburg syndrome Diseases 0.000 description 1
• 201000005928 Weill-Marchesani syndrome Diseases 0.000 description 1
• 230000001594 aberrant effect Effects 0.000 description 1
• 230000004308 accommodation Effects 0.000 description 1
• RXSUFCOOZSGWSW-UHFFFAOYSA-M acetyloxy-(4-aminophenyl)mercury Chemical compound CC(=O)O[Hg]C1=CC=C(N)C=C1 RXSUFCOOZSGWSW-UHFFFAOYSA-M 0.000 description 1
• 229960004150 aciclovir Drugs 0.000 description 1
• MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 description 1
• 239000013543 active substance Substances 0.000 description 1
• 230000001154 acute effect Effects 0.000 description 1
• 125000002252 acyl group Chemical group 0.000 description 1
• 239000000853 adhesive Substances 0.000 description 1
• 230000001070 adhesive effect Effects 0.000 description 1
• 239000002313 adhesive film Substances 0.000 description 1
• 230000002293 adipogenic effect Effects 0.000 description 1
• 238000009098 adjuvant therapy Methods 0.000 description 1
• 230000002411 adverse Effects 0.000 description 1
• 239000000443 aerosol Substances 0.000 description 1
• 229940006546 albon Drugs 0.000 description 1
• FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
• 150000001408 amides Chemical class 0.000 description 1
• APKFDSVGJQXUKY-INPOYWNPSA-N amphotericin B Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-INPOYWNPSA-N 0.000 description 1
• 229960003942 amphotericin b Drugs 0.000 description 1
• 210000003484 anatomy Anatomy 0.000 description 1
• 229920006318 anionic polymer Polymers 0.000 description 1
• 229960002469 antazoline Drugs 0.000 description 1
• REYFJDPCWQRWAA-UHFFFAOYSA-N antazoline Chemical compound N=1CCNC=1CN(C=1C=CC=CC=1)CC1=CC=CC=C1 REYFJDPCWQRWAA-UHFFFAOYSA-N 0.000 description 1
• 210000002159 anterior chamber Anatomy 0.000 description 1
• 239000003242 anti bacterial agent Substances 0.000 description 1
• 230000003266 anti-allergic effect Effects 0.000 description 1
• 230000000844 anti-bacterial effect Effects 0.000 description 1
• 230000003367 anti-collagen effect Effects 0.000 description 1
• 230000000843 anti-fungal effect Effects 0.000 description 1
• 230000003110 anti-inflammatory effect Effects 0.000 description 1
• 230000000840 anti-viral effect Effects 0.000 description 1
• 239000012984 antibiotic solution Substances 0.000 description 1
• 239000003429 antifungal agent Substances 0.000 description 1
• 229940125715 antihistaminic agent Drugs 0.000 description 1
• 239000000739 antihistaminic agent Substances 0.000 description 1
• 229940109449 antisedan Drugs 0.000 description 1
• 239000003443 antiviral agent Substances 0.000 description 1
• 230000005735 apoptotic response Effects 0.000 description 1
• 238000013459 approach Methods 0.000 description 1
• 229960002610 apraclonidine Drugs 0.000 description 1
• IEJXVRYNEISIKR-UHFFFAOYSA-N apraclonidine Chemical compound ClC1=CC(N)=CC(Cl)=C1NC1=NCCN1 IEJXVRYNEISIKR-UHFFFAOYSA-N 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 235000010323 ascorbic acid Nutrition 0.000 description 1
• 239000011668 ascorbic acid Substances 0.000 description 1
• 229960005070 ascorbic acid Drugs 0.000 description 1
• 229960003002 atipamezole Drugs 0.000 description 1
• 239000012298 atmosphere Substances 0.000 description 1
• 229960001671 azapropazone Drugs 0.000 description 1
• WOIIIUDZSOLAIW-NSHDSACASA-N azapropazone Chemical compound C1=C(C)C=C2N3C(=O)[C@H](CC=C)C(=O)N3C(N(C)C)=NC2=C1 WOIIIUDZSOLAIW-NSHDSACASA-N 0.000 description 1
• 229960005364 bacitracin zinc Drugs 0.000 description 1
• 239000007640 basal medium Substances 0.000 description 1
• 230000008901 benefit Effects 0.000 description 1
• 229960005274 benzocaine Drugs 0.000 description 1
• 239000002876 beta blocker Substances 0.000 description 1
• 229960002537 betamethasone Drugs 0.000 description 1
• UREBDLICKHMUKA-DVTGEIKXSA-N betamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-DVTGEIKXSA-N 0.000 description 1
• PLCQGRYPOISRTQ-LWCNAHDDSA-L betamethasone sodium phosphate Chemical compound [Na+].[Na+].C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)COP([O-])([O-])=O)(O)[C@@]1(C)C[C@@H]2O PLCQGRYPOISRTQ-LWCNAHDDSA-L 0.000 description 1
• 229960005354 betamethasone sodium phosphate Drugs 0.000 description 1
• 229960004324 betaxolol Drugs 0.000 description 1
• CHDPSNLJFOQTRK-UHFFFAOYSA-N betaxolol hydrochloride Chemical compound [Cl-].C1=CC(OCC(O)C[NH2+]C(C)C)=CC=C1CCOCC1CC1 CHDPSNLJFOQTRK-UHFFFAOYSA-N 0.000 description 1
• 239000003613 bile acid Substances 0.000 description 1
• 239000003833 bile salt Substances 0.000 description 1
• 229940093761 bile salts Drugs 0.000 description 1
• 230000003851 biochemical process Effects 0.000 description 1
• 230000003115 biocidal effect Effects 0.000 description 1
• 230000008827 biological function Effects 0.000 description 1
• 239000012620 biological material Substances 0.000 description 1
• 239000012472 biological sample Substances 0.000 description 1
• 210000004204 blood vessel Anatomy 0.000 description 1
• 239000008366 buffered solution Substances 0.000 description 1
• 229960003150 bupivacaine Drugs 0.000 description 1
• 238000010804 cDNA synthesis Methods 0.000 description 1
• 238000010805 cDNA synthesis kit Methods 0.000 description 1
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
• LWAFSWPYPHEXKX-UHFFFAOYSA-N carteolol Chemical compound N1C(=O)CCC2=C1C=CC=C2OCC(O)CNC(C)(C)C LWAFSWPYPHEXKX-UHFFFAOYSA-N 0.000 description 1
• 229960001222 carteolol Drugs 0.000 description 1
• 150000001768 cations Chemical class 0.000 description 1
• 229940047495 celebrex Drugs 0.000 description 1
• 229960000590 celecoxib Drugs 0.000 description 1
• 230000030833 cell death Effects 0.000 description 1
• 230000024245 cell differentiation Effects 0.000 description 1
• 208000037887 cell injury Diseases 0.000 description 1
• 230000006727 cell loss Effects 0.000 description 1
• 239000006285 cell suspension Substances 0.000 description 1
• 230000003833 cell viability Effects 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 238000005119 centrifugation Methods 0.000 description 1
• 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
• YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
• 238000012512 characterization method Methods 0.000 description 1
• 238000003889 chemical engineering Methods 0.000 description 1
• RUDATBOHQWOJDD-BSWAIDMHSA-N chenodeoxycholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)CC1 RUDATBOHQWOJDD-BSWAIDMHSA-N 0.000 description 1
• 229960001091 chenodeoxycholic acid Drugs 0.000 description 1
• 210000003837 chick embryo Anatomy 0.000 description 1
• 210000004978 chinese hamster ovary cell Anatomy 0.000 description 1
• 229960005091 chloramphenicol Drugs 0.000 description 1
• WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
• 229960004926 chlorobutanol Drugs 0.000 description 1
• 229960002023 chloroprocaine Drugs 0.000 description 1
• VDANGULDQQJODZ-UHFFFAOYSA-N chloroprocaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1Cl VDANGULDQQJODZ-UHFFFAOYSA-N 0.000 description 1
• CYDMQBQPVICBEU-UHFFFAOYSA-N chlorotetracycline Natural products C1=CC(Cl)=C2C(O)(C)C3CC4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-UHFFFAOYSA-N 0.000 description 1
• CYDMQBQPVICBEU-XRNKAMNCSA-N chlortetracycline Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-XRNKAMNCSA-N 0.000 description 1
• 239000000812 cholinergic antagonist Substances 0.000 description 1
• 238000004587 chromatography analysis Methods 0.000 description 1
• 230000001684 chronic effect Effects 0.000 description 1
• 230000001886 ciliary effect Effects 0.000 description 1
• 229960003405 ciprofloxacin Drugs 0.000 description 1
• 239000004927 clay Substances 0.000 description 1
• 238000004140 cleaning Methods 0.000 description 1
• 238000003776 cleavage reaction Methods 0.000 description 1
• 229960002227 clindamycin Drugs 0.000 description 1
• KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 description 1
• 229960004022 clotrimazole Drugs 0.000 description 1
• VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 description 1
• 229940047766 co-trimoxazole Drugs 0.000 description 1
• AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 1
• 230000037319 collagen production Effects 0.000 description 1
• 229940096422 collagen type i Drugs 0.000 description 1
• 229960002424 collagenase Drugs 0.000 description 1
• 238000004590 computer program Methods 0.000 description 1
• 238000011109 contamination Methods 0.000 description 1
• 238000013270 controlled release Methods 0.000 description 1
• 229910052802 copper Inorganic materials 0.000 description 1
• 239000010949 copper Substances 0.000 description 1
• 201000003046 cornea plana Diseases 0.000 description 1
• 201000004573 corneal ectasia Diseases 0.000 description 1
• 201000004778 corneal edema Diseases 0.000 description 1
• 201000004889 corneal granular dystrophy Diseases 0.000 description 1
• 230000004453 corneal transparency Effects 0.000 description 1
• 229960001334 corticosteroids Drugs 0.000 description 1
• ALEXXDVDDISNDU-JZYPGELDSA-N cortisol 21-acetate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)COC(=O)C)(O)[C@@]1(C)C[C@@H]2O ALEXXDVDDISNDU-JZYPGELDSA-N 0.000 description 1
• 229940111134 coxibs Drugs 0.000 description 1
• 239000002577 cryoprotective agent Substances 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 description 1
• RFWZESUMWJKKRN-UHFFFAOYSA-N dapiprazole Chemical compound CC1=CC=CC=C1N1CCN(CCC=2N3CCCCC3=NN=2)CC1 RFWZESUMWJKKRN-UHFFFAOYSA-N 0.000 description 1
• 229960002947 dapiprazole Drugs 0.000 description 1
• 238000013480 data collection Methods 0.000 description 1
• 229940026692 decadron Drugs 0.000 description 1
• 230000002950 deficient Effects 0.000 description 1
• 230000003412 degenerative effect Effects 0.000 description 1
• 230000003413 degradative effect Effects 0.000 description 1
• 239000012024 dehydrating agents‎ Substances 0.000 description 1
• 210000002555 descemet membrane Anatomy 0.000 description 1
• 238000013461 design Methods 0.000 description 1
• 230000006866 deterioration Effects 0.000 description 1
• 230000001627 detrimental effect Effects 0.000 description 1
• 229950002874 dexamethasone acefurate Drugs 0.000 description 1
• 229950000250 dexamethasone dipropionate Drugs 0.000 description 1
• 229950000812 dexamethasone palmitate Drugs 0.000 description 1
• 229950006825 dexamethasone valerate Drugs 0.000 description 1
• 238000010586 diagram Methods 0.000 description 1
• 229960001259 diclofenac Drugs 0.000 description 1
• DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 description 1
• 229960001193 diclofenac sodium Drugs 0.000 description 1
• 238000009792 diffusion process Methods 0.000 description 1
• 229960000616 diflunisal Drugs 0.000 description 1
• HUPFGZXOMWLGNK-UHFFFAOYSA-N diflunisal Chemical compound C1=C(O)C(C(=O)O)=CC(C=2C(=CC(F)=CC=2)F)=C1 HUPFGZXOMWLGNK-UHFFFAOYSA-N 0.000 description 1
• VKFAUCPBMAGVRG-UHFFFAOYSA-N dipivefrin hydrochloride Chemical compound [Cl-].C[NH2+]CC(O)C1=CC=C(OC(=O)C(C)(C)C)C(OC(=O)C(C)(C)C)=C1 VKFAUCPBMAGVRG-UHFFFAOYSA-N 0.000 description 1
• 239000006185 dispersion Substances 0.000 description 1
• 239000012153 distilled water Substances 0.000 description 1
• 231100000673 dose–response relationship Toxicity 0.000 description 1
• 208000029444 double vision Diseases 0.000 description 1
• 238000012377 drug delivery Methods 0.000 description 1
• 230000004064 dysfunction Effects 0.000 description 1
• 229960003913 econazole Drugs 0.000 description 1
• 230000005489 elastic deformation Effects 0.000 description 1
• 239000003792 electrolyte Substances 0.000 description 1
• 230000009881 electrostatic interaction Effects 0.000 description 1
• 230000008030 elimination Effects 0.000 description 1
• 238000003379 elimination reaction Methods 0.000 description 1
• 229910052876 emerald Inorganic materials 0.000 description 1
• 239000010976 emerald Substances 0.000 description 1
• 206010014801 endophthalmitis Diseases 0.000 description 1
• 210000002889 endothelial cell Anatomy 0.000 description 1
• 230000003511 endothelial effect Effects 0.000 description 1
• 210000000871 endothelium corneal Anatomy 0.000 description 1
• 238000004146 energy storage Methods 0.000 description 1
• 230000007515 enzymatic degradation Effects 0.000 description 1
• 239000002532 enzyme inhibitor Substances 0.000 description 1
• 229960005139 epinephrine Drugs 0.000 description 1
• 210000002919 epithelial cell Anatomy 0.000 description 1
• 210000003743 erythrocyte Anatomy 0.000 description 1
• 229960003276 erythromycin Drugs 0.000 description 1
• 229940011871 estrogen Drugs 0.000 description 1
• 239000000262 estrogen Substances 0.000 description 1
• 229950009769 etabonate Drugs 0.000 description 1
• BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
• 229960003976 etidocaine Drugs 0.000 description 1
• 229960005293 etodolac Drugs 0.000 description 1
• XFBVBWWRPKNWHW-UHFFFAOYSA-N etodolac Chemical compound C1COC(CC)(CC(O)=O)C2=N[C]3C(CC)=CC=CC3=C21 XFBVBWWRPKNWHW-UHFFFAOYSA-N 0.000 description 1
• 201000009819 exposure keratitis Diseases 0.000 description 1
• 231100000013 eye irritation Toxicity 0.000 description 1
• 239000004744 fabric Substances 0.000 description 1
• 206010016256 fatigue Diseases 0.000 description 1
• 229960001419 fenoprofen Drugs 0.000 description 1
• 208000026934 fetal alcohol spectrum disease Diseases 0.000 description 1
• 201000007794 fetal alcohol syndrome Diseases 0.000 description 1
• 239000012894 fetal calf serum Substances 0.000 description 1
• 230000003619 fibrillary effect Effects 0.000 description 1
• 230000003328 fibroblastic effect Effects 0.000 description 1
• RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 description 1
• 229960004884 fluconazole Drugs 0.000 description 1
• XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 description 1
• 229960004413 flucytosine Drugs 0.000 description 1
• 229960003973 fluocortolone Drugs 0.000 description 1
• GAKMQHDJQHZUTJ-ULHLPKEOSA-N fluocortolone Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2C[C@@H](C)[C@H](C(=O)CO)[C@@]2(C)C[C@@H]1O GAKMQHDJQHZUTJ-ULHLPKEOSA-N 0.000 description 1
• 229960001048 fluorometholone Drugs 0.000 description 1
• 229960002390 flurbiprofen Drugs 0.000 description 1
• SYTBZMRGLBWNTM-UHFFFAOYSA-N flurbiprofen Chemical compound FC1=CC(C(C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-UHFFFAOYSA-N 0.000 description 1
• 229960003898 flurbiprofen sodium Drugs 0.000 description 1
• VVIAGPKUTFNRDU-ABLWVSNPSA-N folinic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-ABLWVSNPSA-N 0.000 description 1
• 235000008191 folinic acid Nutrition 0.000 description 1
• 239000011672 folinic acid Substances 0.000 description 1
• 230000006870 function Effects 0.000 description 1
• 125000000524 functional group Chemical group 0.000 description 1
• 230000002538 fungal effect Effects 0.000 description 1
• 229960004675 fusidic acid Drugs 0.000 description 1
• IECPWNUMDGFDKC-MZJAQBGESA-N fusidic acid Chemical compound O[C@@H]([C@@H]12)C[C@H]3\C(=C(/CCC=C(C)C)C(O)=O)[C@@H](OC(C)=O)C[C@]3(C)[C@@]2(C)CC[C@@H]2[C@]1(C)CC[C@@H](O)[C@H]2C IECPWNUMDGFDKC-MZJAQBGESA-N 0.000 description 1
• WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
• 229960002963 ganciclovir Drugs 0.000 description 1
• IRSCQMHQWWYFCW-UHFFFAOYSA-N ganciclovir Chemical compound O=C1NC(N)=NC2=C1N=CN2COC(CO)CO IRSCQMHQWWYFCW-UHFFFAOYSA-N 0.000 description 1
• 238000001879 gelation Methods 0.000 description 1
• 239000003349 gelling agent Substances 0.000 description 1
• 230000002068 genetic effect Effects 0.000 description 1
• 229960002518 gentamicin Drugs 0.000 description 1
• 230000004313 glare Effects 0.000 description 1
• 239000003862 glucocorticoid Substances 0.000 description 1
• 208000014706 granular corneal dystrophy Diseases 0.000 description 1
• 239000008187 granular material Substances 0.000 description 1
• 230000012010 growth Effects 0.000 description 1
• 125000001475 halogen functional group Chemical group 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 201000010884 herpes simplex virus keratitis Diseases 0.000 description 1
• 229960002773 hyaluronidase Drugs 0.000 description 1
• 230000036571 hydration Effects 0.000 description 1
• 238000006703 hydration reaction Methods 0.000 description 1
• 239000000416 hydrocolloid Substances 0.000 description 1
• 229960001067 hydrocortisone acetate Drugs 0.000 description 1
• 239000000017 hydrogel Substances 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• 229950005360 hydroxyamfetamine Drugs 0.000 description 1
• 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
• 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
• 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
• 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
• 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
• 229960001680 ibuprofen Drugs 0.000 description 1
• 229960004716 idoxuridine Drugs 0.000 description 1
• 238000002991 immunohistochemical analysis Methods 0.000 description 1
• 230000001771 impaired effect Effects 0.000 description 1
• 230000001976 improved effect Effects 0.000 description 1
• 230000006872 improvement Effects 0.000 description 1
• 238000012606 in vitro cell culture Methods 0.000 description 1
• 229960000905 indomethacin Drugs 0.000 description 1
• 239000000411 inducer Substances 0.000 description 1
• 230000002458 infectious effect Effects 0.000 description 1
• 208000027866 inflammatory disease Diseases 0.000 description 1
• 230000002757 inflammatory effect Effects 0.000 description 1
• 239000004615 ingredient Substances 0.000 description 1
• 230000005764 inhibitory process Effects 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 201000006904 interstitial keratitis Diseases 0.000 description 1
• 239000007928 intraperitoneal injection Substances 0.000 description 1
• 238000011835 investigation Methods 0.000 description 1
• 239000002555 ionophore Substances 0.000 description 1
• 230000000236 ionophoric effect Effects 0.000 description 1
• 210000000554 iris Anatomy 0.000 description 1
• 230000002427 irreversible effect Effects 0.000 description 1
• 239000002085 irritant Substances 0.000 description 1
• 231100000021 irritant Toxicity 0.000 description 1
• 230000007794 irritation Effects 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 108010011519 keratan-sulfate endo-1,4-beta-galactosidase Proteins 0.000 description 1
• 229960003299 ketamine Drugs 0.000 description 1
• 229960004125 ketoconazole Drugs 0.000 description 1
• DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 description 1
• 229960000991 ketoprofen Drugs 0.000 description 1
• 229960004752 ketorolac Drugs 0.000 description 1
• OZWKMVRBQXNZKK-UHFFFAOYSA-N ketorolac Chemical compound OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 OZWKMVRBQXNZKK-UHFFFAOYSA-N 0.000 description 1
• 229960003630 ketotifen fumarate Drugs 0.000 description 1
• YNQQEYBLVYAWNX-WLHGVMLRSA-N ketotifen fumarate Chemical compound OC(=O)\C=C\C(O)=O.C1CN(C)CCC1=C1C2=CC=CC=C2CC(=O)C2=C1C=CS2 YNQQEYBLVYAWNX-WLHGVMLRSA-N 0.000 description 1
• BBMULGJBVDDDNI-OWKLGTHSSA-N lasalocid Chemical compound C([C@@H]1[C@@]2(CC)O[C@@H]([C@H](C2)C)[C@@H](CC)C(=O)[C@@H](C)[C@@H](O)[C@H](C)CCC=2C(=C(O)C(C)=CC=2)C(O)=O)C[C@](O)(CC)[C@H](C)O1 BBMULGJBVDDDNI-OWKLGTHSSA-N 0.000 description 1
• 229960000320 lasalocid Drugs 0.000 description 1
• 229960001691 leucovorin Drugs 0.000 description 1
• 210000000265 leukocyte Anatomy 0.000 description 1
• IXHBTMCLRNMKHZ-LBPRGKRZSA-N levobunolol Chemical compound O=C1CCCC2=C1C=CC=C2OC[C@@H](O)CNC(C)(C)C IXHBTMCLRNMKHZ-LBPRGKRZSA-N 0.000 description 1
• 229960000831 levobunolol Drugs 0.000 description 1
• 229960004194 lidocaine Drugs 0.000 description 1
• 239000002502 liposome Substances 0.000 description 1
• 239000003589 local anesthetic agent Substances 0.000 description 1
• 230000004807 localization Effects 0.000 description 1
• 230000033001 locomotion Effects 0.000 description 1
• 229960004305 lodoxamide Drugs 0.000 description 1
• RVGLGHVJXCETIO-UHFFFAOYSA-N lodoxamide Chemical compound OC(=O)C(=O)NC1=CC(C#N)=CC(NC(=O)C(O)=O)=C1Cl RVGLGHVJXCETIO-UHFFFAOYSA-N 0.000 description 1
• 229960000558 lodoxamide tromethamine Drugs 0.000 description 1
• 230000007774 longterm Effects 0.000 description 1
• 210000004072 lung Anatomy 0.000 description 1
• 230000000938 luteal effect Effects 0.000 description 1
• 238000010841 mRNA extraction Methods 0.000 description 1
• 208000002780 macular degeneration Diseases 0.000 description 1
• 238000007734 materials engineering Methods 0.000 description 1
• 229940087412 maxidex Drugs 0.000 description 1
• 235000013372 meat Nutrition 0.000 description 1
• 238000011326 mechanical measurement Methods 0.000 description 1
• 229960003803 meclofenamic acid Drugs 0.000 description 1
• VPNGEIHDPSLNMU-UHFFFAOYSA-N medetomidine hydrochloride Chemical compound Cl.C=1C=CC(C)=C(C)C=1C(C)C1=CNC=N1 VPNGEIHDPSLNMU-UHFFFAOYSA-N 0.000 description 1
• 229960003464 mefenamic acid Drugs 0.000 description 1
• HYYBABOKPJLUIN-UHFFFAOYSA-N mefenamic acid Chemical compound CC1=CC=CC(NC=2C(=CC=CC=2)C(O)=O)=C1C HYYBABOKPJLUIN-UHFFFAOYSA-N 0.000 description 1
• 229960002409 mepivacaine Drugs 0.000 description 1
• INWLQCZOYSRPNW-UHFFFAOYSA-N mepivacaine Chemical compound CN1CCCCC1C(=O)NC1=C(C)C=CC=C1C INWLQCZOYSRPNW-UHFFFAOYSA-N 0.000 description 1
• 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
• 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
• 229960002216 methylparaben Drugs 0.000 description 1
• 229960002704 metipranolol Drugs 0.000 description 1
• BLWNYSZZZWQCKO-UHFFFAOYSA-N metipranolol hydrochloride Chemical compound [Cl-].CC(C)[NH2+]CC(O)COC1=CC(C)=C(OC(C)=O)C(C)=C1C BLWNYSZZZWQCKO-UHFFFAOYSA-N 0.000 description 1
• 229960002509 miconazole Drugs 0.000 description 1
• 238000007431 microscopic evaluation Methods 0.000 description 1
• 238000000386 microscopy Methods 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 238000002156 mixing Methods 0.000 description 1
• 230000004342 moderate myopia Effects 0.000 description 1
• 239000003068 molecular probe Substances 0.000 description 1
• 230000000877 morphologic effect Effects 0.000 description 1
• 210000005088 multinucleated cell Anatomy 0.000 description 1
• 229960004270 nabumetone Drugs 0.000 description 1
• 239000002105 nanoparticle Substances 0.000 description 1
• 229960005016 naphazoline Drugs 0.000 description 1
• 229960003255 natamycin Drugs 0.000 description 1
• 239000004311 natamycin Substances 0.000 description 1
• 235000010298 natamycin Nutrition 0.000 description 1
• NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
• 230000008693 nausea Effects 0.000 description 1
• 230000001272 neurogenic effect Effects 0.000 description 1
• 210000002569 neuron Anatomy 0.000 description 1
• 206010069732 neurotrophic keratopathy Diseases 0.000 description 1
• 230000004297 night vision Effects 0.000 description 1
• 229960000965 nimesulide Drugs 0.000 description 1
• HYWYRSMBCFDLJT-UHFFFAOYSA-N nimesulide Chemical compound CS(=O)(=O)NC1=CC=C([N+]([O-])=O)C=C1OC1=CC=CC=C1 HYWYRSMBCFDLJT-UHFFFAOYSA-N 0.000 description 1
• 239000002353 niosome Substances 0.000 description 1
• 229960001180 norfloxacin Drugs 0.000 description 1
• OGJPXUAPXNRGGI-UHFFFAOYSA-N norfloxacin Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 OGJPXUAPXNRGGI-UHFFFAOYSA-N 0.000 description 1
• 229960004110 olsalazine Drugs 0.000 description 1
• QQBDLJCYGRGAKP-FOCLMDBBSA-N olsalazine Chemical compound C1=C(O)C(C(=O)O)=CC(\N=N\C=2C=C(C(O)=CC=2)C(O)=O)=C1 QQBDLJCYGRGAKP-FOCLMDBBSA-N 0.000 description 1
• 239000002997 ophthalmic solution Substances 0.000 description 1
• 230000008520 organization Effects 0.000 description 1
• 230000004792 oxidative damage Effects 0.000 description 1
• 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
• 229960005489 paracetamol Drugs 0.000 description 1
• 230000002445 parasympatholytic effect Effects 0.000 description 1
• 239000000734 parasympathomimetic agent Substances 0.000 description 1
• 230000001499 parasympathomimetic effect Effects 0.000 description 1
• 229940005542 parasympathomimetics Drugs 0.000 description 1
• 239000002245 particle Substances 0.000 description 1
• 230000008506 pathogenesis Effects 0.000 description 1
• 230000007170 pathology Effects 0.000 description 1
• 208000025896 pellucid marginal degeneration Diseases 0.000 description 1
• 239000003961 penetration enhancing agent Substances 0.000 description 1
• 230000000737 periodic effect Effects 0.000 description 1
• 229960001190 pheniramine Drugs 0.000 description 1
• 229960002895 phenylbutazone Drugs 0.000 description 1
• VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
• 229960001802 phenylephrine Drugs 0.000 description 1
• SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 description 1
• 229940067107 phenylethyl alcohol Drugs 0.000 description 1
• 201000001757 phlyctenulosis Diseases 0.000 description 1
• SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 1
• 230000000704 physical effect Effects 0.000 description 1
• 230000035790 physiological processes and functions Effects 0.000 description 1
• 229960002702 piroxicam Drugs 0.000 description 1
• QYSPLQLAKJAUJT-UHFFFAOYSA-N piroxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 QYSPLQLAKJAUJT-UHFFFAOYSA-N 0.000 description 1
• 239000013612 plasmid Substances 0.000 description 1
• 210000001778 pluripotent stem cell Anatomy 0.000 description 1
• 229920001993 poloxamer 188 Polymers 0.000 description 1
• 201000006292 polyarteritis nodosa Diseases 0.000 description 1
• 229950005134 polycarbophil Drugs 0.000 description 1
• 229920000024 polymyxin B Polymers 0.000 description 1
• 229960005266 polymyxin b Drugs 0.000 description 1
• 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
• 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
• 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
• 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
• 229920001451 polypropylene glycol Polymers 0.000 description 1
• 229940068977 polysorbate 20 Drugs 0.000 description 1
• 229940113124 polysorbate 60 Drugs 0.000 description 1
• 229920000053 polysorbate 80 Polymers 0.000 description 1
• 229940068968 polysorbate 80 Drugs 0.000 description 1
• 229920002223 polystyrene Polymers 0.000 description 1
• 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
• 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
• 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
• 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
• 230000002980 postoperative effect Effects 0.000 description 1
• 230000003389 potentiating effect Effects 0.000 description 1
• 229960001621 povidone-iodine Drugs 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 229960001896 pramocaine Drugs 0.000 description 1
• DQKXQSGTHWVTAD-UHFFFAOYSA-N pramocaine Chemical compound C1=CC(OCCCC)=CC=C1OCCCN1CCOCC1 DQKXQSGTHWVTAD-UHFFFAOYSA-N 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 238000001556 precipitation Methods 0.000 description 1
• 239000002243 precursor Substances 0.000 description 1
• 229960002800 prednisolone acetate Drugs 0.000 description 1
• 229960002943 prednisolone sodium phosphate Drugs 0.000 description 1
• 229960004618 prednisone Drugs 0.000 description 1
• XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
• 230000003449 preventive effect Effects 0.000 description 1
• 229960001807 prilocaine Drugs 0.000 description 1
• MVFGUOIZUNYYSO-UHFFFAOYSA-N prilocaine Chemical compound CCCNC(C)C(=O)NC1=CC=CC=C1C MVFGUOIZUNYYSO-UHFFFAOYSA-N 0.000 description 1
• 229960004919 procaine Drugs 0.000 description 1
• MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
• 230000002250 progressing effect Effects 0.000 description 1
• 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
• 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
• 229960003415 propylparaben Drugs 0.000 description 1
• 150000003180 prostaglandins Chemical class 0.000 description 1
• 238000002731 protein assay Methods 0.000 description 1
• 230000002797 proteolythic effect Effects 0.000 description 1
• 230000005180 public health Effects 0.000 description 1
• 210000001747 pupil Anatomy 0.000 description 1
• WKSAUQYGYAYLPV-UHFFFAOYSA-N pyrimethamine Chemical compound CCC1=NC(N)=NC(N)=C1C1=CC=C(Cl)C=C1 WKSAUQYGYAYLPV-UHFFFAOYSA-N 0.000 description 1
• 229960000611 pyrimethamine Drugs 0.000 description 1
• 230000005855 radiation Effects 0.000 description 1
• 239000003642 reactive oxygen metabolite Substances 0.000 description 1
• 238000003259 recombinant expression Methods 0.000 description 1
• 230000001172 regenerating effect Effects 0.000 description 1
• 201000009308 regular astigmatism Diseases 0.000 description 1
• 230000002787 reinforcement Effects 0.000 description 1
• 208000009169 relapsing polychondritis Diseases 0.000 description 1
• 230000002040 relaxant effect Effects 0.000 description 1
• 239000011347 resin Substances 0.000 description 1
• 229920005989 resin Polymers 0.000 description 1
• 230000008458 response to injury Effects 0.000 description 1
• 230000004264 retinal detachment Effects 0.000 description 1
• 230000002441 reversible effect Effects 0.000 description 1
• 229960001487 rimexolone Drugs 0.000 description 1
• QTTRZHGPGKRAFB-OOKHYKNYSA-N rimexolone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CC)(C)[C@@]1(C)C[C@@H]2O QTTRZHGPGKRAFB-OOKHYKNYSA-N 0.000 description 1
• 229960000371 rofecoxib Drugs 0.000 description 1
• RZJQGNCSTQAWON-UHFFFAOYSA-N rofecoxib Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=C(C=2C=CC=CC=2)C(=O)OC1 RZJQGNCSTQAWON-UHFFFAOYSA-N 0.000 description 1
• 201000004700 rosacea Diseases 0.000 description 1
• HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
• 230000007017 scission Effects 0.000 description 1
• 238000007790 scraping Methods 0.000 description 1
• 230000036280 sedation Effects 0.000 description 1
• 238000000926 separation method Methods 0.000 description 1
• 210000002460 smooth muscle Anatomy 0.000 description 1
• 239000011734 sodium Substances 0.000 description 1
• 229940083542 sodium Drugs 0.000 description 1
• 229910052708 sodium Inorganic materials 0.000 description 1
• NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 1
• 229960004025 sodium salicylate Drugs 0.000 description 1
• 229910052938 sodium sulfate Inorganic materials 0.000 description 1
• 235000011152 sodium sulphate Nutrition 0.000 description 1
• JAJWGJBVLPIOOH-IZYKLYLVSA-M sodium taurocholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 JAJWGJBVLPIOOH-IZYKLYLVSA-M 0.000 description 1
• 229940045946 sodium taurodeoxycholate Drugs 0.000 description 1
• JGMJQSFLQWGYMQ-UHFFFAOYSA-M sodium;2,6-dichloro-n-phenylaniline;acetate Chemical compound [Na+].CC([O-])=O.ClC1=CC=CC(Cl)=C1NC1=CC=CC=C1 JGMJQSFLQWGYMQ-UHFFFAOYSA-M 0.000 description 1
• GNMBMOULKUXEQF-UHFFFAOYSA-M sodium;2-(3-fluoro-4-phenylphenyl)propanoate;dihydrate Chemical compound O.O.[Na+].FC1=CC(C(C([O-])=O)C)=CC=C1C1=CC=CC=C1 GNMBMOULKUXEQF-UHFFFAOYSA-M 0.000 description 1
• YXHRQQJFKOHLAP-FVCKGWAHSA-M sodium;2-[[(4r)-4-[(3r,5r,8r,9s,10s,12s,13r,14s,17r)-3,12-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 YXHRQQJFKOHLAP-FVCKGWAHSA-M 0.000 description 1
• UCUGUQPGZNAZKD-UHFFFAOYSA-M sodium;6,8-dioxo-7,9-dihydro-3h-purin-2-olate;hydrate Chemical compound O.[Na+].N1C(=O)NC(=O)C2=C1NC(=O)[N-]2 UCUGUQPGZNAZKD-UHFFFAOYSA-M 0.000 description 1
• 239000007779 soft material Substances 0.000 description 1
• 239000007787 solid Substances 0.000 description 1
• 235000010199 sorbic acid Nutrition 0.000 description 1
• 239000004334 sorbic acid Substances 0.000 description 1
• 229940075582 sorbic acid Drugs 0.000 description 1
• UNFWWIHTNXNPBV-WXKVUWSESA-N spectinomycin Chemical compound O([C@@H]1[C@@H](NC)[C@@H](O)[C@H]([C@@H]([C@H]1O1)O)NC)[C@]2(O)[C@H]1O[C@H](C)CC2=O UNFWWIHTNXNPBV-WXKVUWSESA-N 0.000 description 1
• 210000000952 spleen Anatomy 0.000 description 1
• 230000000087 stabilizing effect Effects 0.000 description 1
• 238000010186 staining Methods 0.000 description 1
• 210000004500 stellate cell Anatomy 0.000 description 1
• 210000001562 sternum Anatomy 0.000 description 1
• 230000003637 steroidlike Effects 0.000 description 1
• 239000011550 stock solution Substances 0.000 description 1
• 201000004181 stromal dystrophy Diseases 0.000 description 1
• 208000025889 stromal keratitis Diseases 0.000 description 1
• 108091007196 stromelysin Proteins 0.000 description 1
• 150000008163 sugars Chemical class 0.000 description 1
• 229960002673 sulfacetamide Drugs 0.000 description 1
• SKIVFJLNDNKQPD-UHFFFAOYSA-N sulfacetamide Chemical compound CC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 SKIVFJLNDNKQPD-UHFFFAOYSA-N 0.000 description 1
• SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
• 229960004306 sulfadiazine Drugs 0.000 description 1
• 229960000654 sulfafurazole Drugs 0.000 description 1
• 229960001940 sulfasalazine Drugs 0.000 description 1
• NCEXYHBECQHGNR-QZQOTICOSA-N sulfasalazine Chemical compound C1=C(O)C(C(=O)O)=CC(\N=N\C=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-QZQOTICOSA-N 0.000 description 1
• NCEXYHBECQHGNR-UHFFFAOYSA-N sulfasalazine Natural products C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 description 1
• 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
• 229960000894 sulindac Drugs 0.000 description 1
• MLKXDPUZXIRXEP-MFOYZWKCSA-N sulindac Chemical compound CC1=C(CC(O)=O)C2=CC(F)=CC=C2\C1=C/C1=CC=C(S(C)=O)C=C1 MLKXDPUZXIRXEP-MFOYZWKCSA-N 0.000 description 1
• 230000001975 sympathomimetic effect Effects 0.000 description 1
• 229940064707 sympathomimetics Drugs 0.000 description 1
• 208000011580 syndromic disease Diseases 0.000 description 1
• 229940037128 systemic glucocorticoids Drugs 0.000 description 1
• 201000000596 systemic lupus erythematosus Diseases 0.000 description 1
• WBWWGRHZICKQGZ-GIHLXUJPSA-N taurocholic acid Chemical compound C([C@@H]1C[C@H]2O)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@H](O)C1 WBWWGRHZICKQGZ-GIHLXUJPSA-N 0.000 description 1
• 229960002871 tenoxicam Drugs 0.000 description 1
• LZNWYQJJBLGYLT-UHFFFAOYSA-N tenoxicam Chemical compound OC=1C=2SC=CC=2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 LZNWYQJJBLGYLT-UHFFFAOYSA-N 0.000 description 1
• 229960002372 tetracaine Drugs 0.000 description 1
• GKCBAIGFKIBETG-UHFFFAOYSA-N tetracaine Chemical compound CCCCNC1=CC=C(C(=O)OCCN(C)C)C=C1 GKCBAIGFKIBETG-UHFFFAOYSA-N 0.000 description 1
• 229960002180 tetracycline Drugs 0.000 description 1
• 229930101283 tetracycline Natural products 0.000 description 1
• 235000019364 tetracycline Nutrition 0.000 description 1
• 150000003522 tetracyclines Chemical class 0.000 description 1
• 229960000337 tetryzoline Drugs 0.000 description 1
• RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
• 229960004906 thiomersal Drugs 0.000 description 1
• 229960004605 timolol Drugs 0.000 description 1
• 229960000707 tobramycin Drugs 0.000 description 1
• NLVFBUXFDBBNBW-PBSUHMDJSA-N tobramycin Chemical compound N[C@@H]1C[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N NLVFBUXFDBBNBW-PBSUHMDJSA-N 0.000 description 1
• 229960001017 tolmetin Drugs 0.000 description 1
• UPSPUYADGBWSHF-UHFFFAOYSA-N tolmetin Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=C(CC(O)=O)N1C UPSPUYADGBWSHF-UHFFFAOYSA-N 0.000 description 1
• 238000003325 tomography Methods 0.000 description 1
• 230000000699 topical effect Effects 0.000 description 1
• 238000012876 topography Methods 0.000 description 1
• 238000002054 transplantation Methods 0.000 description 1
• 239000006163 transport media Substances 0.000 description 1
• 230000008733 trauma Effects 0.000 description 1
• 238000011269 treatment regimen Methods 0.000 description 1
• VSQQQLOSPVPRAZ-RRKCRQDMSA-N trifluridine Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(C(F)(F)F)=C1 VSQQQLOSPVPRAZ-RRKCRQDMSA-N 0.000 description 1
• 229960003962 trifluridine Drugs 0.000 description 1
• 230000001960 triggered effect Effects 0.000 description 1
• LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
• FQCQGOZEWWPOKI-UHFFFAOYSA-K trisalicylate-choline Chemical compound [Mg+2].C[N+](C)(C)CCO.OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O FQCQGOZEWWPOKI-UHFFFAOYSA-K 0.000 description 1
• 229960000281 trometamol Drugs 0.000 description 1
• 102000003390 tumor necrosis factor Human genes 0.000 description 1
• 230000036269 ulceration Effects 0.000 description 1
• 238000002604 ultrasonography Methods 0.000 description 1
• 208000024126 vascular type Ehlers-Danlos syndrome Diseases 0.000 description 1
• 239000013598 vector Substances 0.000 description 1
• 239000003981 vehicle Substances 0.000 description 1
• 238000012795 verification Methods 0.000 description 1
• 229960003636 vidarabine Drugs 0.000 description 1
• 230000003612 virological effect Effects 0.000 description 1
• 208000029257 vision disease Diseases 0.000 description 1
• 230000004393 visual impairment Effects 0.000 description 1
• 235000019155 vitamin A Nutrition 0.000 description 1
• 239000011719 vitamin A Substances 0.000 description 1
• 235000019163 vitamin B12 Nutrition 0.000 description 1
• 239000011715 vitamin B12 Substances 0.000 description 1
• 235000019165 vitamin E Nutrition 0.000 description 1
• 229940046009 vitamin E Drugs 0.000 description 1
• 239000011709 vitamin E Substances 0.000 description 1
• 235000019168 vitamin K Nutrition 0.000 description 1
• 239000011712 vitamin K Substances 0.000 description 1
• 150000003721 vitamin K derivatives Chemical class 0.000 description 1
• 229940045997 vitamin a Drugs 0.000 description 1
• 150000003722 vitamin derivatives Chemical class 0.000 description 1
• 229940046010 vitamin k Drugs 0.000 description 1
• 230000003442 weekly effect Effects 0.000 description 1
• 238000001262 western blot Methods 0.000 description 1
• 230000029663 wound healing Effects 0.000 description 1
• 210000002417 xiphoid bone Anatomy 0.000 description 1
• 229960005332 zileuton Drugs 0.000 description 1
• MWLSOWXNZPKENC-SSDOTTSWSA-N zileuton Chemical compound C1=CC=C2SC([C@H](N(O)C(N)=O)C)=CC2=C1 MWLSOWXNZPKENC-SSDOTTSWSA-N 0.000 description 1
• 239000011701 zinc Substances 0.000 description 1
• 229910052725 zinc Inorganic materials 0.000 description 1
• 235000016804 zinc Nutrition 0.000 description 1
• UCRLQOPRDMGYOA-DFTDUNEMSA-L zinc;(4r)-4-[[(2s)-2-[[(4r)-2-[(1s,2s)-1-amino-2-methylbutyl]-4,5-dihydro-1,3-thiazole-4-carbonyl]amino]-4-methylpentanoyl]amino]-5-[[(2s,3s)-1-[[(3s,6r,9s,12r,15s,18r,21s)-3-(2-amino-2-oxoethyl)-18-(3-aminopropyl)-12-benzyl-15-[(2s)-butan-2-yl]-6-(carbox Chemical compound [Zn+2].C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC([O-])=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2NC=NC=2)C(=O)N[C@H](CC([O-])=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 UCRLQOPRDMGYOA-DFTDUNEMSA-L 0.000 description 1