KR20230122081A - Peg 지질 및 지질 나노입자 - Google Patents
Peg 지질 및 지질 나노입자 Download PDFInfo
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- KR20230122081A KR20230122081A KR1020237023930A KR20237023930A KR20230122081A KR 20230122081 A KR20230122081 A KR 20230122081A KR 1020237023930 A KR1020237023930 A KR 1020237023930A KR 20237023930 A KR20237023930 A KR 20237023930A KR 20230122081 A KR20230122081 A KR 20230122081A
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- Prior art keywords
- alkyl
- compound
- lipid
- sirna
- nucleotides
- Prior art date
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- 150000002632 lipids Chemical class 0.000 title claims abstract description 261
- 239000002105 nanoparticle Substances 0.000 title claims abstract description 59
- 108020004459 Small interfering RNA Proteins 0.000 claims abstract description 225
- 108020004999 messenger RNA Proteins 0.000 claims abstract description 136
- 239000000203 mixture Substances 0.000 claims abstract description 111
- 150000001875 compounds Chemical class 0.000 claims abstract description 108
- 239000003814 drug Substances 0.000 claims abstract description 21
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- 150000007523 nucleic acids Chemical group 0.000 claims description 202
- 102000039446 nucleic acids Human genes 0.000 claims description 181
- 108020004707 nucleic acids Proteins 0.000 claims description 181
- 239000002245 particle Substances 0.000 claims description 163
- 108090000623 proteins and genes Proteins 0.000 claims description 157
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims description 148
- 238000000034 method Methods 0.000 claims description 122
- -1 cationic lipid Chemical class 0.000 claims description 76
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 74
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- 230000002452 interceptive effect Effects 0.000 claims description 54
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- 108700011259 MicroRNAs Proteins 0.000 claims description 50
- 102000004169 proteins and genes Human genes 0.000 claims description 50
- 239000002679 microRNA Substances 0.000 claims description 42
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 29
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 229920001184 polypeptide Polymers 0.000 claims description 24
- 239000008194 pharmaceutical composition Substances 0.000 claims description 22
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 21
- 230000001225 therapeutic effect Effects 0.000 claims description 20
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 18
- 229940124597 therapeutic agent Drugs 0.000 claims description 17
- 239000003937 drug carrier Substances 0.000 claims description 14
- 238000001990 intravenous administration Methods 0.000 claims description 12
- 239000013612 plasmid Substances 0.000 claims description 12
- 229960005486 vaccine Drugs 0.000 claims description 12
- 235000012000 cholesterol Nutrition 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 230000002018 overexpression Effects 0.000 claims description 8
- NRJAVPSFFCBXDT-HUESYALOSA-N 1,2-distearoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC NRJAVPSFFCBXDT-HUESYALOSA-N 0.000 claims description 7
- 150000003904 phospholipids Chemical class 0.000 claims description 7
- 238000011321 prophylaxis Methods 0.000 claims description 7
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- 125000005862 (C1-C6)alkanoyl group Chemical group 0.000 claims description 5
- 230000004071 biological effect Effects 0.000 claims description 5
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
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- XRSXCKHAABAWCH-UHFFFAOYSA-N 1-[2-[bis(2-hydroxydodecyl)amino]ethyl-[2-[4-[2-[bis(2-hydroxydodecyl)amino]ethyl]piperidin-1-yl]ethyl]amino]dodecan-2-ol Chemical compound CCCCCCCCCCC(CN(CCN(CC(CCCCCCCCCC)O)CC(CCCCCCCCCC)O)CCN1CCC(CCN(CC(CCCCCCCCCC)O)CC(CCCCCCCCCC)O)CC1)O XRSXCKHAABAWCH-UHFFFAOYSA-N 0.000 claims description 2
- OHLMHUYMSGNIPE-SUWVGDFQSA-N 2-[methyl-[4-tris[(Z)-dec-4-enoxy]silylbutyl]amino]ethanol Chemical compound CCCCC/C=C\CCCO[Si](CCCCN(C)CCO)(OCCC/C=C\CCCCC)OCCC/C=C\CCCCC OHLMHUYMSGNIPE-SUWVGDFQSA-N 0.000 claims description 2
- ZISVTYVLWSZJAL-UHFFFAOYSA-N 3,6-bis[4-[bis(2-hydroxydodecyl)amino]butyl]piperazine-2,5-dione Chemical compound CCCCCCCCCCC(O)CN(CC(O)CCCCCCCCCC)CCCCC1NC(=O)C(CCCCN(CC(O)CCCCCCCCCC)CC(O)CCCCCCCCCC)NC1=O ZISVTYVLWSZJAL-UHFFFAOYSA-N 0.000 claims description 2
- UMSCHHWDFWCONK-RGLFHLPNSA-N 3,6-bis[4-[bis[(9Z,12Z)-2-hydroxyoctadeca-9,12-dienyl]amino]butyl]piperazine-2,5-dione Chemical compound CCCCC\C=C/C\C=C/CCCCCCC(O)CN(CCCCC1NC(=O)C(CCCCN(CC(O)CCCCCC\C=C/C\C=C/CCCCC)CC(O)CCCCCC\C=C/C\C=C/CCCCC)NC1=O)CC(O)CCCCCC\C=C/C\C=C/CCCCC UMSCHHWDFWCONK-RGLFHLPNSA-N 0.000 claims description 2
- DIIXYZRGUJMAPE-KWXKLSQISA-N 3-[(6z,9z,28z,31z)-heptatriaconta-6,9,28,31-tetraen-19-yl]oxy-n,n-dimethylpropan-1-amine Chemical compound CCCCC\C=C/C\C=C/CCCCCCCCC(OCCCN(C)C)CCCCCCCC\C=C/C\C=C/CCCCC DIIXYZRGUJMAPE-KWXKLSQISA-N 0.000 claims description 2
- ONQFIMPZSCGIJV-PZDDBIFTSA-N 4-[2-[4-[bis[(Z)-dec-4-enoxy]-methylsilyl]butyl]-2,8-diazaspiro[4.5]decan-8-yl]butyl-bis[(Z)-dec-4-enoxy]-methylsilane Chemical compound CCCCC/C=C\CCCO[Si](C)(CCCCN(CC1)CC11CCN(CCCC[Si](C)(OCCC/C=C\CCCCC)OCCC/C=C\CCCCC)CC1)OCCC/C=C\CCCCC ONQFIMPZSCGIJV-PZDDBIFTSA-N 0.000 claims description 2
- FDOXDEFUYQWIRZ-UHFFFAOYSA-N 9-[9-(2-butyloctanoyloxy)nonyl-(4-hydroxybutyl)amino]nonyl 2-butyloctanoate Chemical compound CCCCCCC(CCCC)C(=O)OCCCCCCCCCN(CCCCO)CCCCCCCCCOC(=O)C(CCCC)CCCCCC FDOXDEFUYQWIRZ-UHFFFAOYSA-N 0.000 claims description 2
- JGFLHDDZTNFQCV-ASSJVFBPSA-N C(CCC\C=C/CCCCC)(=O)OC(CCC\C=C/CCCCC)C(CCC\C=C/CCCCC)OC(CCCCCN(C)C)=O Chemical compound C(CCC\C=C/CCCCC)(=O)OC(CCC\C=C/CCCCC)C(CCC\C=C/CCCCC)OC(CCCCCN(C)C)=O JGFLHDDZTNFQCV-ASSJVFBPSA-N 0.000 claims description 2
- CVOTVCISTDBYHB-ZRTCEIMWSA-N C(CC\C=C/CCCCC)O[Si](CCCCN(CCCN(C)CCCC[Si](C)(OCCC\C=C/CCCCC)OCCC\C=C/CCCCC)C)(C)OCCC\C=C/CCCCC Chemical compound C(CC\C=C/CCCCC)O[Si](CCCCN(CCCN(C)CCCC[Si](C)(OCCC\C=C/CCCCC)OCCC\C=C/CCCCC)C)(C)OCCC\C=C/CCCCC CVOTVCISTDBYHB-ZRTCEIMWSA-N 0.000 claims description 2
- XREUYIAIEWJXLH-DNSZEBFCSA-N N,N'-dimethyl-N,N'-bis[4-tris[(Z)-hept-3-enoxy]silylbutyl]propane-1,3-diamine Chemical compound CCC/C=C\CCO[Si](CCCCN(C)CCCN(C)CCCC[Si](OCC/C=C\CCC)(OCC/C=C\CCC)OCC/C=C\CCC)(OCC/C=C\CCC)OCC/C=C\CCC XREUYIAIEWJXLH-DNSZEBFCSA-N 0.000 claims description 2
- ODTJDMBEELIWET-ASSJVFBPSA-N N,N-dimethyl-4-tris[(Z)-dec-4-enoxy]silylbutan-1-amine Chemical compound CCCCC/C=C\CCCO[Si](CCCCN(C)C)(OCCC/C=C\CCCCC)OCCC/C=C\CCCCC ODTJDMBEELIWET-ASSJVFBPSA-N 0.000 claims description 2
- XNHCFCWPCCJPGB-ASSJVFBPSA-N N,N-dimethyl-5-tris[(Z)-dec-4-enoxy]silylpentan-1-amine Chemical compound CCCCC/C=C\CCCO[Si](CCCCCN(C)C)(OCCC/C=C\CCCCC)OCCC/C=C\CCCCC XNHCFCWPCCJPGB-ASSJVFBPSA-N 0.000 claims description 2
- BXGNTOMXXXPXHV-ASSJVFBPSA-N N,N-dimethyl-6-tris[(Z)-dec-4-enoxy]silylhexan-1-amine Chemical compound CCCCC/C=C\CCCO[Si](CCCCCCN(C)C)(OCCC/C=C\CCCCC)OCCC/C=C\CCCCC BXGNTOMXXXPXHV-ASSJVFBPSA-N 0.000 claims description 2
- XWERACRFMCTWCY-UHFFFAOYSA-N OC(CCN(CCCNCCCN(CCC(O)=O)CCC(O)=O)CCC(O)=O)=O Chemical compound OC(CCN(CCCNCCCN(CCC(O)=O)CCC(O)=O)CCC(O)=O)=O XWERACRFMCTWCY-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- ARJCMRWHZPDQJG-ASSJVFBPSA-N [(6z,16z)-12-[(z)-dec-4-enyl]docosa-6,16-dien-11-yl] 5-(dimethylamino)pentanoate Chemical compound CCCCC\C=C/CCCC(CCC\C=C/CCCCC)C(CCC\C=C/CCCCC)OC(=O)CCCCN(C)C ARJCMRWHZPDQJG-ASSJVFBPSA-N 0.000 claims description 2
- WLCODOOBPYTABW-ASSJVFBPSA-N [(6z,16z)-12-[(z)-dec-4-enyl]docosa-6,16-dien-11-yl] 6-(dimethylamino)hexanoate Chemical compound CCCCC\C=C/CCCC(CCC\C=C/CCCCC)C(CCC\C=C/CCCCC)OC(=O)CCCCCN(C)C WLCODOOBPYTABW-ASSJVFBPSA-N 0.000 claims description 2
- NRLNQCOGCKAESA-KWXKLSQISA-N [(6z,9z,28z,31z)-heptatriaconta-6,9,28,31-tetraen-19-yl] 4-(dimethylamino)butanoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCCC(OC(=O)CCCN(C)C)CCCCCCCC\C=C/C\C=C/CCCCC NRLNQCOGCKAESA-KWXKLSQISA-N 0.000 claims description 2
- CHTXXFZHKGGQGX-UHFFFAOYSA-N [2-[3-(diethylamino)propoxycarbonyloxymethyl]-3-(4,4-dioctoxybutanoyloxy)propyl] (9Z,12Z)-octadeca-9,12-dienoate Chemical compound C(CCCCCCCC=C/CC=C/CCCCC)(=O)OCC(COC(CCC(OCCCCCCCC)OCCCCCCCC)=O)COC(=O)OCCCN(CC)CC CHTXXFZHKGGQGX-UHFFFAOYSA-N 0.000 claims description 2
- XNEHCOKBKFCJSM-UHFFFAOYSA-N bis(2-butyloctyl) 10-[3-(dimethylamino)propyl-nonanoylamino]nonadecanedioate Chemical compound CCCCCCCCC(=O)N(CCCN(C)C)C(CCCCCCCCC(=O)OCC(CCCC)CCCCCC)CCCCCCCCC(=O)OCC(CCCC)CCCCCC XNEHCOKBKFCJSM-UHFFFAOYSA-N 0.000 claims description 2
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- VBFYPCGDFUFVCZ-UHFFFAOYSA-N ditridecan-7-yl 10-[3-(dimethylamino)propyl-octanoylamino]nonadecanedioate Chemical compound CCCCCCCC(=O)N(CCCN(C)C)C(CCCCCCCCC(=O)OC(CCCCCC)CCCCCC)CCCCCCCCC(=O)OC(CCCCCC)CCCCCC VBFYPCGDFUFVCZ-UHFFFAOYSA-N 0.000 claims description 2
- ZXVQLTLFYPAIPK-UHFFFAOYSA-N ditridecan-7-yl 10-[decyl-[4-(dimethylamino)butanoyl]amino]nonadecanedioate Chemical compound C(CCCCCCCCC)N(C(CCCN(C)C)=O)C(CCCCCCCCC(=O)OC(CCCCCC)CCCCCC)CCCCCCCCC(=O)OC(CCCCCC)CCCCCC ZXVQLTLFYPAIPK-UHFFFAOYSA-N 0.000 claims description 2
- ABCVHPIKBGRCJA-UHFFFAOYSA-N nonyl 8-[(8-heptadecan-9-yloxy-8-oxooctyl)-(2-hydroxyethyl)amino]octanoate Chemical compound OCCN(CCCCCCCC(=O)OC(CCCCCCCC)CCCCCCCC)CCCCCCCC(=O)OCCCCCCCCC ABCVHPIKBGRCJA-UHFFFAOYSA-N 0.000 claims description 2
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| CN112877275B (zh) * | 2021-02-04 | 2023-03-31 | 中国农业科学院兰州兽医研究所 | Hdac2基因敲除的bhk-21细胞系及其构建方法和应用 |
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| WO2022133344A1 (en) | 2022-06-23 |
| AU2021403156A1 (en) | 2023-07-13 |
| EP4262883A1 (en) | 2023-10-25 |
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