CN114933569A - 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 - Google Patents
鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 Download PDFInfo
- Publication number
- CN114933569A CN114933569A CN202210358677.7A CN202210358677A CN114933569A CN 114933569 A CN114933569 A CN 114933569A CN 202210358677 A CN202210358677 A CN 202210358677A CN 114933569 A CN114933569 A CN 114933569A
- Authority
- CN
- China
- Prior art keywords
- compound
- sirna
- cationic liposome
- sphingolipid
- cationic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002502 liposome Substances 0.000 title claims abstract description 151
- -1 Sphingolipid compound Chemical class 0.000 title claims abstract description 71
- 125000002091 cationic group Chemical group 0.000 claims abstract description 128
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 23
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 8
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
- 125000003277 amino group Chemical group 0.000 claims abstract description 5
- 239000002253 acid Substances 0.000 claims abstract description 4
- 125000003710 aryl alkyl group Chemical class 0.000 claims abstract description 4
- 125000001931 aliphatic group Chemical class 0.000 claims abstract description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- 108020004459 Small interfering RNA Proteins 0.000 claims description 71
- 150000001875 compounds Chemical class 0.000 claims description 68
- 206010028980 Neoplasm Diseases 0.000 claims description 29
- 239000003814 drug Substances 0.000 claims description 29
- 229940079593 drug Drugs 0.000 claims description 24
- 239000008194 pharmaceutical composition Substances 0.000 claims description 22
- 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 20
- 238000002360 preparation method Methods 0.000 claims description 15
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 12
- 235000012000 cholesterol Nutrition 0.000 claims description 10
- 230000014509 gene expression Effects 0.000 claims description 10
- 108020004707 nucleic acids Proteins 0.000 claims description 10
- 102000039446 nucleic acids Human genes 0.000 claims description 10
- 150000007523 nucleic acids Chemical class 0.000 claims description 9
- 208000003721 Triple Negative Breast Neoplasms Diseases 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 8
- 208000022679 triple-negative breast carcinoma Diseases 0.000 claims description 8
- 239000013612 plasmid Substances 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 230000000259 anti-tumor effect Effects 0.000 claims description 6
- 201000011510 cancer Diseases 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- MWRBNPKJOOWZPW-CLFAGFIQSA-N dioleoyl phosphatidylethanolamine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCCCCCC MWRBNPKJOOWZPW-CLFAGFIQSA-N 0.000 claims description 5
- 201000010099 disease Diseases 0.000 claims description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 230000036210 malignancy Effects 0.000 claims description 3
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 2
- 208000035473 Communicable disease Diseases 0.000 claims description 2
- 208000026350 Inborn Genetic disease Diseases 0.000 claims description 2
- 230000003110 anti-inflammatory effect Effects 0.000 claims description 2
- 230000000840 anti-viral effect Effects 0.000 claims description 2
- 208000016361 genetic disease Diseases 0.000 claims description 2
- 108020004999 messenger RNA Proteins 0.000 claims description 2
- 108091070501 miRNA Proteins 0.000 claims description 2
- 239000002679 microRNA Substances 0.000 claims description 2
- 230000001594 aberrant effect Effects 0.000 claims 1
- 208000015181 infectious disease Diseases 0.000 claims 1
- 238000001890 transfection Methods 0.000 abstract description 10
- 230000002209 hydrophobic effect Effects 0.000 abstract description 3
- 231100000053 low toxicity Toxicity 0.000 abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 75
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 71
- 229930012538 Paclitaxel Natural products 0.000 description 70
- 229960001592 paclitaxel Drugs 0.000 description 70
- 239000004055 small Interfering RNA Substances 0.000 description 70
- 238000006243 chemical reaction Methods 0.000 description 66
- 239000000243 solution Substances 0.000 description 54
- 210000004027 cell Anatomy 0.000 description 50
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 36
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- 230000000694 effects Effects 0.000 description 24
- 238000005538 encapsulation Methods 0.000 description 24
- 239000007787 solid Substances 0.000 description 21
- 238000004440 column chromatography Methods 0.000 description 20
- 239000012074 organic phase Substances 0.000 description 20
- 108090000623 proteins and genes Proteins 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 15
- 239000002245 particle Substances 0.000 description 15
- 241000699670 Mus sp. Species 0.000 description 14
- 239000011541 reaction mixture Substances 0.000 description 13
- 108010048367 enhanced green fluorescent protein Proteins 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 11
- 238000001035 drying Methods 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 239000002246 antineoplastic agent Substances 0.000 description 10
- 231100000135 cytotoxicity Toxicity 0.000 description 10
- 230000003013 cytotoxicity Effects 0.000 description 10
- 229940044683 chemotherapy drug Drugs 0.000 description 9
- 239000013583 drug formulation Substances 0.000 description 9
- 229920001427 mPEG Polymers 0.000 description 9
- 239000002609 medium Substances 0.000 description 9
- 238000010791 quenching Methods 0.000 description 9
- 230000000171 quenching effect Effects 0.000 description 9
- 239000000523 sample Substances 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 239000008346 aqueous phase Substances 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 8
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 8
- 230000030279 gene silencing Effects 0.000 description 8
- 230000001965 increasing effect Effects 0.000 description 8
- 238000011068 loading method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 206010059866 Drug resistance Diseases 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 108090000331 Firefly luciferases Proteins 0.000 description 6
- 230000003698 anagen phase Effects 0.000 description 6
- 238000012258 culturing Methods 0.000 description 6
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 6
- 238000011534 incubation Methods 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 238000009210 therapy by ultrasound Methods 0.000 description 6
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 5
- YEDUAINPPJYDJZ-UHFFFAOYSA-N 2-hydroxybenzothiazole Chemical compound C1=CC=C2SC(O)=NC2=C1 YEDUAINPPJYDJZ-UHFFFAOYSA-N 0.000 description 5
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 5
- 206010021143 Hypoxia Diseases 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 239000012043 crude product Substances 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 5
- 230000007954 hypoxia Effects 0.000 description 5
- 230000003834 intracellular effect Effects 0.000 description 5
- 150000002632 lipids Chemical class 0.000 description 5
- 239000012528 membrane Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 210000002966 serum Anatomy 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- RRSNDVCODIMOFX-MPKOGUQCSA-N Fc1c(Cl)cccc1[C@H]1[C@@H](NC2(CCCCC2)[C@@]11C(=O)Nc2cc(Cl)ccc12)C(=O)Nc1ccc(cc1)C(=O)NCCCCCc1cccc2C(=O)N(Cc12)C1CCC(=O)NC1=O Chemical compound Fc1c(Cl)cccc1[C@H]1[C@@H](NC2(CCCCC2)[C@@]11C(=O)Nc2cc(Cl)ccc12)C(=O)Nc1ccc(cc1)C(=O)NCCCCCc1cccc2C(=O)N(Cc12)C1CCC(=O)NC1=O RRSNDVCODIMOFX-MPKOGUQCSA-N 0.000 description 4
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 238000000246 agarose gel electrophoresis Methods 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 229940125773 compound 10 Drugs 0.000 description 4
- 229960000956 coumarin Drugs 0.000 description 4
- 235000001671 coumarin Nutrition 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 4
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000013641 positive control Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 3
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 206010006187 Breast cancer Diseases 0.000 description 3
- 208000026310 Breast neoplasm Diseases 0.000 description 3
- KCBAMQOKOLXLOX-BSZYMOERSA-N CC1=C(SC=N1)C2=CC=C(C=C2)[C@H](C)NC(=O)[C@@H]3C[C@H](CN3C(=O)[C@H](C(C)(C)C)NC(=O)CCCCCCCCCCNCCCONC(=O)C4=C(C(=C(C=C4)F)F)NC5=C(C=C(C=C5)I)F)O Chemical compound CC1=C(SC=N1)C2=CC=C(C=C2)[C@H](C)NC(=O)[C@@H]3C[C@H](CN3C(=O)[C@H](C(C)(C)C)NC(=O)CCCCCCCCCCNCCCONC(=O)C4=C(C(=C(C=C4)F)F)NC5=C(C=C(C=C5)I)F)O KCBAMQOKOLXLOX-BSZYMOERSA-N 0.000 description 3
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 3
- 241000699666 Mus <mouse, genus> Species 0.000 description 3
- OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 238000004113 cell culture Methods 0.000 description 3
- 230000003833 cell viability Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 229940126543 compound 14 Drugs 0.000 description 3
- 229940126086 compound 21 Drugs 0.000 description 3
- 229940125833 compound 23 Drugs 0.000 description 3
- 229940125961 compound 24 Drugs 0.000 description 3
- 229940125846 compound 25 Drugs 0.000 description 3
- 238000012377 drug delivery Methods 0.000 description 3
- 239000012091 fetal bovine serum Substances 0.000 description 3
- 239000012894 fetal calf serum Substances 0.000 description 3
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthene Chemical compound C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 229940015043 glyoxal Drugs 0.000 description 3
- 239000001963 growth medium Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 230000006303 immediate early viral mRNA transcription Effects 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 239000001301 oxygen Chemical group 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- 230000001743 silencing effect Effects 0.000 description 3
- 150000003408 sphingolipids Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- 239000012096 transfection reagent Substances 0.000 description 3
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 3
- 210000004881 tumor cell Anatomy 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- WWUZIQQURGPMPG-UHFFFAOYSA-N (-)-D-erythro-Sphingosine Natural products CCCCCCCCCCCCCC=CC(O)C(N)CO WWUZIQQURGPMPG-UHFFFAOYSA-N 0.000 description 2
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 2
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 2
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 2
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 2
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 108010043121 Green Fluorescent Proteins Proteins 0.000 description 2
- 102000004144 Green Fluorescent Proteins Human genes 0.000 description 2
- 108060001084 Luciferase Proteins 0.000 description 2
- 239000005089 Luciferase Substances 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 101710163270 Nuclease Proteins 0.000 description 2
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 230000001093 anti-cancer Effects 0.000 description 2
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 210000000170 cell membrane Anatomy 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125797 compound 12 Drugs 0.000 description 2
- 229940125758 compound 15 Drugs 0.000 description 2
- 229940126142 compound 16 Drugs 0.000 description 2
- 229940125810 compound 20 Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000005090 green fluorescent protein Substances 0.000 description 2
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 230000000887 hydrating effect Effects 0.000 description 2
- 125000000743 hydrocarbylene group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 230000005917 in vivo anti-tumor Effects 0.000 description 2
- 150000002467 indacenes Chemical class 0.000 description 2
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 230000036457 multidrug resistance Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 210000004940 nucleus Anatomy 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 235000010378 sodium ascorbate Nutrition 0.000 description 2
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 2
- 229960005055 sodium ascorbate Drugs 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 2
- WWUZIQQURGPMPG-KRWOKUGFSA-N sphingosine Chemical compound CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)CO WWUZIQQURGPMPG-KRWOKUGFSA-N 0.000 description 2
- 229910052717 sulfur Chemical group 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- 125000002456 taxol group Chemical group 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 1
- DHXNZYCXMFBMHE-UHFFFAOYSA-N 3-bromopropanoic acid Chemical compound OC(=O)CCBr DHXNZYCXMFBMHE-UHFFFAOYSA-N 0.000 description 1
- FWBHETKCLVMNFS-UHFFFAOYSA-N 4',6-Diamino-2-phenylindol Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 description 1
- GRHQDJDRGZFIPO-UHFFFAOYSA-N 4-bromobutanoic acid Chemical compound OC(=O)CCCBr GRHQDJDRGZFIPO-UHFFFAOYSA-N 0.000 description 1
- 102100033350 ATP-dependent translocase ABCB1 Human genes 0.000 description 1
- 208000031648 Body Weight Changes Diseases 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- AERBNCYCJBRYDG-UHFFFAOYSA-N D-ribo-phytosphingosine Natural products CCCCCCCCCCCCCCC(O)C(O)C(N)CO AERBNCYCJBRYDG-UHFFFAOYSA-N 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 231100000002 MTT assay Toxicity 0.000 description 1
- 238000000134 MTT assay Methods 0.000 description 1
- 108010047230 Member 1 Subfamily B ATP Binding Cassette Transporter Proteins 0.000 description 1
- 241001529936 Murinae Species 0.000 description 1
- 102000043276 Oncogene Human genes 0.000 description 1
- 108700020796 Oncogene Proteins 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- SLGBZMMZGDRARJ-UHFFFAOYSA-N Triphenylene Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 1
- 206010047571 Visual impairment Diseases 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
- SQFPKRNUGBRTAR-UHFFFAOYSA-N acephenanthrylene Chemical group C1=CC(C=C2)=C3C2=CC2=CC=CC=C2C3=C1 SQFPKRNUGBRTAR-UHFFFAOYSA-N 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001028 anti-proliverative effect Effects 0.000 description 1
- 229940041181 antineoplastic drug Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003149 assay kit Methods 0.000 description 1
- 210000001099 axilla Anatomy 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 230000004579 body weight change Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000013592 cell lysate Substances 0.000 description 1
- 210000003855 cell nucleus Anatomy 0.000 description 1
- 230000007541 cellular toxicity Effects 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 238000011260 co-administration Methods 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126208 compound 22 Drugs 0.000 description 1
- 238000004624 confocal microscopy Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000006059 cover glass Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 231100000433 cytotoxic Toxicity 0.000 description 1
- 230000001472 cytotoxic effect Effects 0.000 description 1
- 231100000263 cytotoxicity test Toxicity 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 230000000857 drug effect Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005206 flow analysis Methods 0.000 description 1
- 238000000684 flow cytometry Methods 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 238000001502 gel electrophoresis Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZFGMDIBRIDKWMY-PASTXAENSA-N heparin Chemical compound CC(O)=N[C@@H]1[C@@H](O)[C@H](O)[C@@H](COS(O)(=O)=O)O[C@@H]1O[C@@H]1[C@@H](C(O)=O)O[C@@H](O[C@H]2[C@@H]([C@@H](OS(O)(=O)=O)[C@@H](O[C@@H]3[C@@H](OC(O)[C@H](OS(O)(=O)=O)[C@H]3O)C(O)=O)O[C@@H]2O)CS(O)(=O)=O)[C@H](O)[C@H]1O ZFGMDIBRIDKWMY-PASTXAENSA-N 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 229960001008 heparin sodium Drugs 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 description 1
- 238000000703 high-speed centrifugation Methods 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000036046 immunoreaction Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000005918 in vitro anti-tumor Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000012160 loading buffer Substances 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 239000002539 nanocarrier Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 239000005332 obsidian Substances 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- NQFOGDIWKQWFMN-UHFFFAOYSA-N phenalene Chemical compound C1=CC([CH]C=C2)=C3C2=CC=CC3=C1 NQFOGDIWKQWFMN-UHFFFAOYSA-N 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- AERBNCYCJBRYDG-KSZLIROESA-N phytosphingosine Chemical compound CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@@H](N)CO AERBNCYCJBRYDG-KSZLIROESA-N 0.000 description 1
- 229940033329 phytosphingosine Drugs 0.000 description 1
- DIJNSQQKNIVDPV-UHFFFAOYSA-N pleiadene Chemical compound C1=C2[CH]C=CC=C2C=C2C=CC=C3[C]2C1=CC=C3 DIJNSQQKNIVDPV-UHFFFAOYSA-N 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 150000004579 taxol derivatives Chemical class 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000005580 triphenylene group Chemical group 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 230000002100 tumorsuppressive effect Effects 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/186—Quaternary ammonium compounds, e.g. benzalkonium chloride or cetrimide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/10—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/32—Isothioureas having sulfur atoms of isothiourea groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
Description
技术领域
本发明属于有机合成技术领域,尤其涉及一种鞘脂类化合物、含有鞘脂类化合物的脂质体和应用。
背景技术
乳腺癌,发病率位居女性恶性肿瘤的首位,其中三阴性乳腺癌(triple negativebreast cancer;TNBC)因其复发率高、病死率高和侵袭性强等临床特点成为乳腺癌中恶性程度最高的类型。目前紫杉醇是临床上治疗TNBC的一线药物,但传统的紫杉醇剂型靶向作用差、药物转运效率低且易产生耐药。多项研究表明肿瘤的侵袭、增殖和耐药都和缺氧诱导因子(hypoxia inducible factor-1;HIF-1)有着密切的关系。低氧状态下,HIF-1通过上调多药耐药(multidrug resistance,MDR)与P-糖蛋白从而将紫杉醇等药物泵出细胞外,使细胞内药物浓度降低,杀伤细胞能力减弱。小干扰RNA(siRNA)对目的细胞具有高特异性和低毒性,可以成功沉默恶性致癌基因。然而,裸siRNA在血液中的半衰期不超过1小时,可被血浆中的核酸酶迅速降解或被肾排出。此外,裸siRNA由于其高分子量、亲水性和电荷密度,很难穿透细胞膜。因此,各种可以负载基因药物的载体应运而生,包括胶束、脂质体和无机纳米颗粒。阳离子脂质体已被证明比其他纳米载体具有优势,包括在体液和组织中具有更高的稳定性,更好的生物降解性,能够长时间释放药物。虽然国内外已经报道了多种阳离子脂质体,市面上也有出售的阳离子脂质体如LipofectamineTM2000;Transfection Reagent,但大多数阳离子脂质体表现出了较高的细胞毒性,较低的转染效率,且只能单一的用于递送基因药物。
因此,有必要提供一种新的鞘脂类化合物,克服三阴性乳腺癌对肿瘤化疗药(紫杉醇)的耐药性,提高抗癌药效;且所构建的给药系统具有转染效率高,安全性高,稳定性高的特点。
发明内容
本发明旨在至少解决现有技术中存在的上述技术问题之一。为此,本发明提供了一种鞘脂类化合物。
本发明还提供了一种阳离子脂质体。
本发明还提供了一种阳离子脂质体药物制剂。
本发明还提供了一种阳离子脂质体或阳离子脂质体药物制剂的应用。
本发明的第一方面提供了鞘脂类化合物,所述鞘脂类化合物的结构式如式(Ⅰ)所示:
其中,所述R1和R2独立地选自取代或未取代的C8~22的烷基、取代或未取代的C8~20的烯基;
所述R4选自H、氮杂芳烃基、含胍基取代的脂肪或芳烃基、取代或未取代的C1~10的烷基、杂环基烃基、C2~10的烷基酸;所述R5选自取代或未取代的氨基。
本发明关于鞘脂类化合物的技术方案中的一个技术方案,至少具有以下有益效果:
本发明以长链烷基为疏水尾部,通过(含有三氮唑的共价键、酰胺键、酯键)连接臂,键合氨基酸、季铵盐、叔胺基、仲胺基或伯胺基等亲水头部,设计合成系列新型鞘脂类化合物。将其应用于制备新型阳离子脂质体,得到了转染效率高,稳定性好的低毒性阳离子脂质体。
根据本发明的一些优选的实施方式,所述鞘脂类化合物选自如下结构式中的一种:
本发明的第二方面提供一种阳离子脂质体,所述阳离子脂质体包括上述任一项所述的鞘脂类化合物、胆固醇、二油酰磷脂酰乙醇胺和甲氧基-聚乙二醇-磷脂。
根据本发明的一些实施方式,所述甲氧基-聚乙二醇-磷脂的分子量范围为750~10000,优选的为分子量2000。
根据本发明的一些实施方式,所述鞘脂类化合物、胆固醇、二油酰磷脂酰乙醇胺和甲氧基-聚乙二醇-磷脂的摩尔比为1:(0.5~50):(0.5~50):(0.015~1)。
本发明的第三方面提供一种阳离子脂质体药物制剂,所述药物制剂包括上述所述的阳离子脂质体和药物活性成分,以所述阳离子脂质体中的鞘脂类化合物的摩尔量计算,所述鞘脂类化合物和药物活性成分的摩尔比为(0.1~50):1。
根据本发明的一些实施方式,所述药物活性成分为抗肿瘤化合物、抗病毒化合物、抗炎化合物或类风湿药物中的一种或多种。
根据本发明的一些实施方式,所述药物活性成分为抗肿瘤化合物。
根据本发明的一些实施方式,所述抗肿瘤化合物为紫杉醇或其紫杉醇衍生物。
根据本发明的一些实施方式,所述阳离子脂质体药物制剂还包括核酸。
根据本发明的一些实施方式,所述核酸的量为N/P比1:1~16:1,所述的N/P比是阳离子脂质体中的可电离的氮原子N的摩尔含量和核酸中P的摩尔含量之比。
根据本发明的一些实施方式,所述核酸选自siRNA、miRNA、antagomir、质粒DNA或mRNA。
根据本发明的一些实施方式,所述阳离子脂质体药物制剂的制备方法,包括如下步骤:
S1、将鞘酯类化合物、胆固醇、二油酰磷脂酰乙醇胺、甲氧基-聚乙二醇-磷脂和药物活性成分加入有机溶剂进行溶解得到混合物;
S2、将所述混合物在30~50℃下减压蒸馏至形成脂膜,继续减压蒸馏0.5~2h;
S3、加入无酶水,进行超声至形成乳白色溶液,室温下继续搅拌;
S4、在0~5℃下,将步骤S3的溶液进行探头超声、过滤,即制得阳离子脂质体药物制剂。
根据本发明的一些实施方式,若要加入核酸,还包括步骤S5:将阳离子脂质体药物制剂与核酸复合物和10%胎牛血清混合,将样品置于室温下孵育,即得。
根据本发明的一些实施方式,所述有机溶剂包括氯仿和/或甲醇。
本发明的第四方面提供上述所述的阳离子脂质体、或所述的阳离子脂质体药物制剂在用于治疗由基因异常表达引起的相关疾病的药物制备中的用途,所述疾病包括恶性肿瘤、心血管疾病、类风湿、感染性疾病或遗传病。
根据本发明的一些实施方式,所述恶性肿瘤为三阴性乳腺癌。
本发明的阳离子脂质体共递送基因药物HIF-1αsiRNA和化疗药物紫杉醇表现出协同作用。该阳离子脂质体可以应用于构建共同负载HIF-1αsiRNA和紫杉醇的给药系统,克服三阴性乳腺癌对紫杉醇的耐药性,提高抗癌效果。
定义和一般术语
术语“包括”为开放式表达,即包括本发明所指明的内容,但并不排除其他方面的内容。
本发明中“室温”指的是温度由10℃到40℃。在一些实施例中,“室温”指的是温度由20℃到30℃;在另一些实施例中,“室温”指的是温度由25℃到30℃。
“取代或未取代的C8~20的烷基”表示碳原子总数为8-20的烷基,包括直链烷基、支链烷基和环烷基;并且任选C8-20的烷基中有至少一个H被本文定义的相应基团所取代,例如被羟基、烷氧基或氨基等基团取代。取代或未取代的C1~10的烷基具有相似的定义,其区别在于碳原子数不相同。
“取代或未取代的C8~20的烯基”表示具有一个或多个双键的直链或支链的烃基,且该基团的碳原子总数为8~20,基团中的双键可以在任意位置,并且任选C8-20的烯基中有至少一个H被本文定义的相应基团所取代,例如被羟基、烷氧基等基团取代。
“亚烃基链”仅由碳和氢组成的使分子的其余部分与基团连接的直链或支链的二价烃链,其为饱和的或不饱和的(即,含有一个或多个双键和/或叁键),且具有一至十二个碳原子,例如亚甲基、亚乙基、亚丙基、亚正丁基、亚乙烯基、亚丙烯基、亚正丁烯基、亚丙炔基、亚正丁炔基等。亚烃基链通过单键或双键连接至分子的其余部分且通过单键或双键连接至基团。亚烃基链与分子的其余部分的连接点以及亚烃基链与基团的连接点可通过该链内的一个碳或任两个碳。除非本说明书中另有特定说明,否则亚烃基链是任选取代的。
“芳基”表示包含氢、6至18个碳原子和至少一个芳环的碳环环系统基团。出于本发明的目的,芳基可为单环、双环、三环或四环环系统,其可包括稠合的或桥联的环系统。芳基包括但不限于衍生自苯并苊、苊烯、醋菲烯、蒽、薁、苯、屈、荧蒽、芴、不对称引达省、对称引达省、茚满、茚、萘、非那烯、菲、七曜烯(pleiadene)、芘和苯并菲。除非本说明书中另有特定说明,否则术语“芳基”或前缀“芳-”(如在“芳烃基”中)意指包括任选取代的芳基。
“氮杂芳烃基”表示式-Rb-Rc的基团,其中Rb为亚烃基链且Rc为一个或多个如上文所定义的芳基,其中芳基中有至少一个H被N原子所取代。
“杂环基”表示是指具有一至十二个环碳原子(例如二至十二个)和一至六个选自氮、氧和硫的环杂原子的稳定的3元至18元非芳环基团。除非本说明书中另有特定说明,否则杂环基为单环、双环、三环或四环环系统,其可包括稠合、螺环(“螺-杂环基”)和/或桥联的环系统;且杂环基中的氮、碳或硫原子任选地被氧化;氮原子任选地被季铵化;且杂环基为部分或完全饱和的。
“杂环基烃基”表示式-RbRe的基团,其中Rb为亚烃基链且Re为如上文所定义的杂环基。除非本说明书中另有特定说明,否则杂环基烃基是任选取代的。
“C2~10的烷基酸”表示碳原子总数为2~10的羧酸,烷基包括直链烷基、支链烷基和环烷基。
“取代或未取代的氨基”表示氨基中至少一个H原子被本文所定义的相应基团所取代,例如C1-C8烷基或C3-C8环烷基取代基的基团取代。
附图说明
图1是实施例1~4的鞘脂类化合物的细胞毒性图;
图2是实施例11的阳离子脂质体以及实施例11的阳离子脂质体负载siRNA的细胞毒性图;
图3是实施例11的阳离子脂质体的存储稳定性图;
图4是实施例12制备的阳离子脂质体药物制剂中不同浓度的紫杉醇包封率图;
图5是实施例13制备的阳离子脂质体药物制剂中鞘脂类化合物-胆固醇-DOPE的摩尔比对紫杉醇包封率的影响图;
图6是不同DSPE-mPEG的摩尔比对紫杉醇包封率的影响图;
图7是实施例15制备的阳离子脂质体药物制剂的包封率和载药量图;
图8是实施例15制备的阳离子脂质体药物制剂中的PTX体外释放图;
图9是实施例15制备的阳离子脂质体药物制剂对siRNA-Luc的阻滞作用图;
图10是不同N/P比的负载紫杉醇的阳离子脂质体与siRNA复合物的粒径与电位分析图;
图11是实施例15制备的阳离子脂质体药物制剂与siRNA复合物血清中不同时间点的稳定性图;
图12是实施例11制备的阳离子脂质体递送siRNA-Luc对萤火虫荧光素酶的沉默效率图;
图13是实施例11制备的阳离子脂质体对Cy3-siRNA递送效果图;
图14是采用流式细胞仪定量分析实施例11制备的阳离子脂质体递送Cy3-siRNA效果图;
图15是实施例11制备的阳离子脂质体对EGFP的递送效果图;
图16是实施例11制备的阳离子脂质体共载香豆素C6和Cy3-siRNA的胞内分布图;
图17是MDA-MB-231细胞中HIF-1α蛋白表达量图;
图18是实施例15制备的阳离子脂质体药物制剂和基因药物HIF-1αsiRNA对MDA-MB-231细胞的72h细胞毒性作用图;
图19是荷瘤小鼠体重变化趋势图;
图20是荷瘤小鼠肿瘤体积变化趋势图;
图21是荷瘤小鼠肿瘤体积变化趋势图;
图22是4T1肿瘤模型活体治疗实验结束后对模型中各组肿瘤质量的统计结果图。
具体实施方式
下面将对本发明实施例中的技术方案进行清楚、完整地描述,但本发明的实施方式不限于此。
本发明所采用的试剂、方法和设备,如无特殊说明,均为本技术领域常规试剂、方法和设备。
本发明实施例涉及到的包封率和载药量的计算方法如下:
采用溶解-高速离心法测定紫杉醇包封率。分别吸取100μL Sphy1、Sphy2,Sphy3,Sphy4置于3500Da超速滤管中,加入0.4%吐温80-PBS(0.05mol/L,pH 7.4)溶液1.9mL,涡旋3min后,16000r/min的转速离心30min,取100μL上清液转移至1mL容量瓶中以无水甲醇定容,HPLC测定上清液中游离紫杉醇PTX的量;另分别取适量负载紫杉醇的脂质体至1mL容量瓶中以无水甲醇破乳并定容,进样分析,HPLC测定PTX总量。
载药量(Drug loading efficiency,DLE)和包封率(Encapsulation efficiency,EE)用以下公式计算:
DLE=W1/W×100%
EE=W1/W2×100%
其中,W1和W2分别代表脂质体中被包封PTX的总质量和PTX的投料量,W为脂质总投料量。
实施例1
实施例1提供一种鞘脂类化合物a,结构式如下,制备方法如下:
将化合物1植物鞘氨醇(2.83g,8.9mmol)和tBoc2O(2.23g,10.2mmol)置于反应瓶中,加入tBuOH(60mL)溶液在室温下搅拌8h。待反应完全,减压浓缩反应溶液,以石油醚/乙酸乙酯(v/v,5:1)重结晶得到化合物2,产率为96%,白色固体。
称取产物2(2.55g,6.1mmol)和TsOH(116mg,0.61mmol)于反应瓶中,加入丙酮(20mL)溶液,室温下搅拌,待反应完全。减压浓缩反应溶液,柱层析分离得到化合物3,白色固体,产率89%。
将上述化合物3(2.09g,4.57mmol)置于反应瓶中,加入CH2Cl2(10mL)溶解,在0℃冰浴条件下缓慢滴加甲烷磺酰氯MsCl(0.728mL,9.45mmol),最后加入三乙胺(1.48mL,10.65mmol),将反应混合物在0℃下继续搅拌30分钟,然后在室温下搅拌一小时。反应液中加入H2O进行淬灭,用CH2Cl2萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物4,白色固体,产率为90%。
称取化合物4(1.89g,3.53mmol)于反应瓶中,加入DMF(10mL)溶解,后加入叠氮化钠(1.147g,28.67mmol),反应混合物在65℃下搅拌过夜。反应完全后用H2O猝灭,乙酸乙酯萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物5,白色固体,产率为87%。
称取化合物5(1.8g,3.73mmol)用甲醇(10mL)溶解,再缓慢滴加浓盐酸(0.8mL)。将反应混合物在室温下搅拌过夜至反应完全,将反应溶液减压浓缩,得到粗品。继续加入油酸(1.32g,4.67mmol),EDCI(893mg,4.66mmol),和1-羟基苯并三唑HOBT(629mg,4.66mmol),用二氯甲烷(15mL)溶解,后缓慢滴加三乙胺(0.723mL,5.20mmol),将反应混合物在室温下搅拌16h,然后用二氯甲烷稀释。稀释后的溶液用饱和氯化铵水溶液洗涤。水层用二氯甲烷萃取。收集有机相,无水硫酸钠干燥,减压浓缩,柱层析得到化合物6,白色固体,产率为64%。
称取化合物6(0.1179g,0.19mmol),抗坏血酸钠(94.9mg,0.48mmol),CuSO4(6.7mg,0.04mmol)和化合物7(98.3mg,0.26mmol)于圆底烧瓶中,后加入5.5mL的甲醇/水(10:1,v/v),在室温下搅拌12h。反应液用乙酸乙酯萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到中间体8,白色固体,产率为65%。
称取化合物8(0.127g,0.13mmol)于反应瓶中,加入2mL甲醇溶解,缓慢滴加浓HCl,室温下搅拌至反应完全,反应液用水萃取(3×10mL),收集水相。再向水相缓慢滴加饱和碳酸氢钠,调至PH=7,水层用二氯甲烷萃取,收集有机相,无水硫酸钠干燥,减压浓缩,得到目标化合物a(80mg收率79%)。
目标化合物a的结构鉴定数据:1H NMR(600MHz,CD3OD)δ8.00(s,1H),5.32-5.35(m,2H),4.97-5.00(m,1H),4.69-4.74(m,1H),4.57-4.60(m,1H),4.48-4.52(m,1H),3.92-3.97(m,3H),2.95-2.98(m,2H),2.42-2.45(m,2H),2.00-2.05(m,4H),1.93-1.98(m,1H),1.87-1.91(m,2H),1.71-1.74(m,2H),1.62-1.67(m,3H),1.49-1.54(m,2H),1.29-1.34(m,45H),0.89(t,6H,J=7.2Hz);13C NMR(150MHz,CD3OD)δ175.2,170.2,145.9,131.0,130.8,126.0,74.0,72.4,54.3,54.1,40.4,35.4,33.12,33.11,30.82,30.73,30.68,30.66,30.53,30.50,30.46,30.40,30.39,30.31,28.2,26.2,26.0,23.8,23.0,14.51,14.50.HRMS(ESI):m/z calcd for C45H88N7O4([M+H]+):790.6892,found 790.6972。
其中,化合物1~8的结构式如下
实施例2
实施例2提供一种鞘脂类化合物b,结构式如下,制备方法如下:
将上述实施例1制备的化合物6(0.1845g,0.3mmol)和SnCl2(0.569g,3.0mmol)的5mL乙醇溶液在室温下搅拌12h,二氯甲烷溶解,饱和NaCl溶液洗涤,收集有机相,无水硫酸钠干燥,减压浓缩得到粗产品化合物9,无需进一步提纯。将上述粗品用无水CH2Cl2(7mL)溶解,在0℃搅拌,并缓慢加入三乙胺(0.4mL)和氯化乙酰氯(36μL)。将反应混合物在0℃下搅拌30分钟,然后在室温下下继续搅拌一小时。反应用H2O猝灭,用CH2Cl2萃取,收集有机相,用无水硫酸钠干燥,减压浓缩,柱层析分离,得到化合物10,白色固体,产率为40%。
称取化合物10(41.6mg,0.12mmol)于反应瓶中,加入5mL乙酸乙酯溶解,后加入三甲胺(0.1mL,2M in THF)。在室温下搅拌24小时,产物沉淀为白色固体。将得到的悬浮液冷却到0℃,过滤,用冰冷的乙二醛洗涤,真空干燥,得到目标产物化合物b(45mg,收率65%)。
目标化合物b的结构鉴定数据:1H NMR(600MHz,CDCl3)δ8.73(t,1H,J=6.0Hz,NH),7.52(d,1H,J=8.4Hz,NH),5.32-5.34(m,2H),4.51(s,2H),4.17(s,1H),3.63-3.72(m,3H),3.48-3.52(m,1H),3.42(s,9H),2.19(t,2H,J=7.8Hz),1.99-2.02(m,4H),1.42-1.58(m,8H),1.25-1.34(m,42H),0.88(t,6H,J=7.2Hz);13C NMR(150MHz,CDCl3)δ174.1,163.9,130.1,129.7,74.4,72.3,65.2,54.8,50.1,42.5,40.4,36.6,33.2,32.0,31.92,31.4,30.0,29.93,29.89,29.87,29.83,29.81,29.74,29.59,29.57,29.45,29.42,29.37,29.34,27.3,26.3,25.8,22.71,22.69,14.1.HRMS(ESI):m/z calcd for C41H82N3O4 +([M+]):680.6300,found 680.6286。
其中,化合物9和化合物10的结构式如下:
实施例3
实施例3提供一种鞘脂类化合物c,结构式如下,制备方法如下:
称取化合物10(139.6mg,0.23mmol),赖氨酸(79.7mg,0.23mmol),EDCI(51mg,0.27mmol)和HOBT(37mg,0.27mmol)于反应瓶中,加入2mL无水二氯甲烷溶解,后缓慢滴加三乙胺(0.06mL,0.43mmol),室温下搅拌16h。反应加H2O淬灭,反应液用二氯甲烷萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物11,白色固体,产率为61%。
称取化合物11(0.127g,0.13mmol)于反应瓶中,加入2mL甲醇溶解,缓慢滴加浓HCl,室温下搅拌至反应完全,反应液用水萃取(3×10mL),收集水相。再向水相缓慢滴加饱和碳酸氢钠,调至PH=7,水层用二氯甲烷萃取,收集有机相,无水硫酸钠干燥,减压浓缩,得到的目标产物化合物c(40mg,收率75%)。
目标化合物c的结构鉴定数据:1H NMR(600MHz,CD3OD)δ7.00(s,1H),6.17(d,1H,J=7.2Hz),5.33-5.37(m,2H),4.85-4.91(m,1H),4.04-4.14(m,6H),3.64-3.76(m,2H),3.46-3.48(m,1H),2.17-2.22(m,2H),2.00-2.01(m,4H),1.59-1.73(m,6H),1.25-1.30(m,50H),0.86(t,6H,J=6.6Hz);13C NMR(150MHz,CD3OD)δ174.23,168.52,167.88,130.03,129.72,78.33,72.85,71.58,52.05,50.23,42.42,41.14,41.07,40.83,40.27,36.78,36.69,33.95,31.94,31.92,29.78,29.74,29.71,29.67,29.65,29.59,29.54,29.48,29.37,29.34,29.33,29.26,29.21,29.17,28.86,27.24,27.20,25.63,25.45,22.70,14.13.HRMS(ESI):m/z calcd for C42H85N4O4([M+H]+)709.6565,found 709.6574.
其中,化合物11的结构式如下:
实施例4
实施例4提供一种鞘脂类化合物d,结构式如下,制备方法如下:
称取化合物1鞘氨醇(1.8g,3.73mmol)用甲醇(10mL)溶解,再缓慢滴加浓盐酸(0.8mL)。将反应混合物在室温下搅拌过夜至反应完全,将反应溶液减压浓缩,得到粗品。继续加入油酸(1.32g,4.67mmol),EDCI(893mg,4.66mmol),和HOBT(629mg,4.66mmol),用二氯甲烷(15mL)溶解,后缓慢滴加三乙胺(0.723mL,5.20mmol),将反应混合物在室温下搅拌16h,然后用二氯甲烷稀释。稀释后的溶液用饱和氯化铵水溶液洗涤。水层用二氯甲烷萃取。收集有机相,无水硫酸钠干燥,减压浓缩,柱层析分离得到化合物12,白色固体,产率为72%。
称取化合物12(2.55g,6.1mmol)和TsOH(116mg,0.61mmol)于反应瓶中,加入丙酮(20mL)溶液,室温下搅拌,待反应完全。减压浓缩反应溶液,柱层析分离得到目标化合物13,白色固体,产率89%。
称取化合物13(107.5mg,0.33mmol)于反应瓶中,加入2mL CH2Cl2溶解后在0℃下搅拌,继续加入Et3N(0.05mL)和氯乙酰氯(20μL)。将反应混合物在0℃下搅拌30分钟,然后在室温下再搅拌一小时。反应用H2O猝灭,反应液用二氯甲烷萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压浓缩,硅胶层析纯化,得到化合物14,白色固体,产率为67%,
称取化合物14(42.6mg,0.13mmol)于反应瓶中,加入5mL乙酸乙酯溶解,后加入三甲胺(0.1mL,2M in THF)。在室温下搅拌24小时,产物沉淀为白色固体。将得到的悬浮液冷却到0℃,过滤,用冰冷的乙二醛洗涤,真空干燥,得到目标化合物d(35mg,收率45%)。
目标化合物d的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.96(d,J=8.4Hz,1H,-NH),5.33-5.36(m,2H),4.13-4.19(m,2H),4.09-4.11(m,1H),3.87-3.89(m,1H),3.66-3.68(m,1H),2.50(s,1H),2.17-2.20(m,2H),1.99-2.02(m,3H),1.53-1.64(m,6H),1.46(s,3H),1.33(s,3H),1.25-1.30(m,43H),0.86(t,J=6.6Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.05,130.02,129.73,108.09,78.76,76.80,63.63,50.00,36.83,31.94,31.91,29.78,29.72,29.71,29.67,29.61,29.57,29.54,29.52,29.38,29.34,29.33,29.28,29.15,27.37,27.23,27.18,26.78,25.68,25.02,22.70,22.69,14.13.HRMS(ESI):m/z calcd forC44H85N2O5([M]+)721.6453,found 721.6474.
其中,化合物12,13和14的结构式如下:
实施例5
实施例5提供七种鞘脂类化合物e-k,制备方法如下,结构式如下:
称取化合物14(78.9mg,0.12mmol)于反应瓶中,加入5mL无水二氯甲烷溶解,后加入三乙胺(33.4μL,0.24mmol)和一系列仲胺(0.24mmol)。在室温下搅拌24小时,TLC检测直至反应完全。柱层析分离得到一系列目标化合物e-k(收率29-91%)
目标化合物e的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.87(s,1H,-NH),5.32-5.36(m,2H),4.31-4.36(m,2H),4.20-4.22(m,1H),4.06-4.15(m,2H),3.18(s,2H),2.49(s,4H),2.12(t,J=7.8Hz,2H),1.99-2.02(m,4H),1.61-1.62(m,7H),1.52-1.54(m,3H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.57,170.55,130.08,129.74,108.20,78.78,77.63,64.65,60.38,54.34,48.03,36.85,31.94,31.91,29.78,29.76,29.72,29.69,29.68,29.63,29.59,29.57,29.54,29.38,29.34,29.33,29.30,29.20,29.15,28.98,27.42,27.37,27.23,27.19,26.72,25.73,25.68,25.38,25.02,23.77,22.70,22.69,14.13.HRMS(ESI):m/z calcd forC46H87N2O5([M+H]+)747.6537,found 747.6578.
目标化合物f的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.55(d,J=8.4Hz,1H,-NH),5.32-5.35(m,2H),4.27-4.34(m,3H),4.13-4.16(m,1H),4.02-4.04(m,1H),3.73-3.75(m,4H),3.20(s,2H),2.56-2.58(m,4H),2.12(t,J=8.4Hz,2H),1.99-2.02(m,4H),1.54-1.62(m,4H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13CNMR(150MHz,CDCl3)δ:172.48,170.14,130.05,129.67,108.22,77.63,77.55,66.78,64.75,59.53,53.28,48.19,36.88,31.94,31.91,29.77,29.75,29.71,29.68,29.62,29.57,29.54,29.38,29.34,29.32,29.31,29.29,29.18,28.95,27.25,27.24,27.18,26.79,25.67,25.29,22.70,22.69,14.13.HRMS(ESI):m/z calcd for C45H85N2O6([M+H]+)749.6329,found 749.6370.
目标化合物g的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.60(s,1H,-NH),5.32-5.37(m,2H),4.30-4.34(m,2H),4.19-4.21(m,1H),4.12-4.15(m,1H),4.05-4.07(m,1H),3.32(s,2H),2.51-2.53(m,4H),2.12-2.14(m,2H),1.98-2.02(m,4H),1.53-1.63(m,4H),1.43-1.47(m,6H),1.25-1.31(m,48H),0.86(t,J=6.6Hz,12H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.45,171.79,130.02,129.70,108.16,77.58,77.44,64.26,56.42,55.06,48.23,36.87,31.94,31.91,29.78,29.75,29.71,29.68,29.63,29.57,29.55,29.54,29.38,29.34,29.33,29.30,29.18,28.99,27.35,27.23,27.19,26.73,25.64,25.33,22.70,22.69,20.69,14.12,11.76.HRMS(ESI):m/z calcd for C47H91N2O5([M+H]+)763.6850,found 763.6885.
目标化合物h的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.61(s,1H,-NH),5.31-5.37(m,2H),4.30-4.34(m,2H),4.19-4.20(m,1H),4.12-4.15(m,1H),4.04-4.06(m,1H),3.32(s,2H),2.53-2.56(m,4H),2.12-2.15(m,2H),1.98-2.02(m,4H),1.53-1.61(m,4H),1.39-1.43(m,6H),1.25-1.31(m,52H),0.89(t,J=7.2Hz,12H,-CH2CH3),0.86(t,J=7.2Hz,12H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.44,171.74,130.02,129.70,108.16,77.58,77.42,64.26,55.02,54.15,48.23,36.87,31.94,31.91,29.78,29.76,29.71,29.69,29.68,29.63,29.58,29.55,29.54,29.38,29.34,29.33,29.31,29.19,28.99,27.36,27.23,27.19,26.74,25.64,25.34,22.70,22.69,20.53,14.13,14.05.HRMS(ESI):m/zcalcd for C49H95N2O5([M+H]+)791.7163,found 791.7201.
目标化合物i的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.82(s,1H,-NH),5.31-5.37(m,2H),4.24-4.36(m,3H),4.06-4.15(m,2H),3.35(s,2H),2.65(s,4H),2.12-2.15(m,2H),1.98-2.02(m,4H),1.83(s,2H),1.53-1.63(m,6H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.04,172.56,130.02,129.71,108.16,78.75,77.61,64.70,56.87,54.00,48.14,36.84,31.94,31.91,29.78,29.76,29.71,29.68,29.62,29.58,29.56,29.54,29.38,29.34,29.32,29.30,29.19,28.98,27.38,27.23,27.19,26.74,25.67,25.36,23.77,22.70,22.69,14.13.HRMS(ESI):m/z calcd for C45H85N2O5([M+H]+)733.6380,found 733.6425.
目标化合物j的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.68(s,1H,-NH),5.30-5.37(m,2H),4.29-4.32(m,2H),4.25-4.27(m,1H),4.12-4.15(m,1H),4.06-4.07(m,1H),3.22(s,2H),2.50-2.62(m,8H),2.30(s,3H,-NCH3),2.13(d,J=7.8Hz,2H),1.98-2.02(m,4H),1.53-1.60(m,4H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.52,170.35,130.03,129.69,108.18,77.59,77.39,64.71,59.31,54.83,52.83,48.12,45.95,36.84,31.94,31.91,29.78,29.76,29.72,29.68,29.62,29.59,29.54,29.38,29.34,29.32,29.30,29.19,28.97,27.35,27.24,27.19,26.76,25.67,25.34,22.70,22.69,14.13.HRMS(ESI):m/z calcd for C46H88N3O5([M+H]+)762.6646,found 762.6690.
目标化合物k的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.67(s,1H,-NH),5.31-5.36(m,2H),4.31-4.33(m,2H),4.21-4.23(m,1H),4.12-4.15(m,1H),4.05-4.07(m,1H),3.32(s,2H),2.63-2.65(m,4H),2.12(d,J=7.8Hz,2H),1.98-2.02(m,4H),1.53-1.59(m,4H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,47H),1.04(t,J=7.2Hz,6H,-CH2CH3),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.50,171.58,130.03,129.70,108.17,77.58,77.47,64.44,54.16,48.24,47.74,36.86,31.94,31.91,29.78,29.75,29.71,29.68,29.63,29.58,29.54,29.38,29.34,29.33,29.31,29.30,29.18,28.99,27.33,27.23,27.19,26.74,25.65,25.33,22.70,22.69,14.13,12.20.HRMS(ESI):m/z calcd forC45H87N2O5([M+H]+)735.6537,found 735.6574.
实施例6
实施例6提供七种鞘脂类化合物l-r,制备方法如下,结构式如下:
化合物13(622.0mg,1.0mmol)于反应瓶中,加入4-溴丁酸(1.25mmol),二环己基碳二亚胺(257.5mg,1.25mmol),4-二甲氨基吡啶(12.2mg,0.1mmol)后,用5mL无水二氯甲烷溶解,室温搅拌,TLC检测直至反应完全。将反应浓缩,后经柱层析分离得到中间体化合物15。
称取化合物15(78.9mg,0.12mmol)于反应瓶中,加入5mL无水二氯甲烷溶解,后加入三乙胺(33.4μL,0.24mmol)和一系列仲胺(0.24mmol)。在室温下搅拌24小时,TLC检测直至反应完全。柱层析分离得到一系列目标化合物l-r(收率31-87%)
目标化合物l的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:6.71(s,1H,-NH),5.32-5.34(m,2H),4.36-4.38(m,1H),4.16-4.27(m,4H),2.93(s,2H),2.58-2.59(m,1H),2.49-2.52(m,1H),2.21-2.25(m,4H),1.98-2.02(m,8H),1.53-1.61(m,10H),1.42(s,3H,-C(CH3)2),1.24-1.32(m,47H),0.86(t,J=6.6Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.00,171.87,129.97,129.77,107.99,77.88,76.01,65.05,56.84,53.64,47.84,36.68,31.94,31.91,31.32,29.80,29.79,29.73,29.71,29.68,29.66,29.64,29.54,29.41,29.38,29.35,29.33,29.26,28.79,27.82,27.24,26.85,25.83,25.66,22.69,14.13.HRMS(ESI):m/z calcd for C48H91N2O5([M+H]+)775.6850,found 775.6881.
目标化合物m的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.54(d,J=8.4Hz,1H,-NH),5.32-5.35(m,2H),4.25-4.32(m,2H),4.19-4.22(m,1H),4.12-4.15(m,1H),4.04-4.06(m,1H),3.69-3.70(m,4H),2.34-2.42(m,7H),2.12-2.15(m,2H),1.99-2.02(m,4H),1.79-1.82(m,2H),1.53-1.61(m,4H),1.43(s,3H,-C(CH3)2),1.25-1.32(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.50,172.48,130.05,129.67,108.18,77.57,77.55,66.95,64.42,57.94,53.60,48.28,36.89,31.94,29.77,29.75,29.71,29.69,29.68,29.62,29.57,29.55,29.54,29.37,29.34,29.32,29.31,29.27,29.18,28.96,27.31,27.24,27.19,26.77,25.67,25.33,22.69,21.70,14.13.HRMS(ESI):m/zcalcd for C47H89N2O6([M+H]+)777.6642,found 777.6688.
目标化合物n的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.32-5.35(m,2H),4.24-4.28(m,3H),4.12-4.14(m,2H),2.50-2.60(m,4H),2.38-2.42(m,2H),2.15(t,J=7.8Hz,2H),1.87-2.02(m,6H),1.53-1.60(m,8H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,49H),0.89(t,J=7.8Hz,6H,-CH2CH3),0.86(t,J=6.6Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.14,172.65,130.00,129.72,108.09,77.71,77.57,64.53,55.41,52.85,48.08,36.78,31.94,31.92,31.67,29.78,29.72,29.70,29.68,29.64,29.61,29.59,29.54,29.38,29.35,29.33,29.21,28.91,27.53,27.24,27.21,26.79,25.71,25.47,22.70,14.13,11.73.HRMS(ESI):m/z calcd for C49H95N2O5([M+H]+)791.7163,found 791.7201.
目标化合物o的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.59(s,1H,-NH),5.31-5.37(m,2H),4.27-4.31(m,2H),4.18-4.20(m,1H),4.12-4.15(m,1H),4.05-4.07(m,1H),2.32-2.39(m,8H),2.13-2.15(m,2H),1.98-2.02(m,4H),1.53-1.74(m,8H),1.43(s,3H,-C(CH3)2),1.36-1.39(m,4H),1.25-1.32(m,49H),0.89(t,J=7.8Hz,6H,-CH2CH3),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.77,172.50,130.02,129.70,108.14,77.60,77.35,64.28,53.74,53.19,48.24,36.87,31.99,31.94,31.91,29.78,29.76,29.71,29.69,29.68,29.62,29.59,29.56,29.54,29.38,29.34,29.32,29.28,29.19,28.97,27.37,27.23,27.20,26.75,25.67,25.37,22.70,22.69,20.70,14.13,14.10.HRMS(ESI):m/z calcd for C51H99N2O5([M+H]+)819.7476,found 819.7512.
目标化合物p的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:6.82(d,J=7.8Hz,1H,-NH),5.32-5.34(m,2H),4.41-4.43(m,1H),4.27-4.29(m,2H),4.17-4.21(m,2H),3.16-3.19(m,2H),2.55-2.68(m,2H),2.16-2.26(m,8H),1.99-2.00(m,4H),1.51-1.61(m,8H),1.42(s,3H,-C(CH3)2),1.24-1.32(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.13,171.56,129.97,129.77,107.99,77.90,75.79,65.06,54.55,53.74,47.79,36.64,31.94,31.91,30.89,29.81,29.79,29.73,29.71,29.68,29.65,29.54,29.44,29.38,29.35,29.33,29.27,28.77,27.89,27.24,26.85,25.85,25.72,23.37,22.70,22.69,20.90,14.13.HRMS(ESI):m/z calcd for C47H89N2O5([M+H]+)761.6693,found 761.6732.
目标化合物q的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.56(d,J=8.4Hz,1H,-NH),5.32-5.35(m,2H),4.26-4.31(m,2H),4.18-4.20(m,1H),4.12-4.14(m,1H),4.04-4.06(m,1H),2.33-2.44(m,10H),2.27(s,3H,-NCH3),2.12-2.15(m,2H),1.99-2.00(m,4H),1.78-1.82(m,2H),1.53-1.61(m,4H),1.43(s,3H,-C(CH3)2),1.25-1.31(m,49H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:173.52,172.48,130.03,129.68,108.16,77.58,77.47,64.36,57.53,55.13,53.09,48.26,46.05,36.88,32.07,31.94,31.91,29.77,29.75,29.71,29.68,29.67,29.62,29.58,29.55,29.54,29.37,29.34,29.32,29.31,29.27,29.18,28.97,27.34,27.23,27.19,26.75,25.66,25.34,22.70,22.12,14.13.HRMS(ESI):m/z calcd for C48H92N3O5([M+H]+)790.6959,found 790.6999.
目标化合物r的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.32-5.34(m,2H),4.24-4.31(m,3H),4.14-4.18(m,2H),2.79-2.87(m,4H),2.44-2.50(m,2H),2.17-2.20(m,2H),1.98-2.02(m,6H),1.54-1.60(m,4H),1.43(s,3H,-C(CH3)2),1.24-1.31(m,55H),0.86(t,J=6.6Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.82,172.44,129.99,129.75,108.05,77.80,76.47,64.81,51.35,47.95,46.54,36.71,31.94,31.92,31.39,29.79,29.73,29.71,29.68,29.65,29.62,29.55,29.38,29.35,29.33,29.24,28.84,27.68,27.24,27.22,26.83,25.76,25.56,22.70,14.13,9.75.HRMS(ESI):m/z calcd for C47H91N2O5([M+H]+)763.6850,found 763.6880.
实施例7
实施例7提供七种鞘脂类化合物s-y,制备方法如下,结构式如下:
化合物13(622.0mg,1.0mmol)于反应瓶中,3-溴丙酸(1.25mmol),二环己基碳二亚胺(257.5mg,1.25mmol),4-二甲氨基吡啶(12.2mg,0.1mmol)后,用5mL无水二氯甲烷溶解,室温搅拌,TLC检测直至反应完全。将反应浓缩,后经柱层析分离得到中间体化合物16。
称取化合物16(78.9mg,0.12mmol)于反应瓶中,加入5mL无水二氯甲烷溶解,后加入三乙胺(33.4μL,0.24mmol)和一系列仲胺(0.24mmol)。在室温下搅拌24小时,TLC检测直至反应完全。柱层析分离得到一系列目标化合物s-y(收率30-83%)。
目标化合物s的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.98(s,1H,-NH),5.32-5.36(m,2H),4.48-4.50(m,1H),4.27-4.30(m,1H),4.16-4.18(m,1H),4.10-4.12(m,1H),4.04-4.07(m,1H),2.47-2.69(m,8H),2.10-2.14(m,2H),1.98-2.02(m,4H),1.46-1.61(m,10H),1.43(s,3H,-C(CH3)2),1.25-1.33(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.75,172.37,130.00,129.74,108.14,77.72,76.50,63.96,54.83,54.47,48.08,36.75,32.17,31.94,31.91,29.78,29.72,29.71,29.68,29.64,29.60,29.55,29.38,29.35,29.33,29.22,28.91,27.71,27.24,27.21,26.65,25.57,24.02,22.70,22.69,14.13.HRMS(ESI):m/z calcd for C47H89N2O5([M+H]+)761.6693,found761.6730.
目标化合物t的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.66(d,J=9.6Hz,1H,-NH),5.31-5.36(m,2H),4.29-4.37(m,2H),4.11-4.23(m,2H),4.01-4.04(m,1H),3.68(t,J=4.8Hz,4H),2.67(t,J=7.2Hz,2H),2.46-2.53(m,6H),2.11-2.14(m,2H),1.99-2.02(m,4H),1.52-1.62(m,4H),1.44(s,3H,-C(CH3)2),1.25-1.32(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.55,172.29,130.04,129.68,108.19,77.62,77.23(overlapped with C of CDCl3),66.84,64.33,54.22,53.49,48.22,36.86,32.02,31.94,31.91,29.77,29.75,29.71,29.69,29.67,29.62,29.58,29.56,29.53,29.37,29.33,29.30,29.18,28.94,27.43,27.23,27.19,26.74,25.61,25.40,22.70,14.12.HRMS(ESI):m/z calcd for C46H87N2O6([M+H]+)763.6486,found 763.6526.
目标化合物u的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.74(s,1H,-NH),5.32-5.35(m,2H),4.29-4.34(m,2H),4.20-4.23(m,1H),4.10-4.13(m,1H),4.04-4.06(m,1H),2.77(d,J=7.2Hz,2H),2.38-2.46(m,6H),2.10-2.13(m,2H),1.98-2.02(m,4H),1.60-1.64(m,6H),1.52-1.53(m,2H),1.43(s,3H,-C(CH3)2),1.25-1.32(m,47H),0.85-0.89(m,12H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.79,172.57,130.02,129.71,108.15,77.64,77.10,64.14,55.73,49.59,48.16,36.83,32.56,31.94,31.92,29.78,29.77,29.72,29.69,29.68,29.63,29.59,29.54,29.38,29.33,29.20,28.95,27.49,27.24,27.20,26.71,25.62,25.43,22.70,22.69,19.81,14.13,11.90.HRMS(ESI):m/z calcd for C48H93N2O5([M+H]+)777.7006,found 777.7042.
目标化合物v的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.32-5.35(m,2H),4.29-4.37(m,2H),4.19-4.22(m,1H),4.05-4.12(m,2H),2.82(s,2H),2.48(s,4H),2.11-2.14(m,2H),1.98-2.02(m,4H),1.51-1.62(m,9H),1.43(s,3H,-C(CH3)2),1.25-1.33(m,52H),0.90(t,J=7.2Hz,6H,-CH2CH3),0.86(t,J=6.6Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.66,172.63,130.00,129.72,108.13,77.67,77.23(overlapped with C of CDCl3),64.19,53.43,49.52,48.12,36.80,31.94,31.91,29.78,29.72,29.69,29.68,29.63,29.60,29.56,29.54,29.38,29.35,29.33,29.22,28.92,27.57,27.23,27.20,26.73,25.63,25.48,22.69,20.66,14.12,14.04.HRMS(ESI):m/z calcd for C50H97N2O5([M+H]+)805.7319,found 805.7355.
目标化合物w的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:6.39(d,J=9.0Hz,1H,-NH),5.32-5.35(m,2H),4.65-4.68(m,1H),4.26-4.29(m,1H),4.08-4.12(m,2H),3.99-4.02(m,1H),2.87(s,2H),2.54-2.66(m,6H),1.98-2.10(m,6H),1.48-1.61(m,6H),1.44(s,3H,-C(CH3)2),1.24-1.34(m,49H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.78,171.99,129.98,129.76,108.14,77.87,76.17,63.73,54.28,52.61,47.84,36.60,31.94,29.79,29.72,29.68,29.64,29.61,29.55,29.54,29.40,29.38,29.34,29.33,29.22,28.81,27.91,27.24,27.21,26.62,25.70,25.51,23.45,22.70,14.13.HRMS(ESI):m/z calcd for C46H87N2O5([M+H]+)747.6537,found 747.6578.
目标化合物x的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.75(d,J=9.6Hz,1H,-NH),5.32-5.36(m,2H),4.42-4.44(m,1H),4.27-4.30(m,1H),4.17-4.20(m,1H),4.11-4.13(m,1H),4.02-4.04(m,1H),2.68-2.71(m,2H),2.47-2.55(m,8H),2.28(s,3H,-NCH3),2.10-2.13(m,2H),1.98-2.02(m,4H),1.51-1.61(m,6H),1.43(s,3H,-C(CH3)2),1.25-1.33(m,47H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.59,172.36,130.02,129.70,108.17,77.66,77.23(overlapped with C of CDCl3),64.03,55.00,54.07,53.03,48.17,46.03,36.85,32.30,31.94,31.91,29.78,29.72,29.70,29.68,29.60,29.56,29.54,29.37,29.34,29.20,28.94,27.59,27.24,27.20,26.70,25.57,25.50,22.70,14.13.HRMS(ESI):m/z calcd for C47H90N3O5([M+H]+)776.6802,found 776.6848.
目标化合物y的结构鉴定数据:1H NMR(600MHz,CDCl3)δ:5.32-5.35(m,2H),4.29-4.46(m,2H),4.05-4.20(m,3H),2.50-2.84(m,6H),2.10-2.13(m,2H),1.98-2.02(m,4H),1.50-1.60(m,8H),1.43(s,3H,-C(CH3)2),1.25-1.33(m,51H),0.86(t,J=7.2Hz,6H,-CH2CH3);13C NMR(150MHz,CDCl3)δ:172.68,172.40,130.01,129.74,108.13,78.75,77.71,64.16,48.41,48.11,46.44,36.77,32.33,31.94,29.78,29.72,29.67,29.63,29.59,29.54,29.38,29.34,29.33,29.21,28.89,27.65,27.25,27.21,26.70,25.60,25.54,22.70,14.12,10.86.HRMS(ESI):m/z calcd for C47H89N2O5([M+H]+)749.6693,found749.6736.
实施例8
实施例8提供一种鞘脂类化合物a1,结构式如下,制备方法如下:
将化合物鞘氨醇17(2.67g,8.9mmol)和tBoc2O(2.23g,10.2mmol)置于反应瓶中,加入tBuOH(60mL)溶液在室温下搅拌8h。待反应完全,减压浓缩反应溶液,以石油醚/乙酸乙酯(v/v,5:1)重结晶得到化合物18,产率为93%,白色固体。
将上述化合物18(1.83g,4.57mmol)置于反应瓶中,加入CH2Cl2(10mL)溶解,在0℃冰浴条件下缓慢滴加甲烷磺酰氯MsCl(0.728mL,9.45mmol),最后加入三乙胺(1.48mL,10.65mmol),将反应混合物在0℃下继续搅拌30分钟,然后在室温下搅拌一小时。反应液中加入H2O进行淬灭,用CH2Cl2萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物19,白色固体,产率为93%。
称取化合物19(1.68g,3.53mmol)于反应瓶中,加入DMF(10mL)溶解,后加入叠氮化钠(1.147g,28.67mmol),反应混合物在65℃下搅拌过夜。反应完全后用H2O猝灭,乙酸乙酯萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物20,白色固体,产率为83%。
称取化合物20(1.32g,3.73mmol)用甲醇(10mL)溶解,再缓慢滴加浓盐酸(0.8mL)。将反应混合物在室温下搅拌过夜至反应完全,将反应溶液减压浓缩,得到粗品。继续加入油酸(1.32g,4.67mmol),EDCI(893mg,4.66mmol),和1-羟基苯并三唑HOBT(629mg,4.66mmol),用二氯甲烷(15mL)溶解,后缓慢滴加三乙胺(0.723mL,5.20mmol),将反应混合物在室温下搅拌16h,然后用二氯甲烷稀释。稀释后的溶液用饱和氯化铵水溶液洗涤。水层用二氯甲烷萃取。收集有机相,无水硫酸钠干燥,减压浓缩,柱层析得到化合物21,白色固体,产率为60%。
称取化合物21(0.069g,0.19mmol),抗坏血酸钠(94.9mg,0.48mmol),CuSO4(6.7mg,0.04mmol)和化合物7(98.3mg,0.26mmol)于圆底烧瓶中,后加入5.5mL的甲醇/水(10:1,v/v),在室温下搅拌12h。反应液用乙酸乙酯萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到中间体22,白色固体,产率为57%。
称取化合物22(0.098g,0.13mmol)于反应瓶中,加入2mL甲醇溶解,缓慢滴加浓HCl,室温下搅拌至反应完全,反应液用水萃取(3×10mL),收集水相。再向水相缓慢滴加饱和碳酸氢钠,调至PH=7,水层用二氯甲烷萃取,收集有机相,无水硫酸钠干燥,减压浓缩,得到目标化合物a1(76mg收率78%)。
目标化合物a1的结构鉴定数据:1H NMR(600MHz,CD3OD)δ7.59(s,1H),5.64-5.67(m,2H),5.32-5.35(m,2H),4.80-5.00(m,2H),4.46-4.52(m,2H),3.92-3.97(m,2H),2.95-2.98(m,1H),2.69(m,2H),1.94-2.16(m,8H),1.77(m,2H),1.50-1.53(m,6H),1.25-1.30(m,44H),0.88(t,6H,J=7.2Hz);13C NMR(150MHz,CD3OD)δ173.7,171.2,134.3,130.8,130.6,129.8,122.9,74.0,55.7,54.3,54.1,40.4,35.4,33.12,33.11,30.82,30.73,30.68,30.66,30.53,30.50,30.46,30.40,30.39,30.31,43.0,42.1,36.8,34.1,31.9,29.6,29.3,28.9,27.6,25.7,22.7,22.3,14.10.HRMS(ESI):m/z calcd for C45H85N7O3([M+H]+)772.6714,found 772.6709.
其中,化合物17~22的结构式如下
实施例9
实施例9提供一种鞘脂类化合物b1,结构式如下,制备方法如下:
将上述实施例8制备的化合物21(0.177g,0.3mmol)和SnCl2(0.569g,3.0mmol)的5mL乙醇溶液在室温下搅拌12h,二氯甲烷溶解,饱和NaCl溶液洗涤,收集有机相,无水硫酸钠干燥,减压浓缩得到粗产品化合物23,无需进一步提纯。将上述粗品用无水CH2Cl2(7mL)溶解,在0℃搅拌,并缓慢加入三乙胺(0.4mL)和氯化乙酰氯(36μL)。将反应混合物在0℃下搅拌30分钟,然后在室温下下继续搅拌一小时。反应用H2O猝灭,用CH2Cl2萃取,收集有机相,用无水硫酸钠干燥,减压浓缩,柱层析分离,得到化合物24,白色固体,产率为37%。
称取化合物24(76.6mg,0.12mmol)于反应瓶中,加入5mL乙酸乙酯溶解,后加入三甲胺(0.1mL,2M in THF)。在室温下搅拌24小时,产物沉淀为白色固体。将得到的悬浮液冷却到0℃,过滤,用冰冷的乙二醛洗涤,真空干燥,得到目标产物化合物b1(40mg,收率65%)。
目标化合物b1的结构鉴定数据:1H NMR(600MHz,CDCl3)δ8.14(t,1H,J=6.0Hz,NH),8.01(d,1H,J=8.4Hz,NH),6.18(s,1H,-OH),5.64-5.67(m,2H),5.32-5.34(m,2H),4.80(m,1H),3.48-3.52(m,1H),3.30(s,9H),2.19(t,2H,J=7.8Hz),1.94-2.16(m,8H),1.53(m,2H),1.26-1.33(m,42H),0.88(t,6H,J=7.2Hz);13C NMR(150MHz,CDCl3)δ173.8,170.9,134.3,130.6,129.8,73.6,72.2,58.7,53.8,38.4,36.8,34.0,31.9,29.9,29.7,29.6,29.3,29.0,28.6,27.7,25.6,22.7,14.1;HRMS(ESI):m/z calcd for C41H80N3O3 +([M]+)662.6194,found 662.6194.
其中,化合物23和化合物24的结构式如下:
实施例10
实施例10提供一种鞘脂类化合物c1,结构式如下,制备方法如下:
称取化合物23(129.4mg,0.23mmol),赖氨酸(79.7mg,0.23mmol),EDCI(51mg,0.27mmol)和HOBT(37mg,0.27mmol)于反应瓶中,加入2mL无水二氯甲烷溶解,后缓慢滴加三乙胺(0.06mL,0.43mmol),室温下搅拌16h。反应加H2O淬灭,反应液用二氯甲烷萃取(3×10mL),收集有机相,无水Na2SO4干燥,减压下浓缩,柱层析分离得到化合物25,白色固体,产率为57%。
称取化合物25(89.6mg,0.13mmol)于反应瓶中,加入2mL甲醇溶解,缓慢滴加浓HCl,室温下搅拌至反应完全,反应液用水萃取(3×10mL),收集水相。再向水相缓慢滴加饱和碳酸氢钠,调至PH=7,水层用二氯甲烷萃取,收集有机相,无水硫酸钠干燥,减压浓缩,得到的目标产物化合物c1(37mg,收率72%)。
目标化合物c1的结构鉴定数据:1H NMR(600MHz,CD3OD)δ8.86(s,2H),8.35(s,1H),8.22(s,1H),6.10(s,1H),5.68-5.78(m,2H),5.31-5.39(m,2H),4.78-4.86(m,1H),4.28-4.55(m,1H),3.23-3.31(m,3H),2.62-2.70(m,2H),2.08-2.15(m,4H),2.00(t,J=6.0Hz,2H),1.76-1.91(m,4H),1.58-1.65(m,6H),1.22-1.29(m,44H),0.81(m,6H);13C NMR(150MHz,CD3OD)δ173.8,173.4,134.3,130.6,129.8,73.6,58.7,54.3,42.0,38.7,36.8,34.2,34.0,31.9,29.9,29.7,29.6,29.3,29.0,28.6,27.7,25.6,22.7,22.3,14.1.HRMS(ESI):m/z calcd for C42H83N4O3([M+H]+)691.6460,found 691.6394.
其中,化合物25的结构式如下:
实施例11
将实施例1~4制备的鞘脂类化合物(a、b、c和d)分别制备成阳离子脂质体(Sp1、Sp2、Sp3和Sp4),其制备方法如下:
(1)将鞘脂类化合物(a、b、c和d)分别与胆固醇、辅助磷脂DOPE以及DSPE-mPEG置于圆底烧瓶内,使其摩尔比为1:1:1:0.06。
(2)用2mL氯仿-甲醇(v/v 1:1)溶液充分溶解,置于旋转蒸发仪上,40℃水浴减压蒸馏至圆底烧瓶底部形成均匀的脂膜,继续减压浓缩1h,除尽残留有机试剂。
(3)然后加入2mL纯化水,置于超声仪上超声5min,形成乳白色溶液,常温下继续搅拌水化1h。
(4)冰浴下探头超声120次(工作3s,间歇2s),0.22μm滤膜过滤,即分别制得阳离子脂质体(Sp1)、阳离子脂质体(Sp2)、阳离子脂质体(Sp3)和阳离子脂质体(Sp4)。
实施例12
研究鞘脂类化合物(a、b、c和d)与紫杉醇的比例对包封率的影响,将实施例1~4制备的鞘脂类化合物(a、b、c和d)分别制备成阳离子脂质体药物制剂,制备步骤如下:
1)分别称取摩尔比为1:1:1的鞘脂类化合物(a、b、c和d)、胆固醇、辅助磷脂DOPE于圆底烧瓶内,再加入紫杉醇,以氯仿和甲醇2mL使其充分溶解,其中,鞘脂类化合物(a、b、c和d)和紫杉醇的摩尔比分别均为1:1、2:1、4:1、8:1和16:1。
2)充分溶解后,置于旋转蒸发仪上,40℃减压蒸馏至圆底烧瓶底部形成均匀的脂膜,继续减压蒸馏1h,除尽残留有机试剂。
3)加入适量无酶水,置于超声仪上超声至形成均一的乳白色溶液,常温下继续搅拌水化1h。
4)取出磁子,将上述溶液从圆底烧瓶转移至5mL样品瓶中。冰浴下,探头超声120次。0.22μm滤膜过滤,即可制得一系列阳离子脂质体药物制剂。
实施例13
研究鞘脂类化合物(a、b、c和d)的含量对紫杉醇的包封率的影响,制备方法同实施例12,鞘脂类化合物(a、b、c和d)和紫杉醇的摩尔比为8:1。其区别在于,鞘脂类化合物(a、b、c和d)、胆固醇和辅助磷脂DOPE的摩尔比分别为0.5:1:1、1:1:1、2:1:1和4:1:1。
实施例14
研究DSPE-mPEG的含量对紫杉醇包封率的影响,制备方法同实施例12,其区别在于,鞘脂类化合物(a、b、c和d)和DSPE-mPEG的摩尔比分别为1:0.015、1:0.03、1:0.06和1:0.12。
实施例15
实施例15提供阳离子脂质体药物制剂(Sphy1)、阳离子脂质体药物制剂(Sphy2)、阳离子脂质体药物制剂(Sphy3)和阳离子脂质体药物制剂(Sphy4),其制备方法如下:
1)分别称取摩尔比为1:1:1:0.06的鞘脂类化合物(a、b、c和d)、胆固醇、辅助磷脂DOPE和DSPE-mPEG(分子量2000)于圆底烧瓶内,再加入紫杉醇,以氯仿和甲醇2mL使其充分溶解,其中,鞘脂类化合物(a、b、c和d)和紫杉醇的摩尔比分别均为8:1。
2)充分溶解后,置于旋转蒸发仪上,40℃减压蒸馏至圆底烧瓶底部形成均匀的脂膜,继续减压蒸馏1h,除尽残留有机试剂。
3)加入适量无酶水,置于超声仪上超声至形成均一的乳白色溶液,常温下继续搅拌水化1h。
4)取出磁子,将上述溶液从圆底烧瓶转移至5mL样品瓶中。冰浴下,探头超声120次。0.22μm滤膜过滤,即制得一系列阳离子脂质体药物制剂。
性能测试
鞘脂类化合物的细胞毒性测试:采用MTT法检测实施例1~4的鞘脂类化合物a、鞘脂类化合物b、鞘脂类化合物c和鞘脂类化合物d对MDA-MB-231细胞的增殖的影响,以4×103/孔/100μL将MDA-MB-231细胞接种于96孔板中,培养基分别为含10%FBS1640培养基,在37℃,5%CO2饱和湿度培养箱内培养24h。加入不同浓度的鞘脂类化合物a、鞘脂类化合物b、鞘脂类化合物c和鞘脂类化合物d(80、40、20、10、5、2.5μM),每个浓度设置3个复孔。继续培养72h后,每孔加入10μL MTT溶液,继续孵育4h。吸出上清液,每孔加入100μL二甲基亚砜,置于震荡仪上震荡10min,使甲瓒晶体充分溶解,酶标仪测定吸光值(λ=570nm),据此计算细胞存活率。结果如图1所示。在浓度为2.5-60μM的范围内,四种鞘脂类化合物均未表现出细胞毒性,可以作为安全的载体材料递送化疗药物和基因药物。
阳离子脂质体及其与siRNA-Luc复合物的细胞毒性试验:采用MTT法检测实施例11制备的Sp1、Sp2、Sp3、Sp4、Sp1+siRNA-Luc复合物、Sp2+siRNA-Luc复合物、Sp3+siRNA-Luc复合物、Sp4+siRNA-Luc复合物及free siRNA-Luc对MDA-MB-231细胞活力的影响。因主要为考察阳离子脂质体在载siRNA进行细胞转染过程中是否抑制MDA-MB-231细胞的生长。以4×103/孔/100μL将MDA-MB-231细胞接种于96孔板中,用含10%胎牛血清的1640培养基在37℃,5%CO2饱和湿度培养箱内培养24h。配制N/P为8:1的Sp1、Sp2、Sp3、Sp4、Sp1+siRNA-Luc复合物、Sp2+siRNA-Luc复合物、Sp3+siRNA-Luc复合物、Sp4+siRNA-Luc复合物,siRNA终浓度为50nM,另设置相同浓度的游离siRNA与同等浓度梯度的脂质体、以及Lipo2000、Lipo2000+siRNA-Luc复合物作为对照组。与细胞共孵育4h后,吸去培养基,加入新的完全培养基继续培养72h后,加MTT进行测定,并计算细胞存活率。细胞毒性如图2所示。四种阳离子脂质体及负载siRNA-Luc阳离子脂质体在N/P为8:1的浓度下与细胞进行孵育时,并未产生显著的细胞毒性,与市售转染试剂Lipofectamin 2000(Lipo 2000)相比,也具有相当的存活率。由试验结果可知,阳离子脂质体运载基因进行转染时具有较好的生物兼容性。
将实施例11制备的一系列阳离子脂质体进行储存稳定性测试,取新鲜制备的阳离子脂质体无菌过滤分装至灭菌EP管中,于4℃冰箱存储28天,其存储体系为无菌无RNA酶水,在1、4、7、14、28天取出样品,以激光粒度仪测定其粒径,观察存储期间变化;结果如图3所示,制备的四种空白阳离子脂质体存储28天后,粒径没有明显变化,外观无明显沉淀和絮凝,表现出较高的稳定性。
将实施例11制备的一系列阳离子脂质体和实施例15制备的一系列阳离子脂质体药物制剂进行粒径和电位检测,结果如表1所示,从表中可知,四种阳离子脂质体粒径均不超过100nm,聚分散指数(PDI)均小于0.3。说明实施例1~4的鞘脂类化合物在胆固醇,辅助磷脂DOPE以及DSPE-mPEG的辅助下,能在水溶液中形成脂质体,且其粒径较小,粒径分布较窄,均一性较好。并且四种脂质体均能有效的包载化疗药物紫杉醇,脂质体紫杉醇复合物粒径没有明显变化,且均一性较好。此外这些脂质体及其复合物Zeta电位均大于30mV,较高的表面正电荷说明了该脂质体具有作为阴离子药物载体的特性,且在溶液内较稳定,不易发生聚集。
表1阳离子脂质体和阳离子脂质体药物制剂的粒径、电位和聚分散指数表
将实施例12制备的一系列阳离子脂质体药物制剂进行紫杉醇的包封率测试,研究紫杉醇的含量对包封率效果的影响,结果如图4所示,当PTX与鞘脂类化合物的摩尔比减小到1:8时,Sphy1、Sphy2、Sphy3和Sphy4的包封率分别为83.6%,78.5%,85.4%,73.2%,PTX用量继续减少后,包封率没有明显提高。
将实施例13制备的一系列阳离子脂质体药物制剂进行紫杉醇的包封率测试,结果如图5和表2所示,随着鞘脂类化合物的比例不断增大,包封率也不断增大,鞘脂类化合物-胆固醇-DOPE为1:1:1时,Sphy1、Sphy2、Sphy3和Sphy4的包封率分别为78.6%、68.5%、83.7%和63.2%。鞘脂类化合物的比例进一步增大后,包封率没有明显变化,但是正电荷密度进一步增大,具有增加细胞毒性的风险。
表2不同鞘脂类化合物-胆固醇-DOPE的摩尔比制备的阳离子脂质体药物制剂的表征
将实施例14制备的一系列阳离子脂质体药物制剂进行紫杉醇的包封率测试,由图6和表3可知,随着DSPE-mPEG的增加四种脂质体包封率均进一步增加,当DSPE-mPEG含量与鞘脂的摩尔比例为0.06:1时包封率达到最优,分别为93.6%、90.3%、95.4%、89.7%。同时粒径达到最小,电位均在35mV以上,适合作为阳离子脂质体材料。
表3不同DSPE-mPEG比例制备的阳离子脂质体的表征
将实施例15的一系列阳离子脂质体药物制剂进行包封率和载药量测试,结果如图7所示,Sphy1、Sphy2、Sphy3和Sphy4的包封率均在90%以上,分别为93.6%、90.3%、95.4%和92.7%。载药量分别为4.89%、4.97%、5.21%、4.85%。
将实施例15制备的一系列阳离子脂质体药物制剂进行PTX释放测试,由图8可知,Sphy1、Sphy2、Sphy3和Sphy4均能够缓慢释放紫杉醇。在PH为7.4时,与对照的游离紫杉醇对比,前12h内紫杉醇脂质体没有明显的突释现象,具有良好的稳定性,可以避免由于纳米制剂突释带来的毒副作用,提高紫杉醇用药的安全性。
将实施例15一系列阳离子脂质体药物制剂与siRNA混合孵育并测定结合率:采用琼脂糖凝胶电泳阻滞试验来判断阳离子脂质体药物制剂与siRNA-Luc复合物的结合情况。取siRNA-Luc(10mM),按N/P 1:1、2:1、4:1、8:1和16:1,加入阳离子脂质体药物制剂,孵育20min。以同浓度的游离siRNA-Luc作为对照组。然后与DNA加样缓冲液1:1混匀,上样于1%的琼脂糖凝胶电泳上样槽内,控制电压100V,20min,取出凝胶,用凝胶成像系统拍照分析。结果如图9所示,游离siRNA可在电场作用下完全向正极迁移,随着N/P增加,从上样孔中迁移的siRNA亮度逐渐降低,表明siRNA与阳离子脂质体逐渐结合,当N/P为4:1时,Sphy1、Sphy2、Sphy3和Sphy4几乎将所有的siRNA-Luc阻滞,说明四种脂质体均对siRNA-Luc有较好的结合能力。使用玛尔文纳米粒度分析仪对不同N/P的阳离子脂质体与siRNA复合物进行平均粒径和Zeta电位的测定。如图10所示,在不同N/P下的粒径在84~150nm之间,随着siRNA-Luc的比例增加,粒径呈增大趋势,说明脂质体与siRNA相互结合。当N/P为4:1时,四种阳离子脂质体药物制剂的电位由负转正,电位在15-20mV之间,并且电位随着脂质体的增加而增加。该结果与琼脂糖凝胶电泳结果一致,脂质体复合物的正电性预示了其可以较好地与负电性的细胞膜结合,使基因类药物能更好的进入细胞内。
将实施例15的一系列阳离子脂质体药物制剂与siRNA混合孵育并研究血清稳定性:取实施例15的四种阳离子脂质体药物制剂与siRNA(siRNA-Luc)复合物和10%胎牛血清混合,将样品置于37℃孵育,并以等体积和相同浓度的游离siRNA作为对照。分别取0、6、12、24和48h的样品,在凝胶电泳分析前,在样品中加入2%的肝素钠溶液以提取siRNA,立即与2×Loading Buffer以1:1体积混匀,进行琼脂糖凝胶电泳分析并通过凝胶成像系统拍照。结果如图11所示,游离siRNA在12h基本完全降解,而由脂质体包裹的siRNA虽有降解,但其稳定性相较于游离siRNA己明显提高,在48h时仍然可以看到清晰的siRNA条带,证明四种脂质体在血清存在的条件下均对siRNA有一定的保护作用,避免siRNA被血清中的核酸酶等过快降解。
研究了阳离子脂质体携载萤火虫荧光素酶siRNA对萤火虫荧光素酶的沉默效率:取生长对数期MDA-MB-231-Luc细胞接种于24孔板内,每孔4万个细胞,培养24h。设置实验组:实施例11的Sp1+siRNA-Luc、实施例11的Sp2+siRNA-Luc、实施例11的Sp3+siRNA-Luc、实施例11的Sp4+siRNA-Luc、Lipo2000+siRNA-Luc(N/P 1:1,2:1,4:1,8:1)和游离siRNA-Luc,每孔内siRNA-Luc为50nM,进行转染,孵育4h后,换液继续培养48h。吸去培养液,PBS洗涤一次,加入细胞裂解液,提取萤火虫荧光素酶,按萤火虫荧光素酶测定试剂盒测定,计算荧光素酶沉默效率。结果如图12所示。在孵育时间为48h时四种负载siRNA-Luc的脂质体表现出最强的沉默效率,且随着N/P的增加,沉默效果呈增加趋势,当N/P为4:1时沉默效果达到最佳,而后N/P再增加时,沉默效果却又有所下降。这样的现象可能是脂质体与siRNA-Luc的结合程度引起的,当脂质体相较siRNA-Luc而言出现过量状态时,将siRNA-Luc牢牢结合在多个脂质体的中心,反而不利于siRNA-Luc的逃逸。这四种阳离子脂质体对细胞内荧光素酶的沉默效率分别为83%、68%、75%和63%;Lipo2000沉默效率为78%。
研究了阳离子脂质体对Cy3-siRNA的递送效率、入胞分布及行为:采用Cy3对siRNA进行荧光标记,通过共聚焦显微镜来观察阳离子脂质体对siRNA的递送情况。将呈对数生长期的MDA-MB-231细胞用胰酶消化后,以每孔1×105细胞接种于6孔板中。实验分组分别为实施例11的Sp1+Cy3-siRNA、实施例11的Sp2+Cy3-siRNA、实施例11的Sp3+Cy3-siRNA、实施例11的Sp4+Cy3-siRNA、Lipo2000+Cy3-siRNA、Free Cy3-siRNA和Blank组。各组Cy3-siRNA终浓度为50nM,细胞接种24h后进行转染。4h后,弃去液体,加入含10%血清的1640培养基,继续培养48h后用激光共聚焦显微镜观察细胞内的荧光表达。结果如图13所示,从图中看出:在N/P为4:1时,阳离子脂质体Sp1红色荧光强度最高,表现出对Cy3-siRNA最优的递送效果,但市售阳性对照Lipofectamin 2000却表现出对Cy3-siRNA相对较弱的递送效果,同时阳离子脂质体Sp3也显著超过市售阳性对照Lipofectamin 2000,对siRNA具有优异的递送效果。该实验结果与萤火虫荧光素酶沉默效率基本一致。
将对数生长期MDA-MB-231细胞用胰酶消化,以2×105/孔接种于6孔板中。细胞接种24h后进行转染。实验分组分别为实施例11的Sp1+Cy3-siRNA、实施例11的Sp2+Cy3-siRNA、实施例11的Sp3+Cy3-siRNA、Lipo2000+Cy3-siRNA、Free Cy3-siRNA和Blank组。各组Cy3-siRNA终浓度为50nM,N/P比为4:1。4h后,弃去液体,加入含10%胎牛血清的1640培养基,继续培养48h。弃去培养液,PBS清洗两遍,加入胰酶消化后,收集细胞,用流式细胞仪进行荧光分析。从图14可以看出,使用流式细胞仪定量评估48h时阳离子脂质在MDA-MB-231细胞上对Cy3-siRNA的递送效率,从流式分析图可看出,游离的Cy3-siRNA很难进入细胞,Sp1+Cy3-siRNA和Sp3+Cy3-siRNA组荧光阳性比例可以分别达到86.05%和59.98%,均高于阳性对照Lipo2000+Cy3-siRNA(41.98%)。这些结果与上述共聚焦显微镜观察结果一致。
研究了阳离子脂质体对编码EGFP的质粒DNA(大约含有6300个碱基对)的递送效率:EGFP为绿色荧光蛋白,通过倒置荧光显微镜来观察阳离子脂质体对EGFP质粒DNA的递送情况。将呈对数生长期的MDA-MB-231细胞用胰酶消化后,以每孔1×105细胞接种于6孔板中。实验分组分别为实施例11的Sp1+EGFP、实施例11的Sp2+EGFP、实施例11的Sp3+EGFP、实施例11的Sp4+EGFP、Free EGFP和Blank组。各组EGFP质粒终浓度为7.58nM,细胞接种24h后进行转染。4h后,弃去液体,加入含10%胎牛血清的1640培养基,继续培养48h后用倒置荧光显微镜观察细胞内的绿色荧光蛋白的表达。结果如图15所示,从图中看出:在N/P为4:1时,四种阳离子脂质体均能递送EGFP质粒,其中阳离子脂质体Sp1绿色荧光强度最高,表现出对EGFP质粒最优的递送效果。
研究阳离子脂质体共载香豆素C6和Cy3-siRNA的胞内分布:取对数生长期MDA-MB-231细胞,以每孔1×105个接种于铺有玻璃盖玻片的6孔细胞培养皿内,培养24h。分别加入实施例11的Sp1+C6+Cy3-siRNA、实施例11的Sp2+C6+Cy3-siRNA、实施例11的Sp3+C6+Cy3-siRNA、实施例11的Sp4+C6+Cy3-siRNA、Free C6和C6+FreeCy3-siRNA,使Cy3-siRNA终浓度为50nM,孵育4h后,弃去培养液,PBS轻轻洗涤一次,加入含10%胎牛血清的1640培养基,继续培养48h。取出后,吸去培养液,PBS洗涤两次,加入4%多聚甲醛固定,再加入10μg/mLDAPI进行细胞核染色,15min后吸去染料,PBS洗涤,制作细胞爬片。置于激光共聚焦显微镜下观察红色荧光(λ=550nm),绿色荧光(λ=443nm)与蓝色荧光(λ=364nm),经图像迭合后,确定Cy3-siRNA和C6在细胞内的分布情况。为证明阳离子脂质体可以有效地将siRNA和紫杉醇(PTX)递送进细胞,香豆素C6与PTX均为疏水药物,且香豆素自身可以发出绿色荧光,因此选用C6替代PTX,通过激光共聚焦显微镜确定siRNA和C6的入胞量和胞内分布。结果如图16所示,明场下获得细胞轮廓,与细胞核,C6及Cy3通道重叠后,可发现红色荧光和绿色荧光在细胞内,且部分与蓝色荧光重叠,说明了Cy3-siRNA和C6在阳离子脂质体的递送下,进入了细胞,且有部分已经进入了细胞核内。同时也可以观察到阳离子脂质体Sp1共递送C6和Cy3-siRNA的荧光最强,与单独递送Cy3-siRNA结果基本一致,表现出最优的递送效果。
研究阳离子脂质体递送HIF-1αsiRNA对HIF-1α基因沉默效率:将对数生长期MDA-MB-231细胞用胰酶消化,以2×105/孔接种于6孔板中。细胞接种24小时后进行转染。实验分组分别为实施例11的Sp1+HIF-1αsiRNA、实施例11的Sp2+HIF-1αsiRNA、实施例11的Sp3+HIF-1αsiRNA、实施例11的Sp4+HIF-1αsiRNA、Lipo2000+HIF-1αsiRNA、Free HIF-1αsiRNA和Blank组。各组HIF-1αsiRNA终浓度为50nM,N/P比为4:1。继续在1%O2条件下培养48h,PBS清洗后,用含蛋白酶抑制剂的1×RIPA裂解液对细胞进行裂解和收集。采用BCA检测试剂盒定量测定蛋白浓度。用8%SDS-PAGE分离总蛋白,随后300mA条件下湿转到PVDF膜。膜在封闭缓冲液(5%脱脂牛奶TBS+0.1%Tween 20)中室温封闭1h。与一抗在4℃下孵育过夜后,再将膜用IRDye 800cw标记的山羊抗小鼠IgG二抗在室温下避光孵育1h,扫描检测免疫反应条带。
由图17的结果可以看出,与Blank组相比,阳离子脂质体Sp1、Sp2、Sp3、Sp4和Lipo2000本身并没有敲低HIF-1α蛋白表达的作用。游离的HIF-1αsiRNA组的HIF-1α蛋白表达量与Blank相比也没有降低,证明其很难进入细胞敲低HIF-1α蛋白表达量;而通过转染试剂递送的HIF-1αsiRNA组,HIF-1α蛋白表达量明显被敲低,其中Sp1+HIF-1αsiRNA组蛋白表达量降低最为显著,优于阳性对照Lipo2000。
研究阳离子脂质体共递送化疗药物紫杉醇和基因药物HIF-1αsiRNA的体外抗肿瘤活性:采用SRB法分别检测常氧(21%O2)和低氧(1%O2)条件下,阳离子脂质体共递送化疗药物紫杉醇和基因药物HIF-1αsiRNA对MDA-MB-231细胞的抗增殖作用。实验组设置为:实施例15的阳离子脂质体药物制剂(Sphy1、Sphy2、Sphy3和Sphy4)、实施例15的阳离子脂质体药物制剂(Sphy1、Sphy2、Sphy3和Sphy4)分别与HIF-1αsiRNA的复合物、游离的HIF-1αsiRNA、游离PTX、PTX与HIF-1αsiRNA的复合物。以4×103/孔/100μL将MDA-MB-231细胞接种于96孔板中,培养基分别为含10%FBS1640培养基,在37℃,5%CO2饱和湿度培养箱内培养24h。加入不同组别的药物,每个浓度设置3个复孔。继续培养72h后,每孔加入50μL 4℃预冷的TCA(三氯乙酸)溶液(30%,w/v)固定细胞,TCA溶液的终浓度为10%。静置5min移入4℃冰箱中固定1h,取出用去离子水冲洗5遍,室温晾干。待96孔板室温下晾干后,每孔加入0.4%(w/v)的SRB染液(1%的乙酸配制)70μL,染色30min后倒掉染液,用1%(v/v)乙酸冲洗4次,去除未结合的染料,室温晾干。用100μL三碱基溶液(10mM,pH=10.5)溶解与细胞蛋白结合的染料,水平摇床上振荡20min,采用酶标仪515nm处测定光吸收值,据此计算细胞存活率。
结果如图18所示,在常氧条件下,负载紫杉醇的阳离子脂质体药物制剂组表现出比游离紫杉醇组更强的肿瘤细胞毒性,表明紫杉醇由阳离子脂质体负载后入胞率更高,提升了紫杉醇的药效。而在低氧条件下,游离紫杉醇组的肿瘤细胞毒性较常氧条件下降低,表明在低氧条件下肿瘤细胞对紫杉醇具有一定的耐药性。而共负载紫杉醇和HIF-1αsiRNA的阳离子脂质体药物制剂组,在低氧条件下表现出比游离紫杉醇组和仅负载紫杉醇的阳离子脂质体药物制剂组更强的肿瘤细胞毒性。表明阳离子脂质体共同负载化疗药物紫杉醇和基因药物HIF-1αsiRNA具有明显的协同作用,可以克服肿瘤细胞对紫杉醇的耐药性问题。其中阳离子脂质体药物制剂Sp1作为载体共同负载紫杉醇和HIF-1αsiRNA的效果最好,有潜力作为新型阳离子脂质体共给药系统,克服紫杉醇治疗肿瘤的耐药性的问题。
研究阳离子脂质体共递送化疗药物紫杉醇和基因药物HIF-1αsiRNA的体内抗肿瘤活性:
建立鼠源乳腺癌肿瘤模型:
标准细胞培养间进行4T1细胞培养,待细胞经几次传代且状态稳定时,用胰蛋白酶消化收集,用预冷的PBS重悬收集的细胞,以每只小鼠1×106个4T1(100μL)细胞接种在小鼠右侧腋下,待肿瘤体积约100mm3(体积计算公式:体积=长×宽×宽/2)时,随机分组后开展抗肿瘤药效研究。
抗肿瘤效率研究:
1)小鼠给药治疗处理:设置生理盐水、实施例11的Sp1、游离HIF-1αsiRNA、实施例11的Sp1+HIF-1αsiRNA、游离PTX、实施例15的Sphy1、PTX+HIF-1αsiRNA和实施例15的Sphy1+HIF-1αsiRNA共8组,每两天用一次性无菌胰岛素注射器对小鼠进行尾静脉注射给药一次,连续给药7次后停止给药,在给药停止后的第七天处死;
2)给药当天用游标卡尺对小鼠肿瘤的生长情况进行测量,绘制肿瘤的生长曲线,同时监测小鼠体重的变化情况,并作统计处理分析;
3)在小鼠处死后对其进行解剖,收集肿瘤组织,并对瘤块质量进行测量统计。
在荷瘤小鼠给药的过程中,对小鼠体重进行测量统计,并用游标卡尺实时测量小鼠肿瘤大小,如图19所示,各组小鼠给药期间均未出现死亡,体重没有明显差异,表明脂质体制剂具有很好的生物相容性。由图20可知,与生理盐水组相比,实施例11的Sp1,游离的HIF-1αsiRNA组及Sp1+HIF-1αsiRNA组表现出类似的肿瘤快速生长趋势,没有显著性差异。而游离PTX组和PTX+HIF-1αsiRNA组,实施例15的Sphy1给药组,实施例15的Sphy1+HIF-1αsiRNA给药组,小鼠肿瘤生长趋势均明显减缓,表现出明显的肿瘤抑制活性(*P<0.05,**P<0.01,***P<0.001,****P<0.0001)。如图21所示,与游离紫杉醇组相比,实施例15的负载紫杉醇的脂质体Sphy1和Sphy1+HIF-1αsiRNA组也具有更强的抗肿瘤活性,表现出显著性的差异性(#P<0.05,##P<0.01,###P<0.001,####P<0.0001)。与实施例15的Sphy1组相比,Sphy1+HIF-1αsiRNA组表现出更强的肿瘤抑制活性($P<0.05,$$P<0.01)。
给药结束后,处死荷瘤小鼠并将肿瘤组织分离称重。如图22所示,实施例15的阳离子脂质体药物制剂Sphy1+HIF-1αsiRNA组肿瘤重量最小,实施例15的Sphy1组次之。游离PTX组和PTX+HIF-1αsiRNA组肿瘤重量比生理盐水组、实施例11的阳离子脂质体Sp1组、FreeHIF-1αsiRNA组及实施例11的阳离子脂质体Sp1+HIF-1αsiRNA组小。这些结果表明阳离子脂质体共递送化疗药物紫杉醇和HIF-1αsiRNA具有协同增效作用,克服了三阴性乳腺癌对紫杉醇的耐药性,具有高效的体内抗肿瘤作用。
显然,本发明的上述实施例仅仅是为清楚地说明本发明所作的举例,而并非是对本发明的实施方式的限定。对于所属领域的普通技术人员来说,在上述说明的基础上还可以做出其它不同形式的变化或变动。这里无需也无法对所有的实施方式予以穷举。凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明权利要求的保护范围之内。
Claims (10)
5.一种阳离子脂质体,其特征在于,所述阳离子脂质体包括权利要求1~4任一项所述的鞘脂类化合物、胆固醇、二油酰磷脂酰乙醇胺和甲氧基-聚乙二醇-磷脂。
6.根据权利要求5所述的阳离子脂质体,其特征在于,所述鞘脂类化合物、胆固醇、二油酰磷脂酰乙醇胺和甲氧基-聚乙二醇-磷脂的摩尔比为1:(0.5~50):(0.5~50):(0.015~1)。
7.一种阳离子脂质体药物制剂,其特征在于,所述药物制剂包括如权利要求5或6所述的阳离子脂质体和药物活性成分,以所述阳离子脂质体中的鞘脂类化合物的摩尔量计算,所述鞘脂类化合物和药物活性成分的摩尔比为(0.1~50):1。
8.根据权利要求7所述的阳离子脂质体药物制剂,其特征在于,所述药物活性成分为抗肿瘤化合物、抗病毒化合物、抗炎化合物或类风湿药物中的一种或多种。
9.根据权利要求7所述的阳离子脂质体药物制剂,其特征在于,所述阳离子脂质体药物制剂还包括核酸;
优选地,所述核酸的量为N/P比为1:1~16:1,所述的N/P比是阳离子脂质体中的可电离的氮原子N的摩尔含量和核酸中P的摩尔含量之比;
优选地,所述核酸选自siRNA、miRNA、antagomir、DNA质粒或mRNA。
10.权利要求5或6任一项所述的阳离子脂质体、权利要求7~9任一项所述的阳离子脂质体药物制剂在用于治疗由基因异常表达引起的相关疾病的药物制备中的用途,所述疾病包括恶性肿瘤、心血管疾病、类风湿、感染性疾病或遗传病;
优选地,所述恶性肿瘤为三阴性乳腺癌。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210358677.7A CN114933569A (zh) | 2022-04-07 | 2022-04-07 | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 |
PCT/CN2022/098765 WO2023193341A1 (zh) | 2022-04-07 | 2022-06-14 | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210358677.7A CN114933569A (zh) | 2022-04-07 | 2022-04-07 | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN114933569A true CN114933569A (zh) | 2022-08-23 |
Family
ID=82862677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210358677.7A Pending CN114933569A (zh) | 2022-04-07 | 2022-04-07 | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN114933569A (zh) |
WO (1) | WO2023193341A1 (zh) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995032002A1 (en) * | 1994-05-19 | 1995-11-30 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education On Behalf Of The Oregon Health Sciences University | Covalent microparticle-drug conjugates for biological targeting |
CN1148391A (zh) * | 1995-03-01 | 1997-04-23 | 法玛西雅厄普约翰公司 | 通过与聚吡咯甲酰氨基萘衍生物连接提高生物活性化合物的生物药效性 |
WO2000037046A1 (en) * | 1998-12-22 | 2000-06-29 | University Of Washington | Therapeutic delivery using compounds self-assembled into high axial ratio microstructures |
CN1829535A (zh) * | 2003-06-18 | 2006-09-06 | 耶路撒冷希伯来语大学依苏姆研究开发公司 | 用于接种的sphingoid聚烷基胺缀合物 |
KR20130097465A (ko) * | 2012-02-24 | 2013-09-03 | 주식회사 진영바이오 | 글리코실 세라마이드 화합물 및 그 제조방법 |
CN113121381A (zh) * | 2021-04-19 | 2021-07-16 | 浙江大学 | 一种神经酰胺类化合物及其阳离子脂质体、制备方法和应用 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2743139C (en) * | 2008-11-10 | 2019-04-02 | Alnylam Pharmaceuticals, Inc. | Novel lipids and compositions for the delivery of therapeutics |
-
2022
- 2022-04-07 CN CN202210358677.7A patent/CN114933569A/zh active Pending
- 2022-06-14 WO PCT/CN2022/098765 patent/WO2023193341A1/zh unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995032002A1 (en) * | 1994-05-19 | 1995-11-30 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education On Behalf Of The Oregon Health Sciences University | Covalent microparticle-drug conjugates for biological targeting |
CN1148391A (zh) * | 1995-03-01 | 1997-04-23 | 法玛西雅厄普约翰公司 | 通过与聚吡咯甲酰氨基萘衍生物连接提高生物活性化合物的生物药效性 |
WO2000037046A1 (en) * | 1998-12-22 | 2000-06-29 | University Of Washington | Therapeutic delivery using compounds self-assembled into high axial ratio microstructures |
CN1829535A (zh) * | 2003-06-18 | 2006-09-06 | 耶路撒冷希伯来语大学依苏姆研究开发公司 | 用于接种的sphingoid聚烷基胺缀合物 |
KR20130097465A (ko) * | 2012-02-24 | 2013-09-03 | 주식회사 진영바이오 | 글리코실 세라마이드 화합물 및 그 제조방법 |
CN113121381A (zh) * | 2021-04-19 | 2021-07-16 | 浙江大学 | 一种神经酰胺类化合物及其阳离子脂质体、制备方法和应用 |
Non-Patent Citations (1)
Title |
---|
JAGGAIAH N. GORANTLA ETAL.: ""Design and synthesis of a novel glycosphingolipid derived from polyhydroxy 2-pyrrolidinone and phytoceramide appended by a 1, 2, 3- triazole linker"", 《CHEMISTRY AND PHYSICS OF LIPIDS》, vol. 194, 5 August 2015 (2015-08-05), pages 158 - 164, XP029385806, DOI: 10.1016/j.chemphyslip.2015.08.002 * |
Also Published As
Publication number | Publication date |
---|---|
WO2023193341A1 (zh) | 2023-10-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN115353616B (zh) | 一种聚乙二醇化脂质 | |
EP3538515B1 (en) | Cationic lipids for nucleic acid delivery and preparation thereof | |
KR102262260B1 (ko) | 엔도좀 탈출능을 갖는 펩티드 핵산 복합체 및 이의 용도 | |
CN104922676B (zh) | 聚胺衍生物 | |
AU2011353233B2 (en) | Carrier for negatively charged drugs comprising a cationic lipid and a preparation method thereof | |
EP4328217A1 (en) | Cationic lipid compound, composition containing same and use thereof | |
JP2012509366A (ja) | 核酸送達系のための放出可能ポリマー脂質 | |
WO2010057155A1 (en) | Releasable cationic lipids for nucleic acids delivery systems | |
JP2012509273A (ja) | 核酸送達系のための放出可能融合性脂質 | |
WO2023246074A1 (zh) | 用于递送核酸的阳离子脂质化合物和组合物及用途 | |
KR20100076905A (ko) | 음이온성 약물 함유 약제학적 조성물 및 그 제조방법 | |
CN110433292B (zh) | 一种双靶向材料及其在药物传递中的应用 | |
JP2022531010A (ja) | 薬物送達キャリア及びそれを用いた医薬製剤 | |
CN114380724A (zh) | 用于递送核酸的阳离子脂质化合物和组合物及用途 | |
KR102484332B1 (ko) | 핵산 복합체를 함유하는 피부 투과성 전달체 및 이의 용도 | |
WO2023036311A1 (zh) | 可离子化脂质体、其制备及在基因递送中的应用 | |
CN110917139A (zh) | 多分枝生物素修饰的乳腺癌靶向脂质体的制备和应用 | |
CN114933569A (zh) | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 | |
CN113214171B (zh) | 两亲性树形分子、合成及其作为药物递送系统的应用 | |
EP4321504A1 (en) | Pegylated lipid and liposome modified thereby, and pharmaceutical composition comprising liposome and preparation and use thereof | |
CN115515925A (zh) | 一种聚乙二醇化脂质及其修饰的脂质体、含该脂质体的药物组合物及其制剂和应用 | |
CN110540551B (zh) | 一种脂质体、其制备方法、脂质体组装体及载物脂质体复合体 | |
KR102156323B1 (ko) | 피부 투과성 핵산 복합체를 유효성분으로 함유하는 건선의 예방 또는 치료용 조성물 | |
CN111166892A (zh) | 生物素和穿膜肽共同介导的乳腺癌靶向智能脂质体材料 | |
CN116199646B (zh) | 一种基于Tris的可电离脂质及其制备方法与应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |