WO2013187899A1 - Compositions et procédés pour la stimulation de la cicatrisation des plaies - Google Patents
Compositions et procédés pour la stimulation de la cicatrisation des plaies Download PDFInfo
- Publication number
- WO2013187899A1 WO2013187899A1 PCT/US2012/042414 US2012042414W WO2013187899A1 WO 2013187899 A1 WO2013187899 A1 WO 2013187899A1 US 2012042414 W US2012042414 W US 2012042414W WO 2013187899 A1 WO2013187899 A1 WO 2013187899A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- wound
- insulin
- medium
- nutrient
- media
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 130
- 238000000034 method Methods 0.000 title claims abstract description 41
- 230000029663 wound healing Effects 0.000 title claims description 48
- 230000004936 stimulating effect Effects 0.000 title description 8
- 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 claims abstract description 224
- 102000004877 Insulin Human genes 0.000 claims abstract description 112
- 108090001061 Insulin Proteins 0.000 claims abstract description 112
- 229940125396 insulin Drugs 0.000 claims abstract description 112
- 235000015097 nutrients Nutrition 0.000 claims abstract description 71
- 235000017803 cinnamon Nutrition 0.000 claims abstract description 26
- 230000035876 healing Effects 0.000 claims abstract description 24
- 230000002608 insulinlike Effects 0.000 claims abstract description 19
- 208000027418 Wounds and injury Diseases 0.000 claims description 177
- 206010052428 Wound Diseases 0.000 claims description 171
- 239000002609 medium Substances 0.000 claims description 63
- 238000009472 formulation Methods 0.000 claims description 48
- 238000011282 treatment Methods 0.000 claims description 45
- 229920000642 polymer Polymers 0.000 claims description 42
- 229920000936 Agarose Polymers 0.000 claims description 39
- 239000000499 gel Substances 0.000 claims description 34
- 244000223760 Cinnamomum zeylanicum Species 0.000 claims description 25
- 239000003263 anabolic agent Substances 0.000 claims description 25
- 230000001413 cellular effect Effects 0.000 claims description 25
- 108090000723 Insulin-Like Growth Factor I Proteins 0.000 claims description 19
- 102000013275 Somatomedins Human genes 0.000 claims description 19
- 108010010803 Gelatin Proteins 0.000 claims description 14
- 229920000159 gelatin Polymers 0.000 claims description 14
- 239000008273 gelatin Substances 0.000 claims description 14
- 235000019322 gelatine Nutrition 0.000 claims description 14
- 235000011852 gelatine desserts Nutrition 0.000 claims description 14
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 13
- 239000011669 selenium Substances 0.000 claims description 13
- 229910052711 selenium Inorganic materials 0.000 claims description 13
- 230000003637 steroidlike Effects 0.000 claims description 13
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 12
- 241000407170 Curcuma Species 0.000 claims description 12
- 235000014375 Curcuma Nutrition 0.000 claims description 12
- -1 MCDB153 Substances 0.000 claims description 12
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 claims description 12
- 239000004599 antimicrobial Substances 0.000 claims description 12
- 239000011651 chromium Substances 0.000 claims description 12
- 229910052804 chromium Inorganic materials 0.000 claims description 12
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 claims description 12
- JZRWCGZRTZMZEH-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 claims description 12
- 239000003797 essential amino acid Substances 0.000 claims description 11
- 235000020776 essential amino acid Nutrition 0.000 claims description 11
- 102000008186 Collagen Human genes 0.000 claims description 10
- 108010035532 Collagen Proteins 0.000 claims description 10
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 10
- 239000001913 cellulose Substances 0.000 claims description 10
- 229920002678 cellulose Polymers 0.000 claims description 10
- 229920001436 collagen Polymers 0.000 claims description 10
- 239000008103 glucose Substances 0.000 claims description 10
- 229940088594 vitamin Drugs 0.000 claims description 10
- 229930003231 vitamin Natural products 0.000 claims description 10
- 235000013343 vitamin Nutrition 0.000 claims description 10
- 239000011782 vitamin Substances 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 206010072170 Skin wound Diseases 0.000 claims description 8
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims description 8
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 claims description 6
- QHMQAWNNHVPBQU-UHFFFAOYSA-N 3-(2-hydroxy-3-methylphenyl)-1-phenylprop-2-en-1-one Chemical group CC1=CC=CC(C=CC(=O)C=2C=CC=CC=2)=C1O QHMQAWNNHVPBQU-UHFFFAOYSA-N 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 claims description 6
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 239000011575 calcium Substances 0.000 claims description 6
- 229910052791 calcium Inorganic materials 0.000 claims description 6
- 235000019152 folic acid Nutrition 0.000 claims description 6
- 239000011724 folic acid Substances 0.000 claims description 6
- 229910001410 inorganic ion Inorganic materials 0.000 claims description 6
- 229960003966 nicotinamide Drugs 0.000 claims description 6
- 235000005152 nicotinamide Nutrition 0.000 claims description 6
- 239000011570 nicotinamide Substances 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 235000019192 riboflavin Nutrition 0.000 claims description 6
- 229960002477 riboflavin Drugs 0.000 claims description 6
- 239000002151 riboflavin Substances 0.000 claims description 6
- 235000019157 thiamine Nutrition 0.000 claims description 6
- 239000011721 thiamine Substances 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229940014144 folate Drugs 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229940014662 pantothenate Drugs 0.000 claims description 5
- 235000019161 pantothenic acid Nutrition 0.000 claims description 5
- 239000011713 pantothenic acid Substances 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 229920002307 Dextran Polymers 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 4
- 229920002684 Sepharose Polymers 0.000 claims description 4
- 239000000284 extract Substances 0.000 claims description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 4
- 235000008160 pyridoxine Nutrition 0.000 claims description 4
- 239000011677 pyridoxine Substances 0.000 claims description 4
- 229940011671 vitamin b6 Drugs 0.000 claims description 4
- 239000012980 RPMI-1640 medium Substances 0.000 claims description 2
- 239000004098 Tetracycline Substances 0.000 claims description 2
- 229960002180 tetracycline Drugs 0.000 claims description 2
- 229930101283 tetracycline Natural products 0.000 claims description 2
- 235000019364 tetracycline Nutrition 0.000 claims description 2
- 150000003522 tetracyclines Chemical class 0.000 claims description 2
- 229920000856 Amylose Polymers 0.000 claims 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 2
- 229920002401 polyacrylamide Polymers 0.000 claims 2
- 230000003115 biocidal effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 17
- 239000007758 minimum essential medium Substances 0.000 abstract description 10
- 235000020230 cinnamon extract Nutrition 0.000 abstract description 3
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- NDRKNOADOZHUQR-UHFFFAOYSA-N 1-chloro-4-[cyclohexyloxy(methoxy)phosphoryl]sulfanylbenzene Chemical compound C=1C=C(Cl)C=CC=1SP(=O)(OC)OC1CCCCC1 NDRKNOADOZHUQR-UHFFFAOYSA-N 0.000 abstract 1
- 241000723347 Cinnamomum Species 0.000 abstract 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 28
- 239000011780 sodium chloride Substances 0.000 description 27
- 210000004027 cell Anatomy 0.000 description 20
- 210000002966 serum Anatomy 0.000 description 20
- 206010063560 Excessive granulation tissue Diseases 0.000 description 19
- 210000001126 granulation tissue Anatomy 0.000 description 19
- 230000012010 growth Effects 0.000 description 18
- 210000003491 skin Anatomy 0.000 description 18
- 230000000694 effects Effects 0.000 description 14
- 230000008569 process Effects 0.000 description 13
- 230000001684 chronic effect Effects 0.000 description 12
- 230000006378 damage Effects 0.000 description 11
- 210000001519 tissue Anatomy 0.000 description 11
- 239000003242 anti bacterial agent Substances 0.000 description 10
- 229940088710 antibiotic agent Drugs 0.000 description 10
- 239000000645 desinfectant Substances 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 208000015181 infectious disease Diseases 0.000 description 9
- 208000014674 injury Diseases 0.000 description 9
- 150000008442 polyphenolic compounds Chemical class 0.000 description 9
- 235000013824 polyphenols Nutrition 0.000 description 9
- 230000006870 function Effects 0.000 description 8
- 230000002421 anti-septic effect Effects 0.000 description 7
- 230000002708 enhancing effect Effects 0.000 description 7
- 229940088597 hormone Drugs 0.000 description 7
- 239000005556 hormone Substances 0.000 description 7
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000004113 cell culture Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 229960005369 scarlet red Drugs 0.000 description 6
- 230000000699 topical effect Effects 0.000 description 6
- 230000036770 blood supply Effects 0.000 description 5
- 239000006143 cell culture medium Substances 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 230000002349 favourable effect Effects 0.000 description 5
- 210000002950 fibroblast Anatomy 0.000 description 5
- 239000000017 hydrogel Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000001737 promoting effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 description 5
- 238000001356 surgical procedure Methods 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 206010040799 Skin atrophy Diseases 0.000 description 4
- 229940064004 antiseptic throat preparations Drugs 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 4
- 230000004071 biological effect Effects 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 210000002919 epithelial cell Anatomy 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000013642 negative control Substances 0.000 description 4
- 239000013641 positive control Substances 0.000 description 4
- 230000035755 proliferation Effects 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000011573 trace mineral Substances 0.000 description 4
- 235000013619 trace mineral Nutrition 0.000 description 4
- 239000003981 vehicle Substances 0.000 description 4
- 201000002282 venous insufficiency Diseases 0.000 description 4
- IISHLYLZTYTIJJ-UHFFFAOYSA-N 1-hydroxyethyl 2-methylprop-2-enoate Chemical compound CC(O)OC(=O)C(C)=C IISHLYLZTYTIJJ-UHFFFAOYSA-N 0.000 description 3
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 3
- 208000005230 Leg Ulcer Diseases 0.000 description 3
- 210000001789 adipocyte Anatomy 0.000 description 3
- 238000010171 animal model Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229960002685 biotin Drugs 0.000 description 3
- 235000020958 biotin Nutrition 0.000 description 3
- 239000011616 biotin Substances 0.000 description 3
- 230000004663 cell proliferation Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 210000002615 epidermis Anatomy 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 230000004153 glucose metabolism Effects 0.000 description 3
- 239000003102 growth factor Substances 0.000 description 3
- AGBQKNBQESQNJD-UHFFFAOYSA-N lipoic acid Chemical compound OC(=O)CCCCC1CCSS1 AGBQKNBQESQNJD-UHFFFAOYSA-N 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 230000003278 mimic effect Effects 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000000069 prophylactic effect Effects 0.000 description 3
- 238000007634 remodeling Methods 0.000 description 3
- 231100000241 scar Toxicity 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 230000008736 traumatic injury Effects 0.000 description 3
- 230000035899 viability Effects 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- UDOOPSJCRMKSGL-UHFFFAOYSA-N 3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one Chemical compound OC1=CC=CC=C1C=CC(=O)C1=CC=CC=C1 UDOOPSJCRMKSGL-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- 229930024421 Adenine Natural products 0.000 description 2
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 description 2
- 206010062542 Arterial insufficiency Diseases 0.000 description 2
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 101000976075 Homo sapiens Insulin Proteins 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 2
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 2
- 206010040943 Skin Ulcer Diseases 0.000 description 2
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
- 239000004473 Threonine Substances 0.000 description 2
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- 208000025865 Ulcer Diseases 0.000 description 2
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229960000643 adenine Drugs 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000033115 angiogenesis Effects 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 230000000840 anti-viral effect Effects 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 239000003429 antifungal agent Substances 0.000 description 2
- 239000003443 antiviral agent Substances 0.000 description 2
- 235000009582 asparagine Nutrition 0.000 description 2
- 229960001230 asparagine Drugs 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 210000001772 blood platelet Anatomy 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 230000010261 cell growth Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 210000002808 connective tissue Anatomy 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 229960003067 cystine Drugs 0.000 description 2
- 210000004207 dermis Anatomy 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 210000000416 exudates and transudate Anatomy 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000002695 general anesthesia Methods 0.000 description 2
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 238000010562 histological examination Methods 0.000 description 2
- 235000012907 honey Nutrition 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 2
- PBGKTOXHQIOBKM-FHFVDXKLSA-N insulin (human) Chemical group C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CSSC[C@H]2C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3C=CC(O)=CC=3)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3NC=NC=3)NC(=O)[C@H](CO)NC(=O)CNC1=O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O)=O)CSSC[C@@H](C(N2)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CC=1C=CC=CC=1)C(C)C)C1=CN=CN1 PBGKTOXHQIOBKM-FHFVDXKLSA-N 0.000 description 2
- 229960000310 isoleucine Drugs 0.000 description 2
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 2
- 230000000598 lipoate effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- UICBCXONCUFSOI-UHFFFAOYSA-N n'-phenylacetohydrazide Chemical compound CC(=O)NNC1=CC=CC=C1 UICBCXONCUFSOI-UHFFFAOYSA-N 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 229940049954 penicillin Drugs 0.000 description 2
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 230000002062 proliferating effect Effects 0.000 description 2
- 230000035752 proliferative phase Effects 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 150000003212 purines Chemical class 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 150000003230 pyrimidines Chemical class 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- 238000011272 standard treatment Methods 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- 230000008467 tissue growth Effects 0.000 description 2
- 229960004799 tryptophan Drugs 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 231100000397 ulcer Toxicity 0.000 description 2
- 239000004474 valine Substances 0.000 description 2
- 230000002792 vascular Effects 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- 230000010388 wound contraction Effects 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- CPKVUHPKYQGHMW-UHFFFAOYSA-N 1-ethenylpyrrolidin-2-one;molecular iodine Chemical compound II.C=CN1CCCC1=O CPKVUHPKYQGHMW-UHFFFAOYSA-N 0.000 description 1
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 1
- YXQXLHSRJUFMFD-UHFFFAOYSA-N 3-[(3,4-dihydroxyphenyl)methyl]-2h-chromene-7,8-diol Chemical group C1=C(O)C(O)=CC=C1CC1=CC2=CC=C(O)C(O)=C2OC1 YXQXLHSRJUFMFD-UHFFFAOYSA-N 0.000 description 1
- 229930183010 Amphotericin Natural products 0.000 description 1
- QGGFZZLFKABGNL-UHFFFAOYSA-N Amphotericin A Natural products OC1C(N)C(O)C(C)OC1OC1C=CC=CC=CC=CCCC=CC=CC(C)C(O)C(C)C(C)OC(=O)CC(O)CC(O)CCC(O)C(O)CC(O)CC(O)(CC(O)C2C(O)=O)OC2C1 QGGFZZLFKABGNL-UHFFFAOYSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 244000080208 Canella winterana Species 0.000 description 1
- 235000008499 Canella winterana Nutrition 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- 241000700199 Cavia porcellus Species 0.000 description 1
- 229930186147 Cephalosporin Natural products 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- 235000019743 Choline chloride Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 206010056340 Diabetic ulcer Diseases 0.000 description 1
- IIUZTXTZRGLYTI-UHFFFAOYSA-N Dihydrogriseofulvin Natural products COC1CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 IIUZTXTZRGLYTI-UHFFFAOYSA-N 0.000 description 1
- 239000006145 Eagle's minimal essential medium Substances 0.000 description 1
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 1
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- 102000016359 Fibronectins Human genes 0.000 description 1
- 108010067306 Fibronectins Proteins 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 229930182566 Gentamicin Natural products 0.000 description 1
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 1
- 102000006395 Globulins Human genes 0.000 description 1
- 108010044091 Globulins Proteins 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- UXWOXTQWVMFRSE-UHFFFAOYSA-N Griseoviridin Natural products O=C1OC(C)CC=C(C(NCC=CC=CC(O)CC(O)C2)=O)SCC1NC(=O)C1=COC2=N1 UXWOXTQWVMFRSE-UHFFFAOYSA-N 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
- 206010022489 Insulin Resistance Diseases 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 229930182816 L-glutamine Natural products 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 208000034693 Laceration Diseases 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 206010059240 Lymphostasis Diseases 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- SUHOOTKUPISOBE-UHFFFAOYSA-N O-phosphoethanolamine Chemical compound NCCOP(O)(O)=O SUHOOTKUPISOBE-UHFFFAOYSA-N 0.000 description 1
- 206010057249 Phagocytosis Diseases 0.000 description 1
- 241000233805 Phoenix Species 0.000 description 1
- 229920000153 Povidone-iodine Polymers 0.000 description 1
- 101710096655 Probable acetoacetate decarboxylase 1 Proteins 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 239000006035 Tryptophane Substances 0.000 description 1
- 229930003779 Vitamin B12 Natural products 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000011543 agarose gel Substances 0.000 description 1
- 229940126575 aminoglycoside Drugs 0.000 description 1
- 229940009444 amphotericin Drugs 0.000 description 1
- APKFDSVGJQXUKY-INPOYWNPSA-N amphotericin B Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-INPOYWNPSA-N 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 230000001195 anabolic effect Effects 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002924 anti-infective effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229940121357 antivirals Drugs 0.000 description 1
- 230000006907 apoptotic process Effects 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 229940009098 aspartate Drugs 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 210000001142 back Anatomy 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 239000000022 bacteriostatic agent Substances 0.000 description 1
- 239000007640 basal medium Substances 0.000 description 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 230000002146 bilateral effect Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000012888 bovine serum Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229940124587 cephalosporin Drugs 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 description 1
- 229960003178 choline chloride Drugs 0.000 description 1
- 229940017545 cinnamon bark Drugs 0.000 description 1
- 230000004087 circulation Effects 0.000 description 1
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 1
- FDJOLVPMNUYSCM-UVKKECPRSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7, Chemical compound [Co+3].N#[C-].C1([C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)[N-]\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O FDJOLVPMNUYSCM-UVKKECPRSA-L 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 231100000433 cytotoxic Toxicity 0.000 description 1
- 230000001472 cytotoxic effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 238000005370 electroosmosis Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- 210000005081 epithelial layer Anatomy 0.000 description 1
- 229940014425 exodus Drugs 0.000 description 1
- 210000002744 extracellular matrix Anatomy 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 230000004110 gluconeogenesis Effects 0.000 description 1
- 230000004190 glucose uptake Effects 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 230000034659 glycolysis Effects 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000037313 granulation tissue formation Effects 0.000 description 1
- DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 description 1
- 229960002867 griseofulvin Drugs 0.000 description 1
- 230000003284 homeostatic effect Effects 0.000 description 1
- 230000013632 homeostatic process Effects 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 230000008105 immune reaction Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 210000002510 keratinocyte Anatomy 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 210000004705 lumbosacral region Anatomy 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 239000012577 media supplement Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- FJQXCDYVZAHXNS-UHFFFAOYSA-N methadone hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 FJQXCDYVZAHXNS-UHFFFAOYSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- PMDKYLLIOLFQPO-UHFFFAOYSA-N monocyclohexyl phthalate Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC1CCCCC1 PMDKYLLIOLFQPO-UHFFFAOYSA-N 0.000 description 1
- 230000003562 morphometric effect Effects 0.000 description 1
- 210000000651 myofibroblast Anatomy 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000001338 necrotic effect Effects 0.000 description 1
- 230000001613 neoplastic effect Effects 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 230000037311 normal skin Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 229960000988 nystatin Drugs 0.000 description 1
- VQOXZBDYSJBXMA-NQTDYLQESA-N nystatin A1 Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/CC/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 VQOXZBDYSJBXMA-NQTDYLQESA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000008782 phagocytosis Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229960001621 povidone-iodine Drugs 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 229960004618 prednisone Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000008263 repair mechanism Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012679 serum free medium Substances 0.000 description 1
- 230000008470 skin growth Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229940104230 thymidine Drugs 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 210000003556 vascular endothelial cell Anatomy 0.000 description 1
- 235000019163 vitamin B12 Nutrition 0.000 description 1
- 239000011715 vitamin B12 Substances 0.000 description 1
- 235000008979 vitamin B4 Nutrition 0.000 description 1
- 239000011579 vitamin B4 Substances 0.000 description 1
- 229940045999 vitamin b 12 Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 230000037314 wound repair Effects 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/28—Insulins
-
- 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
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- 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
- A61K31/65—Tetracyclines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/04—Sulfur, selenium or tellurium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/30—Insulin-like growth factors, i.e. somatomedins, e.g. IGF-1, IGF-2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
Definitions
- compositions and methods for stimulating wound healing are provided.
- the purpose of this invention is to improve the microenvironments in and around the wound. Specifically, it comprises of application of tissue and cells culture nutrient media, such as minimum essential media, supplemented with insulin and/or with substances exhibiting insulin-like activity, such as cinnamon or its extract methyl hydroxyl chalcone polymer (MHCP).
- tissue and cells culture nutrient media such as minimum essential media
- insulin and/or with substances exhibiting insulin-like activity such as cinnamon or its extract methyl hydroxyl chalcone polymer (MHCP).
- MHCP methyl hydroxyl chalcone polymer
- Compositions according to the present invention especially compositions which include Insulin or Cinnamon or MHCP or preferably both Cinnamon or MHCP and insulin in effective amounts exhibit synergistic activity in stimulating wound healing, especially including non-healing, chronic wounds, in patients.
- a wound is defined as a break in the continuity of the skin. It can be caused by traumatic injury such as burn, cut or scrape. A prompt treatment will avoid complications such as infection and inflammation.
- the usual and conservative methods of closing a wound are application of various medicaments or alternatively, the wound is closed by surgical procedures of suturing the wounds edges, by grafting cultured skin or by split skin grafts. The aim of all of the above is to promote the growth of granulation tissue that may or may not follow promptly, depending on adequate blood supply bringing into the wound the nutrients that the cells need for growth.
- the concept of this method is to use a proactive rather then protective treatment. That is, following the usage of antiseptic or anti-inflammatory medicaments, that when indicated are the standard treatments, the treatment then should be followed by induction of a stimulatory treatment.
- the idea is to create microenvironment favorable for wound healing after assuring that the wound is clinically clean.
- This method aims to stimulate and support growth of connective tissue components originating from the wound bed and its peripheral walls. The granulation tissue filling the wound space will create the substratum required for re- epithelialization and wound closure.
- Wound healing or wound repair, is an intricate process in which the skin (or another organ-tissue) repairs itself after injury.
- the epidermis the outer or superficial layer and dermis the inner or deeper layer exists in steady-state equilibrium, forming a protective barrier against the external environment. Once the protective barrier is broken, the normal (physiologic) process of wound healing is immediately set in motion.
- the classic model of wound healing is divided into three or four sequential, yet overlapping, phases: (1) homeostatic, (2) inflammatory, (3) proliferative and (4) remodeling.
- the proliferative phase of wound healing is characterized by angiogenesis, collagen formation and deposition, growth of granulation tissue, epithelialization, and wound contraction.
- Angiogenesis involves formation of new blood vessels by the vascular endothelial cells. During the fibroplasia and the granulation tissue formation, the fibroblasts grow and form a new, provisional extra cellular matrix by excreting collagen and fibronectin. Concurrently, re-epithelialization of the epidermis occurs, where epithelial cells proliferate and migrate over the granulation tissue, providing cover for the new tissue.
- Remodeling phase comprises the contraction process where the wound becomes smaller due to contraction of myofibroblasts that grip the wound edges and contract.
- collagen is remodeled and realigned along tension lines and cells that are no longer needed are removed by apoptosis.
- the healing is process that is not only complex but also fragile, and susceptible to interruption or failure leading to the formation of chronic non-healing wounds.
- Factors which may contribute to this include diabetes, topical or systemic venous and/or arterial insufficiencies, old age, and infection.
- a wound is defined as a break in the continuity of the skin. It can be caused by traumatic injury such as burn, cut or scrape. A prompt treatment will avoid complications such as infection and inflammation.
- the usual and conservative methods of closing a wound are application of various medicaments or alternatively, the wound is closed by surgical procedures of suturing the wounds edges, by grafting cultured skin or by split skin grafts. The aim of all of the above is to promote the growth of granulation tissue that may or may not follow promptly, depending primarily on adequate blood supply that brings into the wound the nutrients that the cells need for growth.
- the concept of this method is to use a proactive rather then protective treatment. That is, following the usage of antiseptic or anti-inflammatory medicaments, that when indicated are the standard treatments, the treatment then should be followed by induction of a stimulatory treatment.
- the idea is to create a microenvironment favorable for wound healing after assuring that the wound is clinically clean.
- the wound and its surrounding area will be moisturized, exposed to the rich nutrients, protected from dehydration by the gelling of the media and dressed with sterile gauze which allows the oxygen in the air to penetrate the dressing and reach the wound surface.
- This method aims to stimulate and support growth of connective tissue components originating from the wound bed and its peripheral walls.
- the proliferating granulation tissue filling the wound space will create the substratum required for re- epithelialization leading to wound closure.
- This invention is based on human tissue and cell culture technology of growing fibroblast and epithelial cells in culture. Utilizing similar nutrient media supplements with insulin or alternatively with substances possessing insulin-mimetic features, the milieu in the wound becomes moist and enriched with the nutrients. These are the requirements for cells proliferation and the growth of the granulation tissue including new capillaries into the wound space.
- Serum-free cell culture media supplemented with insulin or substances with insulin-like activity e.g. cinnamon or MHCP or MHCP and insulin-like growth factor, preferably human
- insulin or substances with insulin-like activity e.g. cinnamon or MHCP or MHCP and insulin-like growth factor, preferably human
- a mixture of insulin and a substance with insulin-like activity will supply the cells in the wound with the nutrients required for the process of wound healing.
- Jarville-Taylor et. al. demonstrated the insulin-like activity was found in substances including cinnamon. They report that, in adipocytes cell cultures, Methyl Hydroxy Chalcone Polymer- (MHCP), extracted from cinnamon, acts as a mimetic of insulin. This component that is found in cinnamon affects glucose metabolism and the conversion of glucose to energy that then is utilized to enhance the cells multiplication process. In addition it renders insulin much more efficient and thus acts synergistically with insulin.
- MHCP Methyl Hydroxy Chalcone Polymer-
- Kamath J.V et. al. report the hydroxyproline increase in the granulation tissue content of the wound due to treatment with cinnamum zeylanicum. Anderson R. et.al recently describes the effectiveness of polyphenol type-A polymer extracted from cinnamon as a powerful insulin mimetic substance.
- Karalee J.T. and Stapleton S.R. reported the usage of cinnamon extract to boost insulin sensitivity and that Selenium was implicated in potentiating the insulin-like activity since it stimulates glucose uptake and regulates glycolysis, gluconeogenesis and fatty acids synthesis.
- Alt S. et al. describes using insulin and other agents to work in synergy to accelerate the healing process. However neither of them used serum-free cell culture media such as MEM, DMEM, BGJ or MCDB as a substrate.
- Insulin has been implicates in triggering the cascade of the wound healing process.
- Another object of this invention is to provide compositions and methods to enhance the healing of wounds and of the adjacent tissues surrounding the wound.
- Another object is to treat the wounds by using a combination of readily available and recognizable constituents.
- Another object is to create and support an optimal microenvironment in and around the wound thus creating a favorable optimal moisturized nutrient rich milieu for the process of wound healing.
- Another object to a polymer delivery system is to provide compositions and methods that stimulate the cells in the wound by creating moist environment using a gelled delivery system.
- This invention is based on human cell culture technology that grows fibroblast and epithelial cells in culture.
- the milieu in the wound becomes moist and enriched with nutrients capable of supplying all the requirements the cells need to proliferate and grow into the wound space.
- Preferred aspects of the invention comprise treating wounds in a cellular nutrient medium in combination with a substance possessing insulin-like activity and/or insulin.
- the treatment of wounds may be synergistically enhanced by exposing wounds in a patient to a composition comprising an effective amount of cinnamon or MHCP or polyphenol type- A polymer and/or a non- steroidal anabolic hormone in cellular nutrient medium, optionally and preferably with an effective amount of insulin.
- the formulation of this invention fulfills the requirements needed for promoting wound healing.
- the formulation contains effective amounts of cellular nutrient medium such as minimum essential medium MEM or serum-free cell culture media as otherwise disclosed herein, for example, MEM, DMEM, BGJ or MCDB 153.
- the said media is supplemented with an effective amount of insulin, a non-steroidal anabolic hormone such as insulin-like growth factor (preferably human), or alternatively by insulin-like substances such as cinnamon or its extracts (e.g. MHCP, or polyphenol type-A polymer), chromium, curcuma or selenium.
- the preferred embodiment according to the present invention is the non-steroidal anabolic hormone is insulin.
- the formulation also includes agents that mimic the insulin physiological activity such as cinnamon or its extracts that promote the entry of glucose into cells and converting it to energy. This energy can be utilized for regeneration of granulation tissues.
- insulin is included in compositions according to the present invention at concentrations ranging from about 5 ng/ml (nanograms per milliliter) to about 100 ug/ml (microgram per milliliter) [corresponding to about 120 uUnits/m (micro Units per milliliter) to about 24xl0 5 uUnits/ml— approximately 0.0000005% to about 0.01% by weight], preferably about 500 ng/ml to about 500 ng/ml to about 50-10 ug/ml (about 1.2xl0 4 uUnits/ml to about 1.2xl0 5 uUnits/ml— about 0.00005% to about 0.0005% by weight of the treatment composition based upon the assumption that 1 ml of solution is equal to about t gram in weight).
- the amount of insulin of the instant invention maybe modified according to the length of storage time prior to use.
- compositions that are applied in solid or concentrated form i.e. as a gel, creme, lotion, elixir, powder or the like
- the anabolic hormone is included in concentrations similar to those contained in the solutions, and preferably comprises about 0.00000005% to about 0.000005% by weight of the wound treatment composition (based upon the general assumption that 1 ml of solution is approximately equal to about 1 gram in weight of the final composition). Percent weights may fall outside of these ranges, depending upon the wound treated, the level of stability of the hormone and other factors, as well recognized by one of ordinary skill in the art.
- spices cinnamon is water-soluble and is relatively inexpensive.
- Cinnamon may be a substituted for insulin since it is a substance that mimic insulin physiological activity. According to Anderson et. al, it's most active derivative methyl hydroxy chalcone polymer (MHCP) function as insulin in 3T3 -L adipocytes cell cultures and was most effective in increasing glucose metabolism. Other substances such as the cinnamon derivatives MHCP or polyphenol type-A polymer, selenium, chromium, curcuma and insulin-like growth factor (especially human IGF) also known to mimic insulin activity may also be used as a substitute.
- the biological activity of MHCP at concentrations of about 0.1 mg/ml is about equivalent to the range of activity of lOOnM of insulin.
- Preferred MHCP concentration within the preferred media MCDB 153 ranges from about 0.01 mg/ml to about 1 mg/ml.
- the MHCP in media ranges from about 0.025 mg/ml to about 0.5 mg/ml.
- MHCP and insulin are combined in cellular nutrient medium to provide compositions according to the present invention.
- insulin-like growth factor (IGF) may also be added to the present invention in effective amounts to promote wound healing, especially in chronic wounds.
- IGF insulin-like growth factor
- the inclusion of selenium, chromium and/or curcuma as optional insulin-like agents assists in promoting wound healing of chronic wounds according to the present invention.
- wound is used throughout the specification to describe skin wounds, which are treated, by the formulations and the method according to the present invention.
- a skin wound is defined herein as a breach in the continuity of the skin that is caused by direct injury to the skin.
- Skin wounds are generally characterized by several types: punctures, incisions, including those produced by a variety of surgical procedures, excisions, lacerations, atrophic skin or necrotic wounds and burns, including large burn areas.
- the formulation according to the present invention is used in varying degrees for enhancing the healing of all types of wounds of the skin, including those which occur after a mesh autograph procedure. Compositions according to the present invention are unexpectedly effective to treat chronic wound conditions.
- delivery polymer is used throughout the specification to describe a polymer which can be used in combination with a cellular nutrient medium (preferably, serum free), a non-steroidal anabolic hormone insulin or insulin-like substances and mixtures thereof, and optionally, individually which are preferably used for topical application to the treated wounds according to the present invention.
- a cellular nutrient medium preferably, serum free
- non-steroidal anabolic hormone insulin or insulin-like substances and mixtures thereof preferably used for topical application to the treated wounds according to the present invention.
- These delivery systems polymers include, for example, numerous hydrogels in hydrated or unhydrated form, such as those derived from hydroxyethylmetacrylate (HEMA), glycerolmetacrylate (GMA) and polyvinylpyrrolidone (PVP), polyethylene glycol (PEG) and various carbohydrates, cellulose, and related hydrophilic cellulose polymers, dextran, polyethyleneoxide, dextran-polyethylene, acrylamide, amylase, collagen, gelatin, sepharose, agarose (for example, as an agarose saturated gel), related polymers and mixtures thereof, among numerous others.
- HEMA hydroxyethylmetacrylate
- GMA glycerolmetacrylate
- PVP polyvinylpyrrolidone
- PEG polyethylene glycol
- various carbohydrates cellulose, and related hydrophilic cellulose polymers, dextran, polyethyleneoxide, dextran-polyethylene, acrylamide, amylase, collagen, gelatin, sepharose, agarose (
- delivery polymer is also used to describe polymers that provide slow-release or sustained release characteristics to the wound healing formulations of the invention.
- gelling agent is used to describe those polymers, which may be included in aqueous formulations according to the present invention in effective amounts to gel these formulations.
- MHCP methyl hydroxy chalcone polymer
- Compositions which include effective amounts of MHCP and insulin and optionally, at least one further component selected from the group consisting of insulin-like growth factor (IFG), polyphenol type-A polymer, selenium, chromium, curcuma and mixtures thereof are preferred aspects of the invention because of the synergistic favorable impact such components have on wound healing, especially the healing of chronic wounds.
- IGF insulin-like growth factor
- polyphenol type-A polymer polyphenol type-A polymer
- selenium chromium, curcuma and mixtures thereof
- MHCP is included in compositions according to the present invention in an effective amount, generally at concentration ranging from about O.OOlmg/ml to about 25 mg/ml, about 0.01 mg/ml to about 10 mg/ml, about 0.025 mg/ml to about 5 mg/ml, although concentrations outside of these ranges are . also useful.
- the MHCP ranges from about 0.025 mg/ml to about 0.5-1.0 mg/ml.
- the biological of activity of 0.1 mg/ml of MHCP is approximately equivalent to the biological activity of aboutlOO nM of insulin. Percentage weights may fall outside of these ranges, depending upon the type and size of the wound and other factors, as well recognized by one of ordinary skill in the art.
- the biological activity of MHCP at concentrations of about 0.1 mg/ml is about equivalent to the range of activity of lOOnM of insulin.
- Preferred MHCP concentration within the preferred media MCDB 153 ranges from about 0.01 mg/ml to about 1 mg/ml.
- Preferably the MHCP in MCDB 153 ranges from about 0.025 mg/ml to about 0.5 mg/ml.
- polyphenol type- A polymers found in cinnamon may function as antioxidants, and act as synergistic agents to insulin by potentiating its action and by also contributing to the control of glucose tolerance and diabetes.
- cellular nutrient medium or “cellular nutrient mixture” is used throughout the specification to describe a medium or mixture (generally, at least a minimum essential medium) which preferably contains no serum (is serum-free), and in combination with insulin or insulin-like substances (e.g. MHCP, polyphenolic type-A polymer, insulin-like growth factor, selenium, chromium, curcuma and mixtures thereof), at least one of them comprising the wound healing compositions according to the present invention.
- insulin or insulin-like substances e.g. MHCP, polyphenolic type-A polymer, insulin-like growth factor, selenium, chromium, curcuma and mixtures thereof
- the nutrient medium preferably serum-free, according to the present invention comprises the following elements: (a) essential amino acids; (b) non-essential amino acids; (c) vitamins selected from a group consisting of biotin, folate, lipoate, niacinamide, pantothenate, pyrodine, riboflavin, thiamin and vitamin Bj 2 and mixtures thereof, preferably a vitamin mixture comprising folate, niacinamide, pantothenate, pyrodine, riboflavin and thiamin; (d) glucose; and (e) a mixture of inorganic ions selected from a group consisting of calcium, sodium, potassium, magnesium, chloride and mixtures thereof, preferably a mixture comprising calcium, potassium, magnesium and chloride.
- All of these elements (a), (b), (c), (d) and (e) are included with the anabolic hormone and optionally the insulin like substances in concentrations and/or amounts effective for enhancing the growth of cells which surround, have been injured by or are responsible for healing a wound.
- the preferred concentration of essential and non-essential amino acids used in the present invention is from about 5.0 um (!0 "6 mole) to about 50 mmol. (10 "3 mole).
- the proffered concentration of vitamins used in the present invention ranges from about 1 nanomole (10 "9 mol.) to about 10 um.
- the preferred concentration of glucose used in this invention ranges from about 1 umol. to about 10 or more mmol.
- these organic ions are preferably included in the present compositions are at concentration ranges of about 1 umol to about 50 mmol.
- the nutrient medium according to the present invention optionally contain any one of one or more of the following element: (f) purines and pyrimidines; (g) other organic compounds; (h) other inorganic ions; (i) trace elements; (j) buffers and indicators and (k) other supplements.
- All of the optional elements (f), (g), (h), (i), (j) and (k), when they are included in the nutrient medium according to the present invention are included in the amounts effective for enhancing the growth of cells involved in wound healing processes in combination with insulin or its mimicking substitute cinnamon or MHCP, further including an effective amount of insulin-like growth factor, IGF, selenium, chromium, curcuma and mixtures thereof.
- components (f), (g), (j) and (k) range in concentration from about 1 mmol to about 10 mmol. In the case of components (h) and (j) the concentration preferably ranges from about 1 umol. to about 50 mmol.
- concentration preferably ranges from about 1 umol. to about 50 mmol.
- the present invention may also make use of cellular nutrient medium containing serum, although the use of serum containing cellular nutrient medium is generally less preferred than is serum free medium.
- examples of such nutrient medium include, among numerous others, DMEM, HAM F12 and HAM F10, all containing serum.
- cellular nutrient medium or "nutrient mixture” is used to describe all types of nutrient medium contemplated for the use in the present invenion which contain at least the basic elements (generally, of a minimum essential medium) as described hereinabove, and such term includes serum free cellular nutrient medium.
- the cellular nutrient medium according to the present invention includes one or more commercially available media in solution or lyophilate (solid) form.
- the cellular nutrien medium used may be in the form of a lyophilate which may be reconstructed with water, preferably sterilized, distilled water and then supplemented with the anabolic hormone insulin or cinnamon or hydroxychalcone or polyphenol type-A polymer or mixtures thereof, and optionally, by each one separately and further including optional components IGF, selenium, chromium or curcuma and mixtures thereof.
- the nutrient medium may be used directly in formulations according to the present invention in the form of a lyophilate, or related solid-type material, rather than a solution, especially when gels, creams, elixirs, powders or other delivery vehicles are to be used for delivery. It is clearly preferred when utilizing solid-type materials for delivering the wound healing compositions according to the present invention that the delivery system in the form of a hydrogel or other form containing moistening quantities of water.
- non-steroidal anabolic hormone is used throughout the specification to describe the primary hormone in the instant invention that promotes wound healing in combination with cellular nutrient media.
- the primary hormone is insulin or alternatively a nutrient substitute such as cinnamon, or other natural product which contains effective amounts of MHCP itself or polyphenol type-A polymer.
- nonsteroidal anabolic hormone includes naturally isolated (preferably human) or synthetically produced versions of insulin that are known to function substantially the same as the naturally occurring hormone and includes, where relevant, compounds produced by genetic
- the non-steroidal anabolic hormone that is especially preferred is insulin. While not being limited by way of theory, it is believed that the inclusion of at least one selected from the two, insulin or MHCP and preferably both components, serves to enhance the effect of the nutrient media in increasing the rate and natural process of wound healing. Thus, it is believed that the non-steroidal anabolic hormone actually enables the wound cells to utilize or process the nutrient in the media, which action result in an enhanced rate of wound healing.
- a combination of insulin and MCHP in effective amounts as otherwise described herein is shown to be synergistic in enhancing wound healing.
- each component which is used in the formulation according to the present invention, will depend upon the type and size of the wound, but each component preferably is included in the amount effective for significantly enhancing the healing of a wound relative to traditionally wound healing therapies.
- the formulation include an anabolic hormone or similar agent such as IGF and/or insulin in concentrations of at least about 0.005 ng/ml preferably about 0.5 ng/ml to about 50 ng/ml or more, more preferably about 50 ng/ml to about 20 ng/ml or more.
- the amount of insulin generally falls outside of this range, because of its tendency to degrade and become inactive a more rapid rate then other anabolic hormones.
- the anabolic hormone is insulin and/or a cinnamon extract as insulin substitute such as methylhydroxychalcone polymer or polyphenol type-A polymer, further including one or more of selenium, insulin-like growth factor, chromium, curcuma and mixtures thereof and because of the benefit this hormone or its substitute(s) have in promoting the growth and elaboration of cells and their generally absence of toxicity.
- the preferred anabolic hormone is human insulin, which is well-known protein is readily commercially from a number of sources (for example, Sigma Chemical Co., USA or Novo Nordisk, Copenhagen, Denmark). It is constituted from a number of amino acids (approximately 51) with a total molecular weight of about 5,500. Human insulin for use in the present invention is generally prepared using genetic engineering techniques.
- the insulin may have slightly different activity based upon its weight; however the activity of insulin defined in units is, of course, standard. While not being limited by way of theory, in the present invention, it is believed that the insulin promotes the wound healing by enhancing the transport and utilization of glucose by the cells.
- the cellular nutrient medium used in the present invention, is any nutrient medium having the effect of enhancing the recovery of wounded or atrophic skin tissues when used in combination with the cell growth-stimulating compound.
- the nutrient media is composed of the components set forth herein, it is mixed with effective amounts of the non-steroidal anabolic hormone or its substitute to form the compositions of the present invention.
- the medium is serum-free.
- the cellular media comprises effective amounts of the following constituent: (a) essential; (b) non-essential amino acids; (c) vitamins as previously decribed; (d) inorganic ions as previously described and (e) glucose; optionally, (f) purines and pyrimidines; (g) other organic compounds; (h) other inorganic ions; (i) trace elements; (j) buffers and indicators and (k) other supplements.
- the cellular nutrient medium used herein contains effective amounts of elements (f) through (k).
- Serum free nutrient medium is preferred.
- the preferred serum free nutrient medium is modified MCDB, a well-known medium. Mixtures of standard nutrient media may also be used with favorable results in the instant invention.
- the presence of the anabolic hormone, and in particular, insulin and/or hydroxychalcone (preferably a mixture of at least one of these and most preferably a combination of insulin and MHCP in nutrient medium, further including IGF, cinnamon, selenium, chromium and/or curcuma) in the formulations according to the present invention promotes the utilization of the nutrient medium and consequentially, growth in situ of the granulation tissue, i.e., within the wound itself.
- the novel formulations may also induce the stimulation of the vascular elements and promote the growth of vascularized granulation tissue preparatory to split skin grafting.
- the present formulation may in this same way also be useful to promote the healing, growth and regeneration of atrophic skin and to function as atrophic skin adjuvants.
- the proliferation of vascularized granulation promotes epidermal growth from the peripheral edges of the wound over the vascular granulation tissue substratum and from the deeper layers of the dermis leading to an early closure of the skin over the wound.
- the mechanism which might be assumed, is that in the proliferation phase, new capillaries and fibroblasts appear in the wound from the first day on and reach their maximum levels after one week.
- the new vessels in the granulation tissue originate as budlike structures on nearby vessels, penetrating the wound, become canalized and ramify throughout the wound by cell multiplication.
- the function of the nutrient medium is to provide nutrients to the normal, distressed and injured cells and skin that surround or comprise the wound to be treated, in order to enhance the growth and repair mechanisms that are responsible for the healing of the wound.
- the nutrient medium functions with the anabolic hormone or the nutrient substitute to promote the normal processes of elaboration, synthesis and growth leading to the healing of the wound and adjacent skin areas.
- the gelled media serves to maintain a moist environment surrounding the wound area.
- a number of nutrient media, preferably serum free, alone or in combination may be used in the present invention, including commercially available media or other media well known in the art.
- examples of such media include ADC-1, LPM (BOVINE Serum albumin-free), (10 (HAM), F12 (HAM), DCCM1, DCCM2, RPMI 1640, BGJ Medium (Fitton- Jackson Modification), Basal Medium Eagle (BME with the addition of Earl's salt base), Dulbecco's Modified Eagle Medium (DMEM- without serum), Glasgow Modification Eagle Medium (GMEM), Leibovitz L-15 Medium, McCoy's 5 A medium, Medium Ml 99 (M199E-with Eagle's Minimum Essential Medium (MEM-E with Eagle base), Minimum Essential Medium Eagle (MEM-H-with Hank's salt base) and Minimum Essential Medium Eagle )MEM-NAA-with non essential amino acids), among numerous others.
- These and other useful serum-free nutrient media are available from GIBCO, Grand
- serum-containing nutrient media may also be used in compositions according to the present invention, but the use of the serum-containing media is less preferred because of the possibility that the serum may be contaminated with microbial agents and because the patient may develop immunological reaction to certain antigenic components contained in the serum.
- a preferred but not the only nutrient media for use in the present invention is modified MCDB 153.
- Weights of each of the above in the medium may be varied within the concentration described herein above, to provide formulations workable within the description of the present invention.
- the non-steroidal anabolic hormone to be incorporated into the MCDB 153 composition according to the present invention is a mixture of insulin and/or its substitute at effective concentrations.
- the anabolic hormone insulin (with or without transferring) or the insulin substitute each included in effective concentrations for promoting wound healing.
- the effective amount of insulin generally ranges from about 5 ng/ml to about lOOug/ml and more preferably about 500ng/ml to about 5ug/ml within this range. Higher amounts of insulin may be merited where the formulation is stored for longer periods of time.
- the synergistic activity of insulin and its nutrient substitute suggests that they will enhance the activity of the indigenous natural occurring insulin in and around the wound whether the wound is traumatic or results from atrophic processes and the concomitant sparse blood supply to the area.
- the anabolic hormone insulin was found to impart a maturing stimulus of the growing culture.
- Insulin may be commercially obtained and generally provided in mil quantities (about 41 ng of insulin).
- the Standard Preparation is quantity of purified Zinc Insulin crystals extracted 52% from Bovine and 48% from Porcine pancreas (se Martindale Pharmacopoeia, 26 th Ed.).
- the formulation according to the present invention may also include an effective amount of an antimicrobial agent, for example, antiseptic, antibiotics, antiviral and antifungal agents, such as griseofulvin and nystatin, and the like.
- an antimicrobial agent for example, antiseptic, antibiotics, antiviral and antifungal agents, such as griseofulvin and nystatin, and the like.
- the antimicrobial agent may be added for its ability to treat infections, or alternatively, for its prophylactic effect avoiding an infection.
- an amount effective to treat an infection or a prophylactic amount of such agents is chosen.
- the amount of antimicrobial agent used is that amount typically used in topical application.
- One of ordinary skill in the art can easily determine the type and amount of antimicrobial agents chosen for use in formulations according to the present invention.
- the antimicrobial agent may vary widely depending on the efficacy of the agent to be delivered and the prophylactic treatment or the severity of the infection.
- the amount of antimicrobial agent to be used in the present invention will range from about 0.05 ug/ml to about 250 mg/ml with the preferred range of about 50 to about 200 ug/ml.
- these ranges will vary depending upon the condition of the infection to be treated as well as the strength of the antimicrobial agent employed.
- the amount of amphotericin used generally ranges from about 0.1 ug/ml to about 100 ug/ml with a preferred concentration of about 0.25 ug/ml.
- antibiotics and in particular, penicillin, streptomycin and gentamycin
- these agents are generally utilized within the concentration range of about 0.05 ug/ml to about 250 mg/ml with preferred concentration of about 25ug/ml to about 250 ug/ml.
- antibiotics any number of antibiotics may be used, including sulfa drugs, penicillin, chloramphenicol and aminoglycosides, among others, but it is preferable to use the broad spectrum antibiotics, for example cephalosporin or tetracycline in a prophylactic amount or alternatively, in an amount effective for treating bacterial infection.
- broad spectrum antibiotics for example cephalosporin or tetracycline in a prophylactic amount or alternatively, in an amount effective for treating bacterial infection.
- antibiotics one of ordinary skill in the art will recognize to minimize or avoid the use of antibiotics that may produce allergic reactions in the treated patients.
- the formulations as described herein are further formulated with hydrogels or related delivery polymers for delivering the formulation according to the present invention to the wound.
- the formulations consists of effective amounts of anabolic hormone insulin or it nutrient substitute with a nutrient media, either alone or in addition to other optional components, are admixed with amounts of a delivery polymer effective for producing a gel, for example a hydrogel polymer derived from HEMA (Hydroxyethylmethacrylate) or NVP (N-vinylpyrrlidone), polyethylene glycol (PEG), polyethylene, gelatin, various carbohydrates, sepharose, agarose, methylcellulose, hydroxymethyl and hydroxyethylcelluloseand related hydrophilic cellulose polymers including cellulose, dextran, polyethylene oxide, dextrin- polyethylene, agarose, acrylamide, polyacrilamide, amyloseor collagen to promote wound healing and skin growth.
- HEMA Hydrogel polymer derived from HEMA (Hydroxyeth
- the amount of delivery polymer which is added to the formulations produce a gel generally ranges from about 0.1% by weight to about 20% by weight, preferably about 1% to about 5%or more by weight, depending upon the type of delivery polymer used.
- the gel compositions according to the present invention preferably contain sufficient water or moisture to maintain the wound environment in a moist state - a condition shown to be beneficial to the wound healing.
- the compositions that are formulated with a delivery polymer also exhibit the added .benefit of preventing or slowing the formation of a scab on the wound. While not being limited by way of theory, it is believed that the resultant wound tissue, which remains soft and moist instead of dry and scab-like, produces a beneficial, cosmetically pleasing and increased rate wound healing.
- compositions according to the present invention also may be formulated as creams, elixirs, lotions, powders and the like.
- the various components of the wound treatment compositions according to the present invention may have to be varied in order to maintain effective concentrations for promoting wound healing.
- these compositions may also contain an amount of pharmaceutically acceptable excipient and, in addition, other additive such as diluents, compounding agents, bulking agents, surfactants and the like.
- concentrations of the individual components as a function of the type of delivery vehicle used for the wound treatment compositions in order to facilitate and enhance the wound healing activity of the present formulations.
- the formulations as described hereinabove are topically applied to the wound tissue as a liquid or gel preferably at least once a day and up to six or more times a day.
- the formulations may be administered less frequently then when the formulation are applied as a liquid, for example, once every several days or more.
- a delivery polymer preferably as a moisten delivery polymer
- the formulations may be administered less frequently then when the formulation are applied as a liquid, for example, once every several days or more.
- One of ordinary skill in the art will readily be able to determine the amount and frequency of administering the formulation according to the present invention.
- the amount of material that is spread on the wound as a treatment will be readily apparent to one of ordinary skill in the art.
- about lcc of the formulation is applied per 1 cm 2 of the wound area.
- an amount greater or lesser then the lcc of formulation per 1 cm 2 of the wound surface may be utilized.
- the depth of the formulation on the wound shall be at least about 2 mm and shall cover the whole surface of the wound.
- the preferred media contained essential and non-essential amino acids, Vitamins, other organic constituents, major inorganic salts, trace elements and buffers are supplemented with CaCl, L-glutamine and the non-steroidal anabolic hormone insulin. At concentrations indicated below.
- Folic Acid 1.8 x lO "6 DL-a-lipoic acid 1.0 X 10 "6 Niacinamide 3.0 x lO- 7 D-panto thenate l/20a 1.0 x lO "6 Pyridoxine HC1 3.0 x lO "7 Riboflavin 1.0 x 10 "7 Thiamin HC1 1.0 x 10 "6 Vitamin B 12 3.0 x lO "7
- Insulin-like MHCP 0.5 mg/ml
- EEO electro endosmosis 0/10-0.15
- Hartley-derived albino guinea pigs weighing 300-400 grams were used in this study.
- the animals were housed in individual cages and fed regularly guinea pig chow and water enriched with Oitamin C ad libitum. All Surgical procedures were performed under general anesthesia using Katamin HC1 ([d]-2-(o-chlorophenyl)-2-(methylamino) cyclohexanone hydrochloride, available from Park-Davis) 150 mg/kg i.m. All histological sections were prepared using hematoxylene and Eosin stain as well as Mason's trichrome method for collagen.
- Each animal was anesthetized and four bilateral symmetrical full thickness skin segments measuring 2x3 cm were excised from the dorsum of each animal, two from the scapular region and two from the lumbar region. After washing the wound with warm saline, the wounds were dressed with the gel at a concentration of about 1 cc/cm , covered with a polyethylene base synthetic membrane Omiderm (Omicron, Israel) and anchored with gauze, elastic adhesive and Retelast netting (Medinet, s.p.a., Italy).
- the dressing were changed every 48 hours under general anesthesia, at which time the wounds were washed with warm saline to remove any debris and the remaining gel within the wound, measures, photographed and fresh gel was applied and the wounds dressed as described above.
- days 4, 6, 8, 10, and 12 the animals were sacrificed and the wounds with the surrounding structures were removed and prepared for histological examination.
- the thickness of the newly formed epithelial layer and the underlying granulation tissue were measured using light microscopy (Zeiss) at lOOx magnification.
- the wound micrographs were analyzed using ImageMeasure (Phoenix Corp., Seattle, Wash.) computerized morphometric program and the experimental results were plotted as graphs showing the fractional change in the area (i.e. the closure rate) of the wounds treated with the gel-media + hormone versus the various controls.
- the wound closure rate was tabulated and peak closure day (% closure) was determined.
- Peak closure rate has been used as the measure of wound healing potency. Peak closure rate is the maximum slope of the Vs, time curve.
- Peak closure rate indicate the time after the start of the treatment at which tissue healing or growth rate reaches a maximum value (Maximum rate); i.e. when the treatment is optimal. Seven groups of experiments were performed using various combinations of medicaments as controls:
- Gelatin and Agarose were prepared in saline and the two gels were used to treat experimental wounds.
- the rate of closure of the wounds treated with Agarose was faster than the rate of closure of wounds treated with gelatin.
- Wound closure comparison indicates that the closure of 50% was 31% faster with Agarose in saline as compared to Gelatin in Saline. Peak closure rate occurred 33% earlier with Agarose in Saline treatment.
- Scarlet red dressing (O-Tolylazo-oTolylazi-beta-naphthol plus lanolin, olive oil and petroleum from Chesebrough-Ponds, Inc., hospital Products Division, Greenwich, Conn., USA-an azo dye-containing preparation routinely used in hospitals and claimed to increase epithelialization) was used as a positive control and saline in Agarose was used as negative control.
- Treatment with media + insulin formulation induced accelerated wound healing compared to treatment with media prepared in Agarose without insulin.
- the rate of wound closure using the media alone was similar to that of the wound treated with saline in Agarose.
- the rate of wound closure with the media + disinfectant treatment was initially faster than that of the wounds treated with media alone. However, on the 2 nd day the rate of the wound closure for wounds treated with media + insulin accelerated and was faster than the closure rate of wounds treated with the addition of the disinfectant compress. After the initial period of time, the disinfectant exerted cumulative cytotoxic effect that slows the healing process.
- Scarlet red dressing as a positive control and Saline as a negative control yielded similar results and slower closure when compared with media + Insulin treatment.
- wounds are clean, surgically made and uncomplicated by contamination. This point is important since the gel media may provide a growth substrate for bacteria. It is believed that, in contaminated wounds, a bacteriogram followed by or concomitant with specific antibiotics or disinfectant treatment in combination with the gel media treatment may be indicated.
- moist dressing is used to create optimal environment and to prevent desiccation of the wound bed.
- Enriched cell culture medium supplemented with insulin was gelled in 1% agarose. The gel was applied to the surface of the wound (lml/cm ) once a day. All wound included in the study were clinically clear of infection, following topical antiseptics or antibiotics. Etiology of the wounds was varied from venous and/or arterial insufficiency to insulin-dependant and non- dependant diabetic ulcers, or combinations of the above.
- An 80-year-old male was a non-insulin-dependant patient. He suffered from venous insufficiency, asthma controlled by prednisone, and from siderblastic anemia. He presented with a two years old leg ulcer which previously was treated with antiseptics. The treatment with the gel lasted 4 months partially in the hospital and later on an ambulatory basis.
- the gel treatment aims to change microenvironment of the chronic atrophic wound thereby affecting the metabolic processes in the wound cells.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Inorganic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Chemical & Material Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La présente invention concerne des compositions et des procédés permettant d'améliorer les microenvironnements dans et autour de la plaie dans un effort pour favoriser la cicatrisation. Spécifiquement, la présente invention concerne l'application d'un milieu de culture nutritif de tissus et cellules, comme un milieu essentiel minimum, complété avec de l'insuline et/ou avec des substances présentant une activité de type insulinique, comme la cannelle ou des extraits de cannelle, notamment entre autres MHCP. Le milieu est appliqué sur la plaie pour stimuler les cellules viables dans le lit de la plaie et les cellules adjacentes dans la périphérie de la plaie pour qu'elles prolifèrent et croissent dans la plaie pour aboutir à la fermeture de la plaie.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2012/042414 WO2013187899A1 (fr) | 2012-06-14 | 2012-06-14 | Compositions et procédés pour la stimulation de la cicatrisation des plaies |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2012/042414 WO2013187899A1 (fr) | 2012-06-14 | 2012-06-14 | Compositions et procédés pour la stimulation de la cicatrisation des plaies |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013187899A1 true WO2013187899A1 (fr) | 2013-12-19 |
Family
ID=49758571
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2012/042414 WO2013187899A1 (fr) | 2012-06-14 | 2012-06-14 | Compositions et procédés pour la stimulation de la cicatrisation des plaies |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2013187899A1 (fr) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5461030A (en) * | 1991-02-01 | 1995-10-24 | Life Medical Science, Inc. | Compositions and methods for enhancing wound healing |
US20020122787A1 (en) * | 2000-04-06 | 2002-09-05 | Newell Martha K. | Compositions and methods for promoting wound healing |
US20060258562A1 (en) * | 2000-07-31 | 2006-11-16 | Healor Ltd. | Methods and pharmaceutical compositions for healing wounds |
-
2012
- 2012-06-14 WO PCT/US2012/042414 patent/WO2013187899A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5461030A (en) * | 1991-02-01 | 1995-10-24 | Life Medical Science, Inc. | Compositions and methods for enhancing wound healing |
US20020122787A1 (en) * | 2000-04-06 | 2002-09-05 | Newell Martha K. | Compositions and methods for promoting wound healing |
US20060258562A1 (en) * | 2000-07-31 | 2006-11-16 | Healor Ltd. | Methods and pharmaceutical compositions for healing wounds |
Non-Patent Citations (1)
Title |
---|
KAMATH, J. V. ET AL.: "Pro-healing effect of Cinnamomum zeylanicum Bark", PHYTOTHERAPY RESEARCH, vol. 17, no. ISSUE, 2003, pages 970 - 972 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5591709A (en) | Compositions and methods for treating wounds | |
AU670413B2 (en) | Compositions and methods for treating wounds | |
JP5869219B2 (ja) | 治療および美容適用のためのエリスロポイエチンおよびフィブロネクチン組成物 | |
US20090325861A1 (en) | Dry wound dressing and drug delivery system | |
Dart et al. | Topical treatments in equine wound management | |
CN105107007A (zh) | 一种阳离子医用护创敷料及其制备方法 | |
KR101367340B1 (ko) | 아미노산 및 히알루론산 나트륨에 기반한 멸균 분말 제형의상처-치료용 약학적 조성물 | |
US10292997B2 (en) | Compositions and methods for stimulating wound healing | |
RU2522214C1 (ru) | Способ стимуляции заживления ран различного генеза природным антиоксидантом дигидрокверцетином | |
WO2013187899A1 (fr) | Compositions et procédés pour la stimulation de la cicatrisation des plaies | |
KR20200044434A (ko) | 물질 p를 포함하는 난치성 궤양 치료용 조성물 | |
WO2012095702A1 (fr) | Composition pour régénérer des tissus atrophiques | |
US10232004B2 (en) | Pharmaceutical composition based on Centella asiatica (Hydrocotyle asiatica L.) for the treatment of lower limb ulcers | |
RU2577950C1 (ru) | Способ стимуляции заживления дермальных ожогов | |
Jain et al. | Effect of moist dressing, collagen sheet dressing and epidermal growth factor in healing of chronic wounds | |
RU2369398C2 (ru) | Средство с ранозаживляющей активностью на основе супернатанта человеческих фибробластов | |
EP3000475B1 (fr) | Composition pharmaceutique ou cosmétique pour la régénération et la cicatrisation de la peau | |
RU2278689C2 (ru) | Способ лечения трофических язв и длительно незаживающих гнойных ран | |
Enderami et al. | Applications of blood plasma derivatives for cutaneous wound healing: A mini-review of clinical studies | |
RU2552336C1 (ru) | Средство для лечения гнойных ран, гнойных полостей и трофических язв | |
CA3168280A1 (fr) | Composition de cicatrisation de plaies chroniques et son application | |
AU2021394748A9 (en) | Compositions and methods for treating wounds | |
RU41613U1 (ru) | Устройство для лечения трофических язв и длительно заживающих гнойных ран | |
Stashak et al. | Topical wound treatments | |
WO2002064178A1 (fr) | Utilisation d'extrait de the vert pour soigner des plaies |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12878695 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 12878695 Country of ref document: EP Kind code of ref document: A1 |