US20230277674A1 - Pharmaceutical composition for the parenteral administration of ultrashort-effective beta-adrenoreceptor antagonists - Google Patents
Pharmaceutical composition for the parenteral administration of ultrashort-effective beta-adrenoreceptor antagonists Download PDFInfo
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- US20230277674A1 US20230277674A1 US18/061,562 US202218061562A US2023277674A1 US 20230277674 A1 US20230277674 A1 US 20230277674A1 US 202218061562 A US202218061562 A US 202218061562A US 2023277674 A1 US2023277674 A1 US 2023277674A1
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- United States
- Prior art keywords
- cyclodextrin
- esmolol
- salt
- landiolol
- solution containing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 229940121840 Beta adrenoreceptor antagonist Drugs 0.000 title claims abstract description 22
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 21
- 238000007911 parenteral administration Methods 0.000 title abstract description 6
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229920000858 Cyclodextrin Polymers 0.000 claims abstract description 41
- 150000003839 salts Chemical class 0.000 claims abstract description 41
- 239000000203 mixture Substances 0.000 claims abstract description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229960003745 esmolol Drugs 0.000 claims description 73
- AQNDDEOPVVGCPG-UHFFFAOYSA-N esmolol Chemical compound COC(=O)CCC1=CC=C(OCC(O)CNC(C)C)C=C1 AQNDDEOPVVGCPG-UHFFFAOYSA-N 0.000 claims description 71
- WMDSZGFJQKSLLH-RBBKRZOGSA-N landiolol Chemical compound O1C(C)(C)OC[C@H]1COC(=O)CCC(C=C1)=CC=C1OC[C@@H](O)CNCCNC(=O)N1CCOCC1 WMDSZGFJQKSLLH-RBBKRZOGSA-N 0.000 claims description 53
- 229950005241 landiolol Drugs 0.000 claims description 52
- 229920001450 Alpha-Cyclodextrin Polymers 0.000 claims description 16
- HFHDHCJBZVLPGP-RWMJIURBSA-N alpha-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO HFHDHCJBZVLPGP-RWMJIURBSA-N 0.000 claims description 16
- 229940043377 alpha-cyclodextrin Drugs 0.000 claims description 16
- GDSRMADSINPKSL-HSEONFRVSA-N gamma-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO GDSRMADSINPKSL-HSEONFRVSA-N 0.000 claims description 8
- 229940080345 gamma-cyclodextrin Drugs 0.000 claims description 8
- -1 2-hydroxypropyl Chemical group 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 239000001116 FEMA 4028 Substances 0.000 claims description 5
- 229960004853 betadex Drugs 0.000 claims description 5
- ZPLOQFLCMVIWRY-UHFFFAOYSA-N flestolol Chemical compound NC(=O)NCC(C)(C)NCC(O)COC(=O)C1=CC=CC=C1F ZPLOQFLCMVIWRY-UHFFFAOYSA-N 0.000 claims description 5
- 208000001871 Tachycardia Diseases 0.000 claims description 4
- 229950001315 flestolol Drugs 0.000 claims description 4
- 230000006794 tachycardia Effects 0.000 claims description 4
- 210000001992 atrioventricular node Anatomy 0.000 claims description 3
- 206010003658 Atrial Fibrillation Diseases 0.000 claims description 2
- 206010003662 Atrial flutter Diseases 0.000 claims description 2
- 208000007888 Sinus Tachycardia Diseases 0.000 claims description 2
- 208000007814 Unstable Angina Diseases 0.000 claims description 2
- 206010047281 Ventricular arrhythmia Diseases 0.000 claims description 2
- 206010000891 acute myocardial infarction Diseases 0.000 claims description 2
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 claims description 2
- 235000011175 beta-cyclodextrine Nutrition 0.000 claims description 2
- 208000028867 ischemia Diseases 0.000 claims description 2
- 230000001121 heart beat frequency Effects 0.000 claims 2
- 229940082496 Adrenoreceptor antagonist Drugs 0.000 claims 1
- 208000003734 Supraventricular Tachycardia Diseases 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 58
- 230000015556 catabolic process Effects 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 9
- ODLHGICHYURWBS-LKONHMLTSA-N trappsol cyclo Chemical compound CC(O)COC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)COCC(O)C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1COCC(C)O ODLHGICHYURWBS-LKONHMLTSA-N 0.000 description 9
- 239000000356 contaminant Substances 0.000 description 8
- VZTMYLWJKCAXMZ-UHFFFAOYSA-N 2-[(2-chloroquinazolin-4-yl)amino]ethanol Chemical compound C1=CC=C2C(NCCO)=NC(Cl)=NC2=C1 VZTMYLWJKCAXMZ-UHFFFAOYSA-N 0.000 description 7
- 239000013543 active substance Substances 0.000 description 7
- 229960001015 esmolol hydrochloride Drugs 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000006731 degradation reaction Methods 0.000 description 6
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- 239000007924 injection Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000013112 stability test Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- 230000002666 vasoprotective effect Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000008030 elimination Effects 0.000 description 3
- 238000003379 elimination reaction Methods 0.000 description 3
- 238000004108 freeze drying Methods 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000008215 water for injection Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 229920004482 WACKER® Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000332 adrenergic beta-1 receptor antagonist Substances 0.000 description 2
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- 238000004090 dissolution Methods 0.000 description 2
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- 206010002091 Anaesthesia Diseases 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 238000001949 anaesthesia Methods 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 239000002876 beta blocker Substances 0.000 description 1
- 102000015005 beta-adrenergic receptor activity proteins Human genes 0.000 description 1
- 108040006818 beta-adrenergic receptor activity proteins Proteins 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
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- 239000000470 constituent Substances 0.000 description 1
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- 239000012153 distilled water Substances 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- GEKNCWBANDDJJL-UHFFFAOYSA-N esmolol hydrochloride Chemical compound [Cl-].COC(=O)CCC1=CC=C(OCC(O)C[NH2+]C(C)C)C=C1 GEKNCWBANDDJJL-UHFFFAOYSA-N 0.000 description 1
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- 238000001802 infusion Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- IUBSYMUCCVWXPE-UHFFFAOYSA-N metoprolol Chemical compound COCCC1=CC=C(OCC(O)CNC(C)C)C=C1 IUBSYMUCCVWXPE-UHFFFAOYSA-N 0.000 description 1
- 229960002237 metoprolol Drugs 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003182 parenteral nutrition solution Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 238000012430 stability testing Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 230000000213 tachycardiac effect Effects 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
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- 230000003966 vascular damage Effects 0.000 description 1
- 230000002861 ventricular Effects 0.000 description 1
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Images
Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/40—Cyclodextrins; Derivatives thereof
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
- A61K31/24—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
- A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
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- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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- A61P9/12—Antihypertensives
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Abstract
The present invention relates to a pharmaceutical composition in the form of a storage-stable solution for the parenteral administration of ultrashort-effective β-adrenoreceptor antagonists, comprising a) an ultrashort-effective β-adrenoreceptor antagonist and/or a pharmaceutically acceptable salt thereof, b) water, and c) a cyclodextrin and/or a functional cyclodextrin derivative. The composition according to the invention has high stability, even without the presence of additional adjuvants.
Description
- The present application is a continuation of U.S. patent application Ser. No. 16/860,336, filed Apr. 28, 2020, which is a continuation of U.S. patent application Ser. No. 16/164,926, filed Oct. 19, 2018, which is a continuation of U.S. patent application Ser. No. 15/248,845, filed Aug. 26, 2016, which is a continuation of U.S. patent application Ser. No. 12/809,927, filed Aug. 19, 2010, which is a national phase application under 35 U.S.C. § 371 of International Application No. PCT/AT2008/000470, filed Dec. 22, 2008, which claims priority to Austrian Patent Application No. A2107/2007, filed Dec. 21, 2007. The contents of the aforementioned application as are incorporated into the present application by reference.
- The present invention relates to a pharmaceutical composition for parenteral administration of an ultrashort-effective β-adrenoreceptor antagonist in the form of a solution.
- Due to their very short elimination half-life, ultrashort-effect β-adrenoreceptor antagonists such as esmolol hydrochloride, landiolol hydrochloride (two cardioselective β1 blockers) and flestolol hydrochloride are used in the form of parenteral formulations, particularly in anaesthesia and in emergency and intensive care medicine.
- For the purpose of this invention, the term “ultrashort-effective” is taken to mean an active substance with an elimination half-life which is less than that of the β1 blocker metoprolol (half-life t1/2=90 minutes). More particularly, the elimination half-life of the β-adrenoreceptor antagonists used in accordance with the invention is preferably less than 20 minutes.
- One problem is the low stability of these active substances in aqueous solution as they are hydrolytically split into free acids and alcohol (in the case of esmolol into pure acid and methanol) [e.g. Baaske D M, Dykstra S D, Wagenknecht D M, Karnatz N N Stability of esmolol hydrochloride in intravenous solutions. Am J Hosp Pharm. 1994 Nov. 1; 51 (21): 2693-6; Tamotsu Yasuda, Hiroyuki Kamiya, Yoko Tanaka, Go Watanbe, Ultrashort-acting cardioselective beta-blockade attenuates postischemic cardiac dysfunction in the isolated rat heart. Eur J Cardiothorac Surg 2001; 19:647-652].
- On the other hand the active substance concentration of, for example esmolol, used for administration is so high that these solutions are often hypertonic. In addition, to stabilise these solutions alcohol in concentrations of around 25% is added in many cases. Because of these technical formulation problems, the use of esmolol in intensive care medicine is associated with additional risks.
- Commercially obtainable landiolol is, for example, currently only available in fixed formulations which have to be dissolved before being used in intensive care medicine, leading to an unnecessary loss of time. Freeze-dried compositions containing landiolol are known from CN 1827109A.
- Attempts to solve the problems cited for esmolol include the addition of dextrose [Wiest D B, Garner S S, Childress L M., Stability of esmolol hydrochloride in 5% dextrose injection. Am J Health Syst Pharm 1995 Apr. 1; 52 (7) 716-81, adjusting the pH value to <6 [Rosenberg L S, Hostetler C K, Wagenknecht D M, Aunet D A., An accurate prediction of the pH changes due to degradation: correction for a “produced” secondary buffering system. Pharm. Res. 1988 August; 5(8): 514-71, as well as the addition of propylene glycol in high concentrations [http://www.rxlist.com/cgi/generic3/esmolol.htm].
- WO 85/04580 describes solutions of esmolol in a proportion by weight of 0.1% to 30% which also include a buffer and ethanol in a proportion of 5 to 60%.
- In its
claim 1, EP 0403578 claims an injectable, aqueous composition for treating heart conditions, which has an effective quantity of esmolol (hydrochloride) in a proportion of 1 mg to 250 mg esmolol/ml solution and 0.01 to 0.04 M buffer, and has a pH value in the range 4.5 to 5.5. - International publication WO 02/076446 describes an esmolol solution containing 0.1 to 500 mg/ml esmolol hydrochloride, 0.01 to 2 M buffer and 1 to 500 mg/ml of an osmosis-adjusting agent.
- European publication EP 1417962 describes pharmaceutical compositions consisting of 30 ml to 70 ml dilution with an proportion of 1500 mg to 3500 mg esmolol or a pharmaceutically tolerable salt thereof.
- There are no known attempts to solve the cited problem for landiolol.
- The aim of the present invention is to provide a composition for parenteral administration of ultrashort-effective β-adrenoreceptor antagonist, more particularly for injection or infusion, which on the one hand exhibits a high degree of storage stability and on the other hand an osmolarity which is suitable for administration. The composition should exhibit vaso-protective properties, which is important especially at high active substance concentrations (e.g., in the case of esmolol).
- Surprisingly it was found that the use of a cyclodextrin and/or a functional cyclodextrin derivative to increase the stability of an ultrashort-effective β-adrenoreceptor antagonist and/or a pharmaceutically acceptable salt thereof in a suitable storage-stable aqueous solution for parenteral administration fulfils the aim of the invention in an excellent manner.
- In this aspect of the present invention the solution can also contain other auxiliary substances, in particular buffers, preservation agents, organic solvents that can be mixed with water, salts, sugar alcohols and/or sugar.
- A further aspect of the present invention relates to a pharmaceutical composition for parenteral administration of an ultrashort-effective β-adrenoreceptor antagonist in the form of a storage-stable solution, essentially consisting of a) an ultrashort-effective β-adrenoreceptor antagonist and/or a pharmaceutically acceptable salt thereof b) water and c) a cyclodextrin and/or a functional cyclodextrin derivative
- DE 4207922 and US 2004/0053894 describe in general the use of cyclodextrin in pharmaceutical compositions. The use of cyclodextrin in pharmaceutical compositions is also described in WO 2003/033025, US 2003/021349 and in Ikeda et al., J. Pharm Sci. 2004, 93(7), 1659-1671.
- It was found that by adding cyclodextrin and/or a functional cyclodextrin derivative, the stability of ultrashort-effective β-adrenoreceptor antagonists in pure aqueous solutions can be decisively increased.
- Surprisingly, ultrashort-effective β-adrenoreceptor antagonist solutions consisting solely of the ultrashort-effective β-adrenoceptor antagonist, cyclodextrin and water, are sufficiently storage-stable, even without the presence of other auxiliary substances (such as buffer or osmolarity-adjusting agents known from the prior art) and, in terms of osmolar properties are suitable for administration. This applies particularly in the pH range from 3 to 7.5, preferably from 5 to 7.
- For the purpose of the present invention the term “storage-stable” denotes an aqueous solution, which in contrast to a solution produced through the dissolution of freeze-dried products, can be stored for a longer period of time without any significant breakdown of the contained active substance taking place. Understood as “storage-stable” in particular are aqueous solutions in which after one month less than 5% of the active substance has degraded.
- As has been stated above, the pH value of the solution is preferably 3 to 7.5, particularly preferably 5 to 7.
- The concentration of the cyclodextrin or cyclodextrin derivative in the solution is preferably 0.1% to 20% (w/v), preferably 0.25% to 7% (w/v), particularly preferably 0.5% to 4%.
- The cyclodextrin or the functional cyclodextrin derivative is preferably selected from the group comprising α-cyclodextrin, β-cyclodextrin, γ-cyclodextrin, functional derivatives and mixtures thereof.
- “Functional cyclodextrin derivatives” is taken to mean all pharmaceutically acceptable derivatives of cyclodextrins in which the essential structure and size of the cyclodextrin molecules are retained. Considered as functional cyclodextrin derivatives in particular are esters with pharmaceutically acceptable acids and ethers, especially low-alkyl ethers. Particularly preferred cyclodextrin derivatives are (2-hydroxypropyl)-β-cyclodextrin and (sulfobutylether)-7β-cyclodextrin.
- The ultrashort-effective β-adrenoreceptor antagonist used in the composition in accordance with the invention is preferably an active substance selected from the group comprising esmolol, landiolol and flestolol.
- The concentration of the ultrashort-effective β-adrenoreceptor antagonist or the salt therefore in the solution can be 0.1% to 30% depending on the β-adrenoreceptor antagonist used. Preferred concentrations in the case of esmolol or esmolol salts are 1 to 20%. Preferred concentrations in the case of landiolol or landiolol salts are 1 to 20%. Preferred concentrations in the case of flestolol or flestolol salts are 0.1 to 10%.
- The solution preferably has an osmolarity of 270 mosmol/l to 310 mosmol/l, particularly preferably 280 mosmol/l to 300 mosmol/l. This corresponds to an isotonic solution.
- In the case of esmolol the composition in accordance with the invention is preferably present in the form of a sales unit selected from the group comprising:
-
- 1 ml solution containing 10-20 mg esmolol or a salt thereof
- 2 ml solution containing 10-100 mg esmolol or a salt thereof
- 5 ml solution containing 50-500 mg esmolol or a salt thereof
- 10 ml solution containing 50-5000 mg, more particularly 2500 mg esmolol or a salt thereof
- 50 ml solution containing 50-5000 mg esmolol or a salt thereof [0034] 100 ml solution containing 50-5000 mg esmolol or a salt thereof
- 250 ml solution containing 50-5000 mg esmolol or a salt thereof.
- In the case of conventional products a 10 ml solution containing 100 mg esmolol as a “ready-to-use” product can be used directly for injection. Conventional compositions with high proportions of esmolol (more particularly 10 ml/2500 mg esmolol) must be diluted before administration. In comparison, due to their vasoprotective properties, solutions in accordance with the invention can also be used with higher concentrations of esmolol as “ready-to-use” products.
- In the case of landiolol and/or festolol the composition according to the invention is preferably available in the form of a sales unit selected from the group comprising
-
- 1 ml solution containing 5-20 mg landiolol or festolol or a salt thereof
- 2 ml solution containing 5-100 mg landiolol or festolol or a salt thereof
- 5 ml solution containing 10-500 mg landiolol or festolol or a salt thereof
- 10 ml solution containing 10-5000 mg landiolol or festolol or a salt thereof
- 25 ml solution containing 25-2500 mg landiolol or festolol or a salt thereof
- 50 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof
- 100 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof
- 250 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof.
- In conventional products containing landiolol, 50 mg of landiolol is contained as dry substance. These products must first be made into a solution before injection.
- In the compositions of landiolol according to the invention, the landiolol is already present in solution in a stable form. In general, due to the vasoprotective properties of the compositions according to the invention, comparatively higher concentrations of the ultrashort-effective β-adrenoreceptor antagonists than in the formulations to date can be used.
- The composition according to the invention can be produced in a known manner through mixing and subsequent dissolution of the constituents.
- The composition according to the invention can be used in particular to produce a medicinal product to reduce ventricular frequency in patients with atrial fibrillation, atrial flutter and sinus tachycardia, in atrioventricular and AV node tachycardia, tachycardic supra- and ventricular arrhythmias, in tachycardia and/or hypertension, before, during and after operations as well as in other emergency situations, for the prophylaxis and treatment of perioperative ischaemia, to treat unstable angina pectoris and acute myocardial infarction.
- The invention will be explained in more detail below with the aid of examples of embodiment and figures.
-
FIG. 1 shows the accelerated breakdown of a 5% esmolol reference solution and compositions according to the invention at 75° C. -
FIG. 2 shows the influence of freeze-drying on the accelerated breakdown of esmolol-cyclodextrin complexes in water at 75° C. -
FIG. 3 shows the influence of the concentration of α-cyclodextrin on the stability of esmolol at 75° C. -
FIG. 4 shows the influence of hydroxypropyl-β-cyclodextrin on the stability of esmolol at 75° C. -
FIG. 5 shows the influence of α-cyclodextrin in increasing concentrations on the stability of landiolol in aqueous solution at 70° C. -
FIG. 6 shows the influence of 2-hydroxypropyl-β-cyclodextrin in increasing concentrations on the stability of landiolol in aqueous solution at 70° C. -
FIG. 7 shows the influence of γ-cyclodextrin in increasing concentrations on the stability of landiolol in aqueous solution at 70° C. -
FIG. 8 shows the influence of the pH value on the stability of landiolol in aqueous solution at 70° C. -
FIG. 9 shows the influence of cyclodextrins (2%, w/v) in which landiolol was stored by means of concentrated suspensions on the stability of aqueous landiolol solutions of 0.25% (w/v) at 70° C. - An equimolar quantity of (2-hydroxypropyl)-β-cyclodextrin was added to a 5% esmolol solution and stirred for 6 hours.
- An equimolar quantity of α-cyclodextrin (Cavamax W6 Pharma, manufacturer Wacker Chemie AG) (example 2a) or γ-cyclodextrin (Cavamax W8 Pharma, manufacturer Wacker Chemie AG) example 2b) was added to a 5% esmolol solution and stirred for 18 hours.
- Esmolol and α-cyclodextrin are dissolved in final concentrations of 5% (w/v) (esmolol) and 14% (w/v) α-cyclodextrin) in water for injection purposes and stirred for 24 hours at room temperature.
- Esmolol and optionally additionally α-cyclodextrin are dissolved in a final concentration of 5% (w/v) (esmolol) or 14%, 7%, 4%, 2%, 1% and 0% (w/v) (α-cyclodextrin) in water for injection purposes and stirred for 24 hours at room temperature.
- Esmolol and optionally additionally hydroxypropyl-β-cyclodextrin are dissolved in a final concentration of 5% (w/v) (esmolol) or 7% and 0% (w/v) (hydroxypropyl-β-cyclodextrin) in water for injection purposes and stirred for 24 hours at room temperature.
- A parenteral solution was produced in accordance with the recipe set out in table 1.
-
TABLE 1 Composition of the parenteral esmolol solution Substances Quantity Esmolol HCl 500 mg Sodium acetate 34 mg Glacial acetic acid 3.674 mg Propylene glycol 518 mg Ethanol 402 mg HCl or NaOH for pH 3.5-5.5 q.s. Water ad 10 ml - With solution described in examples 1 to 3, accelerated stability tests were carried out at a temperature of 75° C. After 0, 24, 45 and 70 hours samples were taken which were diluted with distilled water (20 μl sample+180 μl water). The accelerated breakdown was determined by HPLC as follows:
- For the qualitative and quantitative analyses a Hitachi Elite LaChrom HPLC device with a diode array detector and a Waters Nova-
Pak C18 4 μm 3.9×150 mm column were used. The mobile phase consisted of (A) H3PO4 (10 g/l) in water, adjusted to pH 2.35 with triethylamine (TEA) and (B) acetonitrile. The gradient used is set out in table 2. -
TABLE 2 HPLC method Time (min) A (%) B (%) 0 82 18 7 82 18 8 60 40 13 60 40 14 70 30 20 70 30 21 82 18 30 82 18 - The flow rate was 1 ml/minute, the injection volume 200. Esmolol hydrochloride was detected at 274 nm. The retention time of esmolol hydrochloride was on average 3.9 minutes, that of the principal degradation product (“contaminant A” in table 3 below) was 1.7 minutes. To determine degradation the ratio of the principal degradation product to remaining esmolol hydrochloride was calculate and indicated in percent (“degraded esmolol (%)”).
- The results of these studies show a decisively increased stability of the solutions containing cyclodextrin.
-
FIG. 1 shows the accelerated degradation at 75° C. of the 5% esmolol reference solution and esmolol cyclodextrin complexes in water [(⋄) 5% esmolol comparison solution with 0% cyclodextrin—example 3b; (X) 5% esmolol+γ-cyclodextrin—example 2b]; (▪) 5% esmolol+(2-hydroxypropyl)-β-cyclodextrin—example 1); (▴) 5% esmolol+α-cyclodextrin—example 2a]. The values are mean values of 3 tests±SD. -
FIG. 2 shows the influence of freeze drying on the accelerated degradation of esmolol-cyclodextrin complexes in water at 75° C. [(⋄) 5% esmolol comparison solution with 0% cyclodextrin—example 3b; (X) 5% esmolol in 14% α-cyclodextrin solution without freeze drying—example 3a; (▪) 5% esmolol+α-cyclodextrin—example 2a with subsequent freeze drying and reconstitution in water]. The values are mean values of 3 tests±SD. -
FIG. 3 shows the influence of the concentration of α-cyclodextrin on the stability of an aqueous 5% esmolol solution at 75° C. [(Δ) 5% esmolol comparison solution with 0% α-cyclodextrin—example 3b; (+) 5% esmolol+1% α-cyclodextrin—in accordance with example 3b; (∘) 5% esmolol+2% α-cyclodextrin—in accordance with example 3b; (▪) 5% esmolol+4% α-cyclodextrin—in accordance with example 3b; (▴) 5% esmolol+7% α-cyclodextrin—in accordance with example 3b; (●) 5% esmolol+14% α-cyclodextrin—in accordance with example 3b;]. The values are mean values of 3 tests±SD. -
FIG. 4 shows the influence of hydroxypropyl-β-cyclodextrin on the stability of an aqueous 5% esmolol solution at 75° C. [(▪) 5% esmolol comparison solution with 0% hydroxypropyl-β-cyclodextrin—example 3c; (∘) 5% esmolol+7% hydroxypropyl-β-cyclodextrin—in accordance with example 3c]. The values are mean values of 3 tests±SD. - Table 3 shows the storage stability of esmolol cyclodextrin complexes (example 3a) compared with a state-of-the-art formulation (example 4) on the basis of the increase in degradation products (=contaminants).
-
TABLE 3 Stability tests Stability tests 25° C./60% r.h. Storage time 0 months 6 months 0 months 6 months Storage stability tests Esmolol formulation without Esmolol formulation with Contaminants cyclodextrin (example 4) cyclodextrin (example 3a) CONTAMINANT A 0 2.56 ± 0.53 0 1.94 ± 1.06 CONTAMINANT B n.d. n.d. n.d. n.d. CONTAMINANT C n.d n.d. n.d. n.d. CONTAMINANT D n.d. .018 ± 0.01 n.d. n.d. Unknown contaminants 0 0.37 ± 0.04 0 0.38 ± 0.02 Total 0 3.11 0 2.24 - The osmolarity/reduction in freezing point vis-a-vis water was determined with a Knauer semi-micro-osmometer. In order to be able to determine the osmolarity with this osmometer the samples are cooled to freezing in the osmometer.
- The 5% solution with α-cyclodextrin in accordance with example 3a has an osmolarity of 290 mosmol/l. This corresponds to an isotonic solution as the range of isotonia extends from 281 to 297 mosmol/l. Solutions of >310 mosmol/l would be described as hypertonic and solutions of <270 mosmol/l classified as hypotonic.
- Landiolol was dissolved in purified water at a concentration of 0.25% (m/v). Subsequently α-cyclodextrin (Cyclolab, Budapest), 2-hydroxypropyl-β-cyclodextrin (CTD, Inc., Florida) and γ-cyclodextrin (ISP, Germany) was added in final concentrations of 0%, 0.5%, 1%, 2% and 7% (w/v). The solutions were heated to 70° C. and the stability of landiolol determined in accordance with the HPLC method described in example 5. Landiolol was detected at 220 nm. The retention time of landiolol hydrochloride was on average 10.5 minutes, that of the principal degradation product 1.4 minutes. To determine the degradation the ratio of the principal degradation product to the remaining landiolol hydrochloride was calculated and indicated in percent (“degraded landiolol (%)”). The results of this study are shown in
FIG. 5-7 . The shown values are mean values of 3 tests±SD.FIG. 5 shows the influence of 0% (▪), 0.5% (X), 1% (∘), 2% (Δ), 4% (▴) and 7% (□) α-cyclodextrin on the stability of landiolol at 70° C. -
FIG. 6 shows the influence of 0% (▪), 0.5% (X), 1% (∘), 2% (Δ), 4% (▴) and 7% (□) hydroxypropyl-β-cyclodextrin on the stability of landiolol at 70° C. -
FIG. 7 shows the influence of 0% (♦), 0.5% (□), 1% (X), 2% (Δ), 4% (▪) and 7% (∘) γ-cyclodextrin on the stability of landiolol at 70° C. - Landiolol was dissolved in purified water at a concentration of 0.25 (w/v). The pH value was then adjusted to 3; 4; 5; 5.5; 6; 6.5; 7 and 8. The solutions were heated to 70° C. and the stability of landiolol determined with the HPLC method described in examples 5 and 8. The results of these studies are shown in
FIG. 8 . These show the degradation of landiolol at pH 3.0 (⋄), pH 4.0 (X), pH 5.0 (□), pH 5.5 (Δ), ph 6.0 (▴), pH 6.5 (♦), pH 7.0 (∘) and pH 8.0 (▪). The shown values are mean values of 3 tests±SD. - Landiolol and α-cyclodextrin (Cyclolab, Budapest), 2-hydroxypropyl-β-cyclodextrin (CTD Inc., Florida) or γ-cyclodextrin (ISP, Germany) were suspended in purified water in a concentration of 10% landiolol (w/v) and 80% cyclodextrin (w/v) and stirred for two hours at room temperature. After 5 minutes of ultrasound treatment the suspensions were diluted in stages so that the final concentration of landiolol was 0.25% (w/v). These solutions were incubated at 70° C. and the taken sample were analysed by means of the HPLC method described in examples 5 and 8. The results of this study are set out in
FIG. 9 . These show the influence of 2% α-cyclodextrin (▴), 2% 2-hydroxypropyl-β-cyclodextrin (Δ) and 2% γ-cyclodextrin (∘) on the stability of landiolol at 70° C. The shown values are mean values of 3 tests±SD. - Solutions of said β-adrenoreceptor antagonists with or without cyclodextrin were chronically infused into rats via the jugular vein for a longer period. It can be seen that said beta-adreno-receptor antagonists in solutions containing cyclodextrin bring about considerably less endothelial and vascular damage than the use of a conventional solution.
Claims (16)
1. A pharmaceutical composition comprising:
a) an ultrashort-effective β-adrenoreceptor antagonist or a pharmaceutically acceptable salt thereof;
b) water; and
c) a cyclodextrin or a functional cyclodextrin derivative.
2. The pharmaceutical composition of claim 1 , wherein the pH value of the composition is 3 to 7.5.
3. The pharmaceutical composition of claim 2 , wherein the pH value of the composition is 5 to 7.
4. The pharmaceutical composition of claim 1 , wherein the concentration of the cyclodextrin or the functional derivative thereof is 0.1% to 20% (w/v).
5. The pharmaceutical composition of claim 4 , wherein, the concentration of the cyclodextrin or the functional derivative thereof is 0.25% to 7% (w/v).
6. The pharmaceutical composition of claim 5 , wherein the concentration of the cyclodextrin or the functional derivative thereof is 0.5% to 4%.
7. The pharmaceutical composition of claim 1 , wherein the cyclodextrin is selected from the group consisting of α-cyclodextrin, β-cyclodextrin, and γ-cyclodextrin.
8. The pharmaceutical composition of claim 1 , wherein the functional cyclodextrin derivative is selected from the group consisting of (2-hydroxypropyl)-β-cyclodextrin and (sulfobutylether)-7β-cyclodextrin.
9. The pharmaceutical composition of claim 1 , wherein the ultrashort-effective β-adrenoreceptor antagonist is selected from the group consisting of esmolol, landiolol, and flestolol.
19. The pharmaceutical composition of claim 1 , wherein the concentration of the ultrashort-effective β-adrenoreceptor antagonist or salt thereof is 0.1% to 30%.
11. The pharmaceutical composition of claim 1 , wherein the composition has an osmolarity of 270 mosmol/l to 310 mosmol/l.
12. The pharmaceutical composition of claim 11 , wherein the composition has an osmolarity of 280 mosmol/l to 300 mosmol/l.
13. The pharmaceutical composition of claim 1 , wherein the ultrashort-effective (3-adrenoreceptor antagonist is esmolol or a salt thereof, and further wherein the composition is present in the form of a sales unit selected from the group consisting of:
1 ml solution containing 10-20 mg esmolol or a salt thereof,
2 ml solution containing 10-100 mg esmolol or a salt thereof,
5 ml solution containing 50-500 mg esmolol or a salt thereof,
10 ml solution containing 50-5000 mg esmolol or a salt thereof,
10 ml solution containing 2500 mg esmolol or a salt thereof,
50 ml solution containing 50-5000 mg esmolol or a salt thereof,
100 ml solution containing 50-5000 mg esmolol or a salt thereof, and
250 ml solution containing 50-5000 mg esmolol or a salt thereof.
14. The pharmaceutical composition of claim 1 , wherein the ultrashort-effective β-adrenoreceptor antagonist is landiolol or festolol or a salt thereof, and further wherein the composition is present in the form of a sales unit selected from the group consisting of:
1 ml solution containing 5-20 mg landiolol or festolol or a salt thereof,
2 ml solution containing 5-100 mg landiolol or festolol or a salt thereof,
5 ml solution containing 10-500 mg landiolol or festolol or a salt thereof,
10 ml solution containing 10-5000 mg landiolol or festolol or a salt thereof,
25 ml solution containing 25-2500 mg landiolol or festolol or a salt thereof,
50 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof,
100 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof, and
250 ml solution containing 50-5000 mg landiolol or festolol or a salt thereof.
15. A method of reducing heart beat frequency in a patient comprising administering a composition of claim 1 to a patient, whereby the heart beat frequency in the patient is reduced.
16. The method of claim 15 , wherein the patient has atrial fibrillation, atrial flutter, sinus tachycardia, atrioventricular tachycardia, AV node tachycardia, supraventricular tachycardia, ventricular arrhythmias, perioperative ischaemia, unstable angina pectoris, or acute myocardial infarction.
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US16/164,926 US10660964B2 (en) | 2007-12-21 | 2018-10-19 | Pharmaceutical composition for the parenteral administration of ultrashort-effective beta-adrenoreceptor antagonists |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5017609A (en) * | 1984-04-09 | 1991-05-21 | E. I. Du Pont De Nemours And Company | Pharmaceutical composition and method of treatment or prophylaxis of cardiac disorders |
CN1827109A (en) * | 2006-04-14 | 2006-09-06 | 北京润德康医药技术有限公司 | Lyophilized injection powder using Lanluodier and its salt as active ingredients and preparing technique therefor |
US20080293810A1 (en) * | 2007-05-22 | 2008-11-27 | Deepak Tiwari | Multi-dose concentrate esmolol with benzyl alcohol |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4727064A (en) | 1984-04-25 | 1988-02-23 | The United States Of America As Represented By The Department Of Health And Human Services | Pharmaceutical preparations containing cyclodextrin derivatives |
US4857552A (en) * | 1988-06-08 | 1989-08-15 | E. I. Du Pont De Nemours And Co. | Stable pharmaceutical composition |
DE4207922A1 (en) | 1992-03-13 | 1993-09-23 | Pharmatech Gmbh | New water-soluble inclusion complexes contg randomly substd. methyl-beta-cyclodextrin - for admin. of substances which are only sparingly soluble in water |
AU672862B2 (en) * | 1992-12-02 | 1996-10-17 | Insite Vision Incorporated | Cyclodextrin and polymer based drug delivery system |
IL149470A0 (en) | 1999-11-23 | 2002-11-10 | Aderis Pharmaceuticals Inc | Pharmaceutical compositions containing carboxamidoadenosine derivatives |
TWI277414B (en) * | 2001-01-12 | 2007-04-01 | Baxter Int | Esmolol formulation |
WO2003028718A1 (en) * | 2001-10-01 | 2003-04-10 | Smithkline Beecham Corporation | Novel formulations of carvedilol |
EP1443969A2 (en) | 2001-10-18 | 2004-08-11 | Decode Genetics EHF | Non-inclusion cyclodextrin complexes |
ES2318129T3 (en) * | 2002-04-18 | 2009-05-01 | Cv Therapeutics, Inc. | PROCESS OF ARRITMIAS TREATMENT WHICH UNDERSTANDS THE ADMINISTRATION OF AN ADENOSINE A1 AGONIST WITH A BETABLOCKER. |
US7148211B2 (en) * | 2002-09-18 | 2006-12-12 | Genzyme Corporation | Formulation for lipophilic agents |
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US7893040B2 (en) * | 2005-07-22 | 2011-02-22 | Oculis Ehf | Cyclodextrin nanotechnology for ophthalmic drug delivery |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5017609A (en) * | 1984-04-09 | 1991-05-21 | E. I. Du Pont De Nemours And Company | Pharmaceutical composition and method of treatment or prophylaxis of cardiac disorders |
CN1827109A (en) * | 2006-04-14 | 2006-09-06 | 北京润德康医药技术有限公司 | Lyophilized injection powder using Lanluodier and its salt as active ingredients and preparing technique therefor |
US20080293810A1 (en) * | 2007-05-22 | 2008-11-27 | Deepak Tiwari | Multi-dose concentrate esmolol with benzyl alcohol |
Non-Patent Citations (2)
Title |
---|
Lofttson et al (Expert Opin. Drug Deliv. 2005 2(2)), (Year: 2005) * |
Mio, (Masui. 2006 Jul; 55(7):841-8) (Year: 2006) * |
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PL2234614T3 (en) | 2013-03-29 |
AU2008340179B2 (en) | 2014-10-23 |
US20160361422A1 (en) | 2016-12-15 |
US20200323988A1 (en) | 2020-10-15 |
JP5623288B2 (en) | 2014-11-12 |
CN101903024A (en) | 2010-12-01 |
EP2234614A2 (en) | 2010-10-06 |
NZ586200A (en) | 2012-06-29 |
SI2234614T1 (en) | 2013-01-31 |
US10660964B2 (en) | 2020-05-26 |
PT2234614E (en) | 2013-01-25 |
US11517624B2 (en) | 2022-12-06 |
HRP20121045T1 (en) | 2013-01-31 |
EP2234614B1 (en) | 2012-10-17 |
CA2712414A1 (en) | 2009-07-02 |
CY1114951T1 (en) | 2016-12-14 |
US20190046646A1 (en) | 2019-02-14 |
ES2397126T3 (en) | 2013-03-04 |
JP2011506486A (en) | 2011-03-03 |
CA2712414C (en) | 2016-07-12 |
DK2234614T3 (en) | 2013-02-11 |
AU2008340179A1 (en) | 2009-07-02 |
WO2009079679A2 (en) | 2009-07-02 |
WO2009079679A3 (en) | 2009-11-26 |
US20100311738A1 (en) | 2010-12-09 |
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