WO2003026631A1 - Delivery of drug esters through an inhalation route - Google Patents
Delivery of drug esters through an inhalation route Download PDFInfo
- Publication number
- WO2003026631A1 WO2003026631A1 PCT/US2002/018543 US0218543W WO03026631A1 WO 2003026631 A1 WO2003026631 A1 WO 2003026631A1 US 0218543 W US0218543 W US 0218543W WO 03026631 A1 WO03026631 A1 WO 03026631A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ester
- esters
- aerosol
- drug
- drag
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 title claims abstract description 272
- 239000003814 drug Substances 0.000 title claims abstract description 143
- 229940079593 drug Drugs 0.000 title claims abstract description 143
- 239000000443 aerosol Substances 0.000 claims abstract description 151
- 239000002245 particle Substances 0.000 claims abstract description 78
- 239000000203 mixture Substances 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 33
- 241000124008 Mammalia Species 0.000 claims abstract description 24
- 238000010438 heat treatment Methods 0.000 claims abstract description 19
- 238000009833 condensation Methods 0.000 claims abstract description 15
- 230000005494 condensation Effects 0.000 claims abstract description 15
- 238000002664 inhalation therapy Methods 0.000 claims abstract description 4
- -1 norcholine ester Chemical class 0.000 claims description 36
- UEEJHVSXFDXPFK-UHFFFAOYSA-N Norcholine Natural products CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 11
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 claims description 10
- 229960002887 deanol Drugs 0.000 claims description 9
- 229960004752 ketorolac Drugs 0.000 claims description 9
- 208000007848 Alcoholism Diseases 0.000 claims description 8
- 208000019695 Migraine disease Diseases 0.000 claims description 8
- 201000007930 alcohol dependence Diseases 0.000 claims description 8
- 239000003242 anti bacterial agent Substances 0.000 claims description 8
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- 206010027603 Migraine headaches Diseases 0.000 claims description 7
- 229940035678 anti-parkinson drug Drugs 0.000 claims description 7
- 229960000905 indomethacin Drugs 0.000 claims description 7
- 229960000991 ketoprofen Drugs 0.000 claims description 7
- OZWKMVRBQXNZKK-UHFFFAOYSA-N ketorolac Chemical compound OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 OZWKMVRBQXNZKK-UHFFFAOYSA-N 0.000 claims description 7
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- 229940125681 anticonvulsant agent Drugs 0.000 claims description 6
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- 229940005530 anxiolytics Drugs 0.000 claims description 6
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 claims description 6
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- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims description 6
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- PJAGGJPKGNYFJH-QGZVFWFLSA-N [(6ar)-11-acetyloxy-6-methyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinoline-10-yl] acetate Chemical group C([C@H]1N(C)CC2)C3=CC=C(OC(C)=O)C(OC(C)=O)=C3C3=C1C2=CC=C3 PJAGGJPKGNYFJH-QGZVFWFLSA-N 0.000 claims description 4
- 125000004494 ethyl ester group Chemical group 0.000 claims description 4
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- 125000004185 ester group Chemical group 0.000 claims 4
- 125000004492 methyl ester group Chemical group 0.000 claims 2
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- 150000001875 compounds Chemical class 0.000 description 28
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- 238000000354 decomposition reaction Methods 0.000 description 10
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- 125000005907 alkyl ester group Chemical group 0.000 description 8
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- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
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- A61K31/33—Heterocyclic compounds
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/473—Quinolines; Isoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/49—Cinchonan derivatives, e.g. quinine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
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- A—HUMAN NECESSITIES
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- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24V—COLLECTION, PRODUCTION OR USE OF HEAT NOT OTHERWISE PROVIDED FOR
- F24V30/00—Apparatus or devices using heat produced by exothermal chemical reactions other than combustion
Definitions
- the present invention relates to the delivery of drug esters through an inhalation route. Specifically, it relates to aerosols containing drug esters that are used in inhalation therapy.
- the present invention relates to the delivery of drug esters through an inhalation route. Specifically, it relates to aerosols containing drug esters that are used in inhalation therapy.
- the aerosol comprises particles comprising at least 5 percent by weight of drug ester.
- the drug ester has a decomposition index less than 0.15. More preferably, it has a decomposition index less than 0.10 or 0.05.
- the particles comprise at least 10 percent by weight of drag ester. More preferably, the particles comprise at least 20 percent, 30 percent, 40 percent,
- the drug ester is an ester of a drag from one of the following classes: antibiotics, anticonvulsants, antidepressants, antihistamines, antiparkisonian drags, drags for migraine headaches, drugs for the treatment of alcoholism, muscle relaxants, anxiolytics, nonsteroidal anti-inflammatories, other analgesics and steroids.
- the drag ester is an ester of an antibiotic
- it is selected from an ester of one of the following compounds: cefmetazole; cefazolin; cephalexin; cefoxitin; cephacetrile; cephaloglycin; cephaloridine; cephalosporins, such as cephalosporin c; cephalotin; cephamycins, such as cephamycin a, cephamycin b, and cephamycin c; cepharin; cephradine; ampicillin; amoxicillin; hetacillin; carfecillin; carindacillin; carbenicillin; amylpenicillin; azidocillin; benzylpenicillin; clometocillin; cloxacillin; cyclacillin; methicillin; nafcillin; 2-pentenylpenicillin; penicillins, such as penicillin n, penicillin o, penicillin s, and penicillin v; chlorobutin penicillin; diclox
- the drug ester is an ester of an anticonvulsant
- it is selected from an ester of one of the following compounds: 4-amino-3-hydroxybutyric acid, ethanedisulfonate, gabapentin, and vigabatrin.
- the drug ester is an ester of an antidepressant
- it is selected from an ester of one of the following compounds: tianeptine and S-adenosylmethionine.
- the drag ester is an ester of an antihistamine, it is an ester of fexofenadine.
- the drag ester is an ester of an antiparkinsonian drag, it is selected from an ester of one of the following compounds: apomorphine, baclofen, levodopa, carbidopa, and thioctate.
- the drag ester is an ester of a drag for migraine headaches, it is selected from an ester of one of the following compounds: aspirin, diclofenac, naproxen, tolfenamic acid, and valproate.
- the drug ester is an ester of a drug for the treatment of alcoholism, it is an ester of acamprosate.
- the drag ester is an ester of a muscle relaxant, it is an ester of baclofen.
- the drag ester is an ester of an anxiolytic, it is selected from an ester of one of the following compounds: chlorazepate, calcium N-carboamoylaspartate and chloral betaine.
- the drug ester is an ester of a nonsteroidal anti-inflammatory, it is selected from an ester of one of the following compounds: aceclofenac, alclofenac, alminoprofen, amfenac, aspirin, benoxaprofen, bermoprofen, bromfenac, bufexamac, butibufen, bucloxate, carprofen, cinchophen, cinmetacin, clidanac, clopriac, clometacin, diclofenac, diflunisal, etodolac, fenclozate, fenoprofen, flutiazin, flurbiprofen, ibuprofen, ibu
- the drug ester is an ester of an other analgesic, it is selected from an ester of one of the following compounds: bumadizon, clometacin, and clonixin.
- the drug ester is an ester of a steroid, it is selected from an ester of one of the following compounds: betamethasone, chloroprednisone, clocortolone, cortisone, desonide, dexamethasone, desoximetasone, difluprednate, estradiol, fludrocortisone, flumethasone, flunisolide, fluocortolone, fluprednisolone, hydrocortisone, meprednisone, methylprednisolone, paramethasone, prednisolone, prednisone, pregnan-3- alpha-ol-20-one, testosterone, and triamcinolone.
- the ester is selected from an ester of the following type: Cj . -C 6 straight chain substituted or unsubstituted alkyl ester, C t -C ⁇ branched chain substituted or unsubstituted alkyl ester, C -C 6 substituted or unsubstituted cyclic alkyl ester, -C ⁇ substituted or unsubstituted alkenyl ester, C ⁇ -C 6 substituted or unsubstituted alkynyl ester, and substituted or unsubstituted aromatic ester.
- the ester is selected from an ester of the following type: C C ⁇ substituted or unsubstituted straight chain alkanoate, C] . -C 6 substituted or unsubstituted branched chain alkanoate, C ⁇ -C 6 substituted or unsubstituted alkenoate, and C ⁇ -C 6 substituted or unsubstituted alkynoate.
- the drag ester is selected from one of the following: ketoprofen methyl ester, ketoprofen ethyl ester, ketoprofen norcholine ester, ketorolac methyl ester, ketorolac ethyl ester, ketorolac norcholine ester, indomethacin methyl ester, indomethacin ethyl ester, indomethacine norcholine ester, and apomorphine diacetate.
- the aerosol has a mass of at least 0.01 mg.
- the aerosol has a mass of at least 0.05 mg. More preferably, the aerosol has a mass of at least 0.10 mg, 0.15 mg, 0.2 g or 0.25 mg.
- the particles comprise less than 10 percent by weight of drug ester degradation products.
- the particles comprise less than 5 percent by weight of drug ester degradation products. More preferably, the particles comprise less than 2.5, 1, 0.5, 0.1 or 0.03 percent by weight of drug ester degradation products.
- the particles comprise less than 90 percent by weight of water.
- the particles comprise less than 80 percent by weight of water. More preferably, the particles comprise less than 70 percent, 60 percent, 50 percent, 40 percent,
- the aerosol has an mhalable aerosol drug ester mass density of between 0.1 mg/L and 100 mg/L.
- the aerosol has an inhalable aerosol drug mass density of between 0.1 mg/L and 75 mg/L. More preferably, the aerosol has an inhalable aerosol drug mass density of between 0.1 mg/L and 50 mg/L.
- the aerosol has an inhalable aerosol particle density greater than 10 6 particles/mL.
- the aerosol has an inhalable aerosol particle density greater than 10 7 particles/mL or 10 8 particles/mL.
- the aerosol particles have a mass median aerodynamic diameter of less than 5 microns.
- the particles Preferably, the particles have a mass median aerodynamic diameter of less than 3 microns. More preferably, the particles have a mass median aerodynamic diameter of less than 2 or 1 micron(s).
- the geometric standard deviation around the mass median aerodynamic diameter of the aerosol particles is less than 2.
- the geometric standard deviation is less than 1.9. More preferably, the geometric standard deviation is less than 1.8, 1.7, 1.6 or 1.5.
- the aerosol is formed by heating a composition containing drag ester to form a vapor and subsequently allowing the vapor to condense into an aerosol.
- a drug ester is delivered to a mammal through an inhalation route.
- the method comprises: a) heating a composition, wherein the composition comprises at least 5 percent by weight of drag ester, to form a vapor; and, b) allowing the vapor to cool, thereby forming a condensation aerosol comprising particles, which is inhaled by the mammal.
- the drug ester has a decomposition index less than 0.15. More preferably, it has a decomposition index less than 0.10 or 0.05.
- the composition that is heated comprises at least 10 percent by weight of drug ester.
- the composition comprises at least 20 percent, 30 percent, 40 percent, 50 percent, 60 percent, 70 percent, 80 percent, 90 percent, 95 percent, 97 percent, 99 percent, 99.5 percent, 99.9 percent or 99.97 percent by weight of drag ester.
- the drug ester is an ester of a drug from one of the following classes: antibiotics, anticonvulsants, antidepressants, antihistamines, antiparkisonian drugs, drugs for migraine headaches, drugs for the treatment of alcoholism, muscle relaxants, anxiolytics, nonsteroidal anti-inflammatories, other analgesics and steroids.
- the drag ester is an ester of an antibiotic
- it is selected from an ester of one of the following compounds: cefmetazole; cefazolin; cephalexin; cefoxitin; cephacetrile; cephaloglycin; cephaloridine; cephalosporins, such as cephalosporin c; cephalotin; cephamycins, such as cephamycin a, cephamycin b, and cephamycin c; cepharin; cephradine; ampicillin; amoxicillin; hetacillin; carfecillin; carindacillin; carbenicillin; amylpenicillin; azidocillin; benzylpenicillin; clometocillin; cloxacillin; cyclacillin; methicillin; nafcillin; 2-pentenylpenicillin; penicillins, such as penicillin n, penicillin o, penicillin s, and penicillin v; chlorobutin penicillin; diclox
- the drag ester is an ester of an anticonvulsant, it is selected from an ester of one of the following compounds: 4-amino-3-hydroxybutyric acid, ethanedisulfonate, gabapentin, and vigabatrin.
- the drug ester is an ester of an antidepressant
- it is selected from an ester of one of the following compounds: tianeptine and S-adenosylmethionine.
- the drag ester is an ester of an antihistamine, it is an ester of fexofenadine.
- the drag ester is an ester of an antiparkinsonian drag, it is selected from an ester of one of the following compounds: apomorphine, baclofen, levodopa, carbidopa, and thioctate.
- the drug ester is an ester of a drug for migraine headaches
- it is selected from an ester of one of the following compounds: aspirin, diclofenac, naproxen, tolfenamic acid, and valproate.
- the drag ester is an ester of a drug for the treatment of alcoholism, it is an ester of acamprosate.
- the drag ester is an ester of a muscle relaxant, it is an ester of baclofen.
- the drag ester is an ester of an anxiolytic, it is selected from an ester of one of the following compounds: chlorazepate, calcium N-carboamoylaspartate and chloral betaine.
- the drag ester is an ester of a nonsteroidal anti-inflammatory, it is selected from an ester of one of the following compounds: aceclofenac, alclofenac, alminoprofen, amfenac, aspirin, benoxaprofen, bermoprofen, bromfenac, bufexamac, butibufen, bucloxate, carprofen, cinchophen, cinmetacin, clidanac, clopriac, clometacin, diclofenac, diflunisal, etodolac, fenclozate, fenoprofen, flutiazin, flurbiprofen, ibuprofen, ibu
- the drug ester is an ester of an other analgesic
- it is selected from an ester of one of the following compounds: bumadizon, clometacin, and clonixin.
- the drag ester is an ester of a steroid
- it is selected from an ester of one of the following compounds: betamethasone, chloroprednisone, clocortolone, cortisone, desonide, dexamethasone, desoximetasone, difluprednate, estradiol, fludrocortisone, flumethasone, flunisolide, fluocortolone, fluprednisolone, hydrocortisone, meprednisone, methylprednisolone, paramethasone, prednisolone, prednisone, pregnan-3- alpha-ol-20-one, testosterone, and triamcinolone.
- the ester is selected from an ester of the following type: C C ⁇ straight chain substituted or unsubstituted alkyl ester, Ci-C ⁇ branched chain substituted or unsubstituted alkyl ester, C 3 -C 6 substituted or unsubstituted cyclic alkyl ester, Ci-C ⁇ substituted or unsubstituted alkenyl ester, C ⁇ -C 6 substituted or unsubstituted alkynyl ester, and substituted or unsubstituted aromatic ester.
- the ester is selected from an ester of the following type: C ⁇ -C 6 substituted or unsubstituted straight chain alkanoate, C ⁇ -C 6 substituted or unsubstituted branched chain alkanoate, -C ⁇ substituted or unsubstituted alkenoate, and C ⁇ . -C 6 substituted or unsubstituted alkynoate.
- the drug ester is selected from one of the following: ketoprofen methyl ester, ketoprofen ethyl ester, ketoprofen norcholine ester, ketorolac methyl ester, ketorolac ethyl ester, ketorolac norcholine ester, indomethacin methyl ester, indomethacin ethyl ester, indomethacine norcholine ester, and apomorphine diacetate.
- the particles comprise at least 5 percent by weight of drug ester.
- the particles comprise at least 10 percent by weight of drug ester. More preferably, the particles comprise at least 20 percent, 30 percent, 40 percent, 50 percent, 60 percent, 70 percent, 80 percent, 90 percent, 95 percent, 97 percent, 99 percent, 99.5 percent, 99.9 percent or 99.97 percent by weight of drag ester.
- the condensation aerosol has a mass of at least 0.01 mg.
- the aerosol has a mass of at least 0.05 mg. More preferably, the aerosol has a mass of at least 0.10 mg, 0.15 mg, 0.2 g or 0.25 mg.
- the particles comprise less than 10 percent by weight of drug ester degradation products.
- the particles comprise less than 5 percent by weight of drug ester degradation products. More preferably, the particles comprise 2.5, 1, 0.5, 0.1 or 0.03 percent by weight of drug ester degradation products.
- the particles comprise less than 90 percent by weight of water.
- the particles comprise less than 80 percent by weight of water. More preferably, the particles comprise less than 70 percent, 60 percent, 50 percent, 40 percent,
- the particles of the delivered condensation aerosol have a mass median aerodynamic diameter of less than 5 microns.
- the particles have a mass median aerodynamic diameter of less than 3 microns. More preferably, the particles have a mass median aerodynamic diameter of less than 2 or 1 micron(s).
- the geometric standard deviation around the mass median aerodynamic diameter of the aerosol particles is less than 2.
- the geometric standard deviation is less than 1.9. More preferably, the geometric standard deviation is less than 1.8, 1.7, 1.6 or 1.5.
- the delivered aerosol has an inhalable aerosol drug ester mass density of between 0.1 mg/L and 100 mg/L.
- the aerosol has an inhalable aerosol drug mass density of between 0.1 mg/L and 75 mg/L. More preferably, the aerosol has an inhalable aerosol drag mass density of between 0.1 mg/L and 50 mg/L.
- the delivered aerosol has an inhalable aerosol particle density greater than 10 6 particles/mL.
- the aerosol has an inhalable aerosol particle density greater than 10 7 particles/mL or 10 8 particles/mL.
- the rate of inhalable aerosol particle formation of the delivered condensation aerosol is greater than 10 8 particles per second.
- the aerosol is formed at a rate greater than 10 9 inhalable particles per second. More preferably, the aerosol is formed at a rate greater than 10 inhalable particles per second.
- the delivered condensation aerosol is formed at a rate greater than 0.5 mg/second.
- the aerosol is formed at a rate greater than 0.75 mg/second. More preferably, the aerosol is formed at a rate greater than 1 mg/second, 1.5 mg/second or 2 mg/second.
- between 0.1 mg and 100 mg of drug ester are delivered to the mammal in a single inspiration.
- the delivered condensation aerosol results in a peak plasma concentration of drag acid or drug alcohol in the mammal in less than 1 h.
- the peak plasma concentration is reached in less than 0.5 h. More preferably, the peak plasma concentration is reached in less than 0.2, 0.1, 0.05, 0.02 or 0.01 h.
- a kit for delivering a drug ester through an inhalation route to a mammal which comprises: a) a composition comprising at least 5 percent by weight of drug ester; and, b) a device that forms a drag ester aerosol from the composition, for inhalation by the mammal.
- the composition comprises at least 20 percent, 30 percent, 40 percent, 50 percent, 60 percent, 70 percent, 80 percent, 90 percent, 95 percent, 97 percent, 99 percent, 99.5 percent, 99.9 percent or 99.97 percent by weight of drag ester.
- the drag ester has a decomposition index less than 0.15. More preferably, it has a decomposition index less than 0.10 or 0.05.
- the device contained in the kit comprises: a) an element for heating the drag ester composition to form a vapor; b) an element allowing the vapor to cool to form an aerosol; and, c) an element permitting the mammal to inhale the aerosol.
- FIG. 1 shows a cross-sectional view of a device used to deliver drug ester aerosols to a mammal through an inhalation route.
- Aerodynamic diameter of a given particle refers to the diameter of a spherical droplet with a density of 1 g/mL (the density of water) that has the same settling velocity as the given particle.
- “Aerosol” refers to a suspension of solid or liquid particles in a gas. "Aerosol drug ester mass density” refers to the mass of drug ester per unit volume of aerosol.
- Aerosol mass density refers to the mass of particulate matter per unit volume of aerosol.
- Aerosol particle density refers to the number of particles per unit volume of aerosol.
- Condensation aerosol refers to an aerosol formed by vaporization of a substance followed by condensation of the substance into an aerosol.
- Decomposition index refers to a number derived from an assay described in Example 8. The number is determined by substracting the percent purity of the generated aerosol from 1.
- Drug refers to any chemical compound that is used in the prevention, diagnosis, treatment, or cure of disease, for the relief of pain, or to control or improve any physiological or pathological disorder in humans or animals. Such compounds are oftentimes listed in the Physician's Desk Reference (Medical Economics Company, Inc. at
- Drug acid refers to a drag containing a carboxylic acid moiety.
- Drug alcohol refers to a drag containing a hydroxyl moiety.
- Drug Ester refers to a drag acid or drug alcohol, where the carboxylic acid group or hydroxyl group has been chemically modified to form an ester.
- the drag acids and alcohols from which the esters are formed come from a variety of drug classes, including, without limitation, antibiotics, anticonvulsants, antidepressants, antihistamines, antiparkinsonian drugs, drags for migraine headaches, drugs for the treatment of alcoholism, muscle relaxants, anxiolytics, nonsteroidal anti-inflammatories, other analgesics, and steroids.
- antibiotics from which drug esters are formed include cefmetazole; cefazolin; cephalexin; cefoxitin; cephacetrile; cephaloglycin; cephaloridine; cephalosporins, such as cephalosporin c; cephalotin; cephamycins, such as cephamycin a, cephamycin b, and cephamycin c; cepharin; cephradine; ampicillin; amoxicillin; hetacillin; carfecillin; carindacillin; carbenicillin; amylpenicillin; azidocillin; benzylpenicillin; clometocillin; cloxacillin; cyclacillin; methicillin; nafcillin; 2-pentenylpenicillin; penicillins, such as penicillin n, penicillin o, penicillin s, and penicillin v; chlorobutin penicillin; dicloxacillin; diphenicillin; heptylpenicillin; and met
- antidepressants from which drag esters are formed include tianeptine and S-adenosylmethionine.
- antihistamines from which drag esters are formed include fexofenadine.
- antiparkinsonian drugs from which drug esters are formed include apomorphine, baclofen, levodopa, carbidopa, and thioctate.
- anxiolytics from which drug esters are formed include chlorazepate, calcium N-carboamoylaspartate and chloral betaine.
- drags for migraine headache from which drag esters are formed include aspirin, diclofenac, naproxen, tolfenamic acid, and valproate.
- Examples of drugs for the treatment of alcoholism from which drug esters are formed include acamprosate.
- Examples of muscle relaxants from which drug esters are formed include baclofen.
- nonsteroidal anti-inflammatories from which drag esters are formed include aceclofenac, alclofenac, alminoprofen, amfenac, aspirin, benoxaprofen, bermoprofen, bromfenac, bufexamac, butibufen, bucloxate, carprofen, cinchophen, cinmetacin, clidanac, clopriac, clometacin, diclofenac, diflunisal, etodolac, fenclozate, fenoprofen, flutiazin, flurbiprofen, ibuprofen, ibufenac, indomethacin, indoprofen, ketoprofen, ketorolac, loxoprofen, meclofenamate, naproxen, oxaprozin, pirprofen, prodolic acid, salsalate, sulindac, tofen
- Examples of other analgesics from which drug esters are formed include bumadizon, clometacin, and clonixin.
- Examples of steroids from which drag esters are formed include betamethasone, chloroprednisone, clocortolone, cortisone, desonide, dexamethasone, desoximetasone, difluprednate, estradiol, fludrocortisone, flumethasone, flunisolide, fluocortolone, fluprednisolone, hydrocortisone, meprednisone, methylprednisolone, paramethasone, prednisolone, prednisone, pregnan-3-alpha-ol-20-one, testosterone, and triamcinolone.
- drag esters formed from drug acids include C ⁇ -C 6 straight chain substituted or unsubstituted alkyl esters, C ⁇ -C 6 branched chain substituted or unsubstituted alkyl esters, C 3 -C 6 substituted or unsubstituted cyclic alkyl esters, C ⁇ -C 6 substituted or unsubstituted alkenyl esters, C C 6 substituted or unsubstituted alkynyl esters, and substituted or unsubstituted aromatic esters.
- C;[-C 6 straight chain unsubstituted alkyl esters include, for example, methyl ester, ethyl ester and propyl ester.
- C ⁇ -C 6 straight chain substituted alkyl esters include, for example, 2-(dimethylamino)-ethyl ester (- CH 2 CH 2 N(CH 3 ) 2 ).
- C ⁇ -C 6 branched chain unsubstituted alkyl esters include, for example, isopropyl ester and isobutyl ester.
- C ⁇ -C 6 branched chain substituted alkyl esters include, for example, 2-(dimethylamino)-isopropyl ester (-CH(CH 3 )CH 2 N(CH 3 ) ).
- C 3 -C 6 unsubstituted cyclic alkyl esters include, for example, cyclopropyl and cyclohexyl ester.
- C 3 -C 6 substituted cyclic alkyl esters include, for example, 2-(dimethylamino)-cyclopropyl ester.
- C C 6 unsubstituted alkenyl esters include, for example, 2-butenyl ester (- CH 2 CHCHCH 3 ).
- Ci-C 6 substituted alkenyl esters include, for example, 4-
- C ⁇ -C 6 unsubstituted alkynyl esters include, for example, 2-butynyl ester (-CH 2 CCCH 3 ).
- C1-C6 substituted alkynyl esters include, for example, 4-(dimethylamino)-2-butynyl ester (-CH 2 CCCH 2 N(CH 3 ) 2 ).
- Unsubstituted aromatic esters include, for example, phenyl ester and naphthyl ester.
- Substituted aromatic esters include, for example, 4-(dimethylamino)phenyl ester.
- Examples of drug esters formed from drug alcohols include C ⁇ -C 6 substituted or unsubstituted straight chain alkanoates, Cj . -C 6 substituted or unsubstituted branched chain alkanoates, -C ⁇ substituted or unsubstituted alkenoates, and -Ce substituted or unsubstituted alkynoates.
- C C 6 unsubstituted straight chain alkanoates include, for example, methanoate (-C(O)H), ethanoate (-C(O)CH 3 ) and propanoate (-C(O)CH 2 CH 3 ).
- C ⁇ -C 6 substituted straight chain alkanoates include, for example, 2-(phenyl)-ethanoate (- C(O)CH 2 Ph).
- C -C 6 unsubstituted branched chain alkanoates include, for example, isobutanoate (-C(O)CH(CH 3 ) 2 ).
- C ⁇ -C 6 substituted branched chain alkanoates include, for example, 3-(phenyl)-isobutanoate (-C(O)CH(CH 3 )CH 2 Ph).
- C C 6 unsubstituted alkenoates include, for example, 2-butenoate (-C(O)CHCHCH 3 ).
- C C ⁇ substituted alkenoates include, for example, 4-(phenyl)-2-butenoate (-C(O)CHCHCH 2 Ph).
- C ⁇ . -C 6 unsubstituted alkynoates include, for example, 2-butynoate (-C(O)CCCH 3 ).
- C C ⁇ substituted alkynoates include, for example, 4-(phenyl)-2-butynoate.
- Drug ester degradation product refers to a compound resulting from a chemical modification of the drag ester.
- the modification for example, can be the result of a thermally or photochemically induced reaction. Such reactions include, without limitation, oxidation and hydrolysis.
- Inhalable aerosol drug ester mass density refers to the aerosol drug ester mass density produced by an inhalation device and delivered into a typical patient tidal volume.
- “Inhalable aerosol mass density” refers to the aerosol mass density produced by an inhalation device and delivered into a typical patient tidal volume.
- “Inhalable aerosol particle density” refers to the aerosol particle density of particles of size between 100 nm and 5 microns produced by an inhalation device and delivered into a typical patient tidal volume.
- Mass median aerodynamic diameter or “MMAD” of an aerosol refers to the aerodynamic diameter for which half the particulate mass of the aerosol is contributed by particles with an aerodynamic diameter larger than the MMAD and half by particles with an aerodynamic diameter smaller than the MMAD.
- Necholine ester refers to an ester where the portion attached to the ester oxygen is -CH 2 CH 2 N(CH 3 ) 2 .
- Rate of aerosol formation refers to the mass of aerosolized particulate matter produced by an inhalation device per unit time.
- Rate of inhalable aerosol particle formation refers to the number of particles of size between 100 nm and 5 microns produced by an inhalation device per unit time.
- Rate of drug ester aerosol formation refers to the mass of aerosolized, drug ester produced by an inhalation device per unit time.
- Settling velocity refers to the terminal velocity of an aerosol particle undergoing gravitational settling in air.
- Substituted alkyl, alkenyl, alkynyl or aryl refers to the replacement of one or more hydrogen atoms on the moiety (e.g., alkyl) with another group.
- groups include, without limitation, the following: halo, amino, alkylamino, dialkylamino, hydroxyl, cyano, nitro and phenyl.
- Typical patient tidal volume refers to 1 L for an adult patient and 15 mL/kg for a pediatric patient.
- “Vapor” refers to a gas
- vapor phase refers to a gas phase.
- thermal vapor refers to a vapor phase, aerosol, or mixture of aerosol- vapor phases, formed preferably by heating. Formation of Drag Esters from Drag Acids or Drug Alcohols
- Formation of drag esters from drug acids is typically accomplished by reacting the acid, or an activated derivative (e.g., acid chloride or mixed anhydride) with an appropriate alcohol under conditions well known to those of skill in the art. See, for example, Streitweiser, A., Jr. and Heathcock, C. H. (1981) Introduction to Organic Chemistry,
- any suitable method is used to form the aerosols of the present invention.
- a preferred method involves heating a composition comprising a drug ester to form a vapor, followed by cooling of the vapor such that it condenses to provide a drag ester comprising aerosol (condensation aerosol).
- the composition is heated in one of two forms: as pure active compound (i.e., pure drag ester); or, as a mixture of active compound and a pharmaceutically acceptable excipient.
- compositions may be volatile or nonvolatile. Volatile excipients, when heated, are concurrently volatilized, aerosolized and inhaled with drug ester. Classes of such excipients are known in the art and include, without limitation, gaseous, supercritical fluid, liquid and solid solvents. The following is a list of exemplary carriers within the classes: water; terpenes, such as menthol; alcohols, such as ethanol, propylene glycol, glycerol and other similar alcohols; dimethylformamide; dimethylacetamide; wax; supercritical carbon dioxide; dry ice; and mixtures thereof. Solid supports on which the composition is heated are of a variety of shapes.
- Such shapes include, without limitation, cylinders of less than 1.0 mm in diameter, boxes of less than 1.0 mm thickness and virtually any shape permeated by small (e.g., less than 1.0 mm-sized) pores.
- solid supports provide a large surface to volume ratio (e.g., greater than 100 per meter) and a large surface to mass ratio (e.g., greater than 1 cm per gram).
- a solid support of one shape can also be transformed into another shape with different properties. For example, a flat sheet of 0.25 mm thickness has a surface to volume ratio of approximately 8,000 per meter. Rolling the sheet into a hollow cylinder of 1 cm diameter produces a support that retains the high surface to mass ratio of the original sheet but has a lower surface to volume ratio (about 400 per meter).
- a number of different materials are used to construct the solid supports. Classes of such materials include, without limitation, metals, inorganic materials, carbonaceous materials and polymers. The following are examples of the material classes: aluminum, silver, gold, stainless steel, copper and tungsten; silica, glass, silicon and alumina; graphite, porous carbons, carbon yarns and carbon felts; polytetrafluoroethylene and polyethylene glycol. Combinations of materials and coated variants of materials are used as well.
- aluminum foil is a suitable material.
- silica, alumina and silicon based materials include amphorous silica S-5631
- the heating of the drag ester compositions is performed using any suitable method.
- methods by which heat can be generated include the following: passage of current through an electrical resistance element; absorption of electromagnetic radiation, such as microwave or laser light; and, exothermic chemical reactions, such as exothermic solvation, hydration of pyrophoric materials and oxidation of combustible materials.
- Drag ester containing aerosols of the present invention are delivered to a mammal using an inhalation device.
- the aerosol is a condensation aerosol
- the device has at least three elements: an element for heating a drag ester containing composition to form a vapor; an element allowing the vapor to cool, thereby providing a condensation aerosol; and, an element permitting the mammal to inhale the aerosol.
- Various suitable heating methods are described above.
- the element that allows cooling is, in it simplest form, an inert passageway linking the heating means to the inhalation means.
- the element permitting inhalation is an aerosol exit portal that forms a connection between the cooling element and the mammal's respiratory system.
- Delivery device 100 has a proximal end 102 and a distal end 104, a heating module 106, a power source 108, and a mouthpiece 110.
- a drag ester composition is deposited on a surface 112 of heating module 106.
- power source 108 initiates heating of heating module 106 (e.g, through ignition of combustible fuel or passage of current through a resistive heating element).
- the drag ester composition volatilizes due to the heating of heating module 106 and condenses to form a condensation aerosol prior to reaching the mouthpiece 110 at the proximal end of the device 102.
- Air flow traveling from the device distal end 104 to the mouthpiece 110 carries the condensation aerosol to the mouthpiece 110, where it is inhaled by the mammal.
- Devices if desired, contain a variety of components to facilitate the delivery of drag ester containing aerosols.
- the device may include any component known in the art to control the timing of drag aerosolization relative to inhalation (e.g., breath- actuation), to provide feedback to patients on the rate and/or volume of inhalation, to prevent excessive use (i.e., "lock-out” feature), to prevent use by unauthorized individuals, and/or to record dosing histories.
- the ester moiety is typically hydrolyzed to provide the corresponding drag acid or drag alcohol, which produces a desired therapeutic effect.
- hydrolysis is chemically mediated.
- hydrolysis is enzymatically mediated through the action of enzymes endogenous to the animal.
- a typical dosage of a drag ester aerosol is either administered as a single inhalation or as a series of inhalations taken within an hour or less (dosage equals sum of inhaled amounts). Where the drag ester is administered as a series of inhalations, a different amount may be delivered in each inhalation.
- the dosage amount of drug ester in aerosol form is generally no greater than twice the standard dose of the drag acid or drug alcohol given orally.
- I/II clinical trial.
- One animal experiment involves measuring plasma concentrations of drug acid or drug alcohol in an animal after its exposure to the aerosol. Mammals such as dogs or primates are typically used in such studies, since their respiratory systems are similar to that of a human.
- Initial dose levels for testing in humans is generally less than or equal to the dose in the mammal model that resulted in plasma drug levels associated with a therapeutic effect in humans. Dose escalation in humans is then performed, until either an optimal therapeutic response is obtained or a dose-limiting toxicity is encountered.
- Purity of a drug ester containing aerosol is determined using a number of methods, examples of which are described in Sekine et al, Journal of Forensic Science 32:1271- 1280 (1987) and Martin et al, Journal of Analytic Toxicology 13:158-162 (1989).
- One method involves forming the aerosol in a device through which a gas flow (e.g., air flow) is maintained, generally at a rate between 0.4 and 60 L/min.
- the gas flow carries the aerosol into one or more traps.
- the aerosol is subjected to an analytical technique, such as gas or liquid chromatography, that permits a determination of composition purity.
- a variety of different traps are used for aerosol collection.
- the following list contains examples of such traps: filters; glass wool; impingers; solvent traps, such as dry ice-cooled ethanol, methanol, acetone and dichloromethane traps at various pH values; syringes that sample the aerosol; empty, low-pressure (e.g., vacuum) containers into which the aerosol is drawn; and, empty containers that fully surround and enclose the aerosol generating device.
- a solid such as glass wool
- it is typically extracted with a solvent such as ethanol.
- the solvent extract is subjected to analysis rather than the solid (i.e., glass wool) itself.
- the container is similarly extracted with a solvent.
- the gas or liquid chromatograph discussed above contains a detection system (i. e. , detector).
- detection systems are well known in the art and include, for example, flame ionization, photon absorption and mass spectrometry detectors.
- An advantage of a mass spectrometry detector is that it can be used to determine the structure of drug ester degradation products. Particle size distribution of a drug ester containing aerosol is determined using any suitable method in the art (e.g., cascade impaction).
- An Andersen Eight Stage Non- viable Cascade Impactor (Andersen Instruments, Smyrna, GA) linked to a furnace tube by a mock throat (USP throat, Andersen Instruments, Smyrna, GA) is one system used for cascade impaction studies.
- Inhalable aerosol mass density is determined, for example, by delivering a drag- containing aerosol into a confined chamber via an inhalation device and measuring the mass collected in the chamber.
- the aerosol is drawn into the chamber by having a pressure gradient between the device and the chamber, wherein the chamber is at lower pressure than the device.
- the volume of the chamber should approximate the tidal volume of an inhaling patient.
- Inhalable aerosol drag ester mass density is determined, for example, by delivering a drug ester-containing aerosol into a confined chamber via an inhalation device and measuring the amount of non-degraded drag ester collected in the chamber.
- the aerosol is drawn into the chamber by having a pressure gradient between the device and the chamber, wherein the chamber is at lower pressure than the device.
- the volume of the chamber should approximate the tidal volume of an inhaling patient.
- the amount of non- degraded drag ester collected in the chamber is determined by extracting the chamber, conducting chromatographic analysis of the extract and comparing the results of the chromatographic analysis to those of a standard containing known amounts of drug ester.
- Inhalable aerosol particle density is determined, for example, by delivering aerosol phase drug ester into a confined chamber via an inhalation device and measuring the number of particles of given size collected in the chamber.
- the number of particles of a given size may be directly measured based on the light-scattering properties of the particles.
- Number of particles in a given size range Mass in the size range/Mass of a typical particle in the size range.
- Mass of a typical particle in a given size range ⁇ *D 3 * ⁇ /6, where D is a typical particle diameter in the size range (generally, the mean boundary MMADs defining the size range) in microns, ⁇ is the particle density (in g/mL) and mass is given in units of picograms (g "12 ).
- Rate of inhalable aerosol particle formation is determined, for example, by delivering aerosol phase drag ester into a confined chamber via an inhalation device. The delivery is for a set period of time (e.g., 3 s), and the number of particles of a given size collected in the chamber is determined as outlined above. The rate of particle formation is equal to the number of 100 nm to 5 micron particles collected divided by the duration of the collection time.
- Rate of aerosol formation is determined, for example, by delivering aerosol phase drug ester into a confined chamber via an inhalation device.
- the delivery is for a set period of time (e.g., 3 s), and the mass of particulate matter collected is determined by weighing the confined chamber before and after the delivery of the particulate matter.
- the rate of aerosol formation is equal to the increase in mass in the chamber divided by the duration of the collection time.
- the mass of particulate matter may be equated with the mass lost from the device or component during the delivery of the aerosol.
- the rate of aerosol formation is equal to the decrease in mass of the device or component during the delivery event divided by the duration of the delivery event.
- Rate of drag ester aerosol formation is determined, for example, by delivering a drug ester containing aerosol into a confined chamber via an inhalation device over a set period of time (e.g., 3 s). Where the aerosol is pure drug ester, the amount of drag collected in the chamber is measured as described above. The rate of drug ester aerosol formation is equal to the amount of drag ester aerosol collected in the chamber divided by the duration of the collection time. Where the drug ester containing aerosol comprises a pharmaceutically acceptable excipient, multiplying the rate of aerosol formation by the percentage of drug ester in the aerosol provides the rate of drug aerosol formation.
- the drag ester containing aerosols of the present invention are typically used for the same indication as the corresponding drag acid or drag alcohol.
- a drag ester of baclofen would be used to treat parkinsons disease and a drag ester of fexofenadine would be used to treat allergy symptoms.
- Drug acids or drug alcohols are typically commercially available from Simga
- the reaction mixture is diluted with 60 mL dichloromethane and subjected to a series of washings: 50 mL saturated aqueous NaCl followed by 50 mL saturated aqueous NaHCO 3 and 2X 50 mL saturated aqueous NaCl.
- the dichloromethane extract is dried over Na 2 SO 4 , filtered, and concentrated on a rotary evaporator to provide the desired drug ester.
- Apomo ⁇ hine ⁇ CF/ ⁇ O 300 mg was suspended in 600 ⁇ L of acetic acid. The suspension was heated to 100 °C and then cooled to 50 °C. Acetyl chloride (1 mL) was added to the suspension, which was heated at 40 °C for 3 h. The reaction mixture was allowed to cool to room temperature. Dichloromethane (1-2 mL) was added and the mixture was allowed to stir overnight. The reaction mixture was diluted with dichloromethane, and the solvent was removed on a rotary evaporator. Toluene (10 mL) was added to the residue and subsequently removed on a rotary evaporator. The toluene addition/removal was repeated. The resulting solid residue was triturated with ether, providing 430 mg of a solid (mp 158-160 °C).
- Ketorolac 255 mg
- triethylamine 101 mg
- 2-(dimethylamino)ethanol HOCH 2 CH 2 N(CH 3 ) 2 , 380 mg
- BOP 464 mg
- the reaction mixture was gradually allowed to warm to room temperature. See Kim, M. H. and Patel, D. V. (1994) Tet. Lett. 35: 5603-5606.
- the reaction mixture was diluted with 60 mL of dichloromethane and washed sequentially with saturated aqueous NaCl, saturated aquesous NaHCO 3 and then saturated aqueous NaCl.
- the dichloromethane extract was dried over Na SO 4 , filtered, and concentrated on a rotary evaporator to provide 390 mg of the desired material.
- a solution of drug in approximatelyl20 ⁇ L dichloromethane is coated on a 3.5 cm x 7.5 cm piece of aluminum foil (precleaned with acetone). The dichloromethane is allowed to evaporate. The coated foil is wrapped around a 300 watt halogen tube (Feit Electric Company, Pico Rivera, CA), which is inserted into a glass tube sealed at one end with a rubber stopper. Running 60 V of alternating current (driven by line power controlled by a variac) through the bulb for 5-12 s or 90 V for 2.5-3.5 s affords thermal vapor (including aerosol), which is collected on the glass tube walls. (When desired, the system is flushed through with argon prior to volatilization.) Reverse-phase HPLC analysis with detection by absorption of 225 nm light is used to determine the purity of the aerosol.
- Table 1 which follows, provides data from drags volatilized using the above- recited general procedure.
- Drag ester (20 ⁇ L, 10 mM acetonitrile) is added to 1 mL PBS solution (pH 7.5) at room temperature. At intermittent time points, an aliquot of the resulting mixture is injected into an HPLC to obtain the ratio of drag ester to drug acid or drug alcohol. An Arrhenius plot of the data provides a ty 2 for hydrolysis. Table 2 below provides t /2 values for a variety of compounds.
- Human serum (2.34 mL) is placed in a test tube. To the serum is added 260 ⁇ L of a
- Drug ester (1 mg) is dissolved or suspended in a minimal amount of a suitable solvent (e.g. , dichloromethane or methanol).
- a suitable solvent e.g. , dichloromethane or methanol.
- the solution or suspension is pipeted onto the middle portion of a 3 cm by 3 cm piece of aluminum foil.
- the coated foil is wrapped around the end of a 1 Vz cm diameter vial and secured with parafilm.
- a hot plate is preheated to approximately 300 °C, and the vial is placed on it foil side down.
- the vial is left on the hotplate for 10 s after volatilization or decomposition has begun. After removal from the hotplate, the vial is allowed to cool to room temperature.
- the foil is removed, and the vial is extracted with dichloromethane followed by saturated aqueous NaHCO 3 .
- the organic and aqueous extracts are shaken together, separated, and the organic extract is dried over Na SO 4 .
- An aliquot of the organic solution is removed and injected into a reverse- phase HPLC with detection by absorption of 225 nm light.
- a drug ester is preferred for aerosolization where the purity of the drag ester aerosol isolated by this method is greater than 85%.
- Such a drag ester has a decomposition index less than 0.15. The decomposition index is arrived at by substracting the percent purity (i.e., 0.85) from 1.
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PCT/US2002/018543 WO2003026631A1 (en) | 2001-05-24 | 2002-05-13 | Delivery of drug esters through an inhalation route |
JP2003530268A JP2005503425A (en) | 2001-05-24 | 2002-05-13 | Delivery of drug ester by the prescribed inhalation route |
EP02741994A EP1392262A1 (en) | 2001-05-24 | 2002-05-13 | Delivery of drug esters through an inhalation route |
CA002446904A CA2446904A1 (en) | 2001-05-24 | 2002-05-13 | Delivery of drug esters through an inhalation route |
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US29420301P | 2001-05-24 | 2001-05-24 | |
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US31747901P | 2001-09-05 | 2001-09-05 | |
US60/317,479 | 2001-09-05 | ||
PCT/US2002/018543 WO2003026631A1 (en) | 2001-05-24 | 2002-05-13 | Delivery of drug esters through an inhalation route |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003094900A1 (en) * | 2002-05-13 | 2003-11-20 | Alexza Molecular Delivery Corporation | Delivery of drug amines through an inhalation route |
WO2004089374A1 (en) * | 2003-04-14 | 2004-10-21 | Vectura Ltd | Pharmaceutical compositions comprising apomorphine for pulmonary inhalation |
WO2005025559A1 (en) * | 2003-09-12 | 2005-03-24 | Agi Therapeutics Ltd. | Treatment of gastroparesis and nonulcer dyspepsia with gabab agonists |
US8642631B2 (en) | 2008-05-27 | 2014-02-04 | University Of Melbourne | Methods of treating mammals with eustachian tube dysfunctions |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0039369A1 (en) * | 1980-05-02 | 1981-11-11 | Schering Corporation | Beclomethasone ester solvates, process for their preparation, and preparation of a formulation |
US5112598A (en) * | 1988-05-04 | 1992-05-12 | Hermes Fabrik Pharmazeutischer Preparate Franz Gradinger Gmbh & Co. Kg | Vitamin a aerosol-inhalate preparations |
US5126123A (en) * | 1990-06-28 | 1992-06-30 | Glaxo, Inc. | Aerosol drug formulations |
US5607691A (en) * | 1992-06-12 | 1997-03-04 | Affymax Technologies N.V. | Compositions and methods for enhanced drug delivery |
WO2000028979A1 (en) * | 1998-11-13 | 2000-05-25 | Jago Research Ag | Dry powder for inhalation |
-
2002
- 2002-05-13 WO PCT/US2002/018543 patent/WO2003026631A1/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0039369A1 (en) * | 1980-05-02 | 1981-11-11 | Schering Corporation | Beclomethasone ester solvates, process for their preparation, and preparation of a formulation |
US5112598A (en) * | 1988-05-04 | 1992-05-12 | Hermes Fabrik Pharmazeutischer Preparate Franz Gradinger Gmbh & Co. Kg | Vitamin a aerosol-inhalate preparations |
US5126123A (en) * | 1990-06-28 | 1992-06-30 | Glaxo, Inc. | Aerosol drug formulations |
US5607691A (en) * | 1992-06-12 | 1997-03-04 | Affymax Technologies N.V. | Compositions and methods for enhanced drug delivery |
WO2000028979A1 (en) * | 1998-11-13 | 2000-05-25 | Jago Research Ag | Dry powder for inhalation |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003094900A1 (en) * | 2002-05-13 | 2003-11-20 | Alexza Molecular Delivery Corporation | Delivery of drug amines through an inhalation route |
WO2004089374A1 (en) * | 2003-04-14 | 2004-10-21 | Vectura Ltd | Pharmaceutical compositions comprising apomorphine for pulmonary inhalation |
JP2006522785A (en) * | 2003-04-14 | 2006-10-05 | ベクトゥラ・リミテッド | Pharmaceutical composition for pulmonary inhalation comprising apomorphine |
WO2005025559A1 (en) * | 2003-09-12 | 2005-03-24 | Agi Therapeutics Ltd. | Treatment of gastroparesis and nonulcer dyspepsia with gabab agonists |
US8642631B2 (en) | 2008-05-27 | 2014-02-04 | University Of Melbourne | Methods of treating mammals with eustachian tube dysfunctions |
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