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公开(公告)号:NZ526608A
公开(公告)日:2006-06-30
申请号:NZ52660801
申请日:2001-12-20
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , DOTY MARK J , REBBECK CHRISTINE L , BRYNJELSEN SEAN , WERLING JANE , SRIRAM RAJARAM
IPC: C07D407/14 , A61K9/10 , A61K9/14 , A61K9/16 , A61K31/495 , A61K31/496 , A61K47/12 , A61K47/14 , A61K47/18 , A61K47/20 , A61K47/24 , A61K47/28 , A61K47/34 , A61K47/36 , A61K47/38 , A61K47/42 , A61P31/10 , A61K9/20 , A61K9/51
Abstract: A method for preparing submicron sized particles of a pharmaceutically-active compound, the solubility of which is greater in a water-miscible first solvent than in a second solvent which is aqueous is disclosed, wherein the process comprises the steps of: (i) dissolving the pharmaceutically-active compound in the water-miscible first solvent to form a solution, the first solvent being selected from the group consisting of N methyl-2-pyrrolidinone, 2-pyrrolidone, dimethyl sulfoxide, dimethylacetamide, lactic acid, methanol, ethanol, isopropanol, 3-pentanol, n-propanol, glycerol, butylene glycol, ethylene glycol, polypropylene glycol, mono- and diacylated monoglycerides, dimethyl isosorbide, acetone, dimethylformamide, 1,4-dioxane, ethyl acetate, propyl acetate, polyethylene glycol, polyethylene glycol esters, polyethylene glycol sorbitans, polyethylene glycol monoalkyl ethers, polypolypropylene glycol, polypropylene alginate, polypolypropylene glycol-10 butanediol, polypolypropylene glycol-10 methyl glucose ether, polypolypropylene glycol-20 methyl glucose ether, polypolypropylene glycol-15 stearyl ether, polypolypropylene glycol dicaprylate, polypropylene glycol dicaprate, polypropylene glycol laurate; (ii) mixing the solution with the second solvent to define a pre-suspension; and (iii) adding energy to the pre-suspension to form particles having an average effective particle size of less than about 2 micron, and said adding energy step comprises homogenization, counter-current flow homogenization, microfluidization or sonication.
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公开(公告)号:HK1079704A1
公开(公告)日:2006-04-13
申请号:HK05112084
申请日:2005-12-29
Applicant: BAXTER INT
Inventor: WONG JOSEPH CHUNG TAK , KIPP JAMES E , DOTY MARK J , REBBECK CHRISTINE L , PAPADOPOULOS PAVLOS
IPC: A61K20060101 , A61K9/10 , A61K9/14 , A61K9/16 , A61K9/50 , A61K31/495 , A61K31/496
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公开(公告)号:NO20054908L
公开(公告)日:2005-12-21
申请号:NO20054908
申请日:2005-10-24
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , WISLER MONTE , GARCIA RHONDA
Abstract: Methods and apparatuses for comminuting and stabilizing small particles are provided. In one embodiment, an apparatus moves an organic compound dissolved in a solvent to form a suspension of particles in a first fluid stream and moves the suspension in a second fluid stream, wherein the second fluid stream is oriented and positioned with respect to the first stream to cause shearing between the streams and mixing of at least some of the particles in the first and second streams.
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公开(公告)号:NO20055616D0
公开(公告)日:2005-11-28
申请号:NO20055616
申请日:2005-11-28
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , DOTY MARK J , REBBECK CHRISTINE L , SUN CHONG-SON , PAPADOPOULOS PAVLOS , RABINOW BARRETT E , WHITE RANDY
IPC: A61K9/50 , A61K9/51 , A61K31/496 , A61K
Abstract: The present invention relates to compositions of submicron- to micron-size particles of antimicrobial agents. More particularly the invention relates to a composition of an antimicrobial agent that renders the agent potent against organisms normally considered to be resistant to the agent. The composition comprises an aqueous suspension of submicron-tomicron-size particles containing the agent coated with at least one surfactant selected from the group consisting of: ionic surfactants, non-ionic surfactants, biologically derived surfactants, and amino acids and their derivatives. The particles have a volume-weighted mean particle size of less than 5 µm as measured by laser diffractonetry.
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公开(公告)号:NO20054908D0
公开(公告)日:2005-10-24
申请号:NO20054908
申请日:2005-10-24
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , WISLER MONTE , GARCIA RHONDA
Abstract: Methods and apparatuses for comminuting and stabilizing small particles are provided. In one embodiment, an apparatus moves an organic compound dissolved in a solvent to form a suspension of particles in a first fluid stream and moves the suspension in a second fluid stream, wherein the second fluid stream is oriented and positioned with respect to the first stream to cause shearing between the streams and mixing of at least some of the particles in the first and second streams.
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公开(公告)号:NO20052285D0
公开(公告)日:2005-05-10
申请号:NO20052285
申请日:2005-05-10
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , DOTY MARK J , REBBECK CHRISTINE L , PAPADOPOULOS PAVLOS
IPC: A61K9/10 , A61K9/14 , A61K9/16 , A61K9/50 , A61K31/495 , A61K31/496 , A61K
Abstract: The present invention relates to compositions of submicron-to micron-size particles of antifungal agents. More particularly the invention relates to aqueous suspensions of antifungal agents for pharmaceutical use.
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公开(公告)号:CA2523151A1
公开(公告)日:2004-11-11
申请号:CA2523151
申请日:2004-04-29
Applicant: BAXTER INT
Inventor: RABINOW BARRETT E , WHITE RANDY , PAPADOPOULOS PAVLOS , REBBECK CHRISTINE L , SUN CHONG-SON , KIPP JAMES E , WONG JOSEPH CHUNG TAK , DOTY MARK J
IPC: A61K9/50 , A61K9/51 , A61K31/496 , A61K9/14
Abstract: The present invention relates to compositions of submicron- to micron-size particles of antimicrobial agents. More particularly the invention relates t o a composition of an antimicrobial agent that renders the agent potent agains t organisms normally considered to be resistant to the agent. The composition comprises an aqueous suspension of submicron-tomicron-size particles containing the agent coated with at least one surfactant selected from the group consisting of: ionic surfactants, non-ionic surfactants, biologically derived surfactants, and amino acids and their derivatives. The particles ha ve a volume-weighted mean particle size of less than 5 ~m as measured by laser diffractonetry.
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公开(公告)号:BR0212833A
公开(公告)日:2004-10-13
申请号:BR0212833
申请日:2002-09-25
Applicant: BAXTER INT
Inventor: BRYNJELSEN SEAN , STERNBERG SHMUEL , DUNHAM ANDREW J , DOTY MARK J , KIPP JAMES E , JAYSWAL NAILESH , NARAYANAN KRISHNASWAMY
IPC: A61K9/14 , A61K9/19 , A61K9/51 , A61K31/496 , A61K45/00 , A61K47/10 , A61K47/12 , A61K47/14 , A61K47/18 , A61K47/20 , A61K47/24 , A61K47/28 , A61K47/32 , A61K47/34 , A61K47/36 , A61K47/38 , A61K47/42 , B01J13/04
Abstract: The present invention relates to a process for preparing submicron sized nanoparticles of a poorly water soluble compound by lyophilizing a dispersion or microdispersion of a multiphase system having an organic phase and an aqueous phase, the organic phase having the poorly water soluble organic compound therein. The method is preferably used to prepare nanoparticles of a poorly water soluble, pharmaceutically active compound suitable for in vivo delivery, particularly by parenteral routes.
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公开(公告)号:ZA200304742B
公开(公告)日:2004-08-24
申请号:ZA200304742
申请日:2003-06-19
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WONG JOSEPH CHUNG TAK , DOTY MARK J , REBBECK CHRISTINE L , BRYNJELSEN SEAN , WERLING JANE , SPIRAM RAJARAM
IPC: A61K20060101 , A61K9/10 , A61K9/14 , A61K9/16 , A61K31/495 , A61K31/496 , A61K
Abstract: The present invention provides a method for preparing submicron sized particles of an organic compound, the solubility of which is greater in a water-miscible first solvent than in a second solvent which is aqueous, the process including the steps of: (i) dissolving the organic compound in the water-miscible first solvent to form a solution, (ii) mixing the solution with the second solvent to define a pre-suspension; and (iii) adding energy to the pre-suspension to form particles having an average effective particle size of 400 nm to 2 microns.
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50.
公开(公告)号:CA2498043A1
公开(公告)日:2004-07-01
申请号:CA2498043
申请日:2003-08-04
Applicant: BAXTER INT
Inventor: KIPP JAMES E , WERLING JANE , DOTY MARK J , SRIRAM RAJARAM , WONG JOSEPH CHUNG TAK , REBBECK CHRISTINE L
IPC: A61K9/00 , A61K31/495 , A61K9/127 , A61K9/14
Abstract: The present invention provides a method of preparing particles with polymorp h and size control of a pharmaceutical compound, the method including the step s of: (1) providing pharmaceutical compound in a first phase; (2) seeding the compound; (3) causing a phase change in the pharmaceutical compound to a second phase of a desired polymorphic form; and (4) wherein the mean particl e size of the particles is less than 7~m. The present invention further provid es a polymorphic form of itraconazole.
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