专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明申请

US20050202094A1 Nanosuspensions of anti-retroviral agents for increased central nervous system delivery 审中-公开
标题翻译：用于增加中枢神经系统递送的抗逆转录病毒剂的纳米悬浮液
公开(公告)号：US20050202094A1
公开(公告)日：2005-09-15
申请号：US11040910
申请日：2005-01-21
申请人： Jane Werling , Mahesh Chaubal , James Kipp , Barrett Rabinow
发明人： Jane Werling , Mahesh Chaubal , James Kipp , Barrett Rabinow
IPC分类号： A61K9/10 , A61K9/14 , A61K9/51 , A61K31/00 , A61K31/551 , A61K31/7072 , A61K31/7076
CPC分类号： A61K9/10 , A61K9/5123 , A61K31/00 , A61K31/551 , A61K31/7072 , A61K31/7076
摘要： The present invention provides compositions comprising dispersions of anti-retroviral agents and methods of manufacture. The nanosuspensions are made by the process of microprecipitation and energy addition. Preferably, the nanosuspensions are made by the tandem process of microprecipitation-homogenization.
摘要翻译：本发明提供了包含抗逆转录病毒剂分散体和制造方法的组合物。纳米悬浮液是通过微量沉淀和能量添加的过程制成的。优选地，通过微沉淀均质化的串联方法制备纳米悬浮液。

2. 发明申请

US20050048126A1 Formulation to render an antimicrobial drug potent against organisms normally considered to be resistant to the drug 审中-公开
标题翻译：制备抗微生物药物，对抗通常被认为对药物有抗性的生物有效
公开(公告)号：US20050048126A1
公开(公告)日：2005-03-03
申请号：US10834541
申请日：2004-04-29
申请人： Barrett Rabinow , Randy White , Chong-Son Sun , Joseph Chung Wong , James Kipp , Mark Doty , Christine Rebbeck , Pavlos Papadopoulos
发明人： Barrett Rabinow , Randy White , Chong-Son Sun , Joseph Chung Wong , James Kipp , Mark Doty , Christine Rebbeck , Pavlos Papadopoulos
IPC分类号： A61K9/10 , A61K9/14 , A61K9/16 , A61K9/50 , A61K9/51 , A61K31/495 , A61K31/496 , A61K31/4196
CPC分类号： A61K9/10 , A61K9/14 , A61K9/145 , A61K9/146 , A61K9/1688 , A61K9/5015 , A61K9/5031 , A61K9/5036 , A61K9/5042 , A61K9/5123 , A61K9/5138 , A61K9/5146 , A61K9/5192 , A61K31/495 , A61K31/496
摘要： 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- to micron-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 diffractometry.
摘要翻译：本发明涉及抗微生物剂亚微米级微粒的组合物。更具体地，本发明涉及一种抗微生物剂的组合物，其使得该试剂对通常被认为对该试剂具有抗性的生物有效。该组合物包含亚微米级至微米级颗粒的含水悬浮液，其含有涂覆有选自以下的至少一种表面活性剂：离子表面活性剂，非离子表面活性剂，生物衍生的表面活性剂，以及氨基酸及其衍生物。通过激光衍射测量，颗粒的体积加权平均粒度小于5um。

3. 发明申请

US20050048002A1 Method for delivering drugs to the brain 有权
标题翻译：向大脑输送药物的方法
公开(公告)号：US20050048002A1
公开(公告)日：2005-03-03
申请号：US10868680
申请日：2004-06-15
申请人： Barrett Rabinow , James Kipp , Howard Gendelman
发明人： Barrett Rabinow , James Kipp , Howard Gendelman
IPC分类号： A61K9/00 , A61K9/51 , A61K47/48 , A61L9/04 , A61K9/14
CPC分类号： A61K9/00 , A61K9/0085 , A61K9/5123 , A61K9/5146 , A61K47/6901
摘要： The present invention is concerned with delivering a pharmaceutical composition to the brain of a mammalian subject for treating brain diseases or disorders. The process includes the steps of: (i) providing a dispersion of the pharmaceutical composition as particles having an average particle size of from about 150 nm to about 100 microns, and (ii) administering the dispersion to the mammalian subject for delivery to the brain of a portion of the pharmaceutical composition by cells capable of reaching the brain. The dispersion of the pharmaceutical composition as particles, for example, can be phagocytised or adsorbed by the cells prior or subsequent to administration into the mammalian subject. The dispersion of the pharmaceutical composition can be administered to the central nervous system or the vascular system. After administration, the loaded cells transport the pharmaceutical composition as particles into the brain.
摘要翻译：本发明涉及向哺乳动物受试者的脑中递送药物组合物以治疗脑部疾病或病症。该方法包括以下步骤：（i）提供药物组合物的分散体作为平均粒度为约150nm至约100微米的颗粒，和（ii）向哺乳动物受试者施用分散体以递送至脑的药物组合物的一部分能够到达脑的细胞。例如，作为颗粒的药物组合物的分散体可以在给予哺乳动物受试者之前或之后被细胞吞噬或吸附。药物组合物的分散体可以施用于中枢神经系统或血管系统。给药后，负载的细胞将药物组合物作为颗粒输送到脑中。

4. 发明申请

US20060134150A1 Submicron suspensions with polymorph control 审中-公开
标题翻译：具有多态性控制的亚微米悬浮液
公开(公告)号：US20060134150A1
公开(公告)日：2006-06-22
申请号：US11283397
申请日：2006-02-27
申请人： Jane Werling , James Kipp , Rajaram Sriram , Mark Doty
发明人： Jane Werling , James Kipp , Rajaram Sriram , Mark Doty
IPC分类号： A61K9/00
CPC分类号： A61K9/10 , A61K9/14 , A61K9/145 , A61K9/146 , A61K9/1688 , A61K31/495 , A61K31/496
摘要： The present invention provides a method for preparing a suspension of a pharmaceutically active compound, the solubility of which is greater in a water miscible first organic solvent than in a second solvent which is aqueous, The process includes the steps of: (i) dissolving a first quantity of the pharmaceutically active compound in the water miscible first organic solvent to form a first solution; (ii) mixing the first solution with the second solvent to precipitate the pharmaceutically active compound; and (iii) seeding the first solution or the second solvent or the presuspension.
摘要翻译：本发明提供了一种制备药物活性化合物的悬浮液的方法，所述药物活性化合物的溶解度在与水相混溶的第一有机溶剂中大于在水溶液中的溶解度。该方法包括以下步骤：（i）将第一量的药物活性化合物在水混溶的第一有机溶剂中以形成第一溶液; （ii）将第一溶液与第二溶剂混合以沉淀药物活性化合物; 和（iii）接种第一溶液或第二溶剂或预悬浮液。

5. 发明申请

US20050170002A1 Method for preparing submicron particle suspensions 审中-公开
公开(公告)号：US20050170002A1
公开(公告)日：2005-08-04
申请号：US11052276
申请日：2005-02-07
申请人： James Kipp , Joseph Tak Wong , Mark Doty , Jane Werling , Christine Rebbeck , Sean Brynjelsen
发明人： James Kipp , Joseph Tak Wong , Mark Doty , Jane Werling , Christine Rebbeck , Sean Brynjelsen
IPC分类号： A61K9/10 , A61K9/14 , A61K9/16 , A61K31/495 , A61K31/496 , A61K7/32
CPC分类号： A61K9/10 , A61K9/14 , A61K9/145 , A61K9/146 , A61K9/1688 , A61K31/495 , A61K31/496
摘要： The present invention provides a method for preparing a suspension of a pharmaceutically-active compound, the solubility of which is greater in a water-miscible first organic solvent than in a second solvent which is aqueous. The process includes the steps of: (i) dissolving a first quantity of the pharmaceutically-active compound in the water-miscible first organic solvent to form a first solution; (ii) mixing the first solution with the second solvent to precipitate the pharmaceutically-active compound; and (iii) seeding the first solution or the second solvent or the pre-suspension.

6. 发明申请

US20070134341A1 COMPOSITIONS OF LIPOXYGENASE INHIBITORS 审中-公开
标题翻译： LIPOXYGENASE抑制剂的组合物
公开(公告)号：US20070134341A1
公开(公告)日：2007-06-14
申请号：US11560324
申请日：2006-11-15
申请人： James Kipp , Jane Werling , Pramod Gupta , Rita Buresh
发明人： James Kipp , Jane Werling , Pramod Gupta , Rita Buresh
IPC分类号： A61K31/381 , A61K9/14
CPC分类号： A61K9/10 , A61K9/0043 , A61K9/0048 , A61K9/19 , A61K9/5146 , A61K31/38 , A61K31/381
摘要： Pharmaceutical compositions comprising particles of lipoxygenase inhibitor compounds having an effective average size of from about 10 nm to about 50 microns are provided. More particularly, pharmaceutical compositions of particle of a 5-lipoxygenase inhibitor compound having an effective average size of from about 50 nm to about 5 microns are provided. The pharmaceutical compositions are in the form of aqueous suspensions with the particle of the 5-lipoxygenase inhibitor compound present in concentrations of from about 5 to about 200 mg/ml. In addition, methods for making such pharmaceutical compositions are provided. In particular, microprecipitation and direct homogenization in the presence of at least one surfactant are disclosed for making the pharmaceutical compositions.
摘要翻译：提供了包含具有约10nm至约50微米的有效平均尺寸的脂氧合酶抑制剂化合物颗粒的药物组合物。更具体地，提供了具有约50nm至约5微米的有效平均尺寸的5-脂氧合酶抑制剂化合物的颗粒的药物组合物。药物组合物呈水性悬浮液的形式，其中5-脂氧合酶抑制剂化合物的颗粒以约5至约200mg / ml的浓度存在。此外，提供了制备这种药物组合物的方法。特别地，公开了在至少一种表面活性剂存在下的微沉淀和直接均化，用于制备药物组合物。

7. 发明申请

US20060280430A1 Method for delivering particulate drugs to tissues 有权
标题翻译：将颗粒药物递送至组织的方法
公开(公告)号：US20060280430A1
公开(公告)日：2006-12-14
申请号：US11406986
申请日：2006-04-19
申请人： Barrett Rabinow , Howard Gendelman , James Kipp
发明人： Barrett Rabinow , Howard Gendelman , James Kipp
IPC分类号： G11B27/00
CPC分类号： A61K9/0085 , A61K9/10 , A61K9/5123 , A61K9/5146 , A61K47/6901
摘要： The present invention is concerned with delivering a pharmaceutical composition to a tissue target of a mammalian subject for treating brain diseases or disorders. The process includes the steps of: (i) providing a dispersion of the pharmaceutical composition as particles having an average particle size of from about 150 nm to about 100 microns, and (ii) administering the dispersion to the mammalian subject for delivery to the tissue target of a portion of the pharmaceutical composition by cells capable of reaching the tissue target. The dispersion of the pharmaceutical composition as particles, for example, can be phagocytised or adsorbed by the cells prior or subsequent to administration into the mammalian subject. The dispersion of the pharmaceutical composition can be administered to the central nervous system or the vascular system. After administration, the loaded cells transport the pharmaceutical composition as particles into the tissue target.
摘要翻译：本发明涉及将药物组合物递送至哺乳动物受试者的组织靶以治疗脑部疾病或病症。该方法包括以下步骤：（i）提供药物组合物的分散体作为平均粒度为约150nm至约100微米的颗粒，和（ii）向哺乳动物受试者施用分散体以递送至组织通过能够到达组织靶的细胞的一部分药物组合物的靶标。例如，作为颗粒的药物组合物的分散体可以在给予哺乳动物受试者之前或之后被细胞吞噬或吸附。药物组合物的分散体可以施用于中枢神经系统或血管系统。给药后，负载的细胞将药物组合物作为颗粒输送到组织靶中。

8. 发明申请

US20050276861A1 Ex-vivo application of solid microparticulate therapeutic agents 有权
标题翻译：离体应用固体微粒治疗剂
公开(公告)号：US20050276861A1
公开(公告)日：2005-12-15
申请号：US11148453
申请日：2005-06-09
申请人： James Kipp , Barrett Rabinow
发明人： James Kipp , Barrett Rabinow
IPC分类号： A61K9/14 , A61K35/12 , A61K45/00 , A61K47/48 , A61K49/00 , C12N5/06
CPC分类号： A61K49/0002 , A61K9/14 , A61K35/12 , A61K47/6901 , A61K2035/124
摘要： The present invention is concerned with a method of preparing and delivering small particles of a pharmaceutically active material to a mammalian subject for treating diseases or disorders. A preferred embodiment entails: (i) the collection of tissue cells from an animal donor, (ii) selective or non-selective growth of these cells in a cell culture medium to which is added solid particles of a therapeutically active compound, mostly free of a drug carrier (about 10% or less, by weight), and having an average particle size of less than about 100 microns, (iii) contacting the cells in the cell culture medium with the solid particles of therapeutically active compound causing the particles to be taken up by the cells into either the intracellular compartment of the cultured cells, attachment of the active compound as particles to the periphery of such cells, or a combination of intracellular uptake and attachment to the cell surface, (iv) optionally, isolation and/or resuspension of the cells prepared in steps i through iii, (v) administering the cells to the mammalian subject. The pharmaceutically active material can be administered intravenously, intramuscularly, subcutaneously, intradermally, intra-articularly, intrathecally, epidurally, intracerebrally, via buccal route, rectally, topically, transdermally, orally, intranasally, via pulmonary route, intraperitoneally, or combinations thereof. After administration, the loaded cells transport the pharmaceutical composition as particles.
摘要翻译：本发明涉及制备和递送药物活性物质的小颗粒到哺乳动物受试者中用于治疗疾病或病症的方法。优选的实施方案包括：（i）从动物供体收集组织细胞，（ii）这些细胞在细胞培养基中的选择性或非选择性生长，其中加入主要不含药物载体（约10重量％或更少，重量百分比），平均粒径小于约100微米，（iii）使细胞培养基中的细胞与治疗活性化合物的固体颗粒接触，被细胞吸收到培养细胞的细胞内区室中，将活性化合物作为颗粒附着到这种细胞的周边，或细胞内摄取和附着到细胞表面的组合，（iv）任选的分离和 /或在步骤i至iii中制备的细胞的再悬浮，（v）向哺乳动物受试者施用细胞。药物活性物质可以通过静脉内，肌内，皮下，皮内，关节内，鞘内，硬膜外，脑内，经口颊途径，直肠，局部，经皮，口服，鼻内，经由肺途径，腹膜内或其组合施用。给药后，加载的细胞将药物组合物作为颗粒运输。

9. 发明申请

US20060141048A1 (Polyalkoxy)sulfonate surface modifiers 有权
标题翻译：（聚烷氧基）磺酸盐表面改性剂
公开(公告)号：US20060141048A1
公开(公告)日：2006-06-29
申请号：US11304421
申请日：2005-12-15
申请人： James Kipp , Ton Hai , Bennett Melnick
发明人： James Kipp , Ton Hai , Bennett Melnick
IPC分类号： A61K9/14
CPC分类号： C08G65/334 , A61K8/90 , A61K9/146 , A61K47/34 , A61Q19/00 , C08G65/326 , C08L71/02
摘要： The present invention is directed to novel compounds, methods of manufacture and methods of use. The present invention is also directed to solid drug/active agent particles having one or more of the compounds of the present invention associated with the surface thereof. The compounds of the present invention are comprised of a non-polar polyether covalently linked to an anionic sulfonate group. The compounds have an amphipathic quality and preferably, are surface active. Such compounds are preferably useful as surface-active agents to coat and stabilize dispersions of particles in a continuous liquid medium. These surface-active agents may be applied in the stabilization of suspensions, emulsions, or liposome formulations intended for pharmaceutical, medical, cosmetic, or agricultural use. The particles that can be prepared by a variety of methods and will preferably comprise a pharmaceutical agent. Pharmaceutical compositions of the present invention can be used to treat a myriad of conditions and can be administered by many routes, including intravenous, intramuscular, subcutaneous, intrathecal, subdural, intracameral, intracerebral, intralesional, topical, oral, buccal, rectal, transcutaneous, pulmonary, and nasal.
摘要翻译：本发明涉及新化合物，制备方法和使用方法。本发明还涉及具有一种或多种与其表面相关的本发明化合物的固体药物/活性剂颗粒。本发明的化合物由与阴离子磺酸盐基团共价连接的非极性聚醚组成。该化合物具有两性质量，优选表面活性。这些化合物优选用作表面活性剂以涂覆和稳定颗粒在连续液体介质中的分散体。这些表面活性剂可以用于稳定用于制药，医疗，化妆品或农业用途的悬浮液，乳剂或脂质体制剂。可以通过多种方法制备并且优选包含药剂的颗粒。本发明的药物组合物可用于治疗无数的病症，并且可以通过许多途径施用，包括静脉内，肌肉内，皮下，鞘内，硬膜下，阴道内，脑内，肠内，局部，口腔，口腔，直肠，经皮，肺和鼻。

10. 发明申请

US20070212302A1 Preparation and Use of a Stable Formulation of Allosteric Effector Compounds 审中-公开
标题翻译：稳定配方的变构效应剂的制备和应用
公开(公告)号：US20070212302A1
公开(公告)日：2007-09-13
申请号：US11749610
申请日：2007-05-16
申请人： Douglas Johnson , Mark Doty , James Kipp
发明人： Douglas Johnson , Mark Doty , James Kipp
IPC分类号： A61K31/205 , A61B5/055
CPC分类号： A61K31/195 , A61K9/0019 , A61K47/12 , A61K47/18 , A61K47/183 , A61K49/10
摘要： A pharmaceutical composition of 2-[4-[2-[(3,5-dimethylphenyl)amino]-2-oxoethyl]phenoxy]-2-methyl-propionic acid or its physiologically acceptable salts suitable for parenteral administration includes an aqueous formulation of 2-[4-[2-[(3,5-dimethylphenyl)amino]-2-oxoethyl]phenoxy]-2-methyl-propionic acid or its physiologically acceptable salt and a buffer to maintain the pH from about 6 to about 11. The composition in accordance with the invention reduces the amount of particulate matter that forms in solution after heat sterilization. The invention also includes a process for making a pharmaceutical composition of 2-[4-[2-[(3,5-dimethylphenyl)amino]-2-oxoethyl]phenoxy]-2-methyl-propionic acid or its physiologically acceptable salt that has a shelf life in excess of thirty days and is useful in parenteral administration.
摘要翻译： 2- [4- [2 - [（3,5-二甲基苯基）氨基] -2-氧代乙基]苯氧基] -2-甲基 - 丙酸或其适用于胃肠外给药的生理学上可接受的盐的药物组合物包括 2- [4- [2 - [（3,5-二甲基苯基）氨基] -2-氧代乙基]苯氧基] -2-甲基 - 丙酸或其生理上可接受的盐和缓冲液，以将pH保持在约6至约11 根据本发明的组合物减少加热灭菌后在溶液中形成的颗粒物质的量。本发明还包括制备2- [4- [2 - [（3,5-二甲基苯基）氨基] -2-氧代乙基]苯氧基] -2-甲基 - 丙酸或其生理上可接受的盐的药物组合物的方法，保质期超过30天，可用于肠胃外给药。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式