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    • 3. 发明申请
    • Polyamino acids functionalized by at least one hydrophobic group and the therapeutic application thereof
    • 由至少一个疏水基团官能化的聚氨基酸及其治疗应用
    • US20070160568A1
    • 2007-07-12
    • US11509783
    • 2006-08-25
    • Stephanie AngotOlivier BreyneYou-Ping ChanGerard Soula
    • Stephanie AngotOlivier BreyneYou-Ping ChanGerard Soula
    • A61K38/16A61K31/785C07K14/47
    • A61Q19/00A61K8/88A61K47/34A61K47/645A61K47/65C08G69/10C08G69/48
    • The invention relates to novel materials based on biodegradable polyamino acids that are useful for vectorizing active principle/s (AP). The aim of the invention is to supply a new polymeric raw material that is used for vectorizing AP and optimally fulfills all requirements concerning biocompatibility, biodegradability, the ability to be easily associated with numerous active principles or solubilize said active principles and to release the active principles in vivo. Said polymers can also be readily and economically transformed into particles vectorizing active principles according to the grafting rate of the hydrophobic groups, said particles being able to form stable aqueous colloidal suspensions. Said aim is achieved by the inventive amphiphile polyamino acids comprising aspartic and/or glutamic units that carry grafts which encompass at least one hydrophobic unit and are linked to the aspartic and/or glutamic units via a rotula containing two amide functions, more particularly via a spacer of the lysine or ornithine type. Said amide functions ensure better stability during hydrolysis than comparable products known in prior art. The invention also relates to new pharmaceutical, cosmetic, dietetic, or phytosanitary compositions based on the inventive polyamino acids.
    • 本发明涉及可用于向量化活性成分(AP)的可生物降解的聚氨基酸的新型材料。 本发明的目的是提供一种新的聚合物原料,其用于向AP进行载体化,并且最佳地满足关于生物相容性,生物可降解性,易于与许多活性成分相关联的能力或增溶所述活性成分并释放活性成分的所有要求 体内。 所述聚合物也可以容易地和经济地转化成根据疏水基团的接枝速率向量化活性成分的颗粒,所述颗粒能够形成稳定的水性胶体悬浮液。 所述目的通过包含天冬氨酸和/或谷氨酸单元的本发明的两亲性聚氨基酸实现,所述天然氨基酸和/或谷氨酸单元携带包含至少一个疏水单元的移植物,并且通过含有两个酰胺官能团的转运体连接到天冬氨酸和/或谷氨酸单元, 赖氨酸或鸟氨酸类型的间隔物。 所述酰胺功能确保在水解期间比现有技术中已知的可比产品更好的稳定性。 本发明还涉及基于本发明的聚氨基酸的新的药物,化妆品,饮食或植物检疫组合物。
    • 5. 发明授权
    • Telechelic homopolyamino acids functionalized with hydrophobic groups, and their applications, especially therapeutic applications
    • 用疏水基团官能化的远端电泳多聚氨基酸及其应用,特别是治疗应用
    • US07659365B2
    • 2010-02-09
    • US10574475
    • 2004-09-28
    • Rémi SoulaYou-Ping ChanGérard SoulaOlivier Breyne
    • Rémi SoulaYou-Ping ChanGérard SoulaOlivier Breyne
    • C07K14/00
    • A61K8/88A61K9/1075A61K9/5146A61K47/34A61K47/645A61Q19/00C08G69/10C08G73/028C08L79/02
    • The invention relates to novel materials based on biodegradable homopolyamino acids and which can be used for the vectorization of (an) active ingredient(s) (AI). The invention also relates to novel pharmaceutical, cosmetic, dietetic or phytosanitaty compositions based on homopolyamino acids. The invention can produce a novel polymer raw material which can be used for the vectoiization of Al that can optimally be: biocompatible, biodegradable, capable of becoming easily associated with a large number of active ingredients or solubilizing them and releasing the active ingredients in vivo. According to the present invention, which primarily relates to linear homopolyamino acids having aspartic or glutamic units and whose attachments can include hydrophobic groups having 8-30 carbon atoms. The homopolymers are amphiphilic and anionic and can easily be transformed at low cost into particles for the vectorization of active ingredients. The particles can form stable aqueous colloidal suspensions.
    • 本发明涉及基于可生物降解的均聚氨基酸的新型材料,其可用于(a)活性成分(AI)的向量化。 本发明还涉及基于均聚氨基酸的新型药物,化妆品,饮食或植物营养成分。 本发明可以生产出一种新型的聚合物原料,它可以用于最佳的生物相容性,生物降解性,能够容易地与大量活性成分缔合或溶解它们并在体内释放活性成分的Al的促进作用。 根据本发明,其主要涉及具有天冬氨酸或谷氨酸单元的线性均聚氨基酸,并且其连接物可以包括具有8-30个碳原子的疏水基团。 均聚物是两亲性的和阴离子的,并且可以容易地以低成本转化成用于活性成分载体化的颗粒。 颗粒可以形成稳定的水性胶体悬浮液。
    • 6. 发明申请
    • Self-precipitating pharmaceutical formulations for the moified release of an active principle
    • 用于释放活性成分的自沉淀药物制剂
    • US20090011028A1
    • 2009-01-08
    • US12149541
    • 2008-05-05
    • Frederic ChecotCecile Bonnet-GonnetYou-Ping ChanOlivier BreyneRemi Meyrueix
    • Frederic ChecotCecile Bonnet-GonnetYou-Ping ChanOlivier BreyneRemi Meyrueix
    • A61K47/42A61K9/10A61K38/20
    • A61K9/0019A61K9/10A61K9/1641A61K38/02A61K47/645A61K48/00
    • The present invention relates to novel pharmaceutical formulations for the release of an active principle (AP) over a sustained period of time of several days, or even several weeks.The invention relates, in a first aspect, to a liquid formulation comprising at least one active principle (AP) and an aqueous suspension based on colloïdal particles of a polymer (PO), wherein said formulation satisfies the following four conditions:(a) the polymer (PO) is a polyamino acid comprising glutamic residues, wherein some glutamic residues each carry a pendant cationic group (CG), said cationic groups being identical or different from one another, and other glutamic residues each carry a pendent hydrophobic group (GH), said hydrophobic groups (GH) being identical or different from one another, (b) the pHf value of the pH of said formulation is between 3.0 and 6.5; (c) at the pHf value, the polymer (PO) forms a colloïdal solution which associates spontaneously and noncovalently with the active principle (AP); (d) 1 ml of said formulation precipitates during mixing with a volume of 1 ml of a test buffer solution Tp. The invention also relates to a process for the preparation of such formulations and to a process for the preparation of medicaments including such formulations.
    • 本发明涉及用于在持续的几天甚至几周的时间内释放活性成分(AP)的新型药物制剂。 本发明在第一方面涉及包含至少一种活性成分(AP)和基于聚合物(PO)的胶体颗粒的水性悬浮液的液体制剂,其中所述制剂满足以下四个条件:(a) 聚合物(PO)是包含谷氨酸残基的聚氨基酸,其中一些谷氨酸残基各自携带阳离子基团(CG),所述阳离子基团彼此相同或不同,并且其它谷氨酸残基各自携带悬垂疏水基团(GH) ,所述疏水基团(GH)彼此相同或不同,(b)所述制剂的pH值的pHf值为3.0至6.5; (c)在pHf值下,聚合物(PO)形成一种自发和非共价结合活性成分(AP)的胶体溶液; (d)1ml所述制剂在与1ml测试缓冲溶液Tp的体积混合期间沉淀。 本发明还涉及一种制备这些制剂的方法以及制备包括这些制剂的药物的方法。
    • 8. 发明授权
    • Modified-release particles of polyelectrolytes and pharmaceutical formulations thereof
    • US08481019B2
    • 2013-07-09
    • US12149552
    • 2008-05-05
    • Cecile Bonnet-GonnetFrédéric ChecotYou-Ping ChanOlivier Breyne
    • Cecile Bonnet-GonnetFrédéric ChecotYou-Ping ChanOlivier Breyne
    • A61K31/74
    • A61K9/5146A61K9/1641
    • The present invention relates to novel particles comprising polyelectrolyte polymers which are transporters of active principle (AP), in particular protein and peptide active principle, and to novel modified-release pharmaceutical formulations comprising said AP microparticles.These novel particles loaded with AP release the AP over a prolonged period of time of several days, or even several weeks.The invention relates, in a first aspect, to particles comprising: a) a first polyelectrolyte polymer (PE1) in a charged state, carrying side hydrophobic groups (GH), wherein said first polyelectrolyte polymer (PE1) can spontaneously form, in water, a colloidal solution of particles at least one pHm value of the pH of between 3 and 8; b) a second polyelectrolyte polymer (PE2) of opposite polarity to the first polyelectrolyte polymer (PE1), wherein said second polyelectrolyte polymer (PE2) forms, in water, a solution or a colloidal solution at said pHm value of the pH; and c) at least one active principle (AP) associated noncovalently with the particles of the colloidal solution of the first polyelectrolyte polymer (PE1); wherein said particles are obtained by mixing, at a pH equal to pHm, the first polyelectrolyte polymer (PE1), in the form of a colloidal solution of particles associated with the active principle (AP), with the second polyelectrolyte polymer (PE2), in the form of a solution or colloidal solution. The invention also relates to the process for the preparation of these particles, to a pharmaceutical formulation comprising such particles and to a process for the preparation of medicaments.
    • 9. 发明申请
    • Polyglutamic acids functionalized by cationic groups and hydrophobic groups and applications thereof, in particular therapeutic applications thereof
    • 由阳离子基团和疏水基团官能化的聚谷氨酸及其应用,特别是其治疗应用
    • US20090012028A1
    • 2009-01-08
    • US12149542
    • 2008-05-05
    • You-Ping ChanCecile Bonnet-GonnetOlivier Breyne
    • You-Ping ChanCecile Bonnet-GonnetOlivier Breyne
    • A61K47/36A61K31/711A61K31/7105C08G63/685
    • C08G69/10A61K9/10A61K47/34A61K47/645C08G69/48
    • The present invention relates to novel biodegradable materials based on modified polyamino acids that are useful in particular in the vectorization of active principle(s) (APs). The invention is also directed to novel pharmaceutical, cosmetic, health-food or plant-protection compositions based on these polyamino acids.The aim of the invention is to provide a novel polymeric starting material which can be used for AP vectorization and which satisfy all the requirements: biocompatibility, biodegradability, ability to easily associate with or dissolve numerous active principles and to release these active principles in vivo. This goal is achieved by the present invention, which relates to novel polyglutamates modified by cationic groups, which, if they can be deprotonated, exhibit a pKa equal to or greater than 7, and by hydrophobic groups comprising from 8 to 30 carbon atoms.These polyglutamates modified by cationic groups are easily and economically converted into particles for the vectorization of active principles, these particles being themselves capable of forming stable aqueous colloidal suspensions. These modified polyglutamates exhibit the advantage of being less viscous than other analogous polymers while retaining an ability to associate proteins, such as insulin. Some are soluble in water at acidic pH and become insoluble at physiological pH (7.4) and should thus, during subcutaneous injection, precipitate on the site of injection.
    • 本发明涉及基于改性聚氨基酸的新型可生物降解材料,其特别用于活性成分(AP)的向量化。 本发明还涉及基于这些聚氨基酸的新型药物,化妆品,保健食品或植物保护组合物。 本发明的目的是提供一种新颖的聚合起始材料,其可用于AP向量化,并且其满足所有要求:生物相容性,生物降解性,容易地与许多活性成分缔合或溶解的能力,并在体内释放这些活性成分。 该目的通过本发明来实现,本发明涉及由阳离子基团修饰的新的聚谷氨酸,如果它们可以去质子化,表现出等于或大于7的pKa,以及含有8至30个碳原子的疏水基团。 通过阳离子基团改性的这些聚谷氨酸可容易且经济地转化成用于活性成分载体化的颗粒,这些颗粒本身能够形成稳定的水性胶态悬浮液。 这些改性的聚谷氨酸显示出比其它类似聚合物粘稠度较低的优点,同时保留了使蛋白质如胰岛素相关联的能力。 一些在酸性pH下溶于水,在生理pH(7.4)下变得不溶,因此皮下注射时,在注射部位沉淀。