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SOLID FORM OF CELLO-COXYB THAT HAS IMPROVED BIO ACCESSIBILITY

机译:改善了生物可及性的细胞毒素的固体形式

摘要

Developed a selective drug celecoxib, inhibiting cyclooxygenase-2, in amorphous form. A celecoxib drug substance has also been developed, in which celecoxib is present, at least in detectable amounts, in the form of amorphous celecoxib. A composite inhibiting crystallization of celecoxib has also been developed, including particles of an amorphous celecoxib or celecoxib drug substance according to this invention in association with one or more crystallization inhibitors, for example polymers. Also developed a pharmaceutical composition comprising such a composite, inhibiting the crystallization of celecoxib, and one or more formative substances. Methods have also been developed for producing amorphous celecoxib, a celecoxib drug substance in accordance with this invention, a celecoxib crystallization inhibitory composite in accordance with this invention, and a pharmaceutical composition in accordance with this invention. A method has also been developed for treating a medical condition or disorder in a subject to whom treatment with cyclooxygenase-2 inhibitor is indicated, comprising administering, for example, orally a composition according to the invention in a therapeutically effective amount. The international application was published along with an international search report.
机译:开发了选择性药物塞来昔布,以无定形形式抑制环氧合酶-2。还已经开发了塞来昔布药物,其中塞来昔布以无定形塞来昔布的形式至少以可检测的量存在。还已经开发了抑制塞来昔布结晶的复合物,包括与一种或多种结晶抑制剂例如聚合物结合的根据本发明的无定形塞来昔布或塞来昔布药物颗粒。还开发了包含这样的复合物的药物组合物,其抑制塞来昔布的结晶和一种或多种形成性物质。还开发了生产无定形塞来昔布,本发明塞来昔布药物,本发明塞来昔布结晶抑制复合物和本发明药物组合物的方法。还已经开发出一种用于在需要用环加氧酶-2抑制剂治疗的受试者中治疗医学病症或病症的方法,该方法包括例如以治疗有效量口服施用根据本发明的组合物。国际申请与国际检索报告一同发布。

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