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A METHOD FOR THE PREPARATION OF CONTROLLED RELEASE COMPOSITIONS FOR INTERFERON BASED ON PEGT-PBT BLOCK COPOLYMERS

机译:基于PEGT-PBT嵌段共聚物的干扰素可控释成分的制备方法

摘要

The present invention relates to a method for the preparation of a pharamceutical composition for controlled release comprising microparticles including a polymeric carrier and one or more interferons, wherein the polymeric carrier includes one or more block copolymers constructed from poly(ethylene glycol) terephthalate (PEGT) and poly(butylene terephthalate) (PBT), wherein the majority of the microparticles are substantially free of pores having a diameter of more than about 5 urn, comprising the steps of: (a) preparing an emulsion comprising (k) an aqueous inner phase comprising the active compound, and (l) an organic outer phase comprising the biodegradable polymer and at least one organic solvent; (b) solidifying the biodegradable polymer into microparticles by removing at least a fraction of the organic solvent from the emulsion prepared in step (a); (c) collecting and drying the microparticles formed in step (b), wherein step (b) is carried out by emulsifying the emulsion prepared in step (a) in a coherent aqueous phase to obtain a w/o/w-double emulsion, wherein the coherent aqueous phase comprises an osmotic agent
机译:本发明涉及一种用于控制释放的药物组合物的制备方法,该药物组合物包含包含聚合物载体和一种或多种干扰素的微粒,其中该聚合物载体包括一种或多种由聚对苯二甲酸乙二醇酯(PEGT)构成的嵌段共聚物。以及聚对苯二甲酸丁二酯(PBT),其中大多数微粒基本上没有直径大于约5微米的孔,包括以下步骤:(a)制备包含(k)水性内相的乳液包含活性化合物,和(l)包含可生物降解的聚合物和至少一种有机溶剂的有机外相; (b)通过从步骤(a)中制备的乳液中除去至少一部分有机溶剂,将可生物降解的聚合物固化成微粒; (c)收集并干燥步骤(b)中形成的微粒,其中步骤(b)是通过将步骤(a)中制备的乳液在相干水相中乳化以获得w / o / w双乳液而进行的,其中相干水相包含渗透剂

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