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机构地区:[1]山东大学药学院,山东济南250012 [2]兆科药业(合肥)有限公司,安徽合肥230088
出 处:《中国生化药物杂志》2008年第6期403-405,共3页Chinese Journal of Biochemical Pharmaceutics
摘 要:目的研究低分子量肝素钙(LMWH-Ca)口服制剂的制备和口服吸收。方法将LMWH-Ca用聚乙二醇制成微囊、β-环糊精(-βCD)包合和在LMWH-Ca口服液中加入促胃肠道黏膜吸收剂N-[10-(2-羟基苯甲酰基)氨基]癸酸钠(SNAD)等方法制备成不同制剂后,SD大鼠采用灌胃给药,用生色底物法测定不同取样时间的药物浓度。结果在试验的LMWH-Ca口服处方中,加入SNAD的处方具有较好的吸收。结论SNAD对LMWH-Ca口服制剂具有优良的促胃肠道黏膜吸收能力,有助于LMWH-Ca口服制剂的深入研究。Purpose To investigate the oral preparations of low molecular weight heparin calcium(LMWH-Ca) and the absorption of LMWH-Ca in the preparations administered orally. Methods LMWH-Ca preparations were prepared by microeneapsulation with PEG6000, inclusion with β-CD or adding sodium N-[10-(2-hydrox- ybenzoyl)amino]decanoate (SNAD)to enhance the absorption of LMWH-Ca from the gastrointestinal tract, and the concentrations of LMWH-Ca in plasma at varied time after giving the LMWH-Ca preparations to rats intragastrically were determined by chromogenic substrate method. Results Among the preparations of LMWH-Ca, the one containing SNAD had better absorption. Conclusion SNAD has good ability to enhance absorption of oral LMWH-Ca from the gastrointestinal tract. It would be good to have further study on LMWH-Ca oral prepa- rations.
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