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Oral dialysis treatment composition for chronic and end-stage renal disease patients

机译:用于慢性和终末期肾脏疾病患者的口服透析治疗组合物

摘要

The present invention relates to an oral therapeutic composition comprising mannitol as a main component, which is effective for the treatment of chronic and end-stage renal disease patients.;15 to 30 parts by weight of mannitol as a nonabsorbent agent, 2 to 3 parts by weight of NaCl,2SO44.5 to 5.5 parts by weight, KCl 0.7 to 0.8 parts by weight, NaHCO31 to 2 parts by weight. The composition is dissolved in 1 liter of water and taken four times a day, thereby remarkably eliminating the poisonous substance of the patient.;The therapeutic effect of the therapeutic composition for oral use of the present invention is the same as the treatment of hemodialysis or peritoneal dialysis for 12 hours a week (three times a week for 4 hours) in renal failure patients.
机译:本发明涉及一种以甘露醇为主要成分的口服治疗组合物,它对治疗慢性和终末期肾病患者有效; 15-30重量份的甘露醇作为非吸收剂,2-3重量份。按重量计NaCl, 2 SO 4 4.5至5.5重量份,KCl 0.7至0.8重量份,NaHCO 3 1-2份按重量。将该组合物溶于1升水中,每天服用四次,从而明显地消除了患者的有毒物质。本发明的口服用治疗组合物的治疗效果与血液透析或血液透析相同。肾衰竭患者每周进行腹膜透析12小时(每周3次,共4小时)。

著录项

  • 公开/公告号KR940013514A

    专利类型

  • 公开/公告日1994-07-15

    原文格式PDF

  • 申请/专利权人 황일용;

    申请/专利号KR19920024103

  • 发明设计人 황일용;

    申请日1992-12-14

  • 分类号A61K31/715;

  • 国家 KR

  • 入库时间 2022-08-22 04:37:37

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