• 专利标题:   Preparation of drug delivery system involves weighing hyaluronic acid, N-hydroxysuccinimide, phosphate-buffered saline buffer solution, carbodiimide, graphene oxide, chitosan solution and anti-tumor medicine, and precipitating.
  • 专利号:   CN107625964-A
  • 发明人:   LEI Y
  • 专利权人:   LEI Y
  • 国际专利分类:   A61K031/337, A61K031/4745, A61K031/704, A61K033/24, A61K047/04, A61K047/10, A61K047/36, A61P035/00
  • 专利详细信息:   CN107625964-A 26 Jan 2018 A61K-047/04 201817 Pages: 10 Chinese
  • 申请详细信息:   CN107625964-A CN10732335 24 Aug 2017
  • 优先权号:   CN10732335

▎ 摘  要

NOVELTY - Preparation of drug delivery system involves adding hyaluronic acid, N-hydroxysuccinimide, phosphate-buffered saline buffer solution and carbodiimide to a reactor and then mixing, adding amine-polyethylene glycol and phosphate-buffered saline buffer solution to the mixture and then reacting, adding graphene oxide, 2-(N-morpholino)ethanesulfonic acid buffer solution, N-hydroxysuccinimide, carbodiimide and chitosan solution to the mixture and then processing, adding anti-tumor medicine and phosphate-buffered saline buffer solution to the mixture, and precipitating. USE - The method is useful for preparation of drug delivery system. ADVANTAGE - The method enables preparation of drug delivery system with excellent slow release properties, hydrophilicity, biological compatibility, dispersibility and prolonged service life. DETAILED DESCRIPTION - Preparation of drug delivery system involves adding 30 mg hyaluronic acid, 70 mg N-hydroxysuccinimide, 10 ml or 0.01 M phosphate-buffered saline buffer solution and 80 mg carbodiimide to a reactor and then mixing, adding 5 ml amine-polyethylene glycol and 0.01 M phosphate-buffered saline buffer solution to the mixture and then reacting, adding 10-50 mg graphene oxide, 10 ml or 0.01 M 2-(N-morpholino)ethanesulfonic acid buffer solution, 80 mg N-hydroxysuccinimide, 100 mg carbodiimide and 5-10 ml or 5 mg/ml chitosan solution to the mixture and then ultrasonically processing for 10 minutes, filtering the mixture using 0.01 M phosphate-buffered saline buffer solution, adding 50-200 mg anti-tumor medicine and 5 ml phosphate-buffered saline buffer solution to the filtrate and then centrifuging, and precipitating. An INDEPENDENT CLAIM is included for drug delivery system prepared by the method.