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1997 Fiscal Year Final Research Report Summary

Development of Pharmaceutical Additives-Evaluation of Protein and Polysaccharide Hydrolysates as Carrier to Enhance Absorption Rate of Drug

Research Project

Project/Area Number 07557146
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Physical pharmacy
Research InstitutionKumamoto University

Principal Investigator

OTAGIRI Masaki  Kumamoto University, Faculty of Pharmaceutical Science, Professor, 薬学部, 教授 (80120145)

Co-Investigator(Kenkyū-buntansha) NAKAGAMI Hiroaki  Daiichi Pharmaceutical Co., Ltd.Chief Researcher, 製剤センター, 主任研究員
IMAI Teruko  Kumamoto University, Faculty of Pharmaceutical Science, Instructor, 薬学部, 教務員 (70176478)
SUENAGA Ayaka  Kumamoto University, Faculty of Pharmaceutical Science, Assistant Professor, 薬学部, 助手 (20040313)
IMAMURA Yorishige  Kumamoto University, Faculty of Pharmaceutical Science, Assistant Professor, 薬学部, 助教授 (30040314)
Project Period (FY) 1995 – 1997
Keywordspharmaceutical improvement / natural polymer / protein / polysaccharide / drug / absorption / dissolution
Research Abstract

Protein and polysaccharides such as water-soluble gelatin, egg albumin, casein hydrolysate, low molecular chitosan and alginate are the preferred carriers of drugs in various pharmaceutical formulations. However, improvents of the dissolution and absorption of drugs using natural polymers have been not fully studied. Thus, the present study was undertaken to investigate the possible use of natural polymers such as casein hydrolysate, egg albumin as solubilizing agents to improve the absorption of poorly water soluble drugs. The results obtained here are summarized as follows :
1)Two types of fragmented keratin (FKs) were prepared from buffalo horn and hoof using savinase and Na_2S,and their physicochemical and biopharmaceutical properties were examined in mice. The systematic acute toxicity of FKs was significantly lower than that of superoxide dismutase. In plasma, enzymatically fragmented keratin was hydrolyzed slowly, but in liver and kidney homogenates it showed slightly faster hydr … More olysis. In contrast, fragmented gelatin was not hydrolyzed in any of the media used here.
2)The solubility of dl-a-tocopherol (VE) was increased by 300-fold in the presence of egg albumin. The apparent dissolution rate of VE from solid dispersion with egg albumin was markedly enhanced in comparison with VE alone. The mean serum levels of VE following oral administration of egg albumin solid dispersions, especially egg albumin solid dispersion containing myristic acid, were significantly higher than those of the drug alone.
3)Two types of casein hydrolysates, casein A (mean peptide length 3.3) and casein B (mean peptide length 17.4) were prepared by the enzymatic hydrolysis of casein, and their effects on in vitro dissolution rates and oral bioavailability of drugs were evaluated. The in vitro dissolution behavior of the kneaded mixture of three drugs (diclofenac acid, diazepam, and prednisolone) with caseins A and B were significantly improved compared to the drugs alone. The plasma concentration-time profile showed that prednisolone was completely and rapidly absorbed from the casein A kneaded mixture as well as the prednisolone solution. In addition, prednisolone in the kneaded mixture with casein B was more difficult to absorb up to 1 hr after administration in comparison to prednisolone powder. Less

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] 今井 輝子、小田切 優樹(他2名): "Alteration of Pharmacokinetics and Nephrotoxicity of Cisplatin by Alginates" Journal of Pharmaceutical Science. 86.2. 244-247 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 今井 輝子、小田切 優樹(他4名): "Mutual Effect of Albumin and Fatty Acids on Bioavailability of dl-α-tocopherol" International of Pharmaceutics. 155.1. 45-52 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 橋口 照司、小田切 優樹(他2名): "In Vitro Percutaneous Absorption of Prednisolone Derivatives Based on Solibility Parameter" International of Pharmaceutics. 158.1. 11-18 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 川崎 知世、小田切 優樹(他2名): "Preparation and Evaluation of a Suppository Dosage Form Containing Omeprazole" Pharmaceutical Science. 3.9. 431-434 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 今井 輝子、小田切 優樹(他3名): "Casein Hydrolysate as a Rapid and/or Enteric Dissoluing Additive for Oral Drugs" Pharmaceutical Development and Technology. 3.2(in press). (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] M.Fathy、小田切 優樹(他3名): "Preparation and Evaluation of Beads of Different Calcium Alginate Composition for Oral Sustained Relase of Tiaramide" Pharmaceutical Development and Technology. (in press). (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Otagiri Masaki et al: "Alteration of Pharmacokinetics and Nephrotoxicity of Cisplatin by Alginates" Journal of Pharmaceutical Science. 86.2. 244-247 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Otagiri Masaki et al: "Mutual Effect of Albumin and Fatty Acids on Bioavailability of dl-a-tocopherol" International of Pharmaceutics. 155.1. 45-52 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Otagiri Masaki et al: "In Vitro Percutaneous Absorption of Prednisolone Derivatives Based on Solibility Parameter" International of Pharmaceutics. 158.1. 11-18 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Otagiri Masaki et al: "Preparation and Evaluation of a Suppository Dosage Form Containing Omeprazole" Pharmaceutical Science. 3.9. 431-434 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Otagiri Masaki et al: "Casein Hydrolysate as a Rapid and / or Enteric Dissoluing Additive for Oral Drugs" Pharmaceutical Development and Technology. 3.2. (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Otagiri Masaki et al: "Preparation and Evaluation of Beads of Different Calcium Alginate Composition for Oral Sustained Relase of Tiaramide" Pharmaceutical Development and Technology. (1998)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-03-16  

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