Development of a new method for bioavailability assessment using a pharmacokineic/pharmacodynamic model
| Project/Area Number |
05671797
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Physical pharmacy
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| Research Institution | Osaka University of Pharmaceutical Sciences |
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Principal Investigator |
KAKEMI Masawo Osaka University of Pharmaceutical Sciences, Deparment of Pharmaceutics, Professor and Chair, 薬学部, 教授 (00019134)
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| Co-Investigator(Kenkyū-buntansha) |
IWANAGA Kazunori Osaka University of Pharmaceutical Sciences, Deparment of Pharmaceutics, Researc, 薬学部, 助手 (20257900)
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| Project Period (FY) |
1993 – 1994
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| Project Status |
Completed (Fiscal Year 1994)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1994: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1993: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | Blood Pressure Regulation / Plasma Calcium Regulation / Captopril / Salmon-calcitonin / Arginine-vasopressin / Pharmacokinetics / Pharmacodynamics / Optimisation of Dosage Regimen / アルギニン・バソプレッシン / 日内変動 / 抗利尿ホルモン / バイオアベイラビリティー / 投与計画 / サケカルシトニン / フォーマコキネティクス / フォーマコダイナミックス / 日内変動モデル / モデル解析 |
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| Research Abstract |
The rapid development of automated synthetic and recombinant DNA methods of peptide preparation have made available a great variety of peptide and peptide analogs of potential therapeutic value. Example include synthetic peptide hormons (such as insulin, vasopressin, calcitonin, somatostatin, etc.), peptide analogs, renin inhibitors, and angiotensin converting enzyme inhibitors are currently available for clinical use. The usual route of adsministration of these compounds were intravascular, intramuscular or subcutaneous ; however, a number of side effects due to injection have been reported. Although, oral, rectal or nasal route have attracted ateension, because of its potential to improve the side-effects, the assesment of bioavailability after extravascular administration of these drugs are extremely difficult. The objective of this project is to develop a new method for bioavailability assessment and to optimise the dosage regimens after oral nasal administration of these drugs. Captopril (CP), salmon calcitonin (sCT) and arginine vasopressin (AVP) were used as model compounds. A pharmacokinetic (PK) / pharmacodynamic (PD) model, including physiological regulation systems, such as arterial pressure control system, plasma calcium regulation system and/or urinary sodium regulation system was constructued, and the pharmacological data after extravascular administraiton of these drugs were analyzed. Results indicated that the rate and extent of bioavailability of these drugs were precisely estimated by the PK/PD model.
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Report
(3 results)
Research Products
(2 results)
