Abstract |
During recent years, the treatment of pulmonary diseases could be significantly improved due to the introduction of modern retrometabolism-based corticosteroids with improved therapeutic ratio. It is the goal of all inhaled corticosteroids to produce long lasting therapeutic effects at the pulmonary target site and to minimize systemic side effects by rapid clearance of the absorbed drug and low oral bioavailability. The development of PK/PD models allows predictions of drug effects based on the administered dose. For example, the cumulative suppression of endogenous cortisol release (CCS) as one of the major systemic side effects of inhaled corticosteroid therapy can be described with an integrated Emax based PK/PD model. In order to assess the predictive power of this model, a study was conducted to compare the PK/PD-based predictions with CCS data obtained from actual clinical trials for flunisolide, fluticasone propionate, budesonide and triamcinolone acetonide. CCS was predicted for different single doses from different inhaler devices for each drug and a good correlation was observed. Thus, the presented PK/PD model proved to be a valid tool for predicting CCS of inhaled corticosteroids. By fully understanding the underlying mechanisms it will be possible to further improve their therapeutic index.
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Authors | H Derendorf, G Hochhaus, S Krishnaswami, B Meibohm, H Möllmann |
Journal | Die Pharmazie
(Pharmazie)
Vol. 55
Issue 3
Pg. 223-7
(Mar 2000)
ISSN: 0031-7144 [Print] Germany |
PMID | 10756545
(Publication Type: Journal Article)
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Chemical References |
- Adrenal Cortex Hormones
- Hydrocortisone
|
Topics |
- Administration, Inhalation
- Adrenal Cortex Hormones
(administration & dosage, pharmacokinetics, pharmacology)
- Algorithms
- Area Under Curve
- Depression, Chemical
- Humans
- Hydrocortisone
(blood)
- Models, Biological
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