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Featured researches published by Degenhard Marx.


Pharmaceutical Research | 2001

Systemic Delivery of Cetrorelix to Rats by a New Aerosol Delivery System

Rosario Lizio; Thomas Klenner; Antonio Werner Sarlikiotis; Peter Romeis; Degenhard Marx; Thomas Nolte; Wolfgang Jahn; Gerrit Borchard; Claus-Michael Lehr

AbstractPurpose. To study the pulmonary absorption and tolerability of various formulations of the decapeptide cetrorelix acetate in rats by a new aerosol delivery system (ASTA-ADS) for intratracheal application. Methods. Using the ASTA-ADS, cetrorelix liquid formulations (aqueous solutions for ultrasonic nebulization) were firstly selected and subsequently delivered as nebulized aerosol to orotracheally cannulated rats. The pharmacologic effect (decrease of testosterone serum level) of four cetrorelix formulations was determined in rats by enzyme linked immunosorbant assay, and pharmacokinetic data were determined after measurement of cetrorelix serum level by radioimmunoassay. Histological examination of the lung was performed at the end of the experiments, and in a supplementary experiment the respiratory parameters (resistance and compliance) of rats were monitored by a validated pulmonary monitoring system during the aerosol application of the same formulations. Results. After an exposure time of 5 min, the applied formulations reduced the testosterone concentration in serum to subnormal levels (≤1 ng/ml) over a period of 24 h. Comparing the plasma concentration after intratracheal aerosolization with data of intravenous administration, the mean calculated bioavailabilities for the four formulations using the corrected dose (delivered—exhaled amount) were between 48.4 ± 27.0% and 77.4 ± 44.0%. The histologic examination of the lungs revealed different tolerability of the various tested formulations ranging from locally intolerable to well tolerated. The measurement of the lung function parameters did not reveal any compound or formulation related changes. Conclusions. Our studies show that cetrorelix can be effectively administered as aerosol and that intratracheal aerosolization via the ASTA-ADS provides results that are well comparable to other application routes, as demonstrated by statistical comparison of the newly obtained data with previous results from intratracheal instillation of cetrorelix solutions in rats.


Laboratory Animals | 2001

Development of a new aerosol delivery system for systemic pulmonary delivery in anaesthetized and orotracheal intubated rats

Rosario Lizio; Degenhard Marx; Thomas Nolte; Claus-Michael Lehr; Antonio Werner Sarlikiotis; Gerrit Borchard; Wolfgang Jahn; Thomas Klenner

Over the last decade, the systemic absorption of a broad range of therapeutics after pulmonary application has been demonstrated in animals as well as in humans. The most common method used in the laboratory is the intratracheal instillation of drugs in solution. This method is, however, unsatisfactory, because of discrepancies in particle distribution, clearance, kind of injury and bioavailability between instillation and inhalative application. On the other hand, a precise determination of the amount of drug applied by aerosol, and of the aerosol volume retained within the lungs is rather difficult, and is not possible for use with small animals such as mice or rats. We describe a system which allows the delivery of aerosols directly into the animals lungs, and calculation of the amount of drug retained in the lungs. Our system was tested in vitro and in vivo and was shown to allow precise and efficient pharmacokinetic and toxicological studies to be carried out.


Archive | 2002

Hydroxyindoles, their use as inhibitors of phosphodiesterase 4 and processes for their preparation

Norbert Höfgen; Ute Egerland; Hildegard Poppe; Degenhard Marx; Stefan Szelenyi; Thomas Kronbach; Emmanuel Polymeropoulos; Sabine Heer


Archive | 1999

New hydroxyindoles, their use as phosphodiesterase 4 inhibitors and method for producing same

Ute Egerland; Sabine Heer; Norbert Höfgen; Thomas Kronbach; Degenhard Marx; Emmanuel Polymeropoulos; Hildegard Poppe; Stefan Szelenyi


Archive | 2001

Use of pyrido 3,2-e]-pyrazinones as inhibitors of phosphodiesterase 5 for treating erectile dysfunction

Degenhard Marx; Norbert Höfgen; Ute Egerland; Stefan Szelenyi; Thomas Kronbach


Archive | 2001

Novel 7-azaindoles, use thereof as phosphodiesterase 4 inhibitors and method for producing the same

Norbert Höfgen; Ute Egerland; Thomas Kronbach; Degenhard Marx; Stefan Szelenyi; Hildegard Kuss; Emmanuel Polymeropoulos


Drug Research | 2011

Animal models of allergic rhinitis

Istvan Szelenyi; Degenhard Marx; Wolfgang Jahn


Archive | 2000

Combination of loteprednol and antihistamines

Istvan Szelenyl; Degenhard Marx; Sabine Heer; Juergen Engel


Archive | 1999

Neue Kombination von Loteprednol und Antihistaminika

Istvan Szelenyi; Degenhard Marx; Sabine Heer; Juergen Engel


Archive | 2001

Process for the treatment of erectile dysfunction and product therefor

Degenhard Marx; Norbert Höfgen; Ute Egerland; Stefan Szelenyi; Thomas Kronbach

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Stefan Szelenyi

University of Erlangen-Nuremberg

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