Literature DB >> 12007987

Serial cerebrospinal fluid sampling in a rat model to study drug uptake from the nasal cavity.

Mascha P van den Berg1, Stefan G Romeijn, J Coos Verhoef, Frans W H M Merkus.   

Abstract

Drug transport from the nasal cavity to the brain has gained much interest in the last decade. In the present study, a model was developed to determine the uptake of drugs into the cerebrospinal fluid (CSF) after nasal delivery in rats. CSF samples were taken using a cisternal puncture method. In this method, a needle is advanced through the skin and muscles overlying the atlanto-occipital membrane into the cisterna magna, while the rat is fixed in a stereotaxic frame. This method appears to be superior over cannulation of the atlanto-occipital membrane for CSF sampling. The major advantages of the puncture method is the ability of serial and simultaneous CSF and blood sampling for over 2 h in the same rat. To obtain maximal drug absorption from the nasal cavity and uptake into CSF, different positions of the rat's head (upright-90 degrees, supine-90 degrees, supine-45 degrees and supine-70 degrees angles) were tested in nasal delivery studies using hydrocortisone (HC) as a model drug. Putting the rat in the supine-90 degrees angle position increased the absorption of HC into plasma and CSF 2-fold compared to the upright-90 degrees angle position. The supine-70 degrees angle position did not change the HC plasma and CSF levels compared to the supine-90 degrees angle position. However, the supine-70 degrees angle position showed the fastest CSF sampling rate, enabling more accurate CSF sampling and therefore preferred for further studies. In conclusion, the cisternal puncture method using the supine-70 degrees and 90 degrees angle position is a suitable method to study drug transport from the nasal cavity into the CSF, with the ability of multiple CSF sampling.

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Year:  2002        PMID: 12007987     DOI: 10.1016/s0165-0270(02)00033-x

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  19 in total

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3.  Intranasal delivery of N-terminal modified leptin-pluronic conjugate for treatment of obesity.

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Journal:  J Control Release       Date:  2017-03-24       Impact factor: 9.776

4.  Solid microparticles based on chitosan or methyl-β-cyclodextrin: a first formulative approach to increase the nose-to-brain transport of deferoxamine mesylate.

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Journal:  J Control Release       Date:  2015-01-22       Impact factor: 9.776

5.  In vivo contrast-enhanced MR imaging of direct infusion into rat peripheral nerves.

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7.  Uptake of melatonin into the cerebrospinal fluid after nasal and intravenous delivery: studies in rats and comparison with a human study.

Authors:  Mascha P van den Berg; Paul Merkus; Stefan G Romeijn; J Coos Verhoef; Frans W H M Merkus
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9.  Effect of administration method, animal weight and age on the intranasal delivery of drugs to the brain.

Authors:  Jishnu K S Krishnan; Peethambaran Arun; Bhadra Chembukave; Abhilash P Appu; Nivetha Vijayakumar; John R Moffett; Narayanan Puthillathu; Aryan M A Namboodiri
Journal:  J Neurosci Methods       Date:  2017-05-10       Impact factor: 2.390

10.  Sufficient virus-neutralizing antibody in the central nerve system improves the survival of rabid rats.

Authors:  Pi-Hung Liao; Hui-Hua Yang; Ping-Tse Chou; Ming-Hseng Wang; Po-Chun Chu; Hao-Li Liu; Li-Kuang Chen
Journal:  J Biomed Sci       Date:  2012-06-26       Impact factor: 8.410

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