Literature DB >> 12164691

Mixing during intravertebral arterial infusions in an in vitro model.

Robert J Lutz1, Kathy Warren, Frank Balis, Nicholas Patronas, Robert L Dedrick.   

Abstract

Regional delivery of drugs can offer a pharmacokinetic advantage in the treatment of localized tumors. One method of regional delivery is by intra-arterial infusion into the basilar/vertebral artery network that provides local access to infratentorial tumors, which are frequent locations of childhood brain cancers. Proper delivery of drug by infused solutions requires adequate mixing of the infusate at the site of infusion within the artery lumen. Our mixing studies with an in vitro model of the vertebral artery network indicate that streaming of drug solution is likely to occur at low, steady infusion rates of 2 ml/min. Streaming leads to maldistribution of drug to distal perfused brain regions and may result in toxic levels in some regions while concurrently yielding subtherapeutic levels in adjacent regions. According to our model findings, distribution to both brain hemispheres is not likely following infusion into a single vertebral artery even if the infusate is well-mixed at the infusion site. This outcome results from the unique fluid flow properties of two converging channels, which are represented by the left and right vertebral branches converging into the basilar. Fluid in the model remains stratified on the side of the basilar artery served by the infused vertebral artery. Careful thought and planning of the methods of intravertebral drug infusions for treating posterior fossa tumors are required to assure proper distribution of the drug to the desired tissue regions. Improper delivery may be responsible for some noted toxicities or for failure of the treatments.

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Year:  2002        PMID: 12164691     DOI: 10.1023/a:1016034910875

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  16 in total

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Journal:  Neurosurgery       Date:  1986-10       Impact factor: 4.654

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Authors:  D A McDONALD; J M POTTER
Journal:  J Physiol       Date:  1951-07       Impact factor: 5.182

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Authors:  R J Lutz; A H Epstein; J A Cook; R L Dedrick
Journal:  Gynecol Oncol       Date:  1995-11       Impact factor: 5.482

4.  Safety and efficacy of a multicenter study using intraarterial chemotherapy in conjunction with osmotic opening of the blood-brain barrier for the treatment of patients with malignant brain tumors.

Authors:  N D Doolittle; M E Miner; W A Hall; T Siegal; E Jerome; E Osztie; L D McAllister; J S Bubalo; D F Kraemer; D Fortin; R Nixon; L L Muldoon; E A Neuwelt
Journal:  Cancer       Date:  2000-02-01       Impact factor: 6.860

5.  Intravascular streaming and variable delivery to brain following carotid artery infusions in the Sprague-Dawley rat.

Authors:  S C Saris; D C Wright; E H Oldfield; R G Blasberg
Journal:  J Cereb Blood Flow Metab       Date:  1988-02       Impact factor: 6.200

Review 6.  Arterial drug infusion: pharmacokinetic problems and pitfalls.

Authors:  R L Dedrick
Journal:  J Natl Cancer Inst       Date:  1988-03-16       Impact factor: 13.506

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Authors:  D R Shook; L M Beaudet; J L Doppman
Journal:  J Neurosurg       Date:  1987-11       Impact factor: 5.115

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Authors:  R J Lutz; D L Miller
Journal:  Cancer       Date:  1988-09-15       Impact factor: 6.860

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Authors:  J M Collins
Journal:  J Clin Oncol       Date:  1984-05       Impact factor: 44.544

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Authors:  R L Levine; P A Turski; W D Turnipseed; T Grist
Journal:  J Neuroimaging       Date:  1996-04       Impact factor: 2.486

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Journal:  Sci Rep       Date:  2021-03-22       Impact factor: 4.379

Review 3.  Beyond the Blood:Brain Barrier: The Importance of Central Nervous System (CNS) Pharmacokinetics for the Treatment of CNS Tumors, Including Diffuse Intrinsic Pontine Glioma.

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4.  PIV investigation of the flow fields in subject-specific vertebro-basilar (VA-BA) junction.

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  4 in total

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