Literature DB >> 3470138

Distribution of radiolabeled 1-(4-amino-2-methyl-5-pyrimidinyl)methyl-3-(2-chloroethyl)-3-nitros ourea hydrochloride in rat brain tumor: intraarterial versus intravenous administration.

K Yamada, Y Ushio, T Hayakawa, N Arita, T Y Huang, M Nagatani, N Yamada, H Mogami.   

Abstract

To assess the rationale of intraarterial (i.a.) 1-(4-amino-2-methyl-5-pyrimidinyl)methyl-3-(2-chloroethyl)-3-nitrosourea chemotherapy, distribution of 14C-labeled 1-(4-amino-2-methyl-5-pyrimidinyl)methyl-3-(2-chloroethyl)- 3-nitrosourea in rat glioma was studied after i.a. or i.v. infusion. Immediately after infusion, the tumor located in the hemisphere of intracarotid infusion received 4.6-fold higher radioactivity than the tumor located contralaterally to intracarotid infusion and 2.8-fold higher radioactivity than i.v. infusion. The difference was kept up to 30 min after i.a. infusion. Autoradiographic observation indicated rather uniform distribution of the tracer in the central portion of i.a. infusion. However, in the periphery of i.a. infusion, distribution of the tracer was nonhomogenous. The results indicate that i.a. 1-(4-amino-2-methyl-5-pyrimidinyl)methyl-3-(2-chloroethyl)-3-nitrosourea chemotherapy is useful when the tumor has high blood flow and is located in the center of an infused area.

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Year:  1987        PMID: 3470138

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  7 in total

1.  Relationship between drug delivery and the intra-arterial infusion rate of SarCNU in C6 rat brain tumor model.

Authors:  N Takeda; M Diksic
Journal:  J Neurooncol       Date:  1999-02       Impact factor: 4.130

2.  Brain tumor targeting of magnetic nanoparticles for potential drug delivery: effect of administration route and magnetic field topography.

Authors:  Beata Chertok; Allan E David; Victor C Yang
Journal:  J Control Release       Date:  2011-07-07       Impact factor: 9.776

3.  Randomized comparison of intra-arterial versus intravenous infusion of ACNU for newly diagnosed patients with glioblastoma.

Authors:  M Kochii; I Kitamura; T Goto; T Nishi; H Takeshima; Y Saito; K Yamamoto; T Kimura; T Kino; K Tada; S Shiraishi; S Uemura; T Iwasaki; J Kuratsu; Y Ushio
Journal:  J Neurooncol       Date:  2000-08       Impact factor: 4.130

4.  Polyethyleneimine-modified iron oxide nanoparticles for brain tumor drug delivery using magnetic targeting and intra-carotid administration.

Authors:  Beata Chertok; Allan E David; Victor C Yang
Journal:  Biomaterials       Date:  2010-05-21       Impact factor: 12.479

Review 5.  Cytotoxic chemotherapy: advances in delivery, pharmacology, and testing.

Authors:  R Ciordia; J Supko; M Gatineau; T Batchelor
Journal:  Curr Oncol Rep       Date:  2000-09       Impact factor: 5.075

6.  Modification of tumor blood flow and enhancement of therapeutic effect of ACNU on experimental rat gliomas with angiotensin II.

Authors:  K Tokuda; H Abe; T Aida; S Sugimoto; S Kaneko
Journal:  J Neurooncol       Date:  1990-06       Impact factor: 4.130

7.  Delivery of a novel nitrosourea, MCNU, to the brain tissue in glioma-bearing rats. Intracarotid versus intravenous infusion.

Authors:  A Hodozuka; K Sako; H Nakai; M Tomabechi; N Suzuki; Y Yonemasu
Journal:  J Neurooncol       Date:  1993-01       Impact factor: 4.130

  7 in total

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