Literature DB >> 16326078

Plasma antipsychotic concentration and receptor occupancy, with special focus on risperidone long-acting injectable.

Rossella Medori1, Erik Mannaert, Gerhard Gründer.   

Abstract

Although effective plasma concentration ranges have been established for some antipsychotics, conventional and atypical, there is considerable inter-patient pharmacokinetic variation. Positron-emission tomography (PET) can be used to estimate D(2)-like receptor occupancy in the brain needed for an antipsychotic effect and the level above which extrapyramidal side effects (EPS) develop. For conventional antipsychotics, the window occupancy is approximately 70-80%. For the atypical antipsychotic risperidone, the antipsychotic effect starts at approximately 60% occupancy, with occupancy above 80% leading to EPS. The new formulation, risperidone long-acting injectable (RLAI), comprises risperidone in a biodegradable polymer. It is effective long-term at doses of 25 or 50 mg injected i.m. every 2 weeks. The constant and slow release of the long-acting formulation leads to less fluctuation in plasma levels and to a D(2)-like receptor occupancy which is below the threshold for EPS.

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Year:  2005        PMID: 16326078     DOI: 10.1016/j.euroneuro.2005.10.006

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  13 in total

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3.  Predicting pharmacokinetic stability by multiple oral administration of atypical antipsychotics.

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Journal:  Innov Clin Neurosci       Date:  2013-03

Review 4.  Comparative pharmacology of antipsychotics possessing combined dopamine D2 and serotonin 5-HT1A receptor properties.

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6.  Comparison of the peak-to-trough fluctuation in plasma concentration of long-acting injectable antipsychotics and their oral equivalents.

Authors:  John J Sheehan; Kristin R Reilly; Dong-Jing Fu; Larry Alphs
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Review 7.  Clinical utility of drug measurement and pharmacokinetics: therapeutic drug monitoring in psychiatry.

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8.  F15063, a potential antipsychotic with dopamine D(2)/D(3) antagonist, 5-HT(1A) agonist and D(4) partial agonist properties: (IV) duration of brain D2-like receptor occupancy and antipsychotic-like activity versus plasma concentration in mice.

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9.  Induction of Drug Transporters Alters Disposition of Risperidone - A Study in Mice.

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Journal:  Pharmaceutics       Date:  2010-06-02       Impact factor: 6.321

10.  Long-term therapeutic drug monitoring of risperidone and olanzapine identifies altered steady-state pharmacokinetics: a clinical, two-group, naturalistic study.

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