Literature DB >> 30181718

A Clinician's Guide to Oral Extended-Release Drug Delivery Systems in Epilepsy.

James W Wheless, Stephanie J Phelps.   

Abstract

Epilepsy is one of the most common chronic neurologic disorders that affects individuals of all ages. It is primarily managed with antiepileptic drugs (AEDs), with the goal of maintaining complete seizure control combined with minimal or no adverse effects. Oral administration is the mainstay of AED delivery for patients with chronic epilepsy and consists essentially of immediate-release (IR) and modified-release (delayed-release and extended-release [ER]) dosage formulations. Extended-release formulations (hydrophilic or hydrophobic matrix systems, reservoir systems, and osmotic-release systems) release a drug in a controlled manner during an extended period of time following administration. Extended-release formulations have many advantages compared with IR formulations, including simplification of dosing regimens, reduction in pill burden, and reduction in the peak-to-trough fluctuations in serum drug concentration that may be associated with a decreased risk of adverse effects and of seizures. These advantages have the potential to increase adherence to antiepileptic therapy, improve the quality of life of patients, and reduce health care costs. This article, which is intended as a practical guide for clinicians, reviews the properties of the different ER AED formulations currently available and discusses the advantages of ER over IR formulations. Subsequently, an explanation of the technologic basis of the different oral ER formulations, the critical attributes that differentiate ER products, and their individual strengths and weaknesses is provided. Specific recommendations to practitioners on treating patients with ER formulations are included.

Entities:  

Keywords:  antiepileptic drugs; dosage formulations; epilepsy; extended-release; immediate-release; modified-release formulations; seizure; treatment

Year:  2018        PMID: 30181718      PMCID: PMC6117810          DOI: 10.5863/1551-6776-23.4.277

Source DB:  PubMed          Journal:  J Pediatr Pharmacol Ther        ISSN: 1551-6776


  42 in total

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4.  Generic lamotrigine versus brand-name Lamictal bioequivalence in patients with epilepsy: A field test of the FDA bioequivalence standard.

Authors:  Tricia Y Ting; Wenlei Jiang; Robert Lionberger; Jessica Wong; Jace W Jones; Maureen A Kane; Allan Krumholz; Robert Temple; James E Polli
Journal:  Epilepsia       Date:  2015-07-23       Impact factor: 5.864

5.  Impact of nonadherence to antiepileptic drugs on health care utilization and costs: findings from the RANSOM study.

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7.  Improved CNS tolerability following conversion from immediate- to extended-release carbamazepine.

Authors:  A D Miller; G L Krauss; F M Hamzeh
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Journal:  Ther Adv Drug Saf       Date:  2013-04

9.  Prevalence and cost of nonadherence with antiepileptic drugs in an adult managed care population.

Authors:  Keith L Davis; Sean D Candrilli; Heather M Edin
Journal:  Epilepsia       Date:  2007-11-21       Impact factor: 5.864

10.  Bimodal gastroretentive drug delivery systems of lamotrigine: formulation and evaluation.

Authors:  R R Poonuru; C S R Gonugunta
Journal:  Indian J Pharm Sci       Date:  2014 Nov-Dec       Impact factor: 0.975

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8.  Once-nightly sodium oxybate (FT218) demonstrated improvement of symptoms in a phase 3 randomized clinical trial in patients with narcolepsy.

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