Your browser doesn't support javascript.
loading
Chronic, intermittent convection-enhanced delivery devices.
Lewis, Owen; Woolley, Max; Johnson, David; Rosser, Anne; Barua, Neil U; Bienemann, Alison S; Gill, Steven S; Evans, Sam.
Afiliação
  • Lewis O; School of Medical Engineering, Queen's Building, Cardiff University, The Parade, Cardiff, CF24 3AA, UK; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK; Cardiff School of Biosciences, The Sir Martin
  • Woolley M; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK.
  • Johnson D; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK.
  • Rosser A; Cardiff School of Biosciences, The Sir Martin Evans Building, Museum Avenue, Cardiff, CF10 3AX, UK.
  • Barua NU; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK.
  • Bienemann AS; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK.
  • Gill SS; Functional Neurosurgery Research Group, University of Bristol, School of Clinical Sciences, Southmead Hospital, Learning & Research Building, UK.
  • Evans S; School of Medical Engineering, Queen's Building, Cardiff University, The Parade, Cardiff, CF24 3AA, UK.
J Neurosci Methods ; 259: 47-56, 2016 Feb 01.
Article em En | MEDLINE | ID: mdl-26617320
ABSTRACT

BACKGROUND:

Intraparenchymal convection-enhanced delivery (CED) of therapeutics directly into the brain has long been endorsed as a medium through which meaningful concentrations of drug can be administered to patients, bypassing the blood brain barrier. The translation of the technology to clinic has been hindered by poor distribution not previously observed in smaller pre-clinical models. In part this was due to the larger volumes of target structures found in humans but principally the poor outcome was linked to reflux (backflow) of infusate proximally along the catheter track. Over the past 10 years, improvements have been made to the technology in the field which has led to a small number of commercially available devices containing reflux inhibiting features. NEW

METHOD:

While these devices are currently suitable for acute or short term use, several indications would benefit from longer term repeated, intermittent administration of therapeutics (Parkinson's, Alzheimer's, Amyotrophic lateral sclerosis, Brain tumours such as Glioblastoma Multiforme (GBM) and Diffuse intrinsic Pontine Glioma (DIPG), etc.).

RESULTS:

Despite the need for a chronically accessible platform for such indications, limited experience exists in this part of the field. COMPARISON WITH EXISTING METHOD(S) At the time of writing no commercially available clinical platform, indicated for chronic, intermittent or continuous delivery to the brain exists.

CONCLUSIONS:

Here we review the improvements that have been made to CED devices over recent years and current state of the art for chronic infusion systems.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Sistemas de Liberação de Medicamentos / Catéteres Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Sistemas de Liberação de Medicamentos / Catéteres Idioma: En Ano de publicação: 2016 Tipo de documento: Article