Literature DB >> 8544481

Manufacture and release characteristics of Elvax polymers containing glutamate receptor antagonists.

A L Smith1, P M Cordery, I D Thompson.   

Abstract

Implantable sustained-release polymers offer an alternative to osmotic minipumps for the local delivery of drugs to specific brain areas. Here we describe the production of Elvax polymers containing a range of glutamate receptor antagonists and the quantitative characterization of their release properties. Sections of Elvax (200 or 400 microns), prepared by a dimethyl sulphoxide-based method, containing the NMDA antagonist MK-801 or the non-NMDA antagonist CNQX exhibited similar release profiles: an initial 2-week burst followed by a slow decline in release rate over the next 6 weeks. Differences in slice preparation method and thickness or drug concentration and solubility all led to alterations in the level of drug release, but not the overall exponential nature of the release curve. Elvax sections prepared by an aqueous method containing the NMDA antagonists CPP or APV displayed more constant but much lower levels of release than those from the dimethyl sulphoxide-based method. The in vitro release characteristics were compared with in vivo release of MK-801 and the close correspondence observed indicates that the in vitro release data is an accurate predictor of the drug release behaviour of implanted Elvax slices.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8544481     DOI: 10.1016/0165-0270(95)00014-l

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  14 in total

1.  Critical period for activity-dependent synapse elimination in developing cerebellum.

Authors:  S Kakizawa; M Yamasaki; M Watanabe; M Kano
Journal:  J Neurosci       Date:  2000-07-01       Impact factor: 6.167

2.  Bidirectional modulation of visual plasticity by cholinergic receptor subtypes in the frog optic tectum.

Authors:  Chuan-Jiang Yu; Christopher M Butt; Elizabeth A Debski
Journal:  Eur J Neurosci       Date:  2003-03       Impact factor: 3.386

3.  Developmental period for N-methyl-D-aspartate (NMDA) receptor-dependent synapse elimination correlated with visuotopic map refinement.

Authors:  Matthew T Colonnese; Martha Constantine-Paton
Journal:  J Comp Neurol       Date:  2006-02-10       Impact factor: 3.215

4.  Inhibitory plasticity facilitates recovery of stimulus velocity tuning in the superior colliculus after chronic NMDA receptor blockade.

Authors:  Khaleel A Razak; Sarah L Pallas
Journal:  J Neurosci       Date:  2007-07-04       Impact factor: 6.167

5.  Action-based body maps in the spinal cord emerge from a transitory floating organization.

Authors:  Marcus Granmo; Per Petersson; Jens Schouenborg
Journal:  J Neurosci       Date:  2008-05-21       Impact factor: 6.167

6.  Chronic NMDA receptor blockade from birth increases the sprouting capacity of ipsilateral retinocollicular axons without disrupting their early segregation.

Authors:  M T Colonnese; M Constantine-Paton
Journal:  J Neurosci       Date:  2001-03-01       Impact factor: 6.167

7.  Developmental depression of glutamate neurotransmission by chronic low-level activation of NMDA receptors.

Authors:  J Shi; S M Aamodt; M Townsend; M Constantine-Paton
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

8.  Activity-dependent regulation of substance P expression and topographic map maintenance by a cholinergic pathway.

Authors:  S Tu; C M Butt; J R Pauly; E A Debski
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

9.  NMDA antagonists in the superior colliculus prevent developmental plasticity but not visual transmission or map compression.

Authors:  L Huang; S L Pallas
Journal:  J Neurophysiol       Date:  2001-09       Impact factor: 2.714

10.  The behavioral and biochemical effects of BDNF containing polymers implanted in the hippocampus of rats.

Authors:  Rachael W Sirianni; Peter Olausson; Amy S Chiu; Jane R Taylor; W Mark Saltzman
Journal:  Brain Res       Date:  2010-01-21       Impact factor: 3.252

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.