Inclusion of lignocaine base into a polar lipid formulation -in vitrorelease, duration of peripheral nerve block and arterial blood concentrations in the rat-Reference-Cited by-同舟云学术

Inclusion of lignocaine base into a polar lipid formulation -in vitrorelease, duration of peripheral nerve block and arterial blood concentrations in the rat

Published:2001-05 Issue:5 Volume:45 Page:583-589
ISSN:0001-5172
Container-title:Acta Anaesthesiologica Scandinavica
language:en
Short-container-title:

Author:

Dyhre H.,Wallin R.,Björkman S.,Engström S.,Renck H.

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-6576.2001.045005583.x/fullpdf

Reference17 articles.

1. Slow-release formulations of local anesthetics and opioids.;Renck;Curr Opin Anesth,1996

2. Progress in the development of ultra-long-acting local anesthetics.;Kuzma;Reg Anesth,1997

3. Prolonged regional nerve blockade. Injectable biodegradable bupivacaine/polyester microspheres.;Curley;Anesthesiology,1996

4. Glucocorticoids prolong rat sciatic nerve blockade in vivo from bupivacaine microspheres.;Castillo;Anesthesiology,1996

5. A study of polar lipid drug carrier systems undergoing a thermoreversible lamellar-to-cubic phase transition.;Engström;Int J Pharm,1992

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