British Journal of Plastic Surgery 1994-04-01

An evaluation of a new lactic acid polymer drug delivery system: a preliminary report.

Y Sawada, T Ohkubo, M Kudoh, K Sugawara, K Otani, J Sasaki

Index: Br. J. Plast. Surg. 47(3) , 158-61, (1994)

Full Text: HTML

Abstract

A new drug delivery system, made of a mixture of DL-lactic acid polymer and a copoly (L-lactic acid/delta-valerolactone) polymer (LAP) containing varying concentrations of Ofloxacin, has been evaluated. Results revealed that a LAP drug delivery system containing 0.03% Ofloxacin inhibited the in vitro growth of clinically derived Staphylococcus aureus and Pseudomonas aeruginosa. Further, in an in vivo situation in rats, at 1 week after the wound was inflicted, no infection was macroscopically seen in split-thickness wounds that had been covered by LAP drug delivery system containing 0.5 or 0.03% Ofloxacin, and more than 80% of the wound area had epithelialised.


Related Compounds

  • delta-Valerolacton...

Related Articles:

Antimicrobial properties of Kalanchoe blossfeldiana: a focus on drug resistance with particular reference to quorum sensing-mediated bacterial biofilm formation.

2015-07-01

[J. Pharm. Pharmacol. 67 , 951-62, (2015)]

Characterization of the PON1 active site using modeling simulation, in relation to PON1 lactonase activity

2008-01-01

[Bioorg. Med. Chem. 16 , 7504-9, (2008)]

5- and 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors.

2012-01-01

[Bioorg. Med. Chem. Lett. 22 , 267-70, (2012)]

High affinity, stability, and lactonase activity of serum paraoxonase PON1 anchored on HDL with ApoA-I.

2005-09-06

[Biochemistry 44(35) , 11843-54, (2005)]

Switching of polymerization activity of cinnamoyl-alpha-cyclodextrin.

2009-04-21

[Org. Biomol. Chem. 7(8) , 1646-51, (2009)]

More Articles...