## Abstract The purpose of this study was to investigate the antibacterial activity of newly developed amphiphilic lipids and DNA/lipid complexes against two types of oral bacteria and two types of hospital infection bacteria. Nine amphiphilic lipids were quantitatively prepared from the reaction o
Antifungal activity of DNA–lipid complexes and DNA–lipid films against Candida species
✍ Scribed by Y. Inoue; T. Fukushima; T. Hayakawa; R. Ogura; H. Kaminishi; K. Miyazaki; Y. Okahata
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 220 KB
- Volume
- 76A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In this study amphiphilic lipids, DNA–lipid complexes, and DNA–lipid films were prepared, and their antifungal activity against Candida species was examined. The amphiphilic lipids were synthesized from a reaction of glycine or L‐alanine with n‐alkyl alcohol in the presence of p‐toluene sulfonic acid. DNA–lipid complexes, which were prepared by the simple mixing of DNA and amphiphilic lipids, were insoluble in water. Self‐standing, water‐insoluble DNA–lipid films were prepared by casting the DNA–lipid complexes from a chloroform/ethanol solution. The antifungal activities of the lipids and DNA–lipid complexes against the Candida species were evaluated by minimum inhibitory concentrations (MICs); those of DNA–lipid films were evaluated by the disk diffusion method. The seven kinds of lipids, DNA–lipid complexes, and DNA–lipid films showed antifungal activity, and no differences were seen in the antifungal activities between glycine and L‐alanine derivatives. The lipids, DNA–lipid complexes, and DNA–lipid films, which have shorter alkyl chain length in lipids, showed antifungal activity against all Candida species. However, the effect of antifungal activity against Candida species decreased with increased alkyl chain length in lipids. In this study, it was found that lipids, DNA–lipid complexes, and films with a decyl or dodecyl group exhibit more favorable antifungal activity. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
📜 SIMILAR VOLUMES
Cationic lipid-based gene delivery systems have shown promise in transfecting cells both in vitro and in vivo. However, these systems tend to form aggregates in liquid formulation during storage, which has limited their clinical applications. As a result, lyophilization of these systems has recently
## Abstract magnified image A series of 47 novel __N__^1^‐alkylated‐2‐aryl‐5(6)‐substituted‐1__H__‐benzimidazoles and their three novel indole analogues were synthesized and evaluated for __in vitro__ antifungal activities against __Candida__ species by the tube dilution method. The results showed
It is well known that excipients are required to protect nonviral vectors during the lyophilization process. The goal of this study is to describe the stability of lyophilized nonviral vector preparations on pharmaceutically relevant timescales and provide insight into the factors that govern long-t