Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 178-185 
    ISSN: 1435-1536
    Keywords: Cholesterol ; membrane fluidity ; muramyldipeptide ; phospholipid ; vesicle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary The muramyldipeptide derivative B30-MDP has immunoadjuvant activity and vesicleforming ability in aqueous solutions. To assist in the clinical application of B30-MDP to liposomal vaccine, we investigated the physicochemical properties including membrane fluidity, surface charge and particle size of B30-MDP vesicles containing cholesterol, dipalmitoylphosphatidyl-choline (DPPC) or dipalmitoylphosphatidylglycerol (DPPG). The membrane fluidity of B30-MDP/cholesterol vesicles was slightly influenced by cholesterol concentration and temperature. The membrane fluidity of B30-MDP/phospholipid vesicle was dependent on temperature. ESR spectra clearly showed the good miscibility of cholesterol with B30-MDP and the occurrence of phase separation between B30-MDP and phospholipid. The surface charge and particle size of B30-MDP/cholesterol vesicles were hardly influenced by cholesterol concentration in the membrane because the membrane surface was covered with the hydrophilic region of B30-MDP. The effect of this hydrophilic region of B30-MDP on the surface charge and particle size of B30-MDP/phospholipid vesicle was greater than that of phospholipid. This study showed that the membrane structure of B30-MDP/cholesterol vesicle differed from that of B30-MDP/phospholipid vesicle. Further, the hydrophilic region of B30-MDP is considered to play an important role in the physicochemical properties and formation of the vesicle.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1435-1536
    Keywords: Cholesterol ; membrane fluidity ; muramyldipeptide ; phospholipid ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Application of the muramyldipeptide derivative B30-MDP to liposomal vaccines will aid in the development of improved high immunogenicity vaccines. To give full play to the effectiveness of B30-MDP as a liposomal vaccine, it is important to evaluate the effect of cholesterol, dimyristoylphosphatidylcholine (DMPC) or distearoylphosphatidylcholine (DSPC) incorporation on the chemical stability of B30-MDP and physicochemical properties of B30-MDP/lipid mixed vesicles from the view point of pharmaceutics. The observed degradation rate constants of B30-MDP by hydrolysis in B30-MDP/cholesterol mixed vesicles were increased with increasing concentration of cholesterol, however, those in B30-MDP/DMPC and B30-MDP/DSPC mixed vesicles were unchanged with increasing concentration of DMPC and DSPC. The degradation behavior of B30-MDP was then compared with physicochemical properties of B30-MDP/lipid mixed vesicles, such as membrane fluidity and particle size. It was apparent that the degradation of B30-MDP in B30-MDP/cholesterol mixed vesicles was influenced by the particle size, but not by the fluidity of the membranes. In the case of B30-MDP/phospholipid mixed vesicles, MDP/phospholipid mixed vesicles, the degradation of B30-MDP was not influenced by either the membranes' fluidity or the particle size of the mixed vesicles. It is considered that the degradation of B30-MDP in the mixed vesicles is dependent on the membrane state, and the addition of cholesterol to B30-MDP vesicle inhibits the mutual interaction of MDP regions, whereas the addition of phospholipids hardly influences the mutual interaction of MDP regions, possibly owing to phase separation between B30-MDP and phospholipids.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...