High impact information on Myristin

• Lipopolysaccharide- and PMA-activated macrophages from mice fed the trimyristin diet had significantly greater levels of MacMARCKS than LPS- and PMA-activated macrophages of mice fed the safflower oil-containing diet [1].
• The flow behavior of low concentrated dispersions of solid lipid nanoparticles consisting of either trimyristin, tripalmitin or tristearin and different ionic and nonionic stabilizer blends were investigated using a rheometer with cone and plate apparatus and an Ubbelohde type capillary viscometer [2].
• Cytotoxicity studies of Dynasan 114 solid lipid nanoparticles (SLN) on RAW 264.7 macrophages-impact of phagocytosis on viability and cytokine production [3].
• In the present study, the n-hexane extract of Myristica fragrans (MF) seeds, acetone-insoluble part of the n-hexane extract (AIMF) and trimyristin (TM) were assessed for their anxiogenic activity [4].
• Murine peritoneal macrophages were incubated with SLN formulations consisting of Dynasan 114 coated with different surfactants [5].

Associations of Myristin with other chemical compounds

• The levels of MacMARCKS were also greater in lysates of LPS plus rIFNgamma-stimulated macrophages from mice fed the trimyristin diet and mice fed a diet containing a moderate level of myristic acid (12 g/100 g fatty acids) compared with the lysates of macrophages from mice fed the safflower oil diet [1].
• Hamsters were fed diets containing fat (5-20%, w/w) consisting of triolein (TO) alone or 50% triolein plus 50% trimyristin (TM), tripalmitin (TP) or tristearin (TS) for 28 days [6].
• The TM-rich diets produced a concentration-dependent increase in total plasma cholesterol which was a result of significant increases in both VLDL and HDL levels [7].

Analytical, diagnostic and therapeutic context of Myristin

• The rheology and capsule filling properties of molten excipients, Dynafill, Dynasan-114 [8].

References