Sentence examples for two liposome formulations from inspiring English sources

To optimize the size of the liposomal platform, J3 was non-covalently conjugated to the surface of two liposome formulations with diameters of 100 or 200 nm, each with approximately the same Vhh densities.

Consequently, one validated parameter was selected to monitor drug release from two liposome formulations, and compare their ultrasound sensitivity.

Comparing the two liposome formulations, no statistically significant difference was noted.

For initiating Ca2+ signaling, two liposome formulations were prepared encapsulating either 500 μM IP3 or 50 μM AdA in PBS and gold coated.

There was no apparent difference between the two liposome formulations, indicating that the association of RGD-PEG liposomes with tumour endothelium does not improve therapeutic efficacy compared with PEG liposomes, which do not display a specific endothelial cell interaction.

A total of five liposome formulations were prepared.

Three liposome formulations varying in the concentration of DSPE-PEG-maleimide were investigated.

However, the DSPE-PEG2000 liposome, D, showed no cellular internalization, and although the FACS results showed that the percentage of cells that were labelled by liposome D was similar to the three DODEG4 liposome formulations A, B and C, the degree of shift in fluorescence was much lower.

Optimization of formulation variables for the preparation of the liposome was performed and then three liposomal formulations (TPGS-liposome, TPGS-chitosome, chitosome) were prepared with narrow size distribution and high encapsulation efficiency.

The in v itro uptake experiments showed that the three different cancer cell types all labelled and internalised each of the Gd chelated liposome formulations A, B and C containing the oligoethylene glycol spacer lipid DODEG4, although to differing degrees.

Selected liposome formulations [23 25] with encapsulated compound 1 were prepared.