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Additional advantages of polymeric nanocarriers include ease in surface modification, greater encapsulation efficiency of the payload, payload protection, large surface area-to-volume ratio, and the ability to modify the rate of polymer erosion for temporal control over the release of nucleotides [17].
Other advantages include ease in surface modification, greater encapsulation efficiency of the payload, payload protection, large surface area-to-volume ratio, and slow or fast polymer erosion for temporal control over the release of drugs [ 17].
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This procedure yielded a fine powder with at least 70% recovery and protein encapsulation efficiency greater than 94%.
The encapsulation efficiency was greater than 94%, the drug weight content approximately 10% and the yield in the 72.5 90.0% range.
AWP liposomes had slightly lower encapsulation efficiency than encapsulated CWP.
When 0.10 g MPS/g silica was used to modify silica, the encapsulation efficiency of silica was greater than 95%, and the degree of grafting of acrylate polymer onto silica was about 60%.
The characterisation of the nanoparticles (NP) revealed that the encapsulation efficiency (EE) of NLC-rhEGF was significantly greater than obtained with SLN-rhEGF.
The encapsulation efficiency for these batches was 70% or greater (the average size of homogenized LVCN was 83 nm).
Absorbance was converted to amount of drug using a standard graph and the encapsulation efficiency was calculated using the following: (1) Encapsulation Efficiency = Drug encapsulated Total Drug × 100.
encapsulation efficiency.
represents encapsulation efficiency.
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