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Various formulations were prepared using 23 factorial designs.
Formulations were prepared using high-acrylonitrile-content nitrile rubber by employing a two-level experimental design.
The formulations were prepared using Gelucire® 50/13 and Lutrol® F68 as meltable binders.
Various formulations were prepared using different ratios of oils, surfactants and co-surfactants (S&CoS).
Three formulations were prepared using this simple method, including plain liposomes, PEGylated liposomes and folic acid functionalised liposomes, all with a fluorescence dye encapsulated for imaging.
Accordingly, 12 formulations were prepared using a full factorial screening design and monitored over a 3 month period at 40 °C and 75%.
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Theophylline containing pellet formulation was prepared using a matrix consisted of ethylcellulose, microcrystalline cellulose and lactose.
The graft co-polymer-based nanocomposite formulation was prepared using the single-emulsion technique.
PSL formulation was prepared using small unilamellar vesicles of DOPE and CHEMS (6:4 molar ratio) by REV method.
This formulation was prepared using melt-homogenization method, composed of 3-[N(N′,N′-dimethylaminoethane -carbamol] cholesterol (DC-Chol), dioleoylphosphatidylethaN′-dimethylaminoethane -carbamolimyristiN′-dimethylaminoethane -carbamolw).
When the final formulation was prepared using a GMP lyophilizer, radiolabeling yields improved to nearly 90%. Figure 4 Concentration of peptide in a kit versus radiolabeling yield heated 15 min at different temperatures.
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