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The NPs were prepared by multiple solvent emulsification method.
Microparticles were prepared by O/O solvent emulsification method.
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Biodegradable microspheres were prepared by solvent emulsification evaporation method in different polymer:drug ratios (1 1, 2 1 and 3 1).
DHA N/O/W emulsion was prepared by a modified solvent evaporation and membrane emulsification method.
NPs were prepared by an oil/water emulsification method using Eudragit RS or poly(lactide‐co‐glycolide) (PLGA) as matrix polymer and dichloromethane (DCM) or ethyl acetate (EA) as organic solvent while ibuprofen was entrapped as model drug.
The formulation was prepared by a high energy emulsification method and optimized by response surface methodology.
Previously, Varshosaz et al. reported the preparation of carvedilol nanoparticles by emulsification method [19].
Without depending on the wettability changes of the membrane, the CIBs score similarly as membrane emulsification, which is the most energy friendly emulsification method known in literature.
The spontaneous emulsification method was used to prepare different formulations containing 2 mg/mL CBZ.
A series of matrices named Ag Zn were prepared by water-in-oil emulsification method.
The self-emulsification process of oil/surfactant/cosurfactant system was visually inspected after aqueous titration (spontaneous emulsification) method [ 25].
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