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A promethazine (PMZ) molecularly imprinted polymer (MIP) and a non-imprinted polymer (NIP) were synthesized by two different formulations of methacrylic acid ethylene glycol dimethacrylate (MAA EGDMA) and vinyl benzene divinyl benzene (VB DVB).
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Two different formulations of additive-by-additive effects have been presented in the literature [ 23, 24] and both of them were considered.
Tables 4 and 5 show the 90% CIs and the mean ratio of the test-to-reference formulations for Cmax and AUC0 ∞ for gamma and delta tocotrienols in the two different formulations.
Two different formulations of the new method have been explored.
Two different formulations are proposed.
However, two different formulations of this gain have been used.
Two different formulations of the proposed distribution are presented in this section.
A decentralized and a distributed KF are two different formulations of the same KF algorithm[19].
The first is to predict the stAlgorithms next time instance.
The model simulates different therapy adherence scenarios for the two different formulations.
Here, for the first time, we describe how particle size distributions can be modulated differently using two different formulation excipients by shifting size distribution modes to different locations and by modifying the amplitude of the modes.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com