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Optimised liquid formulations were formulated into free flowing granules (S-SNEDDS) by adsorption on the porous materials like Aerosil 200 and Neusilin and thereby compressed into tablet.
All the SLN formulations were formulated into gel using carbopol 934 (carboxyvinyl polymer).
For tissue samples, the tissues were formulated into homogenates using saline solution.
The prepared SLN were formulated into a gel preparation, using carbopol 940.
QSPRs and structural constraints were formulated into an optimization problem which was solved stochastically via Tabu Search.
Two micronized drugs, nitrazepam and flunitrazepam, were formulated into lactose-based interactive mixtures containing a micronized surfactant.
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One of these formulations is Melaleuca alternafolia, or Australian tea tree oil that has been formulated into an oral solution.
Such a drug might be formulated into an extended-release dosage form so that the modified tablet or capsule need be taken only once or twice a day.
Adsorption equilibrium data are formulated into an isotherm model.
Then (3.5) can be formulated into the abstract form (1.1).
The problem is formulated into a bi-level programming problem.
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