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The effect of the skin on drug release were evaluated in vitro.
Sulfide microniches in sediments related to P release were evaluated by computer imaging densitometry (CID).
Viscoelasticity, water uptake, light transmissibility, cytocompatibility, zinc content, and drug loading and release were evaluated.
Their abilities of controlling drug release were evaluated using propranolol (PRO) and zaltoprofen (ZAL) in vitro and in vivo.
The characteristics of soil release were evaluated using two different soils (oil and water based) for its release rating and K/S value.
The effects of Tα1 pre-encapsulation, PLGA molecular weight, PLGA concentration and organic solvents composition on the in vivo Tα1 release were evaluated by subcutaneously injecting Tα1-loaded ISFI into Sprague Dawley Rats.
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Drug release was evaluated spectrophotometrically.
In vitro drug release was evaluated using the dynamic dialysis bag method [19].
This release was evaluated to be in the range 61 72 mol% on initial sulphur basis.
In vitro TA release was evaluated by liquid chromatography mass spectroscopy for 90 days.
Ovariectomized rats were treated for 1 week, and ACh release was evaluated using in vivo microdialysis.
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