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The receptor solution was stirred at room temperature and at suitable time intervals the releasing medium (5.00 mL) was collected.
The PPy film as recognative absorbent has been applied for the selective loading and release of SA to the receptor solution.
The separation step, in turn, was based on a hydrophobic PTFE membrane, which separates the sample from receptor solution (electrolyte) where the electrodes were placed.
Release behavior studies of the pure citrate (equivalent weight is 0.632 g) and citrate-LDH incorporated lotion were carried out using the same method with the receptor solution at pH 4.
The design of the FT cell allowed for monitoring appearance of receptor solution within the donor chamber during the initial equilibration period, allowing for visual inspection of tissue integrity.
The two separate solutions were mixed to obtain a single modified EGF receptor solution.
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During metal ligand interaction the colors of the receptor solutions are significantly changed under UV-light and are promisingly useful in naked eye detection.
The acceptor medium was selected by determining the saturation concentration of vitamin E acetate in different candidate receptor solutions, selecting the one that provided the highest solubility, that is, 24.4 mg/mL.
While polystyrene NPs applied to a MN-treated human epidermal membrane reached receptor solutions in permeation experiments [23,24], poly lactic-co-glycolic (PLGA) NPs could not permeate full thickness human abdominal skin [22], murine [21], or porcine ear skin [10].
The addition of Cu2+ to the receptor 1 solution gave clear colour change from olive green to pink.
This adhesion of ConA to surfaces or molecules can change the concentration and the activity of the receptor in solution.
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