Sentence examples for drug formation from inspiring English sources

It would be noteworthy if smectite clay can be grafted on different surfaces, while its nanospace is accommodated for special requirements such as targeted drug delivery, disintegrated agents in drug formation, selective removal of heavy metal contaminants, applications in high-temperature environments, and conducting polymers in wearable electronics.

Variation in genes that play a role at each step within the gemcitabine metabolic pathway could potentially influence the quantity of drug transported into the cell, metabolic inactivation of the drug, the rate of active drug formation and the quantity of active drug reaching its target(s).

Administration of medications may be compromised when patients require mechanical ventilation and enteral nutrition, but it is possible via an enteral feeding tube if the drug formation is suitable for enteral administration.

The ZnPcF16 offers several advantages over ZnPc for clinical applications, including improved solubility in most solvents, resulting in facilitated drug formation, favourable pharmacokinetics as well as the potential use in fluorine magnetic resonance (F-MR) imaging.

Also, many approaches to flexible polymeric support modification using specially developed LB equipment are described, including examples dealing with the effective ways of capsulation of drugs, formation of hybrid structures, and surface patterning, from the standpoint of medical or plastic electronic applications.

Since PP is a component of biological membranes and can alter the hydrophobicity of a drug after formation of the PC, it is hypothesized that the formation of a drug-PC could increase the permeation of drugs across membranes.

Next, the VP4-coated Fe3O4 NPs were loaded with doxorubicin (DOX), a typical anticancer drug, via formation of amide bond through the EDC approach.

Elastin-like polypeptides (ELPs) are biopolymers capable of in situ drug depot formation through thermally-driven supramolecular complexes at physiological temperatures.

With only a limited range of salmon delousing agents available, all of which have been in use for more than a decade, drug resistance formation has been reported for different products.

The effects of the DM and the multifunctional stabilizer concentration, solvent to anti-solvent ratio, crystallization and storage temperature, and ultrasonic time on drug particle formation during the anti-solvent processing were investigated and the nanosuspension stability was studied.

Thus, these studies may provide tools and strategies to control the effects of drug colloid formation in cell culture and reveal the significance of colloids in cell-based assays.