Sentence examples for release of pharmaceuticals from inspiring English sources

Gold nanoparticles have emerged as one of the delivery systems with most potential for efficient transport and release of pharmaceuticals into diverse cell types.

Waste water treatment plants (WWTPs) have been identified as a major route for release of pharmaceuticals in aquatic bodies where concentrations ranging from ng/L to μg/L are ubiquitously detected.

Thus, using tunable PEG derivatives to encapsulate nanomagnets may facilitate the simultaneous regulation of localized temperature and sustained release of pharmaceuticals to the targeted cells in clinical practice.

Nanocarriers are a leading nanobiotechnology tool with the ability to provide protection, site-specific delivery, enhanced bioavailability and controlled release of pharmaceuticals, genetic material, imaging agents, nutraceuticals and cosmetics to name a few.

Incorporating metal ions into the aluminosilicate layer structure makes the corresponding nanomaterial attractive for various applications, including catalysis [24 26], controlled release of pharmaceuticals [27, 28] as well as lithium ion batteries [29, 30].

Advanced facilities such as these are not currently widespread, but they could be introduced to reduce the release of pharmaceuticals, pesticides, and endocrine disruptors into the aquatic environment.

Magnetic stimulation can be also exploited to regulate the release of pharmaceutical drugs, growth factors, and cells from hydrogels in a controlled manner, on-demand.

Still other materials have biological applications, such as diagnostic sensors that are compatible with living tissue, barriers that control the release of pharmaceutical molecules, and scaffolds for tissue repair.

Furthermore, it demonstrates the feasibility of studying the site of release of pharmaceutical compounds in vivo.

The results from this study therefore point to a potential use of amelogenin in targeted release of pharmaceutical proteins, induced by acidification, but the charge of the entrapped protein may be critical for proper particle formation.

This model is generally used to analyze the release of pharmaceutical polymeric dosage forms when the release mechanism is not well known or when more than one type of release phenomena could be involved (4) [ 38, 40]: (4) M t M ∞ = k t n, where M t / M ∞ is the fraction of drug released, k is the kinetic constants characteristic of the drug/polymer, n is the diffusional exponent for drug release.