Sentence examples for depot release from inspiring English sources

The results showed the capability of properly designed ABC triblock copolymer micelles as reservoirs for drug solubilization and depot release at nanoscale dimensions.

We have developed a hyaluronic acid (HA -based self-polymerizing HA -basedthat serves as a platform for adhesion of structural motifs and a depot release for growthydrogels thatromote transerves stem cell survivas and differentiation.

Instead, olanzapine concentrations increase slowly after the olanzapine LAI injection, and the slow depot release maintains the olanzapine concentration within a range of approximately 5 to 73 ng/mL (10th percentile for 150 mg/2 weeks to 90th percentile for 300 mg/2 weeks at steady state) [ 5], which is within the range resulting from within-label oral olanzapine doses [ 7- 9].

It cannot be excluded that different adipose tissue depots release different combination of cytokines.

HIS cell depots released angiogenic factors which induced directional endothelial cell (EC) migration and tubule formation in a spatially defined assay system.

Fasting causes lipolysis in body fat depots releasing fatty acids, and the liver may increase its fatty acid uptake from the blood in proportion to their concentration in circulation [ 12].

Therefore, our study shows the utility of the PCgel as a depot for release of T lymphocytes and a convenient and valuable in vitro model for studying clinically relevant improvements to glioblastoma immunotherapy.

Adipose tissue, once viewed as simply a storage and release depot for lipids, is now considered an endocrine tissue [ 1, 2] that secretes various substances (adipokines), including tumor necrosis factor-alpha (TNF-α), interleukin (IL -6, leptIL -6diponectin, resistin, visfatin, and omenetin [ 3, 4].

Unlike current depots that release drugs in all direction by an isotropic way, we demonstrate that directional release only to a clinically beneficial direction results in improved disease treatment.

injection, ELP curcumin conjugates underwent a thermally triggered soluble insoluble phase transition, leading to in situ formation of a depot that released curcumin over 4 days post-injection and decreased plasma AUC 7-fold.

To compare final height, change in body mass index (BMI), and time from end of treatment until menarche in girls with central precocious puberty treated with the histrelin implant versus depot gonadotropin releasing hormone agonist injections.