Sentence examples for evaluation in rats of from inspiring English sources

This study describes the preparation, characterization, and in vivo evaluation in rats of nanostructured lipid carriers (NLCs) encapsulating rimonabant (RMN) as prototypical cannabinoid antagonist.

This report described the synthesis of [18F]exendin-4 and its evaluation in rat and human pancreas.

Choi reported information-theoretical quantifier of brain rhythm based on data-driven multiscale representation for neurological deficit evaluation in rat.

Nonetheless, based on the carcinogenic potential of PPAR-activating compounds, current U.S. Food and Drug Administration FDAA) guidance on PPAR agonists requires 2-year carcinogenicity evaluations in rats and mice before initiation of human clinical studies longer than 6 months (U.S. FDA 2008).

The synthesis, radiosynthesis, and evaluation, in vitro and ex vivo in rat, of an 18F-radiotracer designed to image FAAH using positron emission tomography (PET) is described.

I will show that anticipatory mechanisms involved in rats' evaluation of possible routes give rise to satisfaction conditions of contents, and this is why they are representationally relevant for explaining and predicting rats' behavior.

The antidiabetic profiles of the extracts with significant antiradical and antioxidant activities was assessed using two complementary approaches: the glucose intolerance test (hypoglycaemic activity), and the evaluation of activity in rats with induced diabetes.

Additional evaluation of 22 in rats confirmed a significant glucose lowering effect for the high doses already after 10 min and for all doses after 30 min. This was in agreement with an observed increase in plasma insulin concentration, with maximum concentration 15 min after glucose challenge.

The feasibility of PET evaluation of arthritis activity in the rats of group A (0x boost) as compared to the original model was assessed.

The in vivo pharmacokinetic evaluation of PZA-LPPs in rats reveals that intratracheal insufflation of PZA-LPPs leads to a rapid absorption in plasma with an absolute bioavailability of 66%.

Evaluation in a syngeneic rat tumour model showed good targeting of CA20948 tumours (rat pancreatic tumour).