Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
ACS Nano ; 14(3): 3563-3575, 2020 03 24.
Article in English | MEDLINE | ID: mdl-32053346

ABSTRACT

Polymeric nanoparticles (NPs) are an important category of drug delivery systems, and their in vivo fate is closely associated with delivery efficacy. Analysis of the protein corona on the surface of NPs to understand the in vivo fate of different NPs has been shown to be reliable but complicated and time-consuming. In this work, we establish a simple approach for predicting the in vivo fate of polymeric NPs. We prepared a series of poly(ethylene glycol)-block-poly(d,l-lactide) (PEG-b-PLA) NPs with different protein binding behaviors by adjusting their PEG densities, which were determined by analyzing the serum protein adsorption. We further determined the protein binding affinity, denoted as the equilibrium association constant (KA), to correlate with in vivo fate of NPs. The in vivo fate, including blood clearance and Kupffer cell uptake, was studied, and the maximum concentration (Cmax), the area under the plasma concentration-time curve (AUC), and the mean residence time (MRT) were negatively linearly dependent, while Kupffer cell uptake was positively linearly dependent on KA. Subsequently, we verified the reliability of the approach for in vivo fate prediction using poly(methoxyethyl ethylene phosphate)-block-poly(d,l-lactide) (PEEP-b-PLA) and poly(vinylpyrrolidone)-block-poly(d,l-lactide) (PVP-b-PLA) NPs, and the linear relationship between the KA value and their PK parameters further suggests that the protein binding affinity of polymeric NPs can be a direct indicator of their pharmacokinetics.


Subject(s)
Blood Proteins/chemistry , Nanoparticles/chemistry , Polymers/pharmacokinetics , Adsorption , Animals , Injections, Intravenous , Male , Mice , Mice, Inbred C57BL , Mice, Inbred ICR , Nanoparticles/administration & dosage , Particle Size , Polymers/administration & dosage , Polymers/chemistry , Protein Binding , RAW 264.7 Cells , Surface Properties
2.
Food Funct ; 5(1): 42-9, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24162728

ABSTRACT

Various alcoholic beverages containing different concentrations of ethanol are widely consumed, and excessive alcohol consumption may result in serious health problems. The consumption of alcoholic beverages is often accompanied by non-alcoholic beverages, such as herbal infusions, tea and carbonated beverages to relieve drunk symptoms. The aim of this study was to supply new information on the effects of these beverages on alcohol metabolism for nutritionists and the general public, in order to reduce problems associated with excessive alcohol consumption. The effects of 57 kinds of herbal infusions, tea and carbonated beverages on alcohol dehydrogenase and aldehyde dehydrogenase activity were evaluated. Generally, the effects of these beverages on alcohol dehydrogenase and aldehyde dehydrogenase activity are very different. The results suggested that some beverages should not be drank after excessive alcohol consumption, and several beverages may be potential dietary supplements for the prevention and treatment of problems related to excessive alcohol consumption.


Subject(s)
Alcohol Dehydrogenase/analysis , Aldehyde Dehydrogenase/analysis , Beverages/analysis , Plant Preparations/analysis , Alcohol Dehydrogenase/metabolism , Aldehyde Dehydrogenase/metabolism , Carbonated Beverages/analysis , Ethanol/metabolism , Humans , Tea/chemistry , Tea/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL