Physicochemical properties and oral bioavailability of ursolic acid nanoparticles using supercritical anti-solvent (SAS) process

► Nanoscale ursolic acid (UA) was made by a supercritical antisolvent process. ► Mean particle size of processed UA is 139.2±19.7nm, irregularly spherical. ► Dissolution rate and oral bioavailability of nanoscale UA increased significantly. The objective of the study was to prepare ursolic acid (UA)...

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Veröffentlicht in:Food chemistry 2012-05, Vol.132 (1), p.319-325
Hauptverfasser: Yang, Lei, Sun, Zhen, Zu, Yuangang, Zhao, Chunjian, Sun, Xiaowei, Zhang, Zhonghua, Zhang, Lin
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container_end_page 325
container_issue 1
container_start_page 319
container_title Food chemistry
container_volume 132
creator Yang, Lei
Sun, Zhen
Zu, Yuangang
Zhao, Chunjian
Sun, Xiaowei
Zhang, Zhonghua
Zhang, Lin
description ► Nanoscale ursolic acid (UA) was made by a supercritical antisolvent process. ► Mean particle size of processed UA is 139.2±19.7nm, irregularly spherical. ► Dissolution rate and oral bioavailability of nanoscale UA increased significantly. The objective of the study was to prepare ursolic acid (UA) nanoparticles using the supercritical anti-solvent (SAS) process and evaluate its physicochemical properties and oral bioavailability. The effects of four process variables, pressure, temperature, drug concentration and drug solution flow rate, on drug particle formation during SAS process, were investigated. Particles with mean particle size ranging from 139.2±19.7 to 1039.8±65.2nm were obtained by varying the process parameters. The UA was characterised by scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, thermal gravimetric analysis, specific surface area, dissolution test and bioavailability test. It was concluded that physicochemical properties and bioavailability of crystalline UA could be improved by physical modification, such as particle size reduction and generation of amorphous state using SAS process. Further, SAS process was a powerful methodology for improving the physicochemical properties and bioavailability of UA.
doi_str_mv 10.1016/j.foodchem.2011.10.083
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The objective of the study was to prepare ursolic acid (UA) nanoparticles using the supercritical anti-solvent (SAS) process and evaluate its physicochemical properties and oral bioavailability. The effects of four process variables, pressure, temperature, drug concentration and drug solution flow rate, on drug particle formation during SAS process, were investigated. Particles with mean particle size ranging from 139.2±19.7 to 1039.8±65.2nm were obtained by varying the process parameters. The UA was characterised by scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, thermal gravimetric analysis, specific surface area, dissolution test and bioavailability test. It was concluded that physicochemical properties and bioavailability of crystalline UA could be improved by physical modification, such as particle size reduction and generation of amorphous state using SAS process. 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subjects Administration, Oral
Bioavailability
Biological and medical sciences
Biological Availability
Chemical Phenomena
Dissolution
Drugs
Feeding. Feeding behavior
Flow rate
Food industries
Fundamental and applied biological sciences. Psychology
Nanoparticles
Nanoparticles - chemistry
Process parameters
SAS
Solvents - chemistry
Specific surface
Supercritical anti-solvent process
Triterpenes - chemistry
Ursolic Acid
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Physicochemical properties and oral bioavailability of ursolic acid nanoparticles using supercritical anti-solvent (SAS) process
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