Biomimetic adsorbent named as PHBBMA was prepared from lipophilic poly-3-hydroxybutyrate （PHB） by a modified double emulsion solvent evaporation method. PHBBMA, characterized by using scanning electron microscope an...Biomimetic adsorbent named as PHBBMA was prepared from lipophilic poly-3-hydroxybutyrate （PHB） by a modified double emulsion solvent evaporation method. PHBBMA, characterized by using scanning electron microscope and nitrogen adsorption/desorption measurements, is porous spherical particles. The characterization with the thermal gravimetric analysis and differential scanning calorimetry, 1 H nuclear magnetic resonance and Fourier transform infrared spectroscopy showed that PHBBMA preparation was a physical process without chemical reaction. The adsorption of PHBBMA for o-nitrochlorobenzene （o-NCB） was fitted better by Langmuir model than by Freundlich model, while the pseudo second-order model fitting was better than the pseudo first-order model fitting. The maximal adsorption capacity of PHBBMA for o-NCB was 57.83 mg/g at 30°C, although its specific surface area （S BET ） was only 8.45 m 2 /g. PHBBMA is a safe and environmental friendly adsorbent with high adsorption capacity because its component is innocuous and biodegradable PHB produced reusing wastes and contaminants, no byproduct can produced, and its ester and hydrocarbyl groups have strong affinity with organochlorine compounds. The further work will focus on the modification and improvement of PHBBMA in order to increase its S BET and adsorption capacity.展开更多
Abstract: Objective To apply the response surface-central composite design to developing and optimizing the oral fastdisintegrating tablets (ODT) formulation for Jiawei Qing’e, a kind of prescription of Chinese herba...Abstract: Objective To apply the response surface-central composite design to developing and optimizing the oral fastdisintegrating tablets (ODT) formulation for Jiawei Qing’e, a kind of prescription of Chinese herbal medicine.Methods The bitterness of Jiawei Qing’e was masked using Eudragit E-100 by solvent evaporation technique.Response surface approach was applied to investigating the interaction of formulation parameters in optimizing theformulation. The independent variables were Eudragit E-100/drug ratio (X1), amount of disintegrants (X2), and theamount of diluents (X3). The disintegration time (Y1), hardness (Y2), and weight variations of the tablets werecharacterized. Results The models predicted levels of X1= 4.63%, X2= 5.25%, and X3= 34.33%, for the optimalformulation having a hardness of 3.0 kg with the disintegration time of 30 s within experimental region. The observedresponse of Y1= 26.5 s and Y2= 3.14 kg reasonably agreed with the predicted response. Conclusion Responsesurface methodology shows the good predictability and reliability in optimizing the formulation. The optimized ODTof Jiawei Qing’e has acceptable taste, rapid disintegrating ability, and good mechanical strength.展开更多
Biodegradable triblock copolymer PLA/PEG/PLA was synthesized by ring-opening bulk polymerization of D,L-lactide in the presence of poly(ethylene glycol) (PEG), in the molecular structure of which, the length of PEG an...Biodegradable triblock copolymer PLA/PEG/PLA was synthesized by ring-opening bulk polymerization of D,L-lactide in the presence of poly(ethylene glycol) (PEG), in the molecular structure of which, the length of PEG and PLA chain segments was made to be quite different. Nanoparticles were prepared by using the copolymer via a double emulsion-evaporation technique. The paticles tended to form the configuration like capsules, i.e., the nanocapsules, because of the great size difference in PEG and PLA segments of the copolymer. Insulin, chosen as a model drug, was encapsulated into nanocapsules. The effect of preparation conditions on the size, insulin encapsulation efficiency, and in vitro drug release behavour of the nanoparticles were investigated. The experimental results show that the nanocapsules had a smooth spherical surface and the mean diameter was in the range from 180 nm to 350 nm, and the entrapment of insulin achieved up to 78.4. The drug-loaded nanocapsules released their content continuously, remarkably different from the corresponding micelles which gave a significant initial burst release followed by a slow release.展开更多
基金supported by the National Hi-Tech Research and Development Program (863) ofChina (No. 2006AA06Z378)the National Natural Science Foundation of China (No. 20777018, 20977035)+1 种基金the National Key Technology R&D Program of China(No. 2008BAC32B06-1)the Science and Technology Plan Project of Guangdong Province, China (No.2007B030103011)
文摘Biomimetic adsorbent named as PHBBMA was prepared from lipophilic poly-3-hydroxybutyrate （PHB） by a modified double emulsion solvent evaporation method. PHBBMA, characterized by using scanning electron microscope and nitrogen adsorption/desorption measurements, is porous spherical particles. The characterization with the thermal gravimetric analysis and differential scanning calorimetry, 1 H nuclear magnetic resonance and Fourier transform infrared spectroscopy showed that PHBBMA preparation was a physical process without chemical reaction. The adsorption of PHBBMA for o-nitrochlorobenzene （o-NCB） was fitted better by Langmuir model than by Freundlich model, while the pseudo second-order model fitting was better than the pseudo first-order model fitting. The maximal adsorption capacity of PHBBMA for o-NCB was 57.83 mg/g at 30°C, although its specific surface area （S BET ） was only 8.45 m 2 /g. PHBBMA is a safe and environmental friendly adsorbent with high adsorption capacity because its component is innocuous and biodegradable PHB produced reusing wastes and contaminants, no byproduct can produced, and its ester and hydrocarbyl groups have strong affinity with organochlorine compounds. The further work will focus on the modification and improvement of PHBBMA in order to increase its S BET and adsorption capacity.
基金Major Projects of National Science and Technology on"New Drug Creation and Development"(2012ZX09103201-0462012ZX09101212)
文摘Abstract: Objective To apply the response surface-central composite design to developing and optimizing the oral fastdisintegrating tablets (ODT) formulation for Jiawei Qing’e, a kind of prescription of Chinese herbal medicine.Methods The bitterness of Jiawei Qing’e was masked using Eudragit E-100 by solvent evaporation technique.Response surface approach was applied to investigating the interaction of formulation parameters in optimizing theformulation. The independent variables were Eudragit E-100/drug ratio (X1), amount of disintegrants (X2), and theamount of diluents (X3). The disintegration time (Y1), hardness (Y2), and weight variations of the tablets werecharacterized. Results The models predicted levels of X1= 4.63%, X2= 5.25%, and X3= 34.33%, for the optimalformulation having a hardness of 3.0 kg with the disintegration time of 30 s within experimental region. The observedresponse of Y1= 26.5 s and Y2= 3.14 kg reasonably agreed with the predicted response. Conclusion Responsesurface methodology shows the good predictability and reliability in optimizing the formulation. The optimized ODTof Jiawei Qing’e has acceptable taste, rapid disintegrating ability, and good mechanical strength.
文摘Biodegradable triblock copolymer PLA/PEG/PLA was synthesized by ring-opening bulk polymerization of D,L-lactide in the presence of poly(ethylene glycol) (PEG), in the molecular structure of which, the length of PEG and PLA chain segments was made to be quite different. Nanoparticles were prepared by using the copolymer via a double emulsion-evaporation technique. The paticles tended to form the configuration like capsules, i.e., the nanocapsules, because of the great size difference in PEG and PLA segments of the copolymer. Insulin, chosen as a model drug, was encapsulated into nanocapsules. The effect of preparation conditions on the size, insulin encapsulation efficiency, and in vitro drug release behavour of the nanoparticles were investigated. The experimental results show that the nanocapsules had a smooth spherical surface and the mean diameter was in the range from 180 nm to 350 nm, and the entrapment of insulin achieved up to 78.4. The drug-loaded nanocapsules released their content continuously, remarkably different from the corresponding micelles which gave a significant initial burst release followed by a slow release.
