The aim of this study was to prepare arsenic trioxide （ATO）-loaded stealth PEGylated PLGA nanoparticles （PEG-PLGA-NPs） and to assess the merits of PEG-PLGA-NPs as drug carriers for ATO delivery. PEG-PLGA copolymer...The aim of this study was to prepare arsenic trioxide （ATO）-loaded stealth PEGylated PLGA nanoparticles （PEG-PLGA-NPs） and to assess the merits of PEG-PLGA-NPs as drug carriers for ATO delivery. PEG-PLGA copolymer was synthesized with methoxypolyethyleneglycol （Mw=5000）, D, L-lactide, and glycolide by the ring-opening polymerization method. Amorphous ATO was transformed into cubic crystal form to increase its solu-bility in the organic solvent. ATO-loaded PEG-PLGA-NPs were prepared by the modified spontaneous emulsification solvent diffusion （SESD） method, and the main experimental factors influencing the characteristics of nanopar- ticles were investigated, to optimize the preparation. To confirm the escape of PEG-PLGA-NPs from phagocytosis by phagocytes, PEG-PLGA-NPs labeled rhodamine B uptake by murine peritoneal macrophages （MPM） were analyzed by flow cytometry. The results showed that the physicochemical characteristics of PEG-PLGA-NPs were affected by the type and concentration of the emulsifiers, polymer concentration, and drug concentration. ATO-loaded PEG-PLGA-NPs, with particle size of 120.8nm, zeta potential of-10.73mV, encapsulation efficiency of 73.6%, and drug loading of 1.36%, were prepared under optimal conditions. The images of transmission electron micros-copy （TEM） indicated that the optimized nanoparticles were near spherical and without aggregation or adhesion. The release experiments in vitro showed the ATO release from PEG-PLGA-NPs exhibited consequently sustained release for more than 26d, which was in accordance with Higuchi equation. The uptake of PEG-PLGA-NPs by MPM was found to decrease markedly compared to PLGA-NPs. The experimental results showed that PEG-PLGA-NPs were potential nano drug delivery carriers for ATO.展开更多
PbS quantum dots were prepared in the aqueous medium from readily available precursors. The shape of the particles isapproximately spherical, and the average particle size observed from HRTEM image was 7-8 nm. We appl...PbS quantum dots were prepared in the aqueous medium from readily available precursors. The shape of the particles isapproximately spherical, and the average particle size observed from HRTEM image was 7-8 nm. We applied PbS quantumdots and PMMA polymer to fabricate PbS quantum dots-PMMA composites, and investigate the photoluminescence PbSquantum dots in PMMA matrix with different mass ratio. PbS quantum dots in PMMA matrix have broad emission be-tween 900 nm and 1 500 nm and photoluminescence peak at 1 179 nm. Additionally, the photoluminescence intensityincreases with increasing the dopant concentration. PbS quantum dots-PMMA polymer composites can be potentially usedfor polymer optical fiber and electroluminescence (EL) in optical communication.展开更多
A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by...A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by Klebsiella aerogenes were found to be 0.25 mol/L calcium acetate,4%inoculum level,and pH 7.Following that,the monosaccharides and proteins contained in the extracellular polymeric substances(EPS)of Klebsiella aerogenes were identified.The effects of additional identified monosaccharide and proteins on the crystalline form conversion of CaCO_(3) crystals were investigated,and the additional monosaccharides were found to promote the crystalline form conversion of CaCO_(3) crystals from vaterite to calcite.Specifically,adding 1.00 g/L glucuronic acid was observed to enhance the conversion of crystalline phases of CaCO_(3) crystals to calcite completely after 5 d.Meanwhile,additional catalase was observed to contribute to the regular morphology of CaCO_(3) crystals without affecting their crystalline phases.The results indicate that the additional glucuronic acid influences the crystalline forms of CaCO_(3) crystals significantly.展开更多
The objective of this study was to investigate the hemocompatibility and cell responses to some novel poly（L-lactide） （PLA） composites containing surface modified hydroxyapatite particles for potential application...The objective of this study was to investigate the hemocompatibility and cell responses to some novel poly（L-lactide） （PLA） composites containing surface modified hydroxyapatite particles for potential applications as a bone substitute material. The surface of hydroxyapatite （HA） particles was first grafted with L-lactic acid oligomers to form grafted HA （g-HA） particles. The g-HA particles were further blended with PLA to prepare g-HA/PLA composites. Our previous study has shown signifi- cant improvement in tensile properties of these materials due to the enhanced interracial adhesion between the polymer matrix and HA particles. To further investigate the potential applications of these composites in bone repair and other orthopedic sur- geries, a series of in vitro and in vivo experiments were conducted to examine the cell responses and hemocompatibility of the materials. In vitro experiments showed that the g-HA/PLA composites were well tolerated by the L-929 cells. Hemolysis of the composites was lower than that of pure PLA. Subcutaneous implantation demonstrated that the g-HA/PLA composites were more favorable than the control materials for soft tissue responses. The results suggested that the g-HA/PLA composites are promising and safe materials with potential applications in tissue engineering.展开更多
The intestinal epithelium is the main barrier to the oral delivery of poorly water-soluble drugs. Based on the specific transporters expressed on the apical membrane of the intestinal epithelium, novel polymer micelle...The intestinal epithelium is the main barrier to the oral delivery of poorly water-soluble drugs. Based on the specific transporters expressed on the apical membrane of the intestinal epithelium, novel polymer micelles targeting to the organic cation transporter 2（OCTN2） were constructed by combining carnitine conjugated poly（2-ethyl-2-oxazoline）-poly（D,L-lactide）（Car-PEOz-PLA） with monomethoxy poly（ethylene glycol）-poly（D,L-lactide）（mP EG-PLA）. The structure of the synthesized Car-PEOz-PLA was confirmed by -1H NMR, TLC and ammonium reineckate precipitation reaction, and the number-average molecular weight determined by GPC was 7260 g/mol with a low PDI of 1.44. Coumarin 6-loaded carnitine modified polymeric micelles prepared by film hydration method were characterized to have a nano-scaled size of about 31 nm in diameter, uniform spherical morphology, high drug loading content of 0.098%±0.03% and encapsulation efficiency of 92.67%±2.80%. Moreover, the carnitine-modified micelles exhibited the similar in vitro release behavior in SGF and SIF, and evidently enhanced intestinal absorption of poorly water-soluble agent. Therefore, the designed OCTN2-targeted micelles might have a promising potential for oral delivery of poorly water-soluble drugs.展开更多
In the present study, we designed and fabricated pH-sensitive polymeric micelles based on the conjugate of poly（2-ethyl-2-oxazoline）-poly（D,L-lactide）（PEOz-PLA） with doxorubicin（PEOz-PLA-imi-DOX） to efficientl...In the present study, we designed and fabricated pH-sensitive polymeric micelles based on the conjugate of poly（2-ethyl-2-oxazoline）-poly（D,L-lactide）（PEOz-PLA） with doxorubicin（PEOz-PLA-imi-DOX） to efficiently inhibit tumor cell growth. Hence, PEOz-PLA-imi-DOX was successfully synthesized by connecting DOX to the hydrophobic end of pH-sensitive PEOz-PLA via acid cleavable benzoic imine linker and characterized by 1 H NMR spectrum and thin layer chromatography. The critical micelle concentration of PEOz-PLA-imi-DOX was determined to be（14.84±3.85） mg/L. The conjugate micelles（denoted as PP-DOX-PM） formed by PEOz-PLA-imi-DOX using film-hydration method were characterized to have a nano-scaled size of about 21 nm in diameter, and the drug loading content was 1.67%. PP-DOX-PM showed pH-dependent drug release behavior with gradually accelerated release of DOX with decrease of pH value, illustrating the micelles＇ distinguishing feature of endo/lysosomal pH from physiological pH by accelerating drug release. As anticipated, PP-DOX-PM maintained the cytotoxicity of DOX against MDA-MB-231 cells. Collectively, PP-DOX-PM might have great potential for effective suppression of tumor growth.展开更多
基金Supported by the Special Funds for Major State Basic Research Program of China (973 Program, No.2007CB935800)theNational High Technology Research and Development Program of China (863 Program, No.2004AA215162).
文摘The aim of this study was to prepare arsenic trioxide （ATO）-loaded stealth PEGylated PLGA nanoparticles （PEG-PLGA-NPs） and to assess the merits of PEG-PLGA-NPs as drug carriers for ATO delivery. PEG-PLGA copolymer was synthesized with methoxypolyethyleneglycol （Mw=5000）, D, L-lactide, and glycolide by the ring-opening polymerization method. Amorphous ATO was transformed into cubic crystal form to increase its solu-bility in the organic solvent. ATO-loaded PEG-PLGA-NPs were prepared by the modified spontaneous emulsification solvent diffusion （SESD） method, and the main experimental factors influencing the characteristics of nanopar- ticles were investigated, to optimize the preparation. To confirm the escape of PEG-PLGA-NPs from phagocytosis by phagocytes, PEG-PLGA-NPs labeled rhodamine B uptake by murine peritoneal macrophages （MPM） were analyzed by flow cytometry. The results showed that the physicochemical characteristics of PEG-PLGA-NPs were affected by the type and concentration of the emulsifiers, polymer concentration, and drug concentration. ATO-loaded PEG-PLGA-NPs, with particle size of 120.8nm, zeta potential of-10.73mV, encapsulation efficiency of 73.6%, and drug loading of 1.36%, were prepared under optimal conditions. The images of transmission electron micros-copy （TEM） indicated that the optimized nanoparticles were near spherical and without aggregation or adhesion. The release experiments in vitro showed the ATO release from PEG-PLGA-NPs exhibited consequently sustained release for more than 26d, which was in accordance with Higuchi equation. The uptake of PEG-PLGA-NPs by MPM was found to decrease markedly compared to PLGA-NPs. The experimental results showed that PEG-PLGA-NPs were potential nano drug delivery carriers for ATO.
基金This work was supported by the National Key Basic ResearchDevelopment Program of China (Grant 2003CB314906)+1 种基金the Na-tional Natural Science Foundation of China (Grant 10674074)the Natural Science Foundation of Tianjin (Grant07JCYBJC06400)
文摘PbS quantum dots were prepared in the aqueous medium from readily available precursors. The shape of the particles isapproximately spherical, and the average particle size observed from HRTEM image was 7-8 nm. We applied PbS quantumdots and PMMA polymer to fabricate PbS quantum dots-PMMA composites, and investigate the photoluminescence PbSquantum dots in PMMA matrix with different mass ratio. PbS quantum dots in PMMA matrix have broad emission be-tween 900 nm and 1 500 nm and photoluminescence peak at 1 179 nm. Additionally, the photoluminescence intensityincreases with increasing the dopant concentration. PbS quantum dots-PMMA polymer composites can be potentially usedfor polymer optical fiber and electroluminescence (EL) in optical communication.
基金supported by the National Natural Science Foundation of China(Nos.U20A20267,U1967210,12275123)Hunan Provincial Science Fund for Distinguished Young Scholars,China(No.2022JJ10041)the Program of Science and Technology Department of Hunan Province,China(Nos.2020 TJ-Q03,2022SK2077).
文摘A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by Klebsiella aerogenes were found to be 0.25 mol/L calcium acetate,4%inoculum level,and pH 7.Following that,the monosaccharides and proteins contained in the extracellular polymeric substances(EPS)of Klebsiella aerogenes were identified.The effects of additional identified monosaccharide and proteins on the crystalline form conversion of CaCO_(3) crystals were investigated,and the additional monosaccharides were found to promote the crystalline form conversion of CaCO_(3) crystals from vaterite to calcite.Specifically,adding 1.00 g/L glucuronic acid was observed to enhance the conversion of crystalline phases of CaCO_(3) crystals to calcite completely after 5 d.Meanwhile,additional catalase was observed to contribute to the regular morphology of CaCO_(3) crystals without affecting their crystalline phases.The results indicate that the additional glucuronic acid influences the crystalline forms of CaCO_(3) crystals significantly.
基金supported by the Research Fund for the Doctoral Program of Higher Education(Grant No.20060217012)
文摘The objective of this study was to investigate the hemocompatibility and cell responses to some novel poly（L-lactide） （PLA） composites containing surface modified hydroxyapatite particles for potential applications as a bone substitute material. The surface of hydroxyapatite （HA） particles was first grafted with L-lactic acid oligomers to form grafted HA （g-HA） particles. The g-HA particles were further blended with PLA to prepare g-HA/PLA composites. Our previous study has shown signifi- cant improvement in tensile properties of these materials due to the enhanced interracial adhesion between the polymer matrix and HA particles. To further investigate the potential applications of these composites in bone repair and other orthopedic sur- geries, a series of in vitro and in vivo experiments were conducted to examine the cell responses and hemocompatibility of the materials. In vitro experiments showed that the g-HA/PLA composites were well tolerated by the L-929 cells. Hemolysis of the composites was lower than that of pure PLA. Subcutaneous implantation demonstrated that the g-HA/PLA composites were more favorable than the control materials for soft tissue responses. The results suggested that the g-HA/PLA composites are promising and safe materials with potential applications in tissue engineering.
基金The National Natural Science Foundation of China(Grant No.81673366)the National Key Science Research Program of China(973 Program,Grant No.2015CB932100)
文摘The intestinal epithelium is the main barrier to the oral delivery of poorly water-soluble drugs. Based on the specific transporters expressed on the apical membrane of the intestinal epithelium, novel polymer micelles targeting to the organic cation transporter 2（OCTN2） were constructed by combining carnitine conjugated poly（2-ethyl-2-oxazoline）-poly（D,L-lactide）（Car-PEOz-PLA） with monomethoxy poly（ethylene glycol）-poly（D,L-lactide）（mP EG-PLA）. The structure of the synthesized Car-PEOz-PLA was confirmed by -1H NMR, TLC and ammonium reineckate precipitation reaction, and the number-average molecular weight determined by GPC was 7260 g/mol with a low PDI of 1.44. Coumarin 6-loaded carnitine modified polymeric micelles prepared by film hydration method were characterized to have a nano-scaled size of about 31 nm in diameter, uniform spherical morphology, high drug loading content of 0.098%±0.03% and encapsulation efficiency of 92.67%±2.80%. Moreover, the carnitine-modified micelles exhibited the similar in vitro release behavior in SGF and SIF, and evidently enhanced intestinal absorption of poorly water-soluble agent. Therefore, the designed OCTN2-targeted micelles might have a promising potential for oral delivery of poorly water-soluble drugs.
基金National Natural Science Foundation of China(Grant No.81673366)the National Key Science Research Program of China(973 Program,Grant No.2015CB932100)
文摘In the present study, we designed and fabricated pH-sensitive polymeric micelles based on the conjugate of poly（2-ethyl-2-oxazoline）-poly（D,L-lactide）（PEOz-PLA） with doxorubicin（PEOz-PLA-imi-DOX） to efficiently inhibit tumor cell growth. Hence, PEOz-PLA-imi-DOX was successfully synthesized by connecting DOX to the hydrophobic end of pH-sensitive PEOz-PLA via acid cleavable benzoic imine linker and characterized by 1 H NMR spectrum and thin layer chromatography. The critical micelle concentration of PEOz-PLA-imi-DOX was determined to be（14.84±3.85） mg/L. The conjugate micelles（denoted as PP-DOX-PM） formed by PEOz-PLA-imi-DOX using film-hydration method were characterized to have a nano-scaled size of about 21 nm in diameter, and the drug loading content was 1.67%. PP-DOX-PM showed pH-dependent drug release behavior with gradually accelerated release of DOX with decrease of pH value, illustrating the micelles＇ distinguishing feature of endo/lysosomal pH from physiological pH by accelerating drug release. As anticipated, PP-DOX-PM maintained the cytotoxicity of DOX against MDA-MB-231 cells. Collectively, PP-DOX-PM might have great potential for effective suppression of tumor growth.
