We applied a combination of inorganic mesoporous silica material,frequently used as drug carriers,and a natural organic polymer alginate(ALG),to establish a sustained drug delivery system for the poorly water-soluble ...We applied a combination of inorganic mesoporous silica material,frequently used as drug carriers,and a natural organic polymer alginate(ALG),to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin(IND).Mesoporous silica nanospheres(MSNs)were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis.After drug loading into the pores of aninopropyl functionalized MSNs(AP-MSNs),IND loaded AP-MSNs(IND-AP-MSNs)were encapsulated by ALG through the ionic interaction.The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy(SEM),transmission electron microscopy(TEM),nitrogen adsorption,zetapotential analysis and TGA analysis.The surface structure and surface charge changes of the ALG encapsulated AP-MSNs(ALG-AP-MSNs)were also investigated.The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG.We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs.展开更多
A series of Z-schemeβ-Bi_(2)O_(3)/ZrO_(2)hetero-junction composites containing three-dimensional(3D)mesoporous silica nanospheres(MSNs)were synthesized as efficient catalysts for antibiotic remediation.The obtained M...A series of Z-schemeβ-Bi_(2)O_(3)/ZrO_(2)hetero-junction composites containing three-dimensional(3D)mesoporous silica nanospheres(MSNs)were synthesized as efficient catalysts for antibiotic remediation.The obtained MSN/β-Bi_(2)O_(3)/ZrO_(2)ternary composites possess novel lamellar cross structure,which is well constructed byβ-Bi_(2)O_(3)nanosheets,3D MSNs,and ZrO_(2)nanoparticles.The optimal sample BZS-2(Bi∶Zr∶Si=1∶0.4∶0.33)shows an adsorptive-photocatalytic removal efficiency of 92.7%towards levofloxacin(LVF)and a total organic carbon(TOC)removal efficiency of 60.0%under simu-lated solar light irradiation for 100 min.BZS-2 can also remove 90.1%and 91.2%of tetracycline hydrochloride(TC)and oxytetracycline hydrochloride(OTC),respectively,and themaximum adsorptioncapacityof TCover BZS-2is almost 10 times that of-BiO.Theimprovement ofphotocatalytic activitycan bemainly attributed to the enhanced visible-light adsorption capacity and more efficientseparationof photogenerated electron-hole pairs.A possible Z-scheme photocatalytic mechanism of p BiO/ZrOheterojunctions based on valence band offset(AEvBo)andconduction band offset(EcBo)isproposed.This study provides an efficient way to construct novel mesoporous ternary photocatalyst with increased accessible surface area and active sites for treatment of antibiotics by synergistic adsorption and photocatalysis.展开更多
To investigate the influence of mesopores towards the solidification of self-microemulsifying drug delivery system(SMEDDS), mesoporous silica nanospheres(MSNs) and Santa Barbara Amorphous-15(SBA-15) were compared. The...To investigate the influence of mesopores towards the solidification of self-microemulsifying drug delivery system(SMEDDS), mesoporous silica nanospheres(MSNs) and Santa Barbara Amorphous-15(SBA-15) were compared. The MSNs had hydrodynamic size of 195.35 ± 5.82 nm, and pore diameter of 2.70 nm. The SBA-15 had hydrodynamic size of 2312.19 ± 106.93 nm, and pore diameter of 10.91 nm. The MSNs and SBA-15 showed similar loading efficiency of SMEDDS containing sirolimus(SRL). However,MSNs had higher drug dissolution and in vivo absorption, with relative bioavailability of 174.62%. Thus,the length of mesopores played a more important role in solidification of SMEDDS as compared with the pore diameter. This study suggests that the SMEDDS-MSNs can be a potential candidate for oral administration of hydrophobic drugs.展开更多
基金This work was supported by National Basic Research Program of China(973 Program)(2009CB930300)National Natural Science Foundation of China(81072605)Shenyang Special Fund for Exploration of Intellectual Resources.
文摘We applied a combination of inorganic mesoporous silica material,frequently used as drug carriers,and a natural organic polymer alginate(ALG),to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin(IND).Mesoporous silica nanospheres(MSNs)were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis.After drug loading into the pores of aninopropyl functionalized MSNs(AP-MSNs),IND loaded AP-MSNs(IND-AP-MSNs)were encapsulated by ALG through the ionic interaction.The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy(SEM),transmission electron microscopy(TEM),nitrogen adsorption,zetapotential analysis and TGA analysis.The surface structure and surface charge changes of the ALG encapsulated AP-MSNs(ALG-AP-MSNs)were also investigated.The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG.We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs.
基金financially supported by National Natural Science Foundation of China (Nos.21962006, 21607064 and 21707055)the Youth Key Project of Natural Science Foundation of Jiangxi Province (Nos.20192ACBL20014 and 20192ACBL21011)+1 种基金the Natural Science Foundation of Jiangxi Province (Nos.20181BAB203018 and 20181BAB213010)Qingjiang Excellent Young Talents of Jiangxi University of Science and Technology
文摘A series of Z-schemeβ-Bi_(2)O_(3)/ZrO_(2)hetero-junction composites containing three-dimensional(3D)mesoporous silica nanospheres(MSNs)were synthesized as efficient catalysts for antibiotic remediation.The obtained MSN/β-Bi_(2)O_(3)/ZrO_(2)ternary composites possess novel lamellar cross structure,which is well constructed byβ-Bi_(2)O_(3)nanosheets,3D MSNs,and ZrO_(2)nanoparticles.The optimal sample BZS-2(Bi∶Zr∶Si=1∶0.4∶0.33)shows an adsorptive-photocatalytic removal efficiency of 92.7%towards levofloxacin(LVF)and a total organic carbon(TOC)removal efficiency of 60.0%under simu-lated solar light irradiation for 100 min.BZS-2 can also remove 90.1%and 91.2%of tetracycline hydrochloride(TC)and oxytetracycline hydrochloride(OTC),respectively,and themaximum adsorptioncapacityof TCover BZS-2is almost 10 times that of-BiO.Theimprovement ofphotocatalytic activitycan bemainly attributed to the enhanced visible-light adsorption capacity and more efficientseparationof photogenerated electron-hole pairs.A possible Z-scheme photocatalytic mechanism of p BiO/ZrOheterojunctions based on valence band offset(AEvBo)andconduction band offset(EcBo)isproposed.This study provides an efficient way to construct novel mesoporous ternary photocatalyst with increased accessible surface area and active sites for treatment of antibiotics by synergistic adsorption and photocatalysis.
基金supported by the Natural Science Foundation of Fujian Province(Nos.2017J01822 and 2018J01347)Fujian Medical University(No.2017XQ1202)Fuzhou General Hospital(No.2017Q06)
文摘To investigate the influence of mesopores towards the solidification of self-microemulsifying drug delivery system(SMEDDS), mesoporous silica nanospheres(MSNs) and Santa Barbara Amorphous-15(SBA-15) were compared. The MSNs had hydrodynamic size of 195.35 ± 5.82 nm, and pore diameter of 2.70 nm. The SBA-15 had hydrodynamic size of 2312.19 ± 106.93 nm, and pore diameter of 10.91 nm. The MSNs and SBA-15 showed similar loading efficiency of SMEDDS containing sirolimus(SRL). However,MSNs had higher drug dissolution and in vivo absorption, with relative bioavailability of 174.62%. Thus,the length of mesopores played a more important role in solidification of SMEDDS as compared with the pore diameter. This study suggests that the SMEDDS-MSNs can be a potential candidate for oral administration of hydrophobic drugs.