Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-...Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-I were optimized through response surface methodology coupled with central composite design. XPS revealed that the groups of —OH, —COO—, —NH, —NHand —CSS— carried by Hydrogel-Ⅰ were responsible for the uptake of Pb(Ⅱ). Ions exchange, surface complexation, electrostatic attraction and pore-filling effect contributed to the adsorption process. Adsorption performances of Pb(Ⅱ) by Hydrogel-Ⅰ and MAL powders were compared. Although they exhibited similar adsorption rate and maximum adsorption capacity(qm), the reusing ability of Hydrogel-Ⅰ was better and it was easier to be separated from aqueous solution after treatment. Even compared with organic hydrogel materials,Hydrogel-Ⅰ presented relatively quick adsorption speed and high adsorption capacity. It can be concluded that Hydrogel-Ⅰ could be an alternative scavenger for the treatment of Pb(Ⅱ) from aqueous solution.展开更多
A model to correlate and predict the release behavior of drugs from hydrogel nanoparticles is presented in this paper. The nanoparticle is considered as a combination of a shell of an elastic semipermeable membrane an...A model to correlate and predict the release behavior of drugs from hydrogel nanoparticles is presented in this paper. The nanoparticle is considered as a combination of a shell of an elastic semipermeable membrane and a core of a fluid phase （After swelling equilibrium）. The fluid core consists of network building materials and other components that are able to partition in hydrogel nanoparticle phase and surrounding coexisting liquid phase, and is enveloped by the membrane shell. The excess Gibbs energies of the hydrogel nanoparticle phase and the surrounding coexisting fluid phase are expressed e.g. using UNIQUAC equation with ＂free-volume＂ contribution for non-ionic solution and VERS-model for ionic one. The elastic properties of polymer network could be described, for example, by the ＂phanWm network＂ theory.展开更多
The auto-gelling and drug release properties of the thermosensitive chitosan-β-glycerophosphate formulation were investigated. According to rheological study, gelation lag time of chitosan/β-glycerophosphate （GP） ...The auto-gelling and drug release properties of the thermosensitive chitosan-β-glycerophosphate formulation were investigated. According to rheological study, gelation lag time of chitosan/β-glycerophosphate （GP） solutions varied from 2 to 60min with different deacetylation degree of chitosan, pH, gelation temperature, and the particles in the sol. The gelation properties were also found to influence the release profilles of a hydrophilic drug, 5-fluorouracil （5-FU）. Morphological examination by scanning electron microphotography demonstrated that large ＂pores＂ occurred during the gel-forming process, which created hydrophilic environment and led to the rapid initial release of the drug （85% in f＇LrSt 8h）. Poly-3-hydroxybutyrate （PHB）, a biodegradable material, was applied here as scaffold to capture 5-FU into microparticles with high encapsulation efficiency by solvent-nonsolvent method. Combination of these microparticles into the chitosan-β-GP formulation could drop the rapid initial release from 85% down to 29% in the optimized PHB content （75%, by mass）. The release could sustain for about 10 months. Tiffs study provided an understanding of the potential of injectable implant using thermosensitive chitosan-β-GP formulation containing PHB based particles for the water soluble drugs that need the property of long-term delivery.展开更多
基金funded by the National Key Research and Development Project (No.2019YFC1804800)Key R&D Program of Shaanxi Province,China (No.2019SF-253)+3 种基金the Fundamental Research Funds for the Central Universities,China (No.300102291504)the Pearl River S&T Nova Program of Guangzhou,China (No.201710010065)the Science and Technology Program of Guangdong Forestry Administration,China (No.2020-KYXM-08)the Key Laboratory of Resource Chemistry,Ministry of Education,China (No.KLRC_ME2102)。
文摘Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-I were optimized through response surface methodology coupled with central composite design. XPS revealed that the groups of —OH, —COO—, —NH, —NHand —CSS— carried by Hydrogel-Ⅰ were responsible for the uptake of Pb(Ⅱ). Ions exchange, surface complexation, electrostatic attraction and pore-filling effect contributed to the adsorption process. Adsorption performances of Pb(Ⅱ) by Hydrogel-Ⅰ and MAL powders were compared. Although they exhibited similar adsorption rate and maximum adsorption capacity(qm), the reusing ability of Hydrogel-Ⅰ was better and it was easier to be separated from aqueous solution after treatment. Even compared with organic hydrogel materials,Hydrogel-Ⅰ presented relatively quick adsorption speed and high adsorption capacity. It can be concluded that Hydrogel-Ⅰ could be an alternative scavenger for the treatment of Pb(Ⅱ) from aqueous solution.
基金Science and Technology Ministry of Fujian (2005I010 and 2001Z046)
文摘A model to correlate and predict the release behavior of drugs from hydrogel nanoparticles is presented in this paper. The nanoparticle is considered as a combination of a shell of an elastic semipermeable membrane and a core of a fluid phase （After swelling equilibrium）. The fluid core consists of network building materials and other components that are able to partition in hydrogel nanoparticle phase and surrounding coexisting liquid phase, and is enveloped by the membrane shell. The excess Gibbs energies of the hydrogel nanoparticle phase and the surrounding coexisting fluid phase are expressed e.g. using UNIQUAC equation with ＂free-volume＂ contribution for non-ionic solution and VERS-model for ionic one. The elastic properties of polymer network could be described, for example, by the ＂phanWm network＂ theory.
基金Supported by the National Natural Science Foundation of China (No.20376038) and the Research Foundation of the Ministry ofEducation of China (No.2002003056).
文摘The auto-gelling and drug release properties of the thermosensitive chitosan-β-glycerophosphate formulation were investigated. According to rheological study, gelation lag time of chitosan/β-glycerophosphate （GP） solutions varied from 2 to 60min with different deacetylation degree of chitosan, pH, gelation temperature, and the particles in the sol. The gelation properties were also found to influence the release profilles of a hydrophilic drug, 5-fluorouracil （5-FU）. Morphological examination by scanning electron microphotography demonstrated that large ＂pores＂ occurred during the gel-forming process, which created hydrophilic environment and led to the rapid initial release of the drug （85% in f＇LrSt 8h）. Poly-3-hydroxybutyrate （PHB）, a biodegradable material, was applied here as scaffold to capture 5-FU into microparticles with high encapsulation efficiency by solvent-nonsolvent method. Combination of these microparticles into the chitosan-β-GP formulation could drop the rapid initial release from 85% down to 29% in the optimized PHB content （75%, by mass）. The release could sustain for about 10 months. Tiffs study provided an understanding of the potential of injectable implant using thermosensitive chitosan-β-GP formulation containing PHB based particles for the water soluble drugs that need the property of long-term delivery.
