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Preparation Of ZnAl-LDH@SiO2 And Study On The Double Drug Release Behavior

Posted on:2021-03-22Degree:MasterType:Thesis
Country:ChinaCandidate:Z L SunFull Text:PDF
GTID:2381330602972309Subject:Materials Science and Engineering
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The nano-core-shell structure is a material formed by one nano-material coating on another nano-material.These two parts play the role of supporting and protection,respectively.The core-shell structure materials can integrate performance of the two parts and play a certain role that one single part does not have.Its research and application are of great significance to drug carriers and release.In this paper,a dual drug sustained-release system with IBU intercalated LDH as core and mSiO2 and its derivatives as shell was prepared,in order to prepare a drug sustained-release system in which core layer and shell layer are loaded with different drugs,respectively.Firstly,co-precipitation method was used to prepare layered double hydroxide intercalated with ibuprofen?IBU-LDH?.Then three core-shell structures IBU-LDH@SiO2,IBU-LDH@?SiO2+SiO2-NH2?,IBU-LDH@SiO2-NH2 were prepared using IBU-LDH as core and dense SiO2 layer,mSiO2 with high or low amino content coating on the core.The effects of partial exfoliation of IBU-LDH,coating conditions for the shell layer,feeding ratio between shell and core materials on the structure of core-shell structure and its drug sustained release were studied.The results showed that the samples prepared had a core-shell structure with a hexagonal sheet-like morphology as the hydrolytic medium was the volume ratio of formamide:deionized water=1:2 and the pH of the encapsulation solution was 8.Polyhedral oligomeric silsesquioxane is formed in the shell layer of IBU-LDH@SiO2-NH2,which has obvious pore structure.Its pore diameter is 3.5 nm,the specific surface area is 100.00 m2/g.Under the same conditions,the release amounts of the drugs in the shell layer of the three drug carriers are:IBU-LDH@SiO2-NH2>IBU-LDH@?SiO2+SiO2-NH2?>IBU-LDH@SiO2.In terms of release rate,the drug release rate of IBU is slower than that of ferulic acid?FA?.In the three structures,more than 70%of FA release out within 30 minutes,while IBU takes 60 minutes or longer.IBU-LDH@SiO2-NH2 can achieve the step-by-step release of two drugs.On the base of the above results,the structure of LDH@SiO2-NH2 was optimized,the effects of the materials feeding ratio for core-shell layer and encapsulation method on the target products'structure and the drug release of the optimum structure were studied.The results showed that when shell material m APTES+TEOS=0.6 g,APTES:TEOS=20:4,and the outside is further encapsulation with dense SiO2,the drug loading and release of the drug on the shell can be further increased and reduced respectively.Even more drug release equilibrium time can be extended to 80 minutes.
Keywords/Search Tags:IBU-LDH@SiO2-NH2, core-shell structure, dual drug sustained-release, encapsulation, mSiO2
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