marieh ghazaie
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Papers by marieh ghazaie
encapsulating them in organic-inorganic hybrids via sol-gel technique. The assembled
organic-inorganic hybrids had diverse BET surface area, porosity, and high heat resistance.
The synthesized organic-inorganic hybrids were based on zirconium(IV) propoxide, and
tetraethyl orthosilicate as precursor of inorganic network, and chitosan or N-triethylchitosan
as organic or biopolymer components. In these hybrid composites, drug and biopolymer were
coated with a mesoporous inorganic material. FT-IR, FE-SEM, DSC, BET, XRD techniques,
and Zeta potential analysis used for investigating the formation of metformin/chitosan@ZrO2
and sodium naproxen/N-triethylchitosan@SiO2 hybrid composites. Then for investigating the
role of sol-gel process, the release of metformin and sodium naproxen in the prepared hybrid
composites was investigated as model drugs. Compare to drug/biopolymer composite,
incorporation of ZrO2 or SiO2 coating enhanced the drug entrapment appreciably, and
naturally reduced the rate of drug release. For example, the metformin/chitosan composite
without ZrO2 coating released the whole drug in less than10 h in pH 7.4 when the composite
coated with ZrO2 released the entrapped drug after 25 h.
encapsulating them in organic-inorganic hybrids via sol-gel technique. The assembled
organic-inorganic hybrids had diverse BET surface area, porosity, and high heat resistance.
The synthesized organic-inorganic hybrids were based on zirconium(IV) propoxide, and
tetraethyl orthosilicate as precursor of inorganic network, and chitosan or N-triethylchitosan
as organic or biopolymer components. In these hybrid composites, drug and biopolymer were
coated with a mesoporous inorganic material. FT-IR, FE-SEM, DSC, BET, XRD techniques,
and Zeta potential analysis used for investigating the formation of metformin/chitosan@ZrO2
and sodium naproxen/N-triethylchitosan@SiO2 hybrid composites. Then for investigating the
role of sol-gel process, the release of metformin and sodium naproxen in the prepared hybrid
composites was investigated as model drugs. Compare to drug/biopolymer composite,
incorporation of ZrO2 or SiO2 coating enhanced the drug entrapment appreciably, and
naturally reduced the rate of drug release. For example, the metformin/chitosan composite
without ZrO2 coating released the whole drug in less than10 h in pH 7.4 when the composite
coated with ZrO2 released the entrapped drug after 25 h.