Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers
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Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers
Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers
Chinese Journal of Polymer Science2014年32卷第3期 页码:280-291
Affiliations:
Department of Chemistry, Sri Krishnadevaraya University, Anatapur-515 003, India
K. Doraswamy, P. Venkata Ramana. Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers[J]. Chinese Journal of Polymer Science, 2014,32(3):280-291.
K. Doraswamy, P. Venkata Ramana. Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers[J]. Chinese Journal of Polymer Science, 2014, 32(3): 280-291.
K. Doraswamy, P. Venkata Ramana. Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers[J]. Chinese Journal of Polymer Science, 2014,32(3):280-291.DOI: 10.1007/s10118-014-1406-0.
K. Doraswamy, P. Venkata Ramana. Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers[J]. Chinese Journal of Polymer Science, 2014, 32(3): 280-291.DOI: 10.1007/s10118-014-1406-0.
Controlled Drug Release Studies of Atenolol Using Differently Sulfonated Acryloxyacetophenone and Methyl Methacrylate Copolymer Resins as Drug Carriers
2-Acryloxyacetophenone (AAP) was prepared and subjected to suspension polymerization with methyl methacrylate (MMA) using azobisisobutyronitrile (AIBN) as free radical initiator. The differently sulfonated AAP-MMA cross-linked copolymer cationic exchange resins were prepared by sulfonation with concentrated sulphuric acid at 70 ℃. Several characteristics of the prepared resins were evaluated
i.e.
FTIR
the ion-exchange capacity (IEC)
thermo gravimetric analysis (TGA)
particle size distribution and microscopic morphology. The resin characteristics were altered with degree of sulfonation
providing that differently sulfonated resins could be prepared. The behavior of atenolol (ATL) loading and
in vitro
release in the USP stimulated gastric and intestinal fluids of the obtained resins were evaluated. The drug loaded in the resin increased with increasing degree of sulfonation and hence the drug binding site in resin employed. The drug release was lower from the resins with higher content of sulfonic group due to the increase in the diffusive path depth. The drug release was a little lower in stimulated gastric fluid (SGF) than in stimulated intestinal fluids (SIF). The basic groups
ionized to a little greater extent in SGF and preferred binding with the resin rather than releasing. Hence
the differently sulfonated resins could be utilized as novel carriers for drug delivery.
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Polymerization Mechanism of Methyl Methacrylate Initiated by Ethyl Acetate/t-BuP4
Thioxanthene-9-thione Mediated MMA Polymerization
Ambient Temperature Living Radical Copolymerization of Styrene and Methyl Methacrylate with Sodium Hypophosphite as Reducing Agent
Enhancing Processability of Phenylethynyl-terminated Imide Oligomers and Properties of Cured Polyimides via ―CF3 Incorporation
A Paradigm for BF3 Co-initiated Cationic Polymerization with Low Dispersity: Introducing Acetonitrile and Lowering the Reaction Temperature
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Qi-Min Jiang
Wen-Yan Huang
Hong-Jun Yang
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Bi-Biao Jiang
De-Yong Xia
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