pH-sensitive polyvinylpyrrolidone-acrylic acid hydrogels: Impact of material parameters on swelling and drug release

被引:55
|
作者
Sohail, Kashif [1 ]
Khan, Ikram Ullah [2 ,3 ]
Shahzad, Yasser [4 ]
Hussain, Talib [4 ]
Ranjha, Nazar Muhammad [1 ]
机构
[1] Bahauddin Zakariya Univ BZU Multan, Fac Pharm, Multun, Pakistan
[2] Univ Strasbourg, Fac Pharm, Lab Design & Applicat Bioact Mol CAMB, F-67400 Illkirch Graffenstaden, France
[3] Govt Coll GC Univ, Coll Pharm, Faisalabad, Pakistan
[4] Univ Huddersfield, Div Pharm & Pharmaceut Sci, Huddersfield HD1 3DH, W Yorkshire, England
关键词
Drugs/release; Hydrogels/pH sensitive; Polyvinylpyrrolidone-acrilic acid/hidrogels; Tramadol hydrochloride; Methylene bisacrylamide; RADIATION SYNTHESIS; CROSS-LINKING; BEHAVIOR; ENCAPSULATION; MEMBRANES; WATER;
D O I
10.1590/S1984-82502011000100018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we fabricated pH-sensitive polyvinylpyrrolidone/acrylic acid (PVP/AA) hydrogels by a free-radical polymerisation method with variation in the content of monomer, polymer and cross-linking agent. Swelling was performed in USP phosphate buffer solutions of pH 1.2, 5.5, 6.5 and 7.5 with constant ionic strength. Network structure was evaluated by different parameters and FTIR confirmed the formation of cross-linked hydrogels. X-ray crystallography showed molecular dispersion of tramadol HCl. A drug release study was carried out in phosphate buffer solutions of pH 1.2, 5.5 and 7.5 for selected samples. It was observed that swelling and drug release from hydrogels can be modified by changing composition and degree of cross-linking of the hydrogels under investigation. Swelling coefficient was high at higher pH values except for the one containing high PVP content. Drug release increased by increasing the pH of the medium and AA contents in hydrogels while increasing the concentration of cross-linking agent had the opposite effect. Analysis of the drug release mechanism revealed non-Fickian transport of tramadol from the hydrogels.
引用
收藏
页码:173 / 184
页数:12
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