Preparation and characterization of guar gum based biopolymeric hydrogels for controlled release of antihypertensive drug

被引:45
作者
Daud, Hina [1 ,2 ]
Ghani, Ambreen [3 ]
Iqbal, Dure Najaf [4 ]
Ahmad, Nasir [5 ]
Nazir, Saliha [1 ,2 ]
Muhammad, Mahnoor Jan [1 ]
Hussain, Erum Akbar [1 ,6 ]
Nazir, Arif [4 ]
Iqbal, Munawar [4 ]
机构
[1] Lahore Coll Women Univ, Dept Chem, Lahore 54000, Pakistan
[2] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
[3] Univ Educ Lahore, Dept Chem, Vehari Campus, Vehari 61100, Pakistan
[4] Univ Lahore, Dept Chem, Lahore 53700, Pakistan
[5] Natl Univ Sci & Technol, Sch Mech & Mfg Engn, Dept Biomed Engn & Sci, Islamabad, Pakistan
[6] Univ Karachi, HEJ Res Inst Chem, Karachi, Pakistan
关键词
Guar gum; Hydrogels; Solution casting technique; Anti-hypertensive drug; Controlled drug release; PH-SENSITIVE HYDROGELS; SODIUM ALGINATE; ACRYLIC ACID; MICROENCAPSULATION; MICROSPHERES; COMPOSITES; DELIVERY; SALECAN;
D O I
10.1016/j.arabjc.2021.103111
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rapid release and poor drug encapsulation ability limit the use of single biopolymer in water-soluble drugs loading, carrying and release efficiency. In the present study, blended hydrogels based on guar gum, sodium alginate and polyvinyl alcohol (GG/SA/PVA) were prepared by solution casting technique and employed for controlled release of verapamil HCl (VP-HCl). The extent of interaction of all blends was explored by Fourier-transform infrared spectroscopy (FTIR) while surface morphology was determined by Atomic force microscope (AFM) and Scanning electron microscope (SEM). The crystallinity, thermal stability and water absorbing capacity of blends were studied by X-ray diffraction (XRD), Differential scanning calorimeter (DSC), thermogravimetric analysis (TGA) and swelling studies respectively. The results revealed improved crystallinity and stability of all the blends. The prepared blends showed promising drug loading and releasing efficiency with higher GG contents for the controlled release of verapamil HCl and at pH 7.4. Optimum drug release (94%) drug release was achieved in 12 h and followed non-Fickian diffusion mechanism. It has been concluded from the results that GG/SA/PVA blends have potential for drug delivery applications in a controlled manner. (c) 2021 The Authors. Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:14
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