共 45 条
Facile preparation and characterization of pH sensitive Mt/CMC nanocomposite hydrogel beads for propranolol controlled release
被引:67
作者:
Farhadnejad, Hassan
[1
,2
]
Mortazavi, Seyed Alireza
[1
]
Erfan, Mohammad
[1
]
Darbasizadeh, Behzad
[1
]
Motasadizadeh, Hamidreza
[3
]
Fatahi, Yousef
[3
]
机构:
[1] Shahid Beheshti Univ Med Sci, Sch Pharm, Dept Pharmaceut & Pharmaceut Nanotechnol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Students Res Comm, Tehran, Iran
[3] Univ Tehran Med Sci, Dept Pharmaceut Nanotechnol, Fac Pharm, Tehran, Iran
关键词:
Nanocomposite hydrogel;
Carboxymethyl cellulose;
Montmorillonite;
Drug delivery;
DRUG-DELIVERY;
CARBOXYMETHYL CELLULOSE;
IN-VITRO;
EXTENDED-RELEASE;
MATRIX TABLETS;
MONTMORILLONITE;
CHITOSAN;
SODIUM;
HYDROCHLORIDE;
ALGINATE;
D O I:
10.1016/j.ijbiomac.2018.01.061
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The main aim of the present study was to design pH-sensitive nanocomposite hydrogel beads, based on carboxymethyl cellulose (CMC) and montmorillonite (Mt)-propranolol (PPN) nanohybrid, and evaluate whether the prepared nanocomposite beads could potentially be used as oral drug delivery systems. PPN as a model drug-was intercalated into the interlayer space of Mt clay mineral via the ion exchange procedure. The resultant nanohybrid (Mt-PPN) was applied to fabricate nanocomposite hydrogel beads by association with carboxymethyl cellulose. The characterization of test samples was performed using different techniques: X-Ray Diffraction (XRD), IR spectroscopy (FT-IR), thermal gravity analysis (TGA), and scanning electron microscopy (SEM). The drug encapsulation efficiency was evaluated by UV-vis spectroscopy, and was found to be high for Mt/CMC beads. In vitro drug release test was performed in the simulated gastrointestinal conditions to evaluate the efficiency of Mt-PPN/CMC nanocomposite beads as a controlled-release drug carrier. The drug release profiles indicated that the Mt-PPN/CMC nanocomposite beads had high stability against stomach acid and a sustained and controlled-release profile for PPN under the simulated intestinal conditions. (C) 2018 Elsevier B.V. All rights reserved.
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页码:696 / 705
页数:10
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