Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin

被引:102
作者
Angadi, Sudha C. [1 ]
Manjeshwar, Lata S. [1 ]
Aminabhavi, Tejraj M. [1 ,2 ]
机构
[1] Karnatak Univ, Dept Chem, Dharwad 580003, Karnataka, India
[2] All India Council Tech Educ, New Delhi, India
关键词
Gastro-retentive drug delivery; Sodium alginate; Sodium carboxymethyl cellulose; MAS; Composite beads; Amoxicillin; MAGNESIUM ALUMINUM SILICATE; POLYMER NETWORK MICROSPHERES; MUCOADHESIVE MICROSPHERES; DICLOFENAC SODIUM; IN-VITRO; DELIVERY; BEADS; CELLULOSE; FILMS; ERADICATION;
D O I
10.1016/j.ijbiomac.2012.04.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Composite blend microbeads of sodium alginate (NaAlg) with sodium carboxymethyl cellulose (NaCMC) containing magnesium aluminum silicate (MAS) particles and enteric coated with chitosan have been prepared to achieve controlled release (CR) of amoxicillin in stomach environment. The composite beads have been characterized by X-ray diffraction (XRD) to study drug distribution, DSC for understanding thermal stability and Fourier transform infrared (FTIR) spectroscopy to investigate chemical interactions as well as to assess the structure of the drug-loaded formulations. Surface morphology of the beads was investigated by scanning electron microscopy (SEM). The size distribution of beads loaded with drug as studied by particle size analyzer was in the range of 745-889 mu m. The beads exhibited quite widely varying encapsulation efficiencies from 52 to 92%. Equilibrium swelling of the beads measured in water and in vitro release of amoxicillin in pH 1.2 medium suggests that drug release depends on polymer blend composition, concentration of MAS and extent of enteric coating. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 55
页数:11
相关论文
共 55 条
[1]
Albarran M.T., 2004, INT J PHARMACEUT, V273, P121
[2]
Polymer-layered silicate nanocomposites: Preparation, properties and uses of a new class of materials [J].
Alexandre, Michael ;
Dubois, Philippe .
Materials Science and Engineering: R: Reports, 2000, 28 (1-2) :1-63
[3]
DETECTION OF THE INTRAGASTRIC SITES AT WHICH HELICOBACTER-PYLORI EVADES TREATMENT WITH AMOXICILLIN AND CIMETIDINE [J].
ATHERTON, JC ;
COCKAYNE, A ;
BALSITIS, M ;
KIRK, GE ;
HAWKEY, CJ ;
SPILLER, RC .
GUT, 1995, 36 (05) :670-674
[4]
Buzas Gyorgy Miklos, 1999, Orvosi Hetilap, V140, P121
[5]
Nanoparticles Incorporated in pH-Sensitive Hydrogels as Amoxicillin Delivery for Eradication of Helicobacter pylori [J].
Chang, Chiung-Hung ;
Lin, Yu-Hsin ;
Yeh, Chia-Lin ;
Chen, Yi-Chi ;
Chiou, Shu-Fen ;
Hsu, Yuan-Man ;
Chen, Yueh-Sheng ;
Wang, Chi-Chung .
BIOMACROMOLECULES, 2010, 11 (01) :133-142
[6]
New hydrophobically modified carboxymethylcellulose derivatives [J].
Charpentier, D ;
Mocanu, G ;
Carpov, A ;
Chapelle, S ;
Merle, L ;
Muller, G .
CARBOHYDRATE POLYMERS, 1997, 33 (2-3) :177-186
[7]
Preparation of mucoadhesive microspheres containing antimicrobial agents for eradication of H-pylori [J].
Chun, MK ;
Sah, H ;
Choi, HK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 297 (1-2) :172-179
[8]
Ciullo P.A., 1991, COSMET TOILETRIES, V106, P89
[9]
CIULLO PA, 1981, J SOC COSMET CHEM, V32, P275
[10]
LOCAL GASTRIC AND SERUM AMOXICILLIN CONCENTRATIONS AFTER DIFFERENT ORAL APPLICATION FORMS [J].
COOREMAN, MP ;
KRAUSGRILL, P ;
HENGELS, KJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (07) :1506-1509