Al3+ ion cross-linked interpenetrating polymeric network microbeads from tailored natural polysaccharides

被引:49
作者
Bhattacharya, Shiv Sankar [1 ]
Ghosh, Ashoke Kumar [1 ]
Banerjee, Subham [2 ]
Chattopadhyay, Pronobesh [2 ]
Ghosh, Amitava [3 ]
机构
[1] IFTM Univ, Sch Pharmaceut Sci, Moradabad 244001, Uttar Pradesh, India
[2] Def Res Lab, Div Pharmaceut Technol, Tezpur 784001, Assam, India
[3] Bengal Coll Pharmaceut Sci & Res, Durgapur 713212, W Bengal, India
关键词
Carboxymethylation; Aqueous environment; IPN; Microbead; CALCIUM ALGINATE BEADS; IN-VITRO; CONTROLLED-RELEASE; CHITOSAN BEADS; GUM-POLY(VINYL ALCOHOL); HYDROGEL MICROSPHERES; SUSTAINED-RELEASE; DRUG-RELEASE; GUAR GUM; DELIVERY;
D O I
10.1016/j.ijbiomac.2012.08.029
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
Interpenetrating network (IPN) microbeads of sodium carboxymethyl locust bean gum (SCMLBG) and sodium carboxymethyl cellulose (SCMC) containing diclofenac sodium (DS), a non steroidal anti-inflammatory drug were prepared by single water-in-water (w/w) emulsion gelation process using AlCl3 as cross-linking agent in a complete aqueous environment. The influence of different variables like total polymer concentration, gelation time and crosslinker content on in vitro physico-chemical characteristics and drug release rate in different media was investigated. Drug loaded microbeads were evaluated through Fourier transform infra-red (FTIR), X-ray diffraction (XRD) and differential scanning calorimetry (DSC) analyses. Scanning electron microscopy (SEM) micrograph of the beads suggested the formation of spherical particles. FTIR analysis indicated the stable nature of the drug in the blend microbeads. DSC and XRD analysis revealed amorphous state of drug after encapsulation. The drug release profile in acidic medium was considerably less in comparison to alkaline media. Formulations showed non-Fickian type transport mechanism. These tri-valent ion crosslinked beads not only improve drug encapsulation efficiency but also enhance drug release in phosphate buffer. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1173 / 1184
页数:12
相关论文
共 47 条
[1]
Acartürk F, 1999, J MICROENCAPSUL, V16, P291
[2]
Development of novel interpenetrating network gellan gum-poly(vinyl alcohol) hydrogel microspheres for the controlled release of carvedilol [J].
Agnihotri, SA ;
Aminabhavi, TM .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2005, 31 (06) :491-503
[3]
Chitosan-alginate multilayer beads for gastric passage and controlled intestinal release of protein [J].
Anal, AK ;
Bhopatkar, D ;
Tokura, S ;
Tamura, H ;
Stevens, WF .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (06) :713-724
[4]
5-fluorouracil encapsulated alginate beads for the treatment of breast cancer [J].
Arica, B ;
Çalis, S ;
Kas, HS ;
Sargon, MF ;
Hincal, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :267-269
[5]
In vitro and in vivo studies of ibuprofen-loaded biodegradable alginate beads [J].
Arica, B ;
Çalis, S ;
Atilla, P ;
Durlu, NT ;
Çakar, N ;
Kas, HS ;
Hincal, AA .
JOURNAL OF MICROENCAPSULATION, 2005, 22 (02) :153-165
[6]
Chitosan beads for the delivery of salmon calcitonin: Preparation and release characteristics [J].
Aydin, Z ;
Akbuga, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 131 (01) :101-103
[7]
Aydinli M, 2004, TURK J CHEM, V28, P163
[8]
Preparation of sodium alginate-methylcellulose blend microspheres for controlled release of nifedivine [J].
Babu, V. Ramesh ;
Sairam, Malladi ;
Hosamani, Kallappa M. ;
Aminabhavi, Tejraj M. .
CARBOHYDRATE POLYMERS, 2007, 69 (02) :241-250
[9]
Interpenetrating polymer network (IPN) hydrogel microspheres for oral controlled release application [J].
Banerjee, Subham ;
Siddiqui, Lubna ;
Bhattacharya, Shiv Sankar ;
Kaity, Santanu ;
Ghosh, Animesh ;
Chattopadhyay, Pronobesh ;
Pandey, Anurag ;
Singh, Lokendra .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2012, 50 (01) :198-206
[10]
Banerjee S, 2010, J SCI IND RES INDIA, V69, P777