Novel carbon dot coated alginate beads with superior stability, swelling and pH responsive drug delivery

被引:76
作者
Gogoi, Neelam [1 ]
Chowdhury, Devasish [1 ]
机构
[1] Inst Adv Study Sci & Technol, Div Phys Sci, Mat Nanochem Lab, Gauhati 781035, Assam, India
关键词
TETRACYCLINE FIBER THERAPY; CHITOSAN-ALGINATE; MULTICENTER EVALUATION; CONTROLLED-RELEASE; BIOCOMPATIBILITY; MICROCAPSULES; MICROSPHERES; SCAFFOLDS; SURVIVAL; SYSTEM;
D O I
10.1039/c3tb21835j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Novel carbon dot coated alginate beads (CA-CD) exhibiting superior stability and swelling properties have been successfully prepared. CA-CD show exceptional stability in ambient condition and are stable at room atmosphere and temperature even after 60 days. Moreover, CA-CD show excessive swelling in comparison to calcium alginate (CA) beads. The beads were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and optical microscopy. The CA and CA-CD beads were investigated for their use as pH dependent sustained drug delivery vehicles taking tetracycline (TC) and tetracycline associated with beta-cyclodextrin (beta-TC) as model drug systems. It was observed that TC loading was 35% and 77% with CA and CA-CD, respectively. Tetracycline associated with beta-cyclodextrin (beta-TC) shows 48% loading for CA and much greater loading (as high as 90%) for CA-CD. At pH 1, CA-CD and CA beads show maximum drug release with TC cumulative release of 70% and 37% at 96 h, respectively. However, the delivery rates at pH 1 were slower in case of tetracycline associated with beta-cyclodextrin (beta-TC) loading showing 61% release for CA-CD and 22% for CA after 96 h. Thus, CA-CD can be suitably used as an effective drug delivery vehicle with maximum release obtained at pH 1 emphasizing its use in the gastrointestinal tract where pH is low. Also, the use of beta-cyclodextrin with the drug as an inclusion complex renders the CA and CA-CD beads useful for slow and long-term drug administration.
引用
收藏
页码:4089 / 4099
页数:11
相关论文
共 40 条
  • [1] Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin
    Angadi, Sudha C.
    Manjeshwar, Lata S.
    Aminabhavi, Tejraj M.
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2012, 51 (1-2) : 45 - 55
  • [2] [Anonymous], 2012, SCI REP
  • [3] Becker TA, 2001, J BIOMED MATER RES, V54, P76, DOI 10.1002/1097-4636(200101)54:1<76::AID-JBM9>3.0.CO
  • [4] 2-V
  • [5] Burchell T. D., 1999, Carbon Materials for Advanced Technologies
  • [6] Carbon dots for multiphoton bioimaging
    Cao, Li
    Wang, Xin
    Meziani, Mohammed J.
    Lu, Fushen
    Wang, Haifang
    Luo, Pengju G.
    Lin, Yi
    Harruff, Barbara A.
    Veca, L. Monica
    Murray, Davoy
    Xie, Su-Yuan
    Sun, Ya-Ping
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (37) : 11318 - +
  • [7] Cyclodextrins in drug delivery: An updated review
    Challa, R
    Ahuja, A
    Ali, J
    Khar, RK
    [J]. AAPS PHARMSCITECH, 2005, 6 (02)
  • [8] Fluorescent carbon dots obtained from chitosan gel
    Chowdhury, Devasish
    Gogoi, Neelam
    Majumdar, Gitanjali
    [J]. RSC ADVANCES, 2012, 2 (32) : 12156 - 12159
  • [9] Layer-by-layer coating of alginate matrices with chitosan-alginate for the improved survival and targeted delivery of probiotic bacteria after oral administration
    Cook, Michael T.
    Tzortzis, George
    Khutoryanskiy, Vitaliy V.
    Charalampopoulos, Dimitris
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2013, 1 (01) : 52 - 60
  • [10] Electrochemically stimulated drug release from dual stimuli responsive chitin hydrogel
    Ding, Fuyuan
    Shi, Xiaowen
    Jiang, Zhiwei
    Liu, Li
    Cai, Jie
    Li, Zeyong
    Chen, Si
    Du, Yumin
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2013, 1 (12) : 1729 - 1737