Development of a Long-Term Drug Delivery System with Levonorgestrel-Loaded Chitosan Microspheres Embedded in Poly(vinyl alcohol) Hydrogel

被引:22
|
作者
Long, Jingjunjiao [1 ]
Etxabide Etxeberria, Alaitz [1 ,2 ]
Kornelsen, Caroline [3 ]
Nand, Ashveen, V [4 ,5 ]
Ray, Sudip [6 ]
Bunt, Craig R. [7 ]
Seyfoddin, Ali [1 ,8 ]
机构
[1] Auckland Univ Technol, Fac Hlth & Environm Sci, Sch Sci, Drug Delivery Res Grp, Auckland 1142, New Zealand
[2] Univ Basque Country UPV EHU, Engn Coll Gipuzkoa, Dept Chem & Environm Engn, BIOMAT Res Grp, Donostia San Sebastian 48080, Spain
[3] Univ Arkansas Little Rock, Dept Chem, Little Rock, AR 72204 USA
[4] Unitec Inst Technol, Hlth & Community, Auckland 1142, New Zealand
[5] Unitec Inst Technol, Environm & Anim Sci Network, Auckland 1142, New Zealand
[6] Univ Auckland, Sch Chem Sci, MBIE Biocide Toolbox & NZProd Accelerator Program, Auckland 1142, New Zealand
[7] Lincoln Univ, Fac Agr & Life Sci, Dept Agr Sci, Canterbury 7647, New Zealand
[8] Auckland Univ Technol, Fac Hlth & Environm Sci, Sch Interprofess Hlth Studies, Auckland 1010, New Zealand
来源
ACS APPLIED BIO MATERIALS | 2019年 / 2卷 / 07期
关键词
levonorgestrel; controlled release; long-term; microsphere; hydrogel; chitosan; poly(vinyl alcohol);
D O I
10.1021/acsabm.9b00190
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study reports on the fabrication of a controlled release system for the delivery of levonorgestrel (LNG) for long-term contraception. LNG was encapsulated in chemically cross-linked chitosan (CS) microspheres, and microspheres presented a spherical geometry with a good particle size distribution (polydispersity index (PDI) < 0.1). The LNG-CS microspheres were classified based on their particle size range, <63, 63-125, and 125-300 mu m, where the 125-300 mu m particles were selected to be incorporated into a physically cross-linked and annealed PVA hydrogel matrix to prolong the drug release. PVA concentrations and the annealing treatment influenced the swelling behavior of PVA hydrogels. Fourier transform infrared (FTIR) spectroscopy indicated that CS was successfully crosslinked through the formation of a Schiff base; the PVA hydrogel was formed through hydrogen bonding without reacting with LNG, which was only physically entrapped, thus maintaining its stability. Differential scanning calorimetry (DSC) showed that freeze-thaw and annealing processes increased the degree of crystallinity in the PVA hydrogel. In vitro drug release assessments for all formulations showed zero order without any burst release. Over a period of 100 days, 34, 27, and 21% of LNG was released from the CS-LNG microspheres in the size ranges < 63, 63-125, and 125-300 mu m, respectively, while only 14, 11, and 9% of LNG was released when the CS-LNG microspheres were incorporated into 10, 15, and 20% PVA hydrogels, respectively. The drug release kinetics exhibited both diffusion- and swelling-controlled mechanisms following the Korsmeyer-Peppas model. This work presents a promising delivery system for long-term contraception with controlled zero-order release behaviors.
引用
收藏
页码:2766 / 2779
页数:14
相关论文
共 50 条
  • [1] Development of sustained drug delivery system using poly(vinyl alcohol) hydrogel
    Akamatsu, K
    Yamaoka, T
    Ide, H
    Kimura, Y
    23RD INTERNATIONAL SYMPOSIUM ON CONTROLLED RELEASE OF BIOACTIVE MATERIALS, 1996 PROCEEDINGS, 1996, : 793 - 794
  • [2] A thermosensitive chitosan/poly(vinyl alcohol) hydrogel containing nanoparticles for drug delivery
    Tang, Yufeng
    Zhao, Yiyang
    Li, Yan
    Du, Yumin
    POLYMER BULLETIN, 2010, 64 (08) : 791 - 804
  • [3] A thermosensitive chitosan/poly(vinyl alcohol) hydrogel containing nanoparticles for drug delivery
    Yufeng Tang
    Yiyang Zhao
    Yan Li
    Yumin Du
    Polymer Bulletin, 2010, 64 : 791 - 804
  • [4] Long-term regression of experimental endometriosis in a rat model treated with local application of levonorgestrel-loaded biodegradable microspheres
    Yuan, Peng
    Chen, Biliang
    Huang, Yanhong
    Xin, Xiaoyan
    HUMAN REPRODUCTION, 2012, 27 (07) : 2089 - 2095
  • [5] A heterogeneously structured composite based on poly(lactic-co-glycolic acid) microspheres and poly(vinyl alcohol) hydrogel nanoparticles for long-term protein drug delivery
    Wang, N
    Wu, XS
    Li, JK
    PHARMACEUTICAL RESEARCH, 1999, 16 (09) : 1430 - 1435
  • [6] A Heterogeneously Structured Composite Based on Poly(lactic-co-glycolic acid) Microspheres and Poly(vinyl alcohol) Hydrogel Nanoparticles for Long-Term Protein Drug Delivery
    Nuo Wang
    Xue Shen Wu
    Jia Kui Li
    Pharmaceutical Research, 1999, 16 : 1430 - 1435
  • [7] Composite Hydrogel Embedded with Porous Microspheres for Long-Term pH-Sensitive Drug Delivery
    Liu, Xifeng
    Fundora, Kevin A.
    Zhou, Zifei
    Miller, Alan Lee, II
    Lu, Lichun
    TISSUE ENGINEERING PART A, 2019, 25 (3-4) : 172 - 182
  • [8] CHITOSAN/POLY(VINYL ALCOHOL) HYDROGELS FOR ENTRAPMENT OF DRUG LOADED LIPOSOMES
    Ciobanu, Bogdan C.
    Cadinoiu, Anca N.
    Popa, Marcel
    Desbrieres, Jacques
    Peptu, Catalina A.
    CELLULOSE CHEMISTRY AND TECHNOLOGY, 2014, 48 (5-6): : 485 - 494
  • [9] A thermosensitive chitosan/poly(vinyl alcohol) hydrogel containing hydroxyapatite for protein delivery
    Du, Yumin
    Tang, Yufeng
    Wang, Xiaoying
    Hu, Xianwen
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2009, 237
  • [10] A thermosensitive chitosan/poly(vinyl alcohol) hydrogel containing hydroxyapatite for protein delivery
    Tang, Yufeng
    Du, Yumin
    Li, Yan
    Wang, Xiaoying
    Hu, Xianwen
    JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2009, 91A (04) : 953 - 963