An ionically crosslinked hydrogel containing vancomycin coating on a porous scaffold for drug delivery and cell culture

被引:54
作者
Zhang, Li Fang [1 ,2 ]
Yang, De Juan [1 ]
Chen, He Chun [1 ,2 ]
Sun, Rui [1 ]
Xu, Liang [1 ,2 ]
Xiong, Zuo Chun [1 ,2 ]
Govender, Thirumala [3 ]
Xiong, Cheng Dong [1 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Univ KwaZulu Natal, Sch Pharm & Pharmacol, ZA-4000 Durban, South Africa
关键词
biodegradable polymers; porous scaffold; alginate hydrogel; coating; controlled release; cell culture;
D O I
10.1016/j.ijpharm.2007.11.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to prepare and characterize a scaffold with an ionically crosslinked hydrogel coating layer containing a water-soluble drug, vancomycin, via a novel drug loading method for sustained drug delivery and surface modification. The poly(D,L-lactide acid) (PDLLA)/biphasic calcium phosphate (BCP) scaffold with a highly inter-connected porous structurewas fabricated by aparticle-leaching/thermally induced phase separation (TIPS) method. The pre-vacuumized scaffold was immersed into an alginate/vancomycin solution. Following impregnation by the solution, the scaffold was removed and immersed in a CaCl2 solution for 30 min to allow gelation of the alginate solution. In this way, the drug was not exposed to organic solvents or detrimental temperature conditions and it could avoid loss of drug during the leaching process. The water contact angles of the scaffold surface decreased after being coated with the hydrogel. The in vitro drug release profile showed sustained release properties which were influenced by the alginate concentration and the dissolution medium. A standardized bacterial assay showed that the drug was still active after association with the scaffold by this gentle method of drug loading. The in vitro osteoblast culture experiments confirmed the biocompatibility of the scaffold for attachment and proliferation of osteoblasts. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 87
页数:14
相关论文
共 45 条
  • [31] Swelling, erosion and release behavior of alginate-based matrix tablets
    Sriamornsak, Pornsak
    Thirawong, Nartaya
    Korkerd, Kingkarn
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 66 (03) : 435 - 450
  • [32] Modification of fibrous poly(L-lactic acid) scaffolds with self-assembling triblock molecules
    Stendahl, JC
    Li, LM
    Claussen, RC
    Stupp, SI
    [J]. BIOMATERIALS, 2004, 25 (27) : 5847 - 5856
  • [33] A rapid-curing alginate gel system: utility in periosteum-derived cartilage tissue engineering
    Stevens, MM
    Qanadilo, HF
    Langer, R
    Shastri, VP
    [J]. BIOMATERIALS, 2004, 25 (05) : 887 - 894
  • [34] Incorporation of different antibiotics into carbonated hydroxyapatite coatings on titanium implants, release and antibiotic efficacy
    Stigter, M
    Bezemer, J
    de Groot, K
    Layrolle, P
    [J]. JOURNAL OF CONTROLLED RELEASE, 2004, 99 (01) : 127 - 137
  • [35] Sun R., 2004, CHIN J SYN CHEM, V6, P536
  • [36] Tabata Yasuhiko, 2000, Pharmaceutical Science and Technology Today, V3, P80, DOI 10.1016/S1461-5347(00)00242-X
  • [37] Drug release from hydrogel containing albumin as crosslinker
    Tada, D
    Tanabe, T
    Tachibana, A
    Yamauchi, K
    [J]. JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2005, 100 (05) : 551 - 555
  • [38] The fabrication and characterization of poly(lactic acid) scaffolds for tissue engineering by improved solid-liquid phase separation
    Tu, CF
    Cai, Q
    Yang, J
    Wan, YQ
    Bei, JZ
    Wang, S
    [J]. POLYMERS FOR ADVANCED TECHNOLOGIES, 2003, 14 (08) : 565 - 573
  • [39] Webb K, 1998, J BIOMED MATER RES, V41, P422, DOI 10.1002/(SICI)1097-4636(19980905)41:3<422::AID-JBM12>3.0.CO
  • [40] 2-K