Studies on enzymatic degradation of multifunctional composite consisting of chitosan microspheres and shape memory polyurethane matrix

被引:10
作者
Bil, Monika [1 ,2 ]
Hips, Izabela [2 ]
Mrowka, Piotr [3 ,4 ]
Swieszkowski, Wojciech [2 ]
机构
[1] Warsaw Univ Technol, Ctr Adv Mat & Technol CEZAMAT, 19 Poleczki St, PL-02822 Warsaw, Poland
[2] Warsaw Univ Technol, Fac Mat Sci & Engn, 141 Woloska St, PL-02507 Warsaw, Poland
[3] Med Univ Warsaw, Dept Biophys & Human Physiol, 5 Chalubinskiego St, PL-02004 Warsaw, Poland
[4] Inst Hematol & Transfus Med, 14Indiry Gandhi Str, PL-02776 Warsaw, Poland
关键词
Biocomposites; Chitosan; Polyurethane; Lysozyme; Hydrolytic degradation; IN-VIVO DEGRADATION; DRUG-DELIVERY; HYDROLYTIC DEGRADATION; THERMAL-DEGRADATION; MOLECULAR-WEIGHT; CAST FILMS; RELEASE; SCAFFOLDS; VITRO; MECHANISMS;
D O I
10.1016/j.polymdegradstab.2020.109392
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Degradation studies of the multifunctional 3b-PU/CH-M composite consisting of 2.5 (wt.%) chitosan microspheres (CH-M) incorporated into crosslinked poly(caprolactone/lactide-co-glycolide) (PCL/PLGA) - urethane matrix (3b-PU) were performed in vitro in phosphate buffered saline (PBS) with lysozyme (Lys). The degradation process of the composite was monitored and analyzed via scanning electron microscopy (SEM), weight loss, pH measurement, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA-FTIR). FTIR analysis of chemical structure and mechanical properties measurement were also performed. Three stages of degradation were distinguished during 6 months studies: first - lasting the first 4 weeks associated with morphology changes of CH-M embedded in the outer layer of the composite film and 3% mass loss, followed by significant mass loss up to 20% and pH decrease to 6.5 attributed to degradation of PLGA units observed between 4 and 8 weeks of degradation. The last stage that was characterized by lysozyme adhesion on the composite surface and mass loss inhibition. SEM observations revealed that CH-M dispersed in the deeper layer of the polymer matrix preserved 6 months of degradation in PBS/Lys solution. In vitro test on MG-63 cells revealed no significant effect of the degradation products on cell viability and proliferation. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:13
相关论文
共 72 条
  • [31] Jennings JA, 2017, WOODH PUBL SER BIOM, V122, P159, DOI 10.1016/B978-0-08-100230-8.00007-8
  • [32] Chitosan-poly(lactide-co-glycolide) microsphere-based scaffolds for bone tissue engineering: In vitro degradation and in vivo bone regeneration studies
    Jiang, Tao
    Nukavarapu, Syam P.
    Deng, Meng
    Jabbarzadeh, Ehsan
    Kofron, Michelle D.
    Doty, Stephen B.
    Abdel-Fattah, Wafa I.
    Laurencin, Cato T.
    [J]. ACTA BIOMATERIALIA, 2010, 6 (09) : 3457 - 3470
  • [33] Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release
    Kamaly, Nazila
    Yameen, Basit
    Wu, Jun
    Farokhzad, Omid C.
    [J]. CHEMICAL REVIEWS, 2016, 116 (04) : 2602 - 2663
  • [34] Investigation of factors influencing the hydrolytic degradation of single PLGA microparticles
    Keles, Hakan
    Naylor, Andrew
    Clegg, Francis
    Sammon, Chris
    [J]. POLYMER DEGRADATION AND STABILITY, 2015, 119 : 228 - 241
  • [35] Biomaterials for the Delivery of Growth Factors and Other Therapeutic Agents in Tissue Engineering Approaches to Bone Regeneration
    Kowalczewski, Christine J.
    Saul, Justin M.
    [J]. FRONTIERS IN PHARMACOLOGY, 2018, 9
  • [36] Injectable matrices and scaffolds for drug delivery in tissue engineering
    Kretlow, James D.
    Klouda, Leda
    Mikos, Antonios G.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (4-5) : 263 - 273
  • [37] Kumar M.R., 2017, HDB POLYESTER DRUG D
  • [38] Modeling of drug release from bulk-degrading polymers
    Lao, Luciana Lisa
    Peppas, Nicholas A.
    Boey, Freddy Yin Chiang
    Venkatraman, Subbu S.
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 418 (01) : 28 - 41
  • [39] Shape-memory polymers as a technology platform for biomedical applications
    Lendlein, Andreas
    Behl, Marc
    Hiebl, Bernhard
    Wischke, Christian
    [J]. EXPERT REVIEW OF MEDICAL DEVICES, 2010, 7 (03) : 357 - 379
  • [40] Design of biodegradable, implantable devices towards clinical translation
    Li, Chunmei
    Guo, Chengchen
    Fitzpatrick, Vincent
    Ibrahim, Ahmed
    Zwierstra, Myrthe Jasmijn
    Hanna, Philip
    Lechtig, Aron
    Nazarian, Ara
    Lin, Samuel J.
    Kaplan, David L.
    [J]. NATURE REVIEWS MATERIALS, 2020, 5 (01) : 61 - 81