Supercritical CO2 generating chitosan devices with controlled morphology. Potential application for drug delivery and mesenchymal stem cell culture

被引:56
作者
Temtem, Marcio [1 ]
Silva, Ligia M. C. [1 ]
Andrade, Pedro Z. [2 ]
dos Santos, Francisco [2 ]
da Silva, Claudia Lobato [2 ]
Cabral, Joaquim M. S. [2 ]
Abecasis, Manuel M. [3 ]
Aguiar-Ricardo, Ana [1 ]
机构
[1] Univ Nova Lisboa, Dept Quim, Fac Ciencias & Tecnol, REQUIMTE CQFB, P-2829516 Caparica, Portugal
[2] Inst Super Tecn, IBB Ctr Biol & Chem Engn, P-1049001 Lisbon, Portugal
[3] Inst Portugues Oncol Francisco Gentil, Bone Marrow Transplantat Unit, P-1093 Lisbon, Portugal
关键词
Supercritical carbon dioxide; Membranes; Chitosan; Drug delivery and mesenchymal stem cells; CARBON-DIOXIDE; PHASE INVERSION; IN-VITRO; MEMBRANES; BONE; SCAFFOLDS; HYDROGELS; FILMS; INACTIVATION; BIOMATERIALS;
D O I
10.1016/j.supflu.2008.10.020
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, a novel approach involving supercritical carbon dioxide (scCO(2)) induced phase inversion technique was developed to produce chitosan devices using moderate temperatures and three very environmentally acceptable solvents (water, ethanol and CO2). The morphology and three-dimensional (3D) structure were controlled by altering the co-solvent (ethanol) composition in the carbon dioxide non-solvent stream during the demixing induced process. Microarchitectural analysis by scanning electron microscopy identified the production of particulate agglomerates when 10% of ethanol in the scCO(2) stream was used and the ability to make porous membranes with different morphologies and mechanical properties depending on the programmed gradient mode and the entrainer percentage (2.5-5%) added to the scCO2 stream. These structures were characterized in terms of pure water flux, porosity, mechanical properties and biodegradability. These chitosan matrices exhibited low solubility at neutral pH conditions, with no further modifications. We also demonstrated that the current method allows for a single-step preparation of an implantable antibiotic release system by co-dissolving gentamicin with chitosan and the solvent. Finally, the cytotoxicity, as well as the ability of these structures to support the adhesion and proliferation of human mesenchymal stem cells (MSC) in vitro were also addressed. The studies described may provide a starting point for the "green" design and production of chitosan-based materials with potential applications in tissue engineering and regenerative medicine, as well as drug delivery. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
相关论文
共 49 条
  • [21] Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells
    Le Blanc, K
    Rasmusson, I
    Sundberg, B
    Götherström, C
    Hassan, M
    Uzunel, M
    Ringdén, O
    [J]. LANCET, 2004, 363 (9419) : 1439 - 1441
  • [22] Isolation of human marrow-derived mesenchymal stem cells
    Lennon, Donald P.
    Caplan, Arnold I.
    [J]. EXPERIMENTAL HEMATOLOGY, 2006, 34 (11) : 1604 - 1605
  • [23] Over expression of endoglin in human prostate cancer suppresses cell detachment, migration and invasion
    Liu, YQ
    Jovanovic, B
    Pins, M
    Lee, C
    Bergan, RC
    [J]. ONCOGENE, 2002, 21 (54) : 8272 - 8281
  • [24] Porous chitosan scaffolds for tissue engineering
    Madihally, SV
    Matthew, HWT
    [J]. BIOMATERIALS, 1999, 20 (12) : 1133 - 1142
  • [25] Formation of porous flat membrane by phase separation with supercritical CO2
    Matsuyama, H
    Yano, H
    Maki, T
    Teramoto, M
    Mishima, K
    Matsuyama, K
    [J]. JOURNAL OF MEMBRANE SCIENCE, 2001, 194 (02) : 157 - 163
  • [26] Bone tissue engineering using human mesenchymal stem cells: Effects of scaffold material and medium flow
    Meinel, L
    Karageorgiou, V
    Fajardo, R
    Snyder, B
    Shinde-Patil, V
    Zichner, L
    Kaplan, D
    Langer, R
    Vunjak-Novakovic, G
    [J]. ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (01) : 112 - 122
  • [27] Laminin-1 peptide-conjugated chitosan membranes as a novel approach for cell engineering
    Mochizuki, M
    Kadoya, Y
    Wakabayashi, Y
    Kato, K
    Okazaki, I
    Yamada, M
    Sato, T
    Sakairi, N
    Nishi, N
    Nomizu, M
    [J]. FASEB JOURNAL, 2003, 17 (03) : 875 - +
  • [28] Novel approach to fabricate porous sponges of poly(D,L-lactic-co-glycolic acid) without the use of organic solvents
    Mooney, DJ
    Baldwin, DF
    Suh, NP
    Vacanti, LP
    Langer, R
    [J]. BIOMATERIALS, 1996, 17 (14) : 1417 - 1422
  • [29] Evidence for spinodal decomposition and nucleation and growth mechanisms during membrane formation
    Nunes, SP
    Inoue, T
    [J]. JOURNAL OF MEMBRANE SCIENCE, 1996, 111 (01) : 93 - 103
  • [30] Membranes formation of a hydrosoluble biopolymer (PVA) using a supercritical CO2-expanded liquid
    Reverchon, E.
    Cardea, S.
    Rappo, E. Schiavo
    [J]. JOURNAL OF SUPERCRITICAL FLUIDS, 2008, 45 (03) : 356 - 364