In vitro and in vivo ocular biocompatibility of electrospun poly(ε-caprolactone) nanofibers

被引:49
作者
Da Silva, Gisele Rodrigues [1 ]
Lima, Tadeu Henrique [2 ]
Orefice, Rodrigo Lambert [2 ]
Fernandes-Cunha, Gabriella Maria [3 ]
Silva-Cunha, Armando [3 ]
Zhao, Min [4 ,5 ]
Behar-Cohen, Francine [4 ,5 ,6 ]
机构
[1] Fed Univ Sao Joao del Rey, Sch Pharm, BR-35501296 Divinopolis, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Met & Mat Engn, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil
[4] INSERM, Ctr Rech Cordeliers, Team 17, U872, F-75006 Paris, France
[5] Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France
[6] Hotel Dieu Paris, AP HP, F-75004 Paris, France
关键词
Poly(epsilon-caprolactone) nanofibers; Electrospinning; In vitro and in vivo ocular biocompatibility; Retinal pigment epithelial cells (ARPE-19 cells); Muller glial cells (MIO-M1 cells); POLY-EPSILON-CAPROLACTONE; STEM-CELLS; SCAFFOLDS; FABRICATION; DIFFERENTIATION; EXPRESSION; GROWTH;
D O I
10.1016/j.ejps.2015.03.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Biocompatibility is a requirement for the development of nanofibers for ophthalmic applications. In this study, nanofibers were elaborated using poly(epsilon-caprolactone) via electrospinning. The ocular biocompatibility of this material was investigated. MIO-M1 and ARPE-19 cell cultures were incubated with nanofibers and cellular responses were monitored by viability and morphology. The in vitro biocompatibility revealed that the nanofibers were not cytotoxic to the ocular cells. These cells exposed to the nanofibers proliferated and formed an organized monolayer. ARPE-19 and MIO-M1 cells were capable of expressing GFAP, respectively, demonstrating their functionality. Nanofibers were inserted into the vitreous cavity of the rat's eye for 10 days and the in vivo biocompatibility was investigated using Optical Coherence Tomography (OCT), histology and measuring the expression of pro-inflammatory genes (IL-1 beta, TNF-alpha, VEGF and iNOS) (real-time PCR). The OCT and the histological analyzes exhibited the preserved architecture of the tissues of the eye. The biomaterial did not elicit an inflammatory reaction and pro-inflammatory cytokines were not expressed by the retinal cells, and the other posterior tissues of the eye. Results from the biocompatibility studies indicated that the nanofibers exhibited a high degree of cellular biocompatibility and short-term intraocular tolerance, indicating that they might be applied as drug carrier for ophthalmic use. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:9 / 19
页数:11
相关论文
共 38 条
[1]   Poly (ε-caprolactone) nanofibrous ring surrounding a polyvinyl alcohol hydrogel for the development of a biocompatible two-part artificial cornea [J].
Bakhshandeh, Haleh ;
Soleimani, Masoud ;
Hosseini, Saied Shah ;
Hashemi, Hassan ;
Shabani, Iman ;
Shafiee, Abbas ;
Nejad, Amir Houshang Behesht ;
Erfan, Mohammad ;
Dinarvand, Rassoul ;
Atyabi, Fatemeh .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2011, 6 :1509-1515
[2]   Ocular Biocompatibility and Structural Integrity of Micro- and Nanostructured Poly(caprolactone) Films [J].
Bernards, Daniel A. ;
Bhisitkul, Robert B. ;
Wynn, Paula ;
Steedman, Mark R. ;
Lee, On-Tat ;
Wong, Fergus ;
Thoongsuwan, Somanus ;
Desai, Tejal A. .
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2013, 29 (02) :249-257
[3]   Cellular signaling and factors involved in Muller cell gliosis: Neuroprotective and detrimental effects [J].
Bringmann, Andreas ;
Iandiev, Ianors ;
Pannicke, Thomas ;
Wurm, Antje ;
Hollborn, Margrit ;
Wiedemann, Peter ;
Osborne, Neville N. ;
Reichenbach, Andreas .
PROGRESS IN RETINAL AND EYE RESEARCH, 2009, 28 (06) :423-451
[4]   Nanocomposite hydrogels for cartilage tissue engineering: mesoporous silica nanofibers interlinked with siloxane derived polysaccharide [J].
Buchtova, Nela ;
Rethore, Gildas ;
Boyer, Cecile ;
Guicheux, Jerome ;
Rambaud, Frederic ;
Valle, Karine ;
Belleville, Philippe ;
Sanchez, Clement ;
Chauvet, Olivier ;
Weiss, Pierre ;
Le Bideau, Jean .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2013, 24 (08) :1875-1884
[5]  
Chaturvedi T.P., 2013, METHOD MOL BIOL, V1014, P187
[6]   Ocular Delivery of Compacted DNA-Nanoparticles Does Not Elicit Toxicity in the Mouse Retina [J].
Ding, Xi-Qin ;
Quiambao, Alexander B. ;
Fitzgerald, J. Browning ;
Cooper, Mark J. ;
Conley, Shannon M. ;
Naash, Muna I. .
PLOS ONE, 2009, 4 (10)
[7]   Comparative evaluation of chitosan, cellulose acetate, and polyethersulfone nanofiber scaffolds for neural differentiation [J].
Du, Jian ;
Tan, Elaine ;
Hyo Jun Kim ;
Zhang, Allen ;
Bhattacharya, Rahul ;
Yarema, Kevin J. .
CARBOHYDRATE POLYMERS, 2014, 99 :483-490
[8]   Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography [J].
Fischer, M. Dominik ;
Huber, Gesine ;
Beck, Susanne C. ;
Tanimoto, Naoyuki ;
Muehlfriedel, Regine ;
Fahl, Edda ;
Grimm, Christian ;
Wenzel, Andreas ;
Reme, Charlotte E. ;
van de Pavert, Serge A. ;
Wijnholds, Jan ;
Pacal, Marek ;
Bremner, Rod ;
Seeliger, Mathias W. .
PLOS ONE, 2009, 4 (10)
[9]  
Ford KM, 2012, MOL VIS, V18, P519
[10]   Electrospun poly(ε-caprolactone)/gelatin nanofibrous scaffolds for nerve tissue engineering [J].
Ghasemi-Mobarakeh, Laleh ;
Prabhakaran, Molamma P. ;
Morshed, Mohammad ;
Nasr-Esfahani, Mohammad-Hossein ;
Ramakrishna, Seeram .
BIOMATERIALS, 2008, 29 (34) :4532-4539