Literature DB >> 19640157

Controlled vacuum seeding as a means of generating uniform cellular distribution in electrospun polycaprolactone (PCL) scaffolds.

Ming Chen1, Heather Michaud, Sankha Bhowmick.   

Abstract

A major challenge encountered in using electrospun scaffolds for tissue engineering is the non-uniform cellular distribution in the scaffold with increasing depth under normal passive seeding conditions. Because of the small surface pores, typically few microns in diameter, cells tend to congregate and proliferate on the surface much faster compared to penetrating the scaffold interior. In order to overcome this problem, we used a vacuum seeding technique on polycaprolactone electrospun scaffolds while using NIH 3T3 fibroblasts as the model cell system. This serves as a precursor to the bilayer skin model where the fibroblasts would be residing at an intermediate layer and the keratinocytes would be on the top. Vacuum seeding was used in this study to enhance fibroblasts seeding and proliferation at different depths. Our results show that the kinetics of cell attachment and proliferation were a function of varying vacuum pressure as well as fiber diameter. Cell attachment reached a maxima somewhere between 2-8 in. Hg vacuum pressure and fell for lower vacuum pressures presumably because of cell loss through the filtration process. Cell proliferation and collagen secretion over five days indicated that vacuum pressure did not affect cellular function adversely. We also compared the combined impact of scaffold architecture (400 nm versus 1100 nm average diameter fiber scaffolds) and vacuum pressure. At a given pressure, more cells were retained in the 400 nm scaffolds compared to 1100 nm scaffolds. In addition, the cell intensity profile shows cell intensity peak shift from the top to the inner layers of the scaffold by lowering the vacuum pressure from 0 in. Hg to 20 in. Hg. For a given vacuum pressure the cells were seeded deeper within the 1100 nm scaffold. The results indicate that cells can be seeded in electrospun scaffolds at various depths in a controlled manner using a simple vacuum seeding technique. The depth of seeding is a function of pressure and scaffold fiber diameter.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19640157     DOI: 10.1115/1.3173283

Source DB:  PubMed          Journal:  J Biomech Eng        ISSN: 0148-0731            Impact factor:   2.097


  5 in total

1.  In situ gelation for cell immobilization and culture in alginate foam scaffolds.

Authors:  Therese Andersen; Christine Markussen; Michael Dornish; Helene Heier-Baardson; Jan Egil Melvik; Eben Alsberg; Bjørn E Christensen
Journal:  Tissue Eng Part A       Date:  2013-11-28       Impact factor: 3.845

2.  Electrospun biodegradable poly(ε-caprolactone) membranes for annulus fibrosus repair: Long-term material stability and mechanical competence.

Authors:  Dmitriy Alexeev; Melanie Tschopp; Benedikt Helgason; Stephen J Ferguson
Journal:  JOR Spine       Date:  2020-11-27

Review 3.  3D Cell Culture in Alginate Hydrogels.

Authors:  Therese Andersen; Pia Auk-Emblem; Michael Dornish
Journal:  Microarrays (Basel)       Date:  2015-03-24

4.  Design of a Scaffold Parameter Selection System with Additive Manufacturing for a Biomedical Cell Culture.

Authors:  Marc Rabionet; Emma Polonio; Antonio J Guerra; Jessica Martin; Teresa Puig; Joaquim Ciurana
Journal:  Materials (Basel)       Date:  2018-08-14       Impact factor: 3.623

5.  Tissue Engineered Esophageal Patch by Mesenchymal Stromal Cells: Optimization of Electrospun Patch Engineering.

Authors:  Silvia Pisani; Stefania Croce; Enrica Chiesa; Rossella Dorati; Elisa Lenta; Ida Genta; Giovanna Bruni; Simone Mauramati; Alberto Benazzo; Lorenzo Cobianchi; Patrizia Morbini; Laura Caliogna; Marco Benazzo; Maria Antonietta Avanzini; Bice Conti
Journal:  Int J Mol Sci       Date:  2020-03-04       Impact factor: 5.923

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.