<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constructs appeared pink. (B-C) H&E staining of cross sections of constructs. Both AF and NP phases were filled with large amounts of cells (arrows), indicating that cells had a good proliferation in the scaffold. (D-E) SEM of cells in constructs. Both phases were filled with cells (arrows) and large amounts of ECM. (F-G) Live/dead staining of cells in constructs. Cells (arrows) in the constructs displayed green fluorescence, with no red flurescence. (green fluorescence: viable, red fluorescence: necrotic).</p
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>(a) Long, spindle-shaped cells attached to the walls of the scaffold after 3 days (SEM×1000). (b)...
<p>(A) Representative images of MCF-7 cells grown in 2D culture, showing more and denser cells over ...
<p>(A) Macroscopic image of the locations of implanted labeled cell—scaffold constructs in nude mice...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>Specific fluorescent staining of (A) NIH3T3, (B) C2C12 and (C) HeLa mammalian cells within the ce...
<p>A) NIH3T3, C2C12 and HeLa cells were cultured individually in cellulose n = 3 scaffolds for 1, 8 ...
<p>(A,B) Integration and establishment of BM-MSCs on Gelfoam after 3 days of culturing. <i>A</i>, lo...
<p>More than 95% of cells exhibited red fluorescence (A). When the labeled cells were cultured <i>in...
<p>After 7 days in co-culture, imaging of FDA(green)/PI(red) double staining showed that MC3T3-E1 ce...
<p><b>(A)</b> Cell proliferation 12 days after cell seeding, relative to the initial cell number/sca...
<p>(A) Optical microscopy of the morphology of AF cells. AF cells showed a long spindle-like morphol...
<p>(A–B) Low and high magnification images of the NF scaffold respectively. The cells were seeded an...
<p>(A) Diagrams of culture conditions. MDCK I cells were seeded at a density of 2 × 10<sup>5</sup> c...
<p>The PLLA/Col/HA, PLLA/Col, and PLLA/HA scaffold were washed with ice-cold PBS twice and fixed wit...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>(a) Long, spindle-shaped cells attached to the walls of the scaffold after 3 days (SEM×1000). (b)...
<p>(A) Representative images of MCF-7 cells grown in 2D culture, showing more and denser cells over ...
<p>(A) Macroscopic image of the locations of implanted labeled cell—scaffold constructs in nude mice...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>Specific fluorescent staining of (A) NIH3T3, (B) C2C12 and (C) HeLa mammalian cells within the ce...
<p>A) NIH3T3, C2C12 and HeLa cells were cultured individually in cellulose n = 3 scaffolds for 1, 8 ...
<p>(A,B) Integration and establishment of BM-MSCs on Gelfoam after 3 days of culturing. <i>A</i>, lo...
<p>More than 95% of cells exhibited red fluorescence (A). When the labeled cells were cultured <i>in...
<p>After 7 days in co-culture, imaging of FDA(green)/PI(red) double staining showed that MC3T3-E1 ce...
<p><b>(A)</b> Cell proliferation 12 days after cell seeding, relative to the initial cell number/sca...
<p>(A) Optical microscopy of the morphology of AF cells. AF cells showed a long spindle-like morphol...
<p>(A–B) Low and high magnification images of the NF scaffold respectively. The cells were seeded an...
<p>(A) Diagrams of culture conditions. MDCK I cells were seeded at a density of 2 × 10<sup>5</sup> c...
<p>The PLLA/Col/HA, PLLA/Col, and PLLA/HA scaffold were washed with ice-cold PBS twice and fixed wit...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>(a) Long, spindle-shaped cells attached to the walls of the scaffold after 3 days (SEM×1000). (b)...
<p>(A) Representative images of MCF-7 cells grown in 2D culture, showing more and denser cells over ...