Published July 1, 2021 | Version v1
Journal article

Processing variables of direct-write, near-field electrospinning impact size and morphology of gelatin fibers

  • 1. Department of Biomedical Engineering, North Carolina State University, 4130 Engineering Building III, Raleigh, NC 27695 (United States)

Description

Several biofabrication methods are being investigated to produce scaffolds that can replicate the structure of the extracellular matrix. Direct-write, near-field electrospinning of polymer solutions and electrowriting of polymer melts are methods which combine fine fiber formation with computer-guided control. Research with such systems has focused primarily on synthetic polymers. To better understand the behavior of biopolymers used for direct-writing, this project investigated changes in fiber morphology, size, and variability caused by varying gelatin and acetic acid concentration, as well as process parameters such as needle gauge and height, stage speed, and interfiber spacing. Increasing gelatin concentration at a constant acetic acid concentration improved fiber morphology from large, planar structures to small, linear fibers with a median of 2.3 µm. Further varying the acetic acid concentration at a constant gelatin concentration did not alter fiber morphology and diameter throughout the range tested. Varying needle gauge and height further improved the median fiber diameter to below 2 µm and variability of the first and third quartiles to within ±1 µm of the median. Additional adjustment of stage speed did not impact the fiber morphology or diameter. Repeatable interfiber spacings down to 250 µm were shown to be capable with the system. In summary, this study illustrates the optimization of processing parameters for direct-writing of gelatin to produce fibers on the scale of collagen fibers. This system is thus capable of replicating the fibrous structure of musculoskeletal tissues with biologically relevant materials which will provide a durable platform for the analysis of single cell-fiber interactions to help better understand the impact scaffold materials and dimensions have on cell behavior. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1748-605X/abf88b

Additional details

Identifiers

Publishing Information

Journal Title
Biomedical Materials (Bristol. Online)
Journal Volume
16
Journal Issue
4
Journal Page Range
[10 p.]
ISSN
1748-605X

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53053347
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ACETIC ACID; COLLAGEN; GELATIN; POLYMERS
Descriptors DEC
CARBOXYLIC ACIDS; COLLOIDS; DISPERSIONS; MONOCARBOXYLIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PROTEINS; SCLEROPROTEINS