search.noResults

search.searching

saml.title
dataCollection.invalidEmail
note.createNoteMessage

search.noResults

search.searching

orderForm.title

orderForm.productCode
orderForm.description
orderForm.quantity
orderForm.itemPrice
orderForm.price
orderForm.totalPrice
orderForm.deliveryDetails.billingAddress
orderForm.deliveryDetails.deliveryAddress
orderForm.noItems
Biomaterials


common biopolymers used in biofabrication fields. Water and other substances used as food additives, such as acetic acid, are class Q3C. The team found a handful of green solvents


that could not only be used successfully, but that produced fibres with better material properties than those made using organic solvents. These findings are certainly promising. For industry players, they could indicate ways of working that would allow a scale-up in production; for researchers, they may work to further investigation into the sustainability and efficacy of electrospinning. But whether this green electrospinning process could become a reality beyond the lab raises a more complex set of questions: how many in the field can apply these findings to their work, and what does it realistically take for a lab process to translate into industrial manufacturing?


Applying the findings


Because the polymers investigated – collagen, polylactic-co-glycolic acid (PLGA), and polycaprolactone (PCL) – are commonly used in biomedicine, Mosher believes the findings are relevant to most electrospinning labs, and that they could inform workflows across the wider medical device industry.


“I think that almost every lab that does electrospinning uses one of these three polymers ... but there’s others within that chemical family that we think this will also apply to,” he says. “Moving forward, the idea for the industry is just to adapt to these Q3C solvents.”


While many of the Q3C solvents didn’t work with the polymers, there was a handful that did – with acetic acid coming out on top as the most effective. As well as having a low ecological impact, acetic acid can be used for electrospinning under routine fabrication conditions. Helpfully, the paper also includes information on all the parameters used when each polymer was electrospun with each solvent, which Mosher hopes that everyone in the field will use as a blueprint to inform their own work. Researchers could look through the FDA tables and try out a greener solvent, and manufacturers could use the system as a baseline method and add any necessary tweaks. “For someone who has electrospinning experience, this isn’t decades of work,” says Mosher. “You could figure this out in a few runs of electrospinning.” However, green solvents won’t always be an option as many polymers simply won’t dissolve in them. “In most cases, most materials are soluble in organic solvent, not in water or an environmentally- friendly solvent,” says associate professor of fibre science at Cornell University Dr Tamer Uyar, who


Medical Device Developments / www.nsmedicaldevices.com How does Mosher’s green electrospinning work?


Applying sustainability principles to biomaterial production, Mosher and his team developed their ‘green’ electrospinning process by systematically testing biologically benign solvents (US Food and Drug Administration Q3C Class 3). Through trial and error, they identifi ed acetic acid as a solvent that exhibits low ecological impact (global warming potential (GWP) = 1.40 CO2


eq. kg/L) and


supports a stable electrospinning jet under routine fabrication conditions. By tuning electrospinning parameters, such as needle-plate distance and fl ow rate, the researchers updated the fabrication of widely used biomedical polymers (for example, poly--hydroxyesters, collagen), polymer blends, polymer-ceramic composites, and growth factor delivery systems. The resulting ‘green’ fi bres and composites were comparable to traditional meshes in terms of composition, chemistry, architecture, mechanical properties, and biocompatibility. Interestingly, they found the material properties of green synthetic fi bres were more biomimetic than those of traditionally electrospun fi bres, doubling in ductility without compromising yield strength or ultimate tensile strength. Most importantly, green electrospinning proves advantageous for biofabrication, rendering a greater protection of growth factors during fi bre formation and recapitulating native ECM mechanics in the fabrication of biopolymer-based meshes. Mosher and his fellow researchers on the project from Columbia University believe the eco-conscious approach they demonstrated represents a paradigm shift in biofabrication, and will accelerate the translation of scalable biomaterials and biomimetic scaffolds for tissue engineering and regenerative medicine.


is also the editor of the journal Electrospinning. “That’s the chemistry – you cannot avoid it.” However, he believes a helpful future direction for research might be to identify new materials that could be used with green solvents. These could be obtained from nature, as has been seen in electrospun PET bottles formed using plant- based reactants, rather than those from oil sources or petrol.


From lab to industry Translating a lab finding into industrial use is often a journey fraught with practical, commercial, and regulatory challenges. Even if a manufacturer did want to use Mosher’s paper as a blueprint for altering their work, any material changes to a medical device may require approval – which can come with a new set of costs.


in organic solvent, not in water or an environmentally-friendly solvent. That’s the chemistry – you cannot avoid it.”


Tamer Uyar


If there is a change in the materials used to create the device, which would include a change in solvents used during the electrospinning process, the FDA may require a risk assessment of any new or increased biocompatibility concerns. For any changes that may impact a device’s safety and effectiveness, the FDA requires that manufacturers


109


Page 1  |  Page 2  |  Page 3  |  Page 4  |  Page 5  |  Page 6  |  Page 7  |  Page 8  |  Page 9  |  Page 10  |  Page 11  |  Page 12  |  Page 13  |  Page 14  |  Page 15  |  Page 16  |  Page 17  |  Page 18  |  Page 19  |  Page 20  |  Page 21  |  Page 22  |  Page 23  |  Page 24  |  Page 25  |  Page 26  |  Page 27  |  Page 28  |  Page 29  |  Page 30  |  Page 31  |  Page 32  |  Page 33  |  Page 34  |  Page 35  |  Page 36  |  Page 37  |  Page 38  |  Page 39  |  Page 40  |  Page 41  |  Page 42  |  Page 43  |  Page 44  |  Page 45  |  Page 46  |  Page 47  |  Page 48  |  Page 49  |  Page 50  |  Page 51  |  Page 52  |  Page 53  |  Page 54  |  Page 55  |  Page 56  |  Page 57  |  Page 58  |  Page 59  |  Page 60  |  Page 61  |  Page 62  |  Page 63  |  Page 64  |  Page 65  |  Page 66  |  Page 67  |  Page 68  |  Page 69  |  Page 70  |  Page 71  |  Page 72  |  Page 73  |  Page 74  |  Page 75  |  Page 76  |  Page 77  |  Page 78  |  Page 79  |  Page 80  |  Page 81  |  Page 82  |  Page 83  |  Page 84  |  Page 85  |  Page 86  |  Page 87  |  Page 88  |  Page 89  |  Page 90  |  Page 91  |  Page 92  |  Page 93  |  Page 94  |  Page 95  |  Page 96  |  Page 97  |  Page 98  |  Page 99  |  Page 100  |  Page 101  |  Page 102  |  Page 103  |  Page 104  |  Page 105  |  Page 106  |  Page 107  |  Page 108  |  Page 109  |  Page 110  |  Page 111  |  Page 112  |  Page 113  |  Page 114  |  Page 115  |  Page 116  |  Page 117  |  Page 118  |  Page 119  |  Page 120  |  Page 121  |  Page 122  |  Page 123  |  Page 124  |  Page 125  |  Page 126  |  Page 127  |  Page 128  |  Page 129  |  Page 130  |  Page 131  |  Page 132  |  Page 133  |  Page 134  |  Page 135  |  Page 136  |  Page 137  |  Page 138  |  Page 139  |  Page 140  |  Page 141  |  Page 142  |  Page 143  |  Page 144  |  Page 145  |  Page 146  |  Page 147  |  Page 148  |  Page 149  |  Page 150  |  Page 151  |  Page 152  |  Page 153  |  Page 154  |  Page 155  |  Page 156  |  Page 157  |  Page 158  |  Page 159  |  Page 160  |  Page 161  |  Page 162  |  Page 163  |  Page 164  |  Page 165  |  Page 166  |  Page 167  |  Page 168  |  Page 169  |  Page 170