Monday, February 23, 2015

Will 3D Bioprinting Spark a Ethics and Regulatory Debate?

The technology of 3D "bioprinting" (the medical application of 3D printing to produce living tissue and organs) is advancing so quickly that it will spark a major ethical debate on its use by 2016, according to Gartner Inc. At the same time, 3D printing of non-living medical devices such as prosthetic limbs, combined with a burgeoning population and insufficient levels of healthcare in emerging markets, is likely to cause an explosion in demand for the technology by 2015.

"3D bioprinting facilities with the ability to print human organs and tissue will advance far faster than general understanding and acceptance of the ramifications of this technology," said Pete Basiliere, research director at Gartner. Already in August 2013, the Hangzhou Dianzi University in China announced it had invented the biomaterial 3D printer Regenovo, which printed a small working kidney that lasted four months. Earlier in 2013, a two-year-old child in the US received a windpipe built with her own stem cells.

Mr. Basiliere added: "These initiatives are well-intentioned, but raise a number of questions that remain unanswered. What happens when complex 'enhanced' organs involving nonhuman cells are made? Who will control the ability to produce them? Who will ensure the quality of the resulting organs?"

Nevertheless, the day when 3D-bioprinted human organs are readily available is drawing closer, and will result in a complex debate involving a great many political, moral and financial interests.

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