While in Las
Vegas last month, attending the National Association of Tobacco Outlets (NATO)
conference, I attended a number of informative presentations. One of these
presentations was on the “Current State of the E-cigarette” sponsored by the
Smoke Free Alternatives Trade Association (SFATA), an e-cigarette trade
association.
Bill Bartkowski,
one of the pioneers of the U.S. e-cigarette market, provided an interesting
take on the current state and future of the e-cigarette business.
Bartkowski began
his presentation by asking those in attendance to examine the e-cigarettes
currently available on the market. “I can say with some certainty that the
e-cigarettes that are being imported and sold today look nothing like the
e-cigarettes that will be offered for sale five years from now,” he said.
As an analogy,
Bartkowski said to consider the cell phone. The cellular technology that
existed 10 or 15 years ago looks nothing like the smartphones that more than
60% of all U.S. cell phone users have today.
“Technology and
design is always changing, improving and enhancing the consumer experience,” he
said. “It would be naïve to believe that e-cigarette technology and design
would not proceed along the same path.”
Future Perfect
The technology
enhancements that Bartkowski sees coming include excipients beyond today’s
propylene glycol and vegetable glycerin power sources that do not involve
lithium chemistry and devices capable of measuring, monitoring and metering
precise amounts of nicotine per puff.
But, and perhaps most important, he sees devices that are specifically
designed for automated manufacturing, making products manufactured in the U.S.
competitive with those manufactured in Asia.
These
enhancements will not only provide consumers with a more satisfying experience
and retailers with far fewer headaches due to defects and returns, but will
also provide the still nascent industry with a sophisticated, competitive
product that should provide regulators and researchers the necessary data to
support the product claims of safety and modified tobacco risk.
The last point is
especially important in light of comments made by Mitch Zeller, the newly
appointed head of the FDA’s Center for Tobacco Products, who participated in a
panel sponsored by NATO at the conference. While Zeller was reluctant to go
into any specifics about what the FDA was intending to do about e-cigarettes
and pending regulations, he did say that the FDA was eager to learn as much as
they could about the product. “We need
data,” he said emphatically.
Bartkowski made
the point that current e-cigarette technology was not up to the task of
supplying that data. “Virtually all of the research and development done since
this product has been introduced has focused on limiting manufacturing
defects—leaking and battery failures—and on flavorings. Very little, if any
research or product development has centered on achieving more efficient
nicotine uptake via deeper lung
absorption or on electronics and power management that can dispense
predetermined volumes of nicotine. The FDA wants all the data that can be
produced as they evaluate this product and the industry has some obligation to
provide it.”
Some recent
entrants into the e-cigarette category are getting the message. Lorillard, the
owner of Blu Cig, has commented on the record that they are researching deeper
lung absorption. Three weeks after the NATO conference, Reynolds America
reported that their new e-cigarette, Vuse, consists of a proprietary technology
with microchips in both ends that communicate with each other to deliver
consistent nicotine.
This is an
important time in the developing history of the e-cigarette. Bartkowski summed
up the challenge by saying the industry must, “keep the products safe for
users, secure from restrictive regulations, develop better manufacturing
practices and continuously invest in robust research.”
All of this
points to one stark conclusion: Today’s e-cigarette is going to have to change.
Article Credit: http://www.csdecisions.com

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