Clear The Air News Tobacco Blog Rotating Header Image

Nicotine Addiction

Unexpected nicotine in Do-it-Yourself electronic cigarette flavourings

http://tobaccocontrol.bmj.com/content/early/2015/07/26/tobaccocontrol-2015-052468.extract

Electronic cigarette (EC) users often create their own refill fluids by blending bottled nicotine/propylene glycol/glycerol mixtures with Do-it-Yourself (DIY) flavourings.1 Although a complete refill fluid usually contains nicotine, the flavouring solutions themselves are an additive and are presumed to be free of nicotine, which is a known addictive chemical and toxicant.2 To determine if DIY flavourings are nicotine free, we evaluated 30 products from one vendor, using high performance liquid chromatography (HPLC) (figure 1B–D), and confirmed the presence of nicotine via gas chromatography and mass spectrometry (GC-MS) (figure 1E, F). HPLC analysis was performed as previously described in detail.3 Nicotine was extracted from DIY flavorings4 and GC-MS analysis of the extracts was performed using a Hewlett-Packard 5890 Series II gas chromatograph equipped with a Restek Rtx-1MS, 30 m, 0.25 mm column and a Hewlett-Packard 5971A mass selective detector

Low-Nicotine Cigarettes Fail to Sway Smokers

https://www.ucsf.edu/news/2015/07/131046/low-nicotine-cigarettes-fail-sway-smokers

Study Finds Effectiveness of Cessation Aid Slips After 6 Months

By Suzanne Leigh on July 22, 2015

Smokers who successfully lowered their nicotine intake when they were switched to low-nicotine cigarettes were unable to curb their smoking habits in the long term, according to a study by researchers at UCSF and San Francisco General Hospital and Trauma Center.

The study, published online July 22 in the journal Addiction found that levels of cotinine, a derivative of nicotine measured in the blood, plummeted six months after smokers’ regular cigarettes were replaced with low-nicotine ones. But levels started to rebound later into the study when smokers returned to regular cigarettes, suggesting that use of low-nicotine cigarettes alone may be ultimately ineffective in weaning smokers off tobacco.

Researchers led by Neal Benowitz, MD, recruited 135 smokers who had no imminent plans to quit, but were interested in trying low-nicotine cigarettes. Fifty-five of the smokers were told to continue smoking their regular brand, which was provided at no cost, while 80 were instructed to smoke “research cigarettes” with progressively lower levels of nicotine, also provided free of charge. The nicotine was eventually tapered to just 5 percent of that used in regular cigarettes.

Both groups were asked to smoke as desired, but the research cigarette smokers were told to avoid regular cigarettes and other tobacco products. Smoking cessation manuals were given to participants interested in quitting.

At 12 months, provision of both regular and research cigarettes was terminated and both groups’ cotinine levels continued to be monitored for a further year. At the start of the study, the research cigarette group had an average cotinine level of 250ng/ml, which dropped to 113ng/ml at six months. But an upswing was evident at the 12-month mark, which continued to rise as smokers returned to their usual brands, and approximated that of the group that had consistently smoked regular cigarettes.

A total of 68 participants completed the two-year study. Just one participant in the research cigarette group had quit smoking, versus zero in the regular cigarette group.

“We don’t know that very low nicotine cigarettes will not reduce nicotine dependence, but progressively reducing nicotine content of cigarettes in the way that we did, without other means of supporting smokers, did not produce the desired results,” said Benowitz, a professor in the UCSF departments of Medicine and of Bioengineering and Therapeutic Sciences, who conducts research at the San Francisco General Hospital and Trauma Center (SFGH) Division of Clinical Pharmacology and Experimental Therapeutics, Medical Service.

The authors attributed the rebounding cotinine levels in the research cigarette group to noncompliance.

“Cotinine levels were higher than expected given that nicotine content of the very low nicotine cigarettes was only 5 percent of that of conventional cigarettes,” said Benowitz, the paper’s first author. “We know that at six months, 30 percent reported that they had supplemented with conventional cigarettes and this had increased to 43 percent at 12 months.

“The results might have been different if regular cigarettes were not freely available, as would be the case if all cigarettes were mandated to be low in nicotine,” he added.

Smokers who received research cigarettes had stated that they consumed an average 20 cigarettes daily at the start of the study. This fluctuated slightly during the first 12 months and plunged to a reported 13 cigarettes at the two-year mark.

Federal regulation of the nicotine content of cigarettes was proposed in 1994 by Benowitz and colleague Jack Henningfield, PhD, at Johns Hopkins Medicine, as a tool to reduce nicotine dependency. The researchers hypothesized that very low levels of nicotine would prevent new smokers from becoming hooked and facilitate quitting for long-term smokers. The Family Smoking Prevention and Tobacco Act of 2009 authorized the FDA to reduce cigarette nicotine content.

“While reduction of the nicotine content in cigarettes is being considered as a national regulatory intervention to make cigarettes less addictive, our study indicated that this reduction is not likely to be effective if alternative, higher nicotine-containing cigarettes are readily available,” Benowitz said.

“Nicotine reduction would work best in the context of public education, easy access to smoking cessation services and the availability of non-combustible sources of nicotine for those who have difficulty stopping nicotine completely.”

Approximately 18 percent of American adults smoked in 2013, according to the latest figures from the Centers for Disease Control and Prevention.

Co-authors of the study are Natalie Nardone, PhD; Katherine Dains, PhD; Delia Dempsey, MD; and Peyton Jacob, PhD, from the Division of Clinical Pharmacology and Experimental Therapeutics, Medical Service at San Francisco General Hospital and Trauma Center. Jacob and Sharon Hall, PhD, are from the UCSF Department of Psychiatry. Susan Stewart, PhD, is from the Department of Public Health Sciences at UC Davis.

The study was supported by U.S. Public Health Service grants from the National Cancer Institute, National Institute on Drug Abuse and the FDA Center for Tobacco Products. Research cigarettes were provided by Philip Morris, which had no involvement in the design and implementation of the study. First author Benowitz is a consultant to several pharmaceutical companies that market smoking cessation medications. He has served as a paid expert witness in litigation against tobacco companies. Co-author Hall has received material support for a clinical trial from Pfizer. The other authors have no conflicts to declare.

UC San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It includes top-ranked graduate schools of dentistry, medicine, nursing and pharmacy, a graduate division with nationally renowned programs in basic, biomedical, translational and population sciences, as well as a preeminent biomedical research enterprise and two top-ranked hospitals, UCSF Medical Center and UCSF Benioff Children’s Hospital San Francisco.

Randomised clinical trial of snus versus medicinal nicotine among smokers interested in product switching

http://tobaccocontrol.bmj.com/content/early/2015/05/19/tobaccocontrol-2014-052080.full?g=w_tc_open_tab

Abstract

Background

An essential component of evaluating potential modified risk tobacco products is to determine how consumers use the product and resulting effects on biomarkers of toxicant exposure.

Study design

Cigarette smokers (n=391) recruited in Minnesota and Oregon were randomised to either snus or 4 mg nicotine gum for 12 weeks. Participants were instructed to completely switch from cigarettes to these products. Urine samples were collected to analyse for carcinogenic tobacco-specific nitrosamine metabolites (4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and N′-nitrosonornicotine and their glucuronides) and nicotine metabolites (total cotinine and nicotine equivalents) levels.

Results

Of the 391 participants randomised, 52.9% were male, the mean±SD age was 43.9±12.5 years, baseline number of cigarettes/day was 18.0±6.5 and Fagerstrom Test for Nicotine Dependence score was 5.1±2.0. The mean±SD number of snus pouches used/week at week 6 prior to tapering was 39.1±24.0 and nicotine gum pieces used was 37.6±26.3. Dual use of cigarettes and these products were observed in 52.9% and 58.2% of those assigned to snus and nicotine gum, respectively, at week 12. The end of treatment biochemically verified (carbon monoxide, CO <6 ppm) 7-day avoidance of cigarettes was 21.9% in the snus group and 24.6% in the nicotine gum group. Toxicant exposure in the nicotine gum group was significantly less when compared to snus.

Conclusions

Snus performed similarly to nicotine gum in cigarette smokers who were interested in completely switching to these products, but was associated with less satisfaction and greater toxicant exposure than nicotine gum.

Trial registration number NCT: 00710034.

Does smoking reduction worsen mental health? A comparison of two observational approaches

http://bmjopen.bmj.com/content/5/5/e007812.full?g=w_tc_open_tab

Abstract

Objectives

The association between smoking reduction and mental health is of particular interest given that many smokers report that smoking offers mental health benefits. We aimed to assess the association between smoking reduction and change in mental health using two different analytical approaches to determine if there was any evidence of an association. There were no prior hypotheses.

Design

A secondary analysis of prospective individual level patient data from 5 merged placebo-controlled randomised trials of nicotine replacement therapy for smoking reduction.

Participants

All participants were adult smokers, selected because they wanted to reduce but not stop smoking, and had smoked for at least 3 years. Participants were excluded if they were pregnant, breastfeeding, under psychiatric care, deemed to be unfit by a general practitioner, or part of a cessation programme. 2066 participants were enrolled in the trials, 177 participants were biologically validated as prolonged reducers, and 509 as continuing smokers at both 6-week and 18-week follow-ups.

Primary outcome

Change in mental health from baseline to an 18-week follow-up was measured using the emotional well-being subscale on the Short Form Health Survey-36.

Results

After adjustment for confounding variables, the differences for reducers compared with continuing smokers were: regression modelling −0.6 (95% CI −4.4 to 3.2) and propensity score matching 1.1 (95% CI −2.0 to 4.1).

Conclusions

Smoking reduction, sustained for at least 12 weeks, was not associated with change in mental health, suggesting that reducing smoking was no better or worse for mental health than continuing smoking. Clinicians offering smoking reduction as a route to quit can be confident that, on average, smoking reduction is not associated with negative change in mental health.

Flavour chemicals in electronic cigarette fluids

Download (PDF, 523KB)

Mayo Clinic, Nicotine Dependence Center: A Provider of Hope & Healing

Tobacco giant to launch nicotine inhaler designed to help smokers stub out their habit

http://www.mirror.co.uk/news/technology-science/technology/tobacco-giant-launch-nicotine-inhaler-5218279

British American Tobacco’s new Voke device wins license to be sold as a medicine

Cigarette manufacturer British American Tobacco is preparing to release a new nicotine inhaler.

The Voke device is licensed as a medicine and produces no heat, working more like an asthma inhaler than an electronic cigarette.

BAT has reached the second stage of its bid to bring the device to market, after being awarded a variation to its license from the UK Medicines and Healthcare products regulatory agency.

The first stage of this medical license was granted in September 2014.

A production line has been set up near King’s Lynn and the device will be built by Nicoventures, a subsidary of BAT.

A spokeswoman for Nicoventures told Mirror Online: “The work towards full scale-up continues and until it has been completed we will not be able to confirm timing, but we will be launching Voke as soon as we can.”

It is understood that Voke could one day be prescribed as a way to give up smoking.

The device is different from e-cigarettes, which work by heating liquid to produce cloud of nicotine-rich vapour.

Tom Pruen, chief scientific officer at the The Electronic Cigarette Industry Trade Association, welcomed the arrival of the inhaler.

“The Voke isn’t really a competitor product for e-cigs, rather it is some much needed innovation in the somewhat stagnant nicotine replacement market.”

However, one disadvantage of the devices lies in the fact they do not deliver clouds of flavoured vapour.

“They apparently deliver nicotine well, but don’t have the flavour or sensation that an e-cig does,” Pruen added.

“The Voke is another choice for smokers who want to quit so it’s a win for everyone, except possibly the combustible arm of BAT [which produces cigarettes].”

Using e-cigarettes is known to be healthier than smoking real tobacco, although recent research has controversially highlighted health concerns.

Addicted to Pleasure: Tobacco

Jury finds Philip Morris liable in Engle-Progeny Cigarette case

http://www.ourgazette.com/article/20150122/MN01/150129832/1014/OG/jury-finds-philip-morris-liable-in-engle-progeny-cigarette-case&source=RSS

A Florida federal jury found that Philip Morris USA is liable to Florida resident Donna Brown and awarded her $17.2 million in compensatory and punitive damages in the first federal court Engle-progeny cigarette trial of 2015. Ms. Brown began smoking cigarettes as a minor, became addicted, and now suffers from a painful disease that cost her the loss of her legs.

Motley Rice LLC, the law firm behind the landmark Tobacco Master Settlement Agreement, represented the plaintiff, together with Lieff Cabraser Heimann & Bernstein, LLP, and The Wilner Firm, P.A.

Ms. Brown began smoking Marlboro cigarettes around 16-years-old and subsequently developed an addiction to nicotine. As a result of this addiction, she has experienced life-altering health issues. Following her diagnosis of peripheral vascular disease (PVD) in 1992—a disease that typically causes a narrowing of the large arteries and blood restriction, most commonly in the lower extremities—Ms. Brown has endured more than two dozen surgeries, including surgeries to remove both of her legs in 2003. She has also suffered multiple strokes.

Ms. Brown hasn’t allowed these obstacles to stand in her way, however. In 1972 she was one of the first women in the southeast to work as an electronics technician for a telephone company and maintained that job until late 2004. Though the loss of both of her limbs was life altering, she continued for some time to find ways to enjoy some of her favorite hobbies, including golfing and fishing.

“The jury’s decision was just and fair, and a recognition that every person has the right not to be hurt by the careless, reckless or intentional acts of another,” said Motley Rice attorney Nathan D. Finch. “The jury recognized that Ms. Brown was hurt very badly by Philip Morris’ decisions over many years to repeatedly put its own profits over people’s health, decisions which unfortunately harmed a whole generation of Americans. Philip Morris and other tobacco companies now have to face the realities of their actions and answer to hundreds of people like Ms. Brown who they intentionally tried to get addicted.”

Ms. Brown’s case is one of the thousands of suits filed against tobacco companies following the 2006 landmark ruling of Engle v. Ligget Group Inc.

Motley Rice tobacco attorneys Nathan D. Finch, James W. Ledlie, Robert T. Haefele and Lisa M. Saltzburg were trial counsel for the plaintiff. The case is Donna Brown v. Philip Morris USA et al, United States District Court Middle District of Florida Jacksonville Division, No. 3:09-CV-10687-WGY-HTS.

Cone snail venom holds promise for medical treatments for cancer, addiction

14 Jan 2015

While considered a delicacy in some parts of the world, snails have found a more intriguing use to scientists and the medical profession offering a plethora of research possibilities. Cone snails are marine mollusks, just as conch, octopi and squid, but they capture their prey using venom. The venom of these marine critters provides leads for detection and possible treatment of some cancers and addictions.

Frank Marí, Ph.D., professor in the Department of Chemistry and Biochemistry in FAU’s Charles E. Schmidt College of Science at Florida Atlantic University, has focused his research on cone snail venom and has published a study in the current issue of the Journal of Biological Chemistry.

“The venom produced by these animals immobilizes prey, which can be worms, other snails and fish,” said Marí. “The venom is an extraordinary complex mixture of compounds with medicinal properties.”

The venom components selectively target cells in the body and make them valuable drug leads and powerful molecular tools for understanding the human body’s processes. One class of venom components is the alpha-conotoxins, named so because they target nicotinic receptors that are central to a range of diseases such as Alzheimer’s disease, schizophrenia, tobacco addiction and lung cancer.

The venom of a particular species of cone snail, Conus regius, collected by the Marí group at the Florida Keys, is particularly rich in alpha conotoxins. Aldo Franco, Ph.D., who worked in Marí’s lab, described more than ten new alpha-conotoxins in his Ph.D. dissertation at FAU. Among these, they found RegIIA, a compound that potently blocked the alpha3beta4 nicotinic receptor. This particular receptor when activated can be associated with lung cancer and nicotine addiction.

“We investigated in detail how RegIIA interacts with the alpha3beta4 nicotinic receptors and embarked on engineering new compounds that were more specific toward alpha3beta4 receptors and not other nicotinic receptors,” said Marí. “Our aim is to open new avenues for cancer and addiction research inspired on compounds from marine animals.”

Cone snails can be found throughout the Florida coast at different depths. Marí and his team regularly collect these animals using SCUBA and sometimes using deep-water submarines.

http://www.sciencedaily.com/releases/2015/01/150114090815.htm