Wicked Wizard Eliquid Electronic cigarettes and vaping: a new challenge in clinical medicine and public health. A literature review.
Electronic Cigarettes and Vaping: A New Challenge in Clinical Medicine and Public Health. A Literature Review
Electronic cigarette (e-cigarette) use, or vaping, in the United States and worldwide is increasing. Their use is highly controversial from scientific, political, financial, psychological, and sociological ideologies. Given the controversial nature of e-cigarettes and vaping, how should medical care providers advise their patients? To effectively face this new challenge, health care professionals need to become more familiar with the existing literature concerning e-cigarettes and vaping, especially the scientific literature. Thus, the aim of this article is to present a review of the scientific evidence-based primary literature concerning electronic cigarettes and vaping. A search of the most current literature using the pubmed database dating back to 2008, and using electronic cigarette(s) or e-cigarette(s) as key words, yielded a total of 66 highly relevant articles. These articles primarily deal with (1) consumer-based surveys regarding personal views on vaping, (2) chemical analysis of e-cigarette cartridges, solutions, and mist, (3) nicotine content, delivery, and pharmacokinetics, and (4) clinical and physiological studies investigating the effects of acute vaping. When compared to the effects of smoking, the scant available literature suggests that vaping could be a “harm reduction” alternative to smoking and a possible means for smoking cessation, at least to the same degree as other Food and Drug Administration-approved nicotine replacement therapies. However, it is unclear if vaping e-cigarettes will reduce or increase nicotine addiction. It is obvious that more rigorous investigations of the acute and long-term health effects of vaping are required to establish the safety and efficacy of these devices; especially parallel experiments comparing the cardiopulmonary effects of vaping to smoking. Only then will the medical community be able to adequately meet the new challenge e-cigarettes and vaping present to clinical medicine and public health.
Keywords: electronic cigarettes, nicotine addiction, nicotine replacement, smoking cessation, vaping, harm reduction
Use of electronic cigarettes (e cigarettes), referred to as vaping, is a relatively new phenomenon that is quickly gaining the interest of many long-time tobacco smokers. According to a report by UBS Securities LLC (1), sales from the e cigarette market doubled from $250 to $500 million between 2011 and 2012, and are expected to quadruple by 2014. E cigarettes are becoming a preferred alternative for nicotine delivery among many smokers because of their realistic look, feel, and taste compared to traditional cigarettes. Furthermore, many cigarette smokers have turned to vaping because e cigarette vendors have previously marketed their product as a cheaper and safer smokeless alternative to traditional cigarettes, and a possible smoking cessation tool. The Food and Drug Administration (FDA) rejected these claims, and in September of 2010 they informed the President of the Electronic Cigarette Association (2) that warning letters had been issued to five distributors of e cigarettes for “violations of good manufacturing practices, making unsubstantiated drug claims, and using the devices as delivery mechanisms for active pharmaceutical ingredients.” Many web sites still claim that use of e cigarettes is safe because tobacco is not burned and hence there is no inhalation of the many toxins found in cigarette smoke. For example, Electronic Cigarette Consumer Reviews (3), an e cigarette website, is filled with anecdotal consumer claims relating how e cigarettes helped them to quit smoking and improved their overall health.
The FDA has reported that e cigarette cartridges and solutions contain nitrosamines, diethylene glycol, and other contaminants potentially harmful to humans (4). From their analysis, the FDA reasons that the sale of e cigarettes should be prohibited or regulated as dangerous nicotine delivery systems that comply with the safety standards of the Federal Food Drug and Cosmetic Act (FDCA) (5). This presents an obvious dilemma since traditional cigarettes, which include nicotine, are proven to be harmful to human health, but are exempt from the FDCA safety standards. After Smoking Everywhere, Inc., filed an injunction against the FDA for restricting the sale of their e cigarettes in the United States (6), the US Court of Appeals (7) decided that e cigarettes may not be marketed as a safer alternative to cigarettes, or as a smoking cessation device, but instead must be sold as a smokeless tobacco product subject to the same rules and regulations of other tobacco products. What makes this ruling so controversial is that e cigarettes contain no tobacco other than a miniscule quantity found in the tobacco flavoring. Despite the court’s decision, e cigarette vendors have embraced this ruling, and are happy to sell their devices as alternatives to conventional cigarettes, so long as the FDA does not interfere with the sale of their products. Nevertheless, the potential harmful effects of vaping have led the FDA to issue Internet warnings regarding the risks of vaping (8). While the FDA has serious concerns regarding their use, Health New Zealand Ltd. (HNZ), a private enterprise which analyzed the safety of the Ruyan® e cigarette with Ruyan® financial support, recommends the use of e cigarettes as an alternative to traditional smoking (9). HNZ bases its recommendation on the likelihood that vaping is potentially less dangerous than traditional smoking; in other words, their message is “harm reduction.” Cahn and Siegel (10) support HNZ’s recommendation, concluding that “electronic cigarettes show tremendous promise in the fight against tobacco-related morbidity and mortality.” In addition to reducing tobacco-related morbidity and mortality, vaping may also reduce harm incurred from second hand smoke and benefit the environment (11).
Foulds et al. (12, 13) believe that more research needs to be conducted to determine the safety and efficacy of e cigarettes as a smoking cessation tool. However, they also state that individuals who have successfully quit smoking in favor of vaping should continue to use e cigarettes as a healthier alternative to conventional cigarettes. Although there are clear perceptions among e cigarette users that e cigarettes can be used as both a smoking cessation tool, and a safer alternative to smoking, they can be marketed as neither. The FDCA (5) precludes their use as a smoking cessation tool, and the Family Smoking Prevention and Tobacco Control Act (14) precludes their use as a reduced-risk alternative; therefore, e cigarettes must be sold as a tobacco product. E cigarettes could play an important role in the future of smoking cessation, but their use is currently clouded by a tangle of legal and political issues. It is evident that more research on the safety and efficacy of e cigarettes needs to be conducted, and that more stringent quality control measures should be implemented in order for the legal and political ramifications surrounding these products can be untangled.
The medical community must prepare itself to face the new challenge concerning e cigarettes and vaping as a “harm reduction” tool. As a consequence of past lessons learned from “Big Tobacco” companies, the medical community is suspicious of e cigarettes and has routinely advised against their use (15). The medical community advises on the side of caution, indicating that very little scientific evidence is available to show, one way or the other, that e cigarettes are safe to use, or that they help in the smoking cessation process. In addition, many physicians fear that patients who vape are merely substituting one form of nicotine addiction for another. While there are certainly potential perils associated with vaping, smoking, the leading cause of preventable disease in the United States, is likely to be more dangerous than vaping, especially when considering the myriad of known toxins found in cigarette smoke and the diseases which they promote. Assuming this premise is true, what should the primary medical focus be for a patient who has successfully transitioned from conventional cigarettes to e cigarettes? Should it be to maintain smoking abstinence, or should it be to quit vaping? Would it not be prudent for a patient who is unwilling to quit smoking or give up nicotine to vape instead of smoke? Given these circumstances, how should patients be advised? The potential health hazards of nicotine addiction from smokeless tobacco products have previously been reviewed in a policy statement by the American Heart Association and include hemodynamic effects, endothelial dysfunction, thrombogenesis, systemic inflammation, and other metabolic effects (16). Understandably, the medical community (15) is concerned that increased availability of e cigarettes could increase worldwide nicotine dependence, especially among the young as they are enticed by the various flavor options e cigarettes have to offer. Since vaping does not produce smoke from burning tobacco, the opponents of e cigarettes fear that traditional smokers will substitute vaping for smoking in settings where smoking is not permitted without any real intention of quitting conventional cigarettes. Furthermore, vaping in public places, coupled with recent e cigarette commercials on national television, could possibly undermine or weaken current antismoking regulations. Health care professionals will need to consider and weigh what is more harmful to the public, continued smoking or increased nicotine addiction. As e cigarettes gain greater popularity among smokers, these challenges will undoubtedly occur with increasing frequency.
In order to face this new challenge, health care professionals will need to become familiar with the available scientific evidence-based literature concerning e cigarettes and vaping. Currently, this literature is sparse, but growing fast, and primarily deals with (1) consumer-based surveys regarding personal views on vaping, (2) chemical analysis of e cigarette cartridges, solutions, and mist, (3) nicotine content, delivery, and pharmacokinetics, and (4) clinical and physiological studies investigating the acute effects of vaping. Only after reviewing the current literature can physicians and other health care providers give appropriate counsel regarding the role of e cigarettes and vaping as a safer alternative to smoking, and as a smoking cessation tool (17). Consequently, the aim of this article is to provide a review of the current literature concerning e cigarettes and vaping so that the medical community can better prepare for the new challenge these devices bring to clinical medicine and public health. The search for relevant scientific literature was accomplished using the pubmed database in which the key words electronic cigarette(s) or e cigarette(s) were used. The search for articles extended back to 2008 and only highly relevant evidence-based primary literature was retrieved for review. Sixty-six articles dealing with surveys soliciting personal views on vaping; studies analyzing potential toxins and contaminants in e cigarette cartridges, solutions, and mist; reports profiling nicotine content, delivery, and pharmacokinetics; and clinical and physiological studies investigating the effects of acute vaping were ultimately used. Of these articles, two were published between 2008 and 2009. Six, ten, and fifteen articles were published in 2010, 2011, and 2012, respectively. Thus far, 33 highly relevant articles have been published in 2013, indicating a progressive increase in e cigarette related research.
Surveys have shown that awareness of e cigarettes has quadrupled between 2009 and 2011 (18) and that they have a high adoption rate among traditional smokers (19, 20). Many current and ex-smokers use e cigarettes as a nicotine replacement therapy (NRT) to help them reduce or quit smoking (13, 21–25) while others use e cigarettes as a less harmful alternative to smoking (21, 23, 26, 27). At the end of 6 months, Polosa et al. found that vaping e cigarettes decreased consumption of conventional cigarettes by 80% after 6 months (28) and 50% after 24 months (29). Caponnetto et al. reported similar reductions in cigarette consumption and cigarette abstinence after a year-long trial of using e cigarettes in both normal smokers (30) and in chronic schizophrenic smokers (31). The authors claim that withdrawal symptoms were minimal and that the perception and acceptance of e cigarettes was satisfactory, even in the schizophrenic patients. The results of Vickerman et al. (32) are less optimistic. They reported that nearly a third of 2758 callers to six state tobacco quit lines had ever used e cigarettes of which 61.7% used the e cigarettes for <1 month. Barbeau et al. (26) reported that using e cigarettes, in comparison to other FDA-approved NRTs, such as nicotine gum, patches, and inhalers, had less annoying side effects and were more effective in preventing relapse, primarily because vaping retained the psychosocial aspects of real smoking better than the FDA-approved NRTs. Hua et al. (33) found a total of 405 different health-related effects (78 positive, 326 negative, and 1 neutral) reported by e cigarette users in three different online forums. Users reporting negative health-related effects often reported multiple symptoms, while users reporting positive health-related effects usually reported a single symptom. Additionally, negative health-related effects occurred most frequently in the respiratory, neurological, sensory, and digestive systems while the positive health-related effects occurred solely in the respiratory system.
It is possible that the decreased daily consumption of conventional cigarettes among e cigarette users, as seen in some studies (28–31), is at least partially due to a psychological element involving smokers’ motivation to quit. Support for this idea is seen in a recent Hawaiian multiethnic study (34) involving 1567 traditional smokers of which 13% were also e cigarette users attempting to quit smoking. This survey reported that smokers who used e cigarettes as a smoking cessation tool were more serious about wanting to quit smoking as compared to smokers who did not use e cigarettes. In addition, e cigarettes were also viewed as a viable option to other FDA-approved smoking cessation tools. Sutfin et al. (35) surveyed 4444 students from eight North Carolina colleges and found that 216 of these students had experimented with e cigarettes (ever e cigarette users) while 4228 had never used e cigarettes (never e cigarette users). Of the ever e cigarette users, 12% were never smokers, 30% were former or experimental smokers, 33% were current non-daily smokers, and 9% were current daily smokers compared to 53, 19, 14, and 4%, for the never e cigarette users, respectively. When the ever e cigarette users were asked about e cigarette harm perception, 17% indicated e cigarettes are as harmful as conventional cigarettes, 45% responded with less harmful, 3% thought e cigarettes to be more harmful, and 23% were unsure. The never e cigarette users responded with 16, 22, 2, and 51%, respectively. This data suggest that vaping is more common, but not exclusive, among traditional smokers. Another statistic revealed that vaping among young college students (mean age 20.7 ± 2.9 years) does not appear to be motivated by any intention to quit smoking. This is somewhat in contrast to Pokhrel et al. (34) who indicated more serious intentions toward smoking cessation among an older population of smokers using e cigarettes (mean age 42.3 ± 1.02 years) compared to smokers not using e cigarettes (mean age 45.63 ± 0.35 years). They also reported that individuals who took up vaping as a means to quit smoking were significantly younger and had smoked for less years than those who never vaped.
A concern of the FDA (8) and the medical community (15) is that availability of e cigarettes will entice teens and young adults toward vaping, which could ultimately lead to smoking conventional cigarettes. Currently, there is little or no concrete evidence confirming the validity of this concern. Cho et al. (36) used data collected from a Korean Health Project to determine awareness and use of e cigarettes. They found that 10.2% of 4353 students were aware of e cigarettes, but only 0.5% of those students had actually tried e cigarettes. Pepper et al. (37) conducted a national online survey of 228 male adolescents (ages 11–19) and determined that <1% of these individuals actually tried e cigarettes. On the other hand, 67% of the respondents were aware of e cigarettes with awareness being higher among the older boys. Of those individuals who never tried e cigarettes, 18% were willing to experiment with no preference toward flavored versus unflavored e cigarettes. Additionally, smokers were more amiable to experiment with e cigarettes than non-smokers. In contrast, discussions with 11 focus groups involving 66 young adults (ages 18–26) revealed that young adults favorably perceive e cigarettes and other new tobacco products specifically because they come in different flavors and that eliminating these flavors may reduce intentions to try these products (38). Another study surveyed 2624 US Midwestern young adults (ages 20–28) and indicated that 69.9% of the respondents were aware of e cigarettes, but that only 7% actually tried vaping (39). Goniewicz et al. (40) conducted a survey of students enrolled at 176 nationally representative Polish high schools (ages 15–19) and universities (ages 20–24) and reported that 23.5% of high school students and 19% of university students had ever tried e cigarettes. Of all the students who tried e cigarettes, only 3.2% were non-smokers, which compares closely to the 4.9% reported by Sutfin et al. (35). Other strong correlates of e cigarette use among adolescents include male gender, and having parents who smoke (36, 40). While a small percentage of young non-smokers experiment with e cigarettes, it is more likely that young smokers will experiment with e cigarettes. One fact emerges from these studies; as e cigarette popularity increases, so does awareness of them among young individuals. How increasing awareness will ultimately affect e cigarette usage by adolescent and young adults remains to be seen.
A number of studies (41–43) indicate that all forms of NRT are at least initially successful in maintaining cigarette abstinence. However, the successful long-term smoking cessation rate still remains relatively low. Employing a meta-analysis study, Hughes et al. (41) found the 6-month smoking quit rates for NRTs to be between 1 and 11% in seven studies as compared to between 3 and 5% in smokers who tried to quit on their own (44). Rennard et al. (42) reported a quit rate of 8% among smokers who used the nicotine inhaler for 15 months. In contrast, few studies have tested e cigarettes as a smoking cessation tool (28, 29, 45). From an online survey, Siegal et al. (45) reported that 31% (69 of 216) of the respondents were no longer smoking cigarettes after 6 months of using e cigarettes. Of those respondents who quit smoking, 57% were still using e cigarettes, 9% were using other tobacco free nicotine products, and 34% were completely nicotine free. Polosa et al. (28) investigated the effect of e cigarettes on smoking cessation and discovered that 22.5% (9 of 40) of the participants had not had a cigarette in 6 months. Of that cohort, 67% were still using e cigarettes while 33% were nicotine free. Similar results were reported in a 24-month study by Polosa et al. (29). These studies and others (46, 47) suggest that e cigarettes could play a role in smoking reduction and cessation, and as a result could reduce the harm incurred by smoking as effectively as any FDA-approved NRT. However, the role of e cigarettes on total nicotine abstinence is still highly questionable, and it has been suggested that one form of nicotine addiction is simply replacing another (26). A summary of the studies involving consumer-based surveys regarding personal views of vaping are shown in Table Table11.
Studies involving consumer-based surveys regarding personal views on vaping.
Chemical Analysis of E cigarette Cartridges, Solutions, and Mist
The ingredients found in e cigarette cartridges and solutions are relatively few, and for the most part non-toxic and non-carcinogenic, especially in the low quantities delivered. They include nicotine, propylene glycol, glycerin, and tobacco flavoring (4, 48). Propylene glycol, an FDA-approved solvent used in foods, a vehicle for intravenous diazepam, and as the major ingredient found in e cigarette fluids, makes up about 90% of the solution (9). Certain contaminates, most of which are derived from tobacco flavoring, have been detected in e cigarettes. A small amount of diethylene glycol (approximately 1%), a known carcinogen and an ingredient in anti-freeze, was also detected in one out of 18 cartridges analyzed by the FDA (4). The source of the diethylene glycol contamination is not clear but could reflect the use of non-pharmaceutical grade propylene glycol (10). In comparison, cigarette smoke from burned tobacco products contains thousands of compounds, many of which have been shown to induce or promote carcinogenesis (49); specifically the trace metals (i.e., cadmium, arsenic, chromium, nickel, and lead), the tobacco specific N-nitrosamines (TSNA), the polycyclic aromatic hydrocarbons (PAHs), and the volatile organic compounds (VOCs). While investigations have shown some of these hazardous compounds to be present in e cigarette cartridges, solutions, and mist, there are only a few reports detecting levels of these contaminates high enough to be of significant risk to humans. The HNZ study (9) found levels of arsenic cadmium, chromium, nickel, and lead to be undetectable in e cigarette cartridge liquid. In contrast, Williams at al. (50) found levels of lead, chromium, and nickel in e cigarette aerosol to be equivalent to, and in some cases higher than, what has been reported for cigarette smoke. They indicate that the primary source of these trace metals are the filaments inside the e cigarette cartomizer (i.e., the aerosolizing component of the e cigarette), and conclude that improved quality control of e cigarette design and manufacturing would greatly reduce the presence of these trace metals. The FDA (4) and HNZ (9) both reported that e cigarettes contain trace amounts of TSNAs, but the levels found in the e cigarettes represent only a very small fraction (0.008 μg/e cigarette cartridge containing 16 mg of nicotine) of what is typically found in traditional cigarettes (6.3 μg/full flavor Marlboro cigarette) (51). To put this into perspective, an e cigarette cartridge is good for about 150–300 puffs while a single conventional cigarette is good for about 10–15 puffs (52). The amount of total TSNAs found in other FDA-approved nicotine products was roughly equivalent to the total amount of TSNAs found in e cigarettes (9, 10). Other studies (11, 53–56) confirm the low levels of TSNAs present in e cigarette solutions and vapor, as well as the low or undetectable levels of particulate matter, trace metals, VOCs, and PAHs, especially when compared to the amounts present in cigarette smoke.
As previously mentioned (2), the FDA issued warnings to several e cigarette companies for selling e-cartridges and refill solutions containing active pharmaceutical ingredients such as rimonabant (Zimulti®) for the purpose of losing weight and reducing smoking addiction, and tadalafil (the active ingredient in Cialis®) for the purpose of increasing sexual capacity. FDA analyses of these e-cartridges and solutions revealed the presence of amino-tadalafil and not tadalafil, and the presence of an oxidative product of rimonabant, as well as rimonabant (57), although the amount of either of these substances that is able to transfer from liquid to vapor phase is low (58). Table Table22 summarizes the studies involving chemical analyses of e cigarette cartridges, solutions, and mist.
Studies involving chemical analysis of e cigarette cartridges, solutions, and mist.
Nicotine Content, Delivery, and Pharmacokinetics
E cigarettes are designed to deliver nicotine in an aerosolized manner that simulates an authentic smoking experience without the real smoke. In this respect, e cigarettes are similar to the FDA-approved nicotine inhaler. Bullen et al. (59) determined the Ruyan® e cigarette had a nicotine pharmacokinetic profile very similar to the Nicotrol® inhaler, but the study’s participants thought the e cigarettes were more pleasant to use and produced less irritation to the mouth and throat. For e cigarettes, the nicotine is delivered through cartridges prefilled with a nicotine solution or cartridges that the user fills with a nicotine refill solution. In either case, the nicotine concentration of the solutions or cartridges can be purchased in strengths ranging from 0 to 24 mg or more, according to user preference. Unfortunately, the amounts of nicotine specified on the labels of various brands of e-cartridges and solutions have not always been accurate or consistent (60). The FDA (4, 57, 58) confirmed the ability of e cigarettes to deliver nicotine, but stated there is too much variability in the amount of nicotine delivered per puff of any e cigarette cartridge for them to be considered safe. Repeated analysis of a menthol high strength Njoy® e cigarette cartridge (18 mg of nicotine) yielded nicotine deliveries of 26.8, 34.9, and 43.2 μg/100 ml puff. The medium strength Smoking Everywhere® e cigarette cartridge (11 mg of nicotine) and the medium strength Njoy® e cigarette cartridge (12 mg of nicotine) delivered 15.7 and 10.6 μg nicotine/100 ml puff, respectively, and were found to be similar to the 10-mg Nicotrol® inhaler shown to deliver 15.2 μg nicotine/100 ml puff. Of major concern is that some e-cartridges and solutions that were labeled as containing 0 mg of nicotine did in fact contain some nicotine (4,57). The FDA (4, 58) also detected small quantities of cotinine, a metabolite of nicotine, and several nicotine related impurities to include, anabasine, anatabine, myosmine, and β-nicotyrine in some, but not all, e-cartridge solutions and mist samples analyzed. Flouris and Oikonomou (61) question the rigor by which the FDA conducted these analyses, indicating that these analyses “cannot be used to draw conclusions or inferences about potential effects on health” until more rigorous chemical analyses, followed by extensive animal and clinical trials in humans, are conducted. Two other studies have also found discrepancies in the labeled nicotine content compared to the actual nicotine content in a number of e cigarette brands (52, 62). Goniewicz et al. (52) reported relative percent differences between the labeled and actual nicotine concentration per cartridges (or refill fluids) to range between −89 and 28% in 30 popular brands of e cigarettes. Cameron et al. (62) found the actual nicotine concentration in e cigarette cartridges and refill fluids to range from 1.8 to 23.7 mg/ml less than the labeled nicotine concentration. However, a more recent study analyzing several brands of e cigarette refill solutions did find nicotine content to be accurate and consistent to what was printed on the label (63). Inconsistencies reported in nicotine concentrations, and hence deliveries, could be a reason why some e cigarette users and not others report adverse reactions such as mouth and throat irritation, vertigo, headache, and nausea (21, 26, 33). Incidentally, some of these same adverse reactions have also been reported for various FDA-approved NRTs (64). In a study evaluating design features, accuracy and clarity of labeling, and quality of printed materials and instruction manuals for e cigarettes it was concluded that design flaws, inadequate product labeling, and lack of quality control in the manufacturing of e cigarettes are an indication that stricter oversight and regulation are required for these devices (65). Accurate production, safe packaging, and proper storage of e cigarette refill solutions are critical. Typically, a 5-ml vial of e cigarette refill solution could contain a nicotine concentration of 20 mg/ml or 100 mg/vial, and the known lethal dose of nicotine has been estimated to be about 10 mg in children and between 30 and 60 mg in adults (62). Given the potential health hazards of nicotine (16), inadvertent skin contact, or consumption of just one of these vials by children or pets could have tragic consequences. It is important that extreme caution be used when storing nicotine solutions.
Regardless of the inaccuracies and inconsistencies in the production of e cigarette cartridges and solutions, puff-for-puff, the amount of nicotine finding its way into the blood stream from vaping an e cigarette has been shown to be less than what you would expect from smoking a conventional cigarette with comparable nicotine content (59, 66, 67). These studies report little or no increases in blood nicotine levels of naive subjects after acute predefined use of e cigarettes compared to conventional cigarettes. According to Bullen et al. (59), serum levels of nicotine were similar after use of either the Nicotrol® inhaler or a Ruyan® e cigarette. They found serum nicotine levels to peak at 1.3 ng/ml after 19.6 min of vaping an e cigarette, and 2.1 ng/ml after 32 min of using the Nicotrol® inhaler, compared to 13.4 ng/ml after 14.3 min of smoking a cigarette. The Nicotrol® inhaler is said to be inappropriately named since it does not deliver significant quantities of nicotine directly to the lungs (68, 69). This is because the particle size of the delivered nicotine is too large to effectively reach pulmonary alveoli (70, 71). With each puff, the inhaler delivers nicotine to the oral cavity which is subsequently absorbed by the buccal mucosa and pharyngeal mucosa. It is not clear where most of the nicotine from e cigarettes is primarily absorbed; the alveoli, the airways or the oral cavity.In vitro evidence suggests that e cigarette aerosol particle size and distribution in the respiratory system is similar to conventional cigarette smoke (72–74). Sahu et al. (72) found the particle size of mainstream cigarette smoke to range between 186 and 198 nm and deliveries to the pulmonary alveoli, tracheal, and bronchiolar airways, and oral cavity were predicted to be 29.8, 15.2, and 16.3%, respectively. Zhang et al. (73) determined average e cigarette aerosol particle diameters to be approximately 400 nm, and alveolar deliveries to be between 7 and 18%. Zhang et al. (73) also indicate that nicotine delivery is highly dependent on a number of factors, including vaping technique, particle evolution, and cloud effects. It is very likely that aerosol particle size and nicotine delivery via e cigarettes may have similar distribution profiles that are intermediate between conventional cigarettes and the Nicotrol® inhaler.
In contrast to the aforementioned investigations (59, 66, 67), three other study (75–77) found increased blood levels of nicotine in experienced e cigarette users within 5 min of the first puff of an e cigarette. Dawkins et al. (76) reported blood nicotine levels to increase from 0.74 ng/ml baseline to 6.77 ng/ml 10 min after 10 puffs of an e cigarette, achieving a mean 13.91 ng/ml by the end of a 1-h ad libitum vaping period. It has also been reported that cotinine in the saliva (78) and serum (79) of e cigarette users is significantly elevated to levels commonly found in cigarette smokers. Vansickel and Eissenberg (75) also reported an increase in heart rate, which is not surprising since smoking and nicotine have long been known to stimulate heart rate and blood pressure (80, 81). It is interesting to note that the 2010 Vansickel et al. (67) study, and in Czogala et al. (82), heart rate and nicotine levels were significantly increased in smokers, but not vapers. However, the 2013 Vansickel and Eissenberg study (75) reported that both smoking and vaping-induced similar concomitant increases in heart rate and blood levels of nicotine. As suggested by Farsalinos et al. (83), this discrepancy could be attributed to differences in experimental design, and puffing topography of the participants in each study (i.e., different daily durations of vaping, experience with e cigarette devices, personal puffing characteristics to include the amount of vacuum created on every puff, and the vaping-induced deposition of nicotine into the oral cavity and/or size of the aerosolized particles). Trtchounian et al. (84), determined that smoke/aerosol density remained fairly constant while puffing on a conventional cigarette from start to finish (approximately 10 puffs), although variations did exist between brands of conventional cigarettes. The aerosol density for e cigarettes, while higher than conventional cigarettes in three out of the four brands tested, also remained fairly constant for the first 10 puffs of a new e cigarette cartridge. However, a decremental decrease in aerosol density was observed as each cartridge approached its terminal life. Consequently, this decrease in aerosol density would require the person vaping to generate more vacuum to maintain an aerosol density equivalent to the initial puffs and could be a reason contributing to longer puff duration for electronic cigarettes than for conventional cigarettes (85). Similar variations in the rate of airflow required to produce aerosol between and within brands of e cigarettes were also reported by Williams and Talbot (86). According to Goniewicz et al. (52), these studies demonstrate the importance of the initial nicotine content, the efficiency of the vaporization process that determines how much of the nicotine gets aerosolized, and the individual’s puffing topography on the efficacy of nicotine delivery from e cigarettes.
Many smokers claim that smoking cigarettes increases cognitive awareness, reduces stress, and induces a pleasurable feeling of wellbeing. Consequently, this is what makes smoking cigarettes so enjoyable and addictive. It is suggested that smoking has some psychological beneficial effects relating to job performance, vigilance, and mnemonic tasks, and that these effects are induced by nicotine, the addictive ingredient in tobacco (87). Similar effects have also been noted in non-smokers after a single dose of nicotine (88), and it is also worth mentioning that nicotine may have an ameliorating effect on both Parkinson’s and Alzheimer’s patients (89). Dawkins et al. (90, 91) found a decrease in the desire to smoke and reduced withdrawal symptoms associated with tobacco abstinence (1–10 h) among smokers vaping e cigarettes with nicotine in comparison to e cigarettes without nicotine. Furthermore, the nicotine from the e cigarette also improved prospective memory and working memory performance. Nicotine is a central nervous system (CNS) stimulant, and as such it is possible that a psychological need to enhance cognitive functioning reinforces addiction in smokers (92). Nicotine is also known to stimulate adrenergic and dopaminergic neurons in mesolimbic areas of the brain involved with reinforcing pleasurable reward behavior (93). Monoamine oxidases (MAO) normally reduce nicotine-induced adrenergic and dopaminergic activities by oxidizing them to inactive metabolites, and thereby limiting reward behavior. For cigarette smokers, however, nicotine is made even more addictive by synergizing with MAO inhibitors known to be present in cigarette smoke (94). Supporting evidence has been shown by Fowler et al. (95, 96) in which the activities of both MAO-A and MAO-B were reduced in various brain regions of smokers but not of non-smokers. Lewis et al. (94) indicate that there are at least six different MAO inhibitors present in cigarette smoke. In contrast, Laugesen et al. (9) were unable to detect any MAO inhibitors in e cigarette cartridges or the inhaled aerosol mist. These studies suggest that nicotine from e cigarettes and other FDA-approved NRTs may be less addictive than nicotine from burned tobacco products, and may be the reason why e cigarette users report a suppression of smoking and nicotine cravings (59, 66, 67, 90, 91). These investigations support the rationale behind NRT treatment for smoking cessation, which is that nicotine from NRTs, and possibly e cigarettes, does not occupy the nicotinic receptors to the same extent as nicotine from tobacco smoke (97). The effect is reducing withdrawal symptoms and cravings for cigarettes (71, 98) while possibly still providing some enhanced cognitive awareness and pleasurable reward (92, 93). A summary of the studies involving nicotine content, delivery, and pharmacokinetics are listed in Table Table33.
Studies involving nicotine content, delivery, and pharmacokinetics.
Clinical and Physiological Effects of Acute Vaping
The harmful effects of smoking on human health are obvious and well documented. In contrast, effects of vaping on human health are inconclusive due to the extreme paucity of empirical research investigating the presence of vaping-induced health hazards and/or benefits. Few studies have actually reported deleterious effects of vaping. In one report, McCauley et al. (99) present a case study concerning a 42-year-old woman diagnosed with exogenous lipoid pneumonia due to e cigarette use. She presented with a 7-month history of dyspnea, productive cough, and fevers which coincided with her use of e cigarettes. Samples of her sputum, and bronchoalveolar lavage revealed lipid-laden macrophages. Glycerin, an ingredient added to e cigarette solutions for the purpose of producing visual smoke when vaping, was thought to be the causative agent. Computed axial tomography (CAT) images of her lungs revealed areas of patchy ground glass superimposed on interlobular septal thickening, a pattern typical of a restrictive ventilatory defect with diffusion impairment, and consistent with the patient’s diagnosis. Cessation of e cigarette use resulted in improvement of her symptoms that was verified by follow-up lung radiography, however, pulmonary function testing still indicated mild diffusion impairment. Since the case study does not reveal if the patient is a current or ex-smoker and for how long, it is unclear whether the persistent diffusion impairment is a result of a concurrent or previous smoking habit, the use of e cigarettes, or the after effects of lipoid pneumonia per se. In another report, Vardavas et al. (100) found that 5 min of acute vaping among healthy smokers had no effect on basic pulmonary parameters [i.e., forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), peak expiratory flow (PEF), or midexpiratory flows at 50 (MEF50) and 75 (MEF75) percent]. This is in agreement Flouris et al. (79) who reported the FEV1/FVC ratio after acute vaping to be non-significantly reduced by 3.0% (79). This study, also reported the FEV1/FVC ratio after acute tobacco smoking to be significantly reduced by 7.2%. Vardavas et al. (100) did find decreased amounts of exhaled nitric oxide and increased peripheral airway resistance and impedance in smokers who vaped for 5 min. From these results they concluded that acute vaping has “immediate adverse physiological effects similar to some of the effects observed with smoking” but that the long-term health effects of vaping are not known and potentially harmful. The authors went on to qualify their conclusion by stating that although the differences in exhaled nitric oxide, airway resistance, and impedance were statistically significant, the differences are probably not clinically important. It is possible that the increased airway resistance and impedance demonstrated by Vardavas et al. (100) is partially due to the nicotine inhaled from the e cigarettes. Evidence for this is seen in a study reporting that non-smokers who inhaled nicotine (0–64 mg/ml) showed a dose-dependent increase in both the amount of coughing and airway obstruction, suggesting that nicotine stimulates afferent nerve endings in the bronchial mucosa which then triggers parasympathetic cholinergic pathways leading to bronchoconstriction (101).
In recent years there has been an effort to clinically use exhaled nitric oxide as an important non-invasive adjunct to pulmonary function testing (102) in order to monitor the degree of airway inflammation and eosinophilia (103, 104) commonly observed in conditions such as asthma. Unfortunately, interpretation of exhaled nitric oxide levels in the clinical setting is complex and confusing requiring adjustments for gender, age, height, respiratory infection, allergies, and smoking (105, 106). Given these difficulties, its validity is controversial. The major consensus in the literature is that the amount of exhaled nitric oxide is reduced in long-time smokers, as compared to non-smokers (105–109). In addition, it has been shown that smoking cessation is associated with an increase in exhaled nitric oxide back toward non-smoker levels (110). A possible mechanism of action for the opposing relationship of exhaled nitric oxide in smokers versus non-smokers could be the high levels of carbon monoxide present in cigarette smoke since there is strong evidence suggesting that carbon monoxide inhibits nitric oxide production by blocking nitric oxide synthase activity (111, 112). This mechanism is unlikely to occur with long-term vaping since carbon monoxide levels in e cigarette mist are negligible (9). In any case, there is no available literature showing the long-term effects of vaping on exhaled nitric oxide or carbon monoxide, although Caponnetto et al. (113) did show exhaled carbon monoxide levels to decrease from 31 to 4 ppm, 29 to 2 ppm, and 35 to 5 ppm in three individuals who first successfully transitioned from conventional cigarettes to e cigarettes and then quit e cigarettes altogether. The first time carbon monoxide was measured, all individuals were heavy smokers (45 pack/year, 28 pack/year, and 89 pack/year histories). The final time that exhaled carbon monoxide was measured all individuals had been smoke- and vape-free for nearly 2 years. Using an experimental group of “healthy” smokers, Vardavas et al. (100) reported a decreased fraction of exhaled nitric oxide (FENO) after just 5 min of vaping (from 13.02 to 10.89 ppb) which they correlated with airway inflammation and oxidative stress. In their introduction they state that “smokers have significantly lower concentrations of FENO – a non-invasive marker of bronchial inflammation – compared with non-smokers.” On the other hand, in their discussion they state that “nitric oxide is an additional marker that has been implicated in the pathophysiology of airway diseases associated with smoking, is strongly correlated with eosinophilic inflammation and bronchial hyperactivity, and has become an established marker for assessing oxidative stress, indicating the immediate effect e cigarette usage might have on pulmonary homeostasis.” From these two statements and from their FENO results, it is unclear whether they mean that smoking and vaping produce less bronchial inflammation and oxidative stress or more bronchial inflammation and oxidative stress when compared to not smoking or not vaping.
Although base levels of nitric oxide tend to be lower in smokers compared to non-smokers, Chambers et al. (114) observed significant increases in exhaled nitric oxide from 2.6 ppb before smoking to 4.8 ppb 1 min and 3.2 ppb 10 min after smoking a cigarette. Buda et al. (115) reported FENO to be 18, 29, and 16% higher than baseline 30, 45, and 60 min after smoking a cigarette, respectively. The findings of Vardavas et al. (100) concerning FENO levels after acute vaping are in direct opposition to what has been observed immediately after smoking a cigarette (114, 115). These results clearly demonstrate that acute vaping and acute smoking affect pulmonary nitric oxide metabolism, and the associated airway inflammatory responses, differently. From the available literature it is not clear how vaping might affect pulmonary inflammatory processes, but, as previously indicated, glycerin has been linked to lipoid pneumonia (99), and nicotine is known to generate endothelial dysfunction and systemic inflammation (16). Propylene glycol mist has been shown to produce ocular and respiratory irritation (116), and increase the risk of acquiring asthma (117), although Robertson et al. (118) reported that long-term inhalation of propylene glycol vapor by both monkeys and rats produced no deleterious pulmonary effects and Laugesen et al. (9) found no ill effects in humans. Bahl et al. (119) investigated the effects of a number of e cigarette refill fluids on cultured human embryonic stem cells (hESCs), and human pulmonary fibroblasts (hPFs) and found that nicotine in e cigarette refill fluids had no effect on hESC or hPF cytotoxicity at any concentration. However, they did report a positive correlation between hESC cytotoxicity, and the number and concentration of other chemicals used to flavor e cigarette refill fluids. Similar results were published by Romagna et al. (120) who demonstrated that an extract of e cigarette mist was less cytotoxic to cultured murine fibroblasts than an extract of tobacco cigarette smoke. A further indication that there are differences in the inflammatory responses between vapers and smokers is illustrated in a study reporting an absence of increased inflammatory indices in smokers asked to vape for 30 min compared to smokers who were asked to smoke for 30 min (121). Acute smoking has long been known to increase white blood cell count, which is a sign of acute inflammatory load (122). Flouris et al. (121) were able to confirm elevations of white blood cell count, lymphocyte count, and granulocyte count in active smokers but not in active vapers. Support for this is seen in a recently published case report (123) where a 36-year-old male with a nine pack-year history of smoking exhibited reversal of chronic idiopathic neutrophilia symptoms after he quit smoking and started vaping. Table Table44 summarizes the studies involving clinical and physiological effects of acute vaping.
Studies involving clinical and physiological effects of acute vaping.
Despite the popularity e cigarettes have gained worldwide, very little rigorous research has been done regarding the effects these devices have on human health. This article reviews the existing evidence-based literature, dealing with surveys soliciting personal views on vaping; studies analyzing potential toxins and contaminants in e cigarette cartridges, solutions, and mist; reports profiling nicotine content, delivery, and pharmacokinetics; and clinical and physiological studies investigating the effects of acute vaping. When compared to the harmful effects of smoking, these studies suggest that vaping could be used as a possible “harm reduction” tool. There is evidence supporting e cigarettes as an aide for smoking cessation, at least as successful as currently available FDA-approved NRTs. Less evidence exists to suggest that e cigarettes are effective in recovery from nicotine dependence. More rigorous research is essential before any solid conclusions can be drawn about the dangers, or usefulness of e cigarettes. In particular, more rigorous research is required delving into both acute and long-term cardiopulmonary effects of vaping, especially those experiments comparing the effects of vaping with those of smoking. E cigarettes are fast becoming a new “tobacco” industry (124) that could reduce the incidence of traditional smoking. It is also possible that e cigarettes may either decrease or increase the incidence of nicotine addiction. Given these uncertainties, will the availability of e cigarettes provide for healthier U.S. and world populations, as harm reductionists hope, or will other more dangerous ill effects ultimately emerge? Health care professionals must remain current with the literature concerning e cigarettes and vaping. Only then can they make informed decisions aimed at maximizing human safety and minimizing the potential ill effects e cigarettes may have on their patients and the public. Only then can the new challenge regarding e cigarettes and vaping in clinical medicine and public health be adequately addressed.
Conflict of Interest Statement
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author would like to thank the faculty and staff of the DeBusk College of Osteopathic Medicine, Lincoln Memorial University for graciously providing constructive criticism, comments, and editorial assistance in the preparation of this manuscript.