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Forensic chemical profiling of flavouring additives in seized mu’assel (shisha) by gas chromatography-mass spectrometry (GC-MS)

  • Deepak Middha
  • Archna NegiEmail author
Open Access
Original Article

Abstract

Background

Water-pipe tobacco smoking obsession has again spread worldwide. Especially, the younger generation is besotted with mu’assel (shisha) and avidly use these for smoking. Numbers of additives are being added in commercial brands of mu’assel (shisha) to impart diverse taste with amusing aroma. The name of only one of the masking flavours like strawberry, chocolate, vanilla etc. and not the chemical ingredients are printed on the packets of mu’assel. The manufactures remain silent about mentioning the chemical ingredients used for flavourings as they may not have scientific data about chemical compounds attributing to multiple flavours. There is also a shortfall in quality control owing to non-availability of technical procedure(s) to identify masking multiple flavouring additives. Many of these flavoured additives are either carcinogenic or potentially hazardous for human health. Ignoring health hazards, the avaricious manufacturers are intentionally adding multiple additives to make their products more addictive in order to increase their sales. The need of the hour is to unequivocally establish a technique for chemical profiling of the flavouring additives in mu’assel. In this paper, seven popular commercial brands of mu’assel were extracted, sonicated and analysed by GC-MS technique for detection of flavouring additives.

Results

Twenty-eight flavouring additives, i.e. camphor, linalool, benzyl ethanol, β-citronellol, menthol, vanillin, ethyl vanillin, eugenol, eucalptol, patchouli alcohol, nerol, rheosmin, musk ambrette, musk ketone, phenyl ethyl methyl ether, anethole, estragole, limonene, benzaldehyde, terpineol, phenyl ethyl butyrate, phenethyl isobutyrate, piperonal, methyl isobutyrate, methyl dihydro jasmonate, anisyl alcohol, trans-geraniol and sabinene along with nicotine were detected in varied proportions by GC-MS technique in seven seized popular commercial brands of mu’assel.

Conclusion

A study on chemical profiling of flavouring additives in commercial mu’assel has yet not been reported. Henceforth, this forensic attempt was aimed to secure public health by chemically profiling the flavouring additives of mu’assel. Many of the detected additives may cause severe health problems. Moreover, the smoker may suffer from neuroticism and psychoticism that may lead to a number of cases pertaining to physical assaults and sexual harassment.

Keywords

Forensic chemistry Carcinogenic Flavour GC-MS Nicotine Smoking Mu’assel Hookah Psychoticism Public health 

Abbreviations

CNS

Central nervous system

COPTA

Cigarette and Other Tobacco Product Act

EC

European community

EU

European Union

GC-MS

Gas chromatography-mass spectrometry

LC

Liquid chromatography

MSD

Mass selective detector

R.V

Representative variety

TIC

Total ion chromatogram

WHO

World Health Organization

Background

Tobacco is one of the most widely abused substances in the world and is found to be highly addictive for its major alkaloid stimulant—nicotine (Ralapati and Lu 1998). The tobacco plant is a part of the genus Nicotiana and of the Solanaceae (nightshade) family. While more than 70 species of tobacco are known, the chief commercial crop is Nicotiana Tabacum (Fig. 1).
Fig. 1

Nicotiana Tabacum (Wikipedia 2015)

Dried cured tobacco leaves are consumed by various ways such as in cigarettes, cigars, mu’assel, flavoured tobacco, snuff, chewing tobacco, dipping tobacco and snus. Among these, the most popular way to consume tobacco is mu’assel through a hookah or water pipe (Fig. 2) in which the vapour or smoke of mu’assel is passed through a water basin before inhalation (Wikipedia 2015). Mu’assel or shisha is becoming increasingly popular due to its flavoured tobacco smoke. It is a syrupy tobacco mix with molasses and vegetable glycerol as moisturiser. Some specific flavours are also added to it. Typical flavours of mu‘assel include strawberry, chocolate, vanilla, apple, grape, guava, lemon and mint, as well as many other fruit-based mixtures. In this form, the user gets nicotine along with multi-flavour smoke.
Fig. 2

Hookah (Wikipedia 2015)

Additives are used primarily for flavours and smoothing the smoker’s experience (Rabinoff et al. 2007). Ninety-five percent of chemicals used in fragrances are synthetic compounds derived from petroleum. Smoking them can cause cancer, birth defects, CNS disorders and allergic reactions, e.g. limonene—carcinogenic, benzyl alcohol—CNS depressants, camphor—CNS stimulant and linalool—CNS depressants (EPA 2015).

Some of these chemicals are also found addictive, e.g. menthol increases nicotine receptor density (Callier V 2014). Henceforth, the Tobacco Products Directive (2001/37/EC) was provided for EU member states to regulate tobacco products so as to protect public health. This directive included the prohibition of ingredients which increase the addictiveness of tobacco products (Europa 2015). Owing to the short falls in quality control norms and non-availability of a reliable facility to identify flavouring additives, avaricious manufacturers are intentionally adding additives without considering the adverse effect of these chemicals. Moreover, these manufacturers are only printing the name of the masking flavour and not the details of the other additives on the cover of the commercial mu’assel. Due to these unfair practices, smokers remain unaware about the health hazard of flavouring additives present in mu’assel. Some methods were developed for the detection of nicotine from tobacco leaves by GC-MS (Hossain AM et al. 2013) and for detection of furanic compounds in the smoke of the water pipe (Schubert et al. 2011).

Study on chemical profiling of flavouring additives in mu’assel has not yet been reported. Henceforth, a forensic attempt is made to secure public health by chemically profiling flavouring additives in mu’assel. Forensic study was mainly targeted to give complete forensic chemical profiling of mu’assel so as to make smokers aware of the hidden health hazards of these products. In this study, representative samples from a large number of commercial varieties of mu’assel were subjected to forensic chemical analysis. These commercial varieties of mu’assel were seized during raids conducted in different hookah bars in Chandigarh by Chandigarh Police under COPTA Act, 2003, and were submitted at the Central Forensic Science Laboratory, Chandigarh, for the detection of nicotine. The samples of commercial varieties of mu’assel were ultrasonicated (Verma and Middha 2010) and analysed by using gas chromatography-mass spectrometry (GC-MS) technique. Twenty-eight flavouring additives apart from nicotine were identified by the mass spectral chemical profiling.

Materials and method

Representative varieties and reagents

The representative samples were taken from seven commercial varieties of mu’assel seized by Chandigarh police and were marked as R.V-1 to R.V-7.

Variety

Brand

Representative samples

1

Aladdin “Lady Dragon”

R.V-1

2

Aladdin “Sweet 16”

R.V-2

3

Aladdin “Brain Freezer”

R.V-3

4

Aladdin “X on Beach”

R.V-4

5

Qehwa “Pan Salsa”

R.V-5

6

Mya“Bombay Blue Pan ”

R.V-6

7

Mya “Pan Rasna”

R.V-7

The packets of all the seized varieties of mu’assel were printed with only details of nicotine and tar, whereas the details of other multiple flavouring additives were not mentioned on any of the packets of mu’assel.

The solvent used for extraction was of LC grade (Merck, German).

Equipment

Ultrasonicator of PCi, Mumbai, India; Balance-AB104S of Mettler, Toledo, Switzerland; Thermo Finnigan Trace GC Ultra coupled with a Thermo DSQ Quadrupole MS and Thermo autosampler 3000 were used (directive 2001/37/EC).

Ultrasonic extractions of mu’assel for flavouring additives

Ten millilitres of chloroform was added to a 2-g representative sample of each variety in a round bottom flask and kept for 8  h in a refrigerator. These were then ultrasonicated for 1 followed by filtration through Whatman No.1 filter paper (GE Healthcare, UK). The filtrated samples were concentrated to 2 ml and stored at 4 °C.

Instrumentation conditions

A Thermo Finnigan Trace GC Ultra coupled with a Thermo DSQ Quadrupole MS and Thermo autosampler 3000 was used. The column was a 30-m BP-5 with 0.3- mm I.D. and 0.5-μm film thickness. Helium was used as a carrier gas at a constant flow of 1.2  ml/min. Splitless injection was used with a splitless time of 60 s. The injector and interface line temperature were held at 250 °C and 330 °C respectively. Oven temperature was held at 90 °C for 1 min and increased to 310 °C at the rate of 20 °CC/min and held at this temperature for 10 min.

The MSD conditions: ionisation energy 70 eV, ion source temperature 200 °C, mass range 41–410 amu, electron multiplier voltage (Auto tune + 200 V).

Sample injection volume: 1 μl

Compound identification

Xcaliber 1.4 software was used for data acquisition and processing and results were screened using the library of National Institute of Standard and Technology.

Results

Various chemicals apart from nicotine were detected in R.V-1 to R.V-7 by GC-MS technique. Out of these, 28 flavouring additives/ chemicals were found responsible for flavour in these representative varieties. These 28 flavouring chemicals are tabulated against their respective detected retention time (Rt) in Tables 1, 2, 3, 4, 5, 6 and 7 and their resulting total ion chromatogram are depicted in Figs. 3, 4, 5, 6, 7, 8 and 9 respectively. Combined chemical profiling of these 28 flavouring additives detected in R.V-1 to R.V-7 are summarised in Table 8 and the flavour of each detected chemical along with its chemical structure is summarised in Table 9.
Table 1

Detected flavouring additives in R.V-1

R t

Chemical compound

Molecular weight (g/mol)

Important fragments

5.54

Limonene

136.24

68, 67, 93, 53, 94, 136

6.30

Linalool

154.25

71, 93, 55 ,121 ,136 ,139

6.51

Benzene ethanol

108.14

91, 92, 122, 65, 39, 123

6.91

camphor

152.24

95, 81, 69, 108, 152, 153

7.16

Menthol

156.27

71, 81, 95, 55, 123, 138

7.65

β-Citronellol

156.27

41, 69 ,81 ,82 ,123 ,138

7.93

Nerol

154.25

41, 69, 93, 123, 136, 154

8.31

Anethole

148.21

148, 147, 133, 77, 51, 149

8.96

Nicotine

162.2

84, 45, 133, 162, 55, 119

8.98

Eugenol

164.20

164, 149, 77, 55, 103, 165

9.40

Vanillin

152.15

151, 152, 81, 123, 53, 153

9.89

Ethyl Vanillin

166.18

137, 166, 109, 81, 29, 167

10.66

Rheosmin

164.20

107, 164, 43, 121, 94, 165

11.75

Patchouli alcohol

222.36

83, 138, 98, 222, 81, 55

Table 2

Detected flavouring additives in R.V-2

R t

Chemical compound

Molecular weight (g/mol)

Important fragments

5.58

Eucalptol

154.249

81, 71, 108, 69, 111, 154

6.16

Phenyl ethyl methyl ether (Kewda ether)

136.19

45, 91, 136, 104, 65, 137

6.53

Benzeneethanol

108.14

91, 92, 65, 122, 39, 123

6.93

Camphor

152.24

95, 81, 69, 108, 41, 152

7.16

Menthol

156.27

71, 81, 95, 41, 123, 138

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.98

Estragole

148.20

148, 147, 77, 121, 91, 51

8.33

Anethole

148.21

148, 147, 117, 77, 51, 149

8.84

Piperonal

150.13

149, 150, 63, 121, 65, 62

8.95

Nicotine

162.2

84, 133,162,42,119,65

8.98

Eugenol

164.20

164, 149, 77, 103, 55, 165

9.42

Vanillin

152.15

151, 152, 81, 123, 153, 154

9.89

Ethyl vanillin

166.18

137, 166, 109, 81, 29, 167

11.75

Patchouli alcohol

222.36

83, 138, 98, 222, 81, 55

12.91

Musk ambrette

268.26

253, 43, 91, 77, 268, 115

Table 3

Detected flavoured additives in R.V-3

R t

Chemical compound

Molecular weight (g/mol)

Important fragments

5.54

Limonene

136.24

68, 67, 93, 94, 136, 137

5.86

Sabinene

136.23

93, 91, 71, 41, 136, 137

6.30

Linalool

154.25

71, 93, 43, 121, 136, 139

6.51

Benzene ethanol

108.14

91, 92, 65, 122, 39, 123

6.91

Camphor

152.24

95, 81, 108, 41, 152, 55

7.16

Menthol

156.27

71, 81, 95, 55, 123, 138

7.35

Terpineol

154.25

59, 93, 121, 136, 81, 139

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.91

Trans-gerniol

154.25

69, 41, 68, 93, 123, 139

8.95

Nicotine

162.2

84, 133, 162, 42, 119, 65

8.98

Eugenol

164.20

164, 149, 77, 103, 55, 39

9.40

Vanillin

152.15

151, 152, 81, 123, 53, 153

9.72

Phenyl ethyl butyrate

192.25

104, 105, 71, 91, 106, 161

9.91

Ethyl vanillin

166.18

137, 138, 166, 109, 81, 167

10.66

Rheosmin

164.20

107, 43, 164, 77, 121, 165

12.91

Musk ambrette

268.26

253, 43, 91, 77, 268, 115

13.93

Musk ketone

294.30

43, 279, 128, 294, 115, 129

Table 4

Detected flavouring additives in R.V-4

R t

Chemical compound

Molecular weight (g/mol)

Important fragments

5.60

Eucalptol

154.249

43, 81, 71, 108, 111, 154

5.81

Methyl isobutyrate

102.13

43, 40, 71, 87, 102, 103

6.16

Phenyl ethyl methyl ether

136.19

91, 136, 104, 65, 137, 138

6.30

Linalool

154.25

71, 43, 93, 55, 121, 136

6.51

Benzene ethanol

108.14

91, 92, 65, 122, 39, 123

6.93

Camphor

152.24

95, 81, 41, 108, 109, 152

7.16

Menthol

156.27

71, 81, 95, 55, 67, 123

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.93

Nerol

154.25

41, 69, 68, 93, 123, 136

8.31

Anethole

148.21

148, 147, 117, 77, 105, 51

8.96

Nicotine

162.2

84, 133, 162, 92, 82, 163

8.98

Eugenol

164.20

164, 149, 77, 103, 55, 165

9.40

Vanillin

152.15

151, 152, 81, 123, 53, 153

9.74

Phenethyl isobutyrate

192.254

104, 43, 71, 105, 106, 42

10.66

Rheosmin

164.20

107, 43, 164, 77, 121, 65

11.45

Methyl dihydro jasmonate

226.32

83, 156, 153, 82, 55, 96

11.73

Patchouli alcohol

222.36

41, 43, 83, 98, 138, 222

12.89

Musk ambrette

268.2

253, 268, 91, 77, 115, 145

13.93

Musk ketone

294.30

43, 279, 128, 294, 115, 129

Table 5

Detected flavouring additives in R.V-5

R t

Chemical compound

Molecular weight

(g/mol)

Important fragments

5.60

Eucalptol

154.249

81, 71, 108, 111, 154, 69

6.16

Phenyl ethyl methyl ether (Kewda ether)

136.19

91, 136, 45, 65, 104, 137

6.53

Benzene ethanol

108.14

91, 92, 65, 122, 64, 123

7.16

Menthol

156.27 l

71, 81, 95, 123, 138, 67

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.93

Trans-gerniol

154.25

69, 41, 93, 123, 139, 154

8.96

Nicotine

162.2

84, 133, 162, 42, 119, 163

9.40

Vanillin

152.15

151, 152, 153, 81, 123, 53

11.75

Patchouli alcohol

222.36

83, 138, 98, 222, 81, 55

12.91

Musk ambrette

268.2

253, 43, 91, 268, 77, 115

Table 6

Detected flavouring additives in R.V-6

R t

Chemical compound

Molecular weight

(g/mol)

Important fragments

4.75

Benzaldehyde

106.12

105, 106, 77, 78, 107

5.60

Eucalptol

154.249

43, 81, 71, 108, 111, 154

6.17

Phenyl ethyl methyl ether

136.19

91, 136, 45, 65, 104, 103

6.30

Linalool

154.25

71, 93, 55, 69, 121, 136

6.53

Benzene ethanol

108.14

91, 92, 122, 65, 39, 93

6.93

Camphor

152.24

95, 81, 69, 108, 41, 152

7.16

Menthol

156.27

71, 81, 95, 82, 123, 138

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.93

Trans-gernaniol

154.25

69, 41, 68, 93, 123, 139

8.28

Anisyl alcohol

138.17

138, 137, 109, 77, 94, 39

8.96

Nicotine

162.2

84, 133, 162, 42, 119, 163

8.98

Eugenol

164.20

164, 149, 77, 103, 131, 55

9.40

Vanillin

152.15

151, 152, 81, 109, 53, 50

9.89

Ethyl vanillin

166.18

137, 166, 138, 109, 81, 167

10.66

Rheosmin

164.20

107, 164, 43, 77, 121, 65

11.75

Patchouli alcohol

222.36

83, 138, 98, 222, 81, 55

Table 7

Detected flavouring additives in R.V-7

R t

Chemical compound

Molecular weight (g/mol)

Important fragments

5.60

Eucalptol

154.249

43, 81, 108, 71, 111, 154

6.16

Phenylethylmethylether (Kewda ether)

136.19

45, 91, 136, 104, 65, 137

6.30

Linalool

154.25

71, 93, 55, 68, 121, 136

6.53

Benzene ethanol

108.14

91, 92, 122, 65, 39, 123

6.93

Camphor

152.24

95, 81, 69, 108, 41, 152

7.17

Menthol

156.27

71, 81, 95, 55, 123, 138

7.65

β-Citronellol

156.27

41, 69, 81, 82, 123, 138

7.91

Trans-geraniol

154.25

69, 41, 93, 123, 139, 154

8.31

Estragole

148.20

148, 147, 77, 121, 91, 51

8.95

Nicotine

162.2

84, 133, 162, 82, 92, 163

8.98

Eugenol

164.20

164, 149, 77, 103, 55, 165

9.40

Vanillin

152.15

151, 152, 81, 123, 53, 153

11.75

Patchouli alcohol

222.36

41, 43, 83, 98, 138, 222

12.91

Musk ambrette

268.26

253, 268, 43, 91, 77, 115

13.93

Musk Ketone

294.30

43, 279, 128, 294, 115, 129

Table 8

Combined chemical profiling of detected flavouring additives

S.No.

R.V-1

R.V-2

R.V-3

R.V-4

R.V-5

R.V-6

R.V-7

1

Camphor

Camphor

Camphor

Camphor

Camphor

Camphor

2

Linalool

Linalool

Linalool

Linalool

Linalool

3

Benzene ethanol

Benzene ethanol

Benzene ethanol

Benzene ethanol

Benzene ethanol

Benzene ethanol

Benzene ethanol

4

β-Citronellol

β-Citronellol

β-Citronellol

β-Citronellol

β-Citronellol

β-Citronellol

β-Citronellol

5

Menthol

Menthol

Menthol

Menthol

Menthol

Menthol

Menthol

6

Vanillin

Vanillin

Vanillin

Vanillin

Vanillin

Vanillin

Vanillin

7

Ethyl vanillin

Ethyl vanillin

Ethyl vanillin

Ethyl vanillin

8

Eugenol

Eugenol

Eugenol

Eugenol

Eugenol

Eugenol

9

Eucalptol

Eucalptol

Eucalptol

Eucalptol

Eucalptol

10

Patchouli alcohol

Patchouli alcohol

Patchouli alcohol

Patchouli alcohol

Patchouli alcohol

Patchouli alcohol

11

Nerol

Nerol

12

Rheosmin

Rheosmin

Rheosmin

Rheosmin

13

Musk ambrette

Musk ambrette

Musk ambrette

Musk ambrette

Musk ambrette

14

Musk ketone

Musk ketone

Musk ketone

15

Phenyl ethyl methyl ether (Kewda ether)

Phenyl ethyl methyl ether (Kewda ether)

Phenyl ethyl methyl ether (Kewda ether)

Phenyl ethyl methyl ether (Kewda ether)

Phenyl ethyl methyl ether (Kewda ether)

16

Anethole

Anethole

Anethole

17

Estragole

Estragole

18

Limonene

Limonene

19

Benzaldehyde

20

Terpineol

21

Phenyl ethyl butyrate

22

Phenethyl isobutyrate

23

Piperonal

24

Methyl iso Butyrate

 

25

Methyl dihydro jasmonate

26

Anisyl alcohol

27

Trans-geraniol

Trans-geraniol

Trans-geraniol

Trans-geraniol

28

Sabinene

Table 9

Chemicals detected in R.V-1 to R.V-7 imparting the flavour

Fig. 3

Total ion chromatogram of R.V-1

Fig. 4

Total ion chromatogram of R.V-2

Fig. 5

Total ion chromatogram of R.V-3

Fig. 6

Total ion chromatogram of R.V-4

Fig. 7

Total ion chromatogram of R.V-5

Fig. 8

Total ion chromatogram of R.V-6

Fig. 9

Total ion chromatogram of R.V-7

Discussion

Twenty-eight flavouring additives were detected in seven representative varieties of mu’assel by GC-MS technique summarised in Tables 1, 2, 3, 4, 5, 6, ,7 and 8 and TICs of R.V-1 to R.V-7 are depicted in Figs. 3, 4, 5, 6, 7, 8 and 9 respectively. Some of these detected chemicals are derived from plants origin, some are synthesised and some are both: These are categorised as under:
  1. 1.

    Plant origin: camphor, linalool, benzyl alcohol, β-citronellol, menthol, vanillin, eugenol, patchouli alcohol, nerol, eucalptol, rheosmin, anethole, estragole, limonene, benzaldehyde, terpineol, trans-geraniol and sabinene

     
  2. 2.

    Synthetic: musk ambrette, musk ketone, ethyl vanillin, methyl isobutyrate, phenyl ethyl butyrate, phenethyl isobutyrate, phenyl ethyl methyl ether and methyl dihydro jasmonate

     
  3. 3.

    Both (plant origin as well as synthetic): piperonal and anisyl alcohol

     

These chemicals are added for imparting flavour into the mu’assel by the manufacturers. These detected chemicals owe specific properties for impartinga characteristic flavour. The flavour of each detected chemical is summarised in Table 9. Some of these chemicals impart similar flavours. The manufacturers inadvertently added on multiple chemicals imparting the same flavour in mu’assel, i.e for vanilla flavour—vanillin and ethyl vanillin in R.V-1, R.V-2, R.V-3 and R.V-6; for spicy flavour—eugenol and eucalptol in R.V-2, R.V-4, R.V-6 and R.V-7 and for musk aroma—musk ambrette and musk ketone in R.V-3, R.V-4 and R.V-7 and for aroma of mixture of citrus and floral—β-citronellol and methyl dihydro jasmonate in R.V-4.

TICs of seven representative varieties are depicted in Figs. 3, 4, 5, 6, 7, 8 and 9. Menthol was computed to have high proportion in R.V-1, R.V-3, R.V-5, R.V-6 and R.V-7, whereas anethole was in high proportion in R.V-2 and R.V-4. Patchouli alcohol, benzene ethanol and camphor were detected in R.V-1, R.V-4, R.V-6 and R.V-7; eucalptol in R.V-2 and R.V-4 to R.V-7; linalool in R.V-1, R.V-3, R.V-4, R.V-6 and R.V-7 and musk ambrette in R.V-2 to R.V-5 and R.V-7. β-citronellol, menthol, vanillin and benzene ethanol were detected in all seven representative varieties of mu’assel.

The collective flavour of these chemicals in seven representative varieties of mu’assel are summarised in Table 10.
Table 10

Collective flavour (taste and aroma) by flavouring additives in mu’assel varieties

Representative sample

Collective taste

Collective aroma

R.V-1

Cool mint, vanilla, anise, fennel, citrus-rosy with spiciness

Strong penetrating odour of orange, anise, fennel, sweet rose, raspberry and patchouli

R.V-2

Cool mint, citrus-rosy, vanilla, licorice with spiciness

Strong penetrating odour of musk, green floral jasmine metallic fresh rose note, anise and fennel anisic type odour.

R.V-3

Cool mint, citrus-rosy, vanilla, woody with spiciness of black pepper

Strong penetrating odour of musk, vanilla, raspberry, orange, lilac and rose

R.V-4

Cool mint, citrus-rosy, vanilla with spiciness

Strong penetrating odour of patchouli, rose, spicy, raspberry, musk, green floral jasmine metallic fresh rose note, anise, fennel, fruity odour of apple or pineapple, sweet fruity-rose honey floral odour, mixture of floral and citrus

R.V-5

Cool mint, vanilla with spiciness

Citrus-rosy, patchouli, spicy, musk, green floral jasmine metallic fresh rose note

R.V-6

Cool mint, vanilla, spicy, rose-like floral

Strong penetrating odour of citrus-rosy, patchouli, spicy, vanilla, fruity odour of raspberry, green floral jasmine metallic fresh rose note and almond odour-like hawthorn

R.V-7

Floral, cool mint, vanilla, spicy, musk, licorice type and rose-like floral

Strong penetrating, floral with touch of spiciness, citrus-rosy, vanilla, spicy, patchouli, musk, green floral jasmine metallic fresh rose note and anisic-type odour

For imparting higher flavour notes, the avaricious manufacturers add multiple chemicals un-proportionally to mu’assel without considering their hazardous consequences. Moreover, to increase the sales of their products, manufacturers have been adding multiple chemical compounds having alike flavour. Owing to these, the fusion of flavours of these multiple chemical compounds in mu’assel does not have any specific pleasant flavour due to interference of flavours of various chemicals.

Conclusion

Twenty-eight chemicals responsible for flavour were detected in seven representative varieties of mu’assel. The presence of these flavoured additives varies in each of the seven representative varieties. A difference in the flavoured additives causes a difference in the flavour of these samples. These flavoured additives not only add flavour to these mu’assel products but also make the person more addictive for its taste. Moreover, buyers are not aware of these chemicals and their harmful effects as the details of these flavoured chemicals are not printed on covers of any of these representative varieties. Therefore, the manufacturer should print the name of all the added chemicals on covers of mu’assel packets.

The users while using hookah inhale nicotine along with these chemicals. Some of the chemicals along with nicotine are accumulated inthe human body while some are converted to new compounds during the heating process and also get accumulated in the human body. These chemicals and their new converted chemicals are harmful to the body. Some of these chemicals have been approved as additives to food but these are not tested by burning. The aforementioned health hazards need utmost attention by the public authorities; on our part, we have indeed carried out an in-depth analysis on the burnt flavouring additives of Mu’assel vis-à-vis health issues. The findings are being critically reviewed before making in public.

Forensic significance

Production and consumption of flavoured mu’assel are based on various economic, social, cultural and government policies. Due to loopholes in the government policy, they are commercially available in plenty in the market/online purchase and especially in hookah bars. The consumption of hookah along with flavoured additives is a major issue related to health as these are so hazardous that their exposure to the human body can cause inflammation to monocytes and can cause severe health problems. Some of these are neurotoxic and some are even carcinogenic. Another aspect of the flavoured mu’assel is the increasing mortalities due to the disease caused by smoking hookah and by consumption of flavoured additives.

The hookah smokers tend to be more extroverted, tensed, impulsive, depressive, anxious and suffered from traits of neuroticism and psychoticism which results in a number of cases pertaining to physical assault and sexual harassment. To make the situation worse, there is no internationally accepted standard method for analysing flavoured mu’assel in forensic cases along with any type of database.

This research publication does have a societical outreach as it makes the public at large aware about the hazardous effects of flavouring additives in a mu’assel and will aid the public authority to make a smoke-free world.

Notes

Acknowledgements

The authors express their gratitude to the researchers engaged in restoring public health and safety and to the public authorities striving to make a smoke-free world.

The authors are thankful to the Chief Forensic Scientist, DFSS, MHA, Govt. of India, and Director, CFSL, DFSS, MHA, Govt. of India, Chandigarh, for constant scientific support and encouragements.

Authors’ contributions

Dr. DM has planned, reviewed, guided the research experimentations, interpretation and publication frame work. Mrs. AN has participated in methodology development, experimentations, interpretation and wrote the manuscript. Both authors have read and approved the final manuscript.

Funding

The authors received no specific funding for this work

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Copyright information

© The Author(s) 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Central Forensic Science Laboratory, Directorate of Forensic Science ServicesMinistry of Home Affairs, Govt. of IndiaChandigarhIndia

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