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1  acetate-, xylitol-, and sorbitol-containing chewing gum.
2 liva substitutes, and sugar-free lozenges or chewing gum.
3  protein (FRIL) formulated in clinical-grade chewing gum.
4 tent of TiO(2) included candies, sweets, and chewing gums.
5                                              Chewing gum (2 g) containing plant cells expressed CTB-A
6 ut chewing gum were 5.7 (1.7-13.5) and, with chewing gum, 3.6 (0.3-7.3), respectively (p = 0.001).
7    Patients in the intervention arm received chewing gum 4 times a day postoperatively.
8  in the lablab bean powder (683 days) and in chewing gum (790 days), and fully functional (794 days)
9 ng diluted samples, computer keyboard swabs, chewing gum, and cigarette butts.
10 st model explaining the menthol release from chewing gum, and it was found that the release was mostl
11 s suggest that regular use of CHX-containing chewing gum appears useful to control dental plaque form
12       Lastly, the role of vagal signaling or chewing gum as potential treatment strategies of allevia
13 sults suggest spices infused into sugar-free chewing gum bolster the antioxidant capacity of saliva,
14 ies on elective procedures demonstrates that chewing gum can lessen the duration of ileus.
15 ssify IC in various foods including cookies, chewing gum, cheese, and bread.
16  amplitude was significantly decreased after chewing gum containing 4 mg of nicotine.
17 tude responses decreased significantly after chewing gum containing both 2 and 4 mg of nicotine.
18                                              Chewing gum could induce increased swallowing frequency,
19  instructed to use 5 pieces of the unlabeled chewing gum daily (containing 5.0 mg CHX acetate/piece;
20   The null hypothesis of this study was that chewing gum does not have any effect on the clearance of
21 stered four 200 mg doses of caffeine-infused chewing-gum during night-time circadian trough and monit
22 f postoperative ileus was 21.5 h less in the chewing gum group (28.5 versus 50.0, P = 0.002), while t
23 th of hospital stay was 2.5 days less in the chewing gum group (5.4 versus 7.9, P = 0.007).
24                            Sham feeding with chewing gum has been shown to accelerate the return of g
25 ations and industrial products like candies, chewing gums, mouthwash and toothpaste.
26 andomized controlled trials on the impact of chewing gum on the duration of ileus in patients undergo
27    This trial aimed to examine the effect of chewing gum on the length of the postoperative ileus whi
28 owels (OR = 3.1, 95% CI 2.1-4.5), sharing of chewing gum or partially eaten candies (OR = 3.4, 95% CI
29  and could be used as an active component in chewing gums or mouthwashes for both caries and gingivit
30 dents were assigned a random ordering of the chewing gum products and received professional tooth cle
31 phosphate-fortified (alpha-TCP) experimental chewing gum released sufficient calcium and phosphate to
32                           The CHX-containing chewing gum showed significantly reduced plaque values (
33            These techniques include nicotine chewing gum, skin patches, nasal sprays, and inhalers, a
34                                              Chewing gum that is readily available and reasonably pri
35 H < 4 during the postprandial period without chewing gum were 5.7 (1.7-13.5) and, with chewing gum, 3
36                                Two pieces of chewing gum were used following each morning and evening
37  release mechanism and quality of sugar-free chewing gums were investigated.
38           Group A received routine care with chewing gum, while group B only received routine care.
39                                              Chewing gum with virus-trapping proteins offers a genera