Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14708
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dc.contributor.authorTundulawessa Y.
dc.contributor.authorYongchaiyud P.
dc.contributor.authorChutrthong W.
dc.contributor.authorTundulawessa K.
dc.date.accessioned2021-04-05T03:36:40Z-
dc.date.available2021-04-05T03:36:40Z-
dc.date.issued2010
dc.identifier.issn1252208
dc.identifier.other2-s2.0-77952909091
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14708-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77952909091&partnerID=40&md5=0b6c7b5a654e2ca144d8a85be63573e0
dc.description.abstractObjective: To compare the absorption rate of nicotine in volunteer blood, and determine the clinical trial on smoking cessation. Material and Method: This method using reverse phase C18 column and buffer pH 5.05 as the mobile phase, flow rate 0.9 ml/min. The UV-visible detector found the retention time of nicotine in gum and volunteer blood was 5.0756 min. The linear calibration curves of nicotine in human blood were obtained over the concentration range of 2.0-20.0 μg/ml. The coefficient variability for Nicotine gum 6.74% (2 mg/g). Extraction recovery was over 86% in blood, correlation coefficient of determination (r2) > 0.9999 and the detection limit 0.0060 μg/ml. The 24 healthy volunteer men, 27 to 55 years of age, were habitual cigarette smokers. They were randomized into two groups,12 subjects chewed two 2 mg pieces, Nicomild-2 Sugar Free Gum (Millimed, Thailand), the other chewed two 2 mg, pieces, Nicorette Sugar Free(Pharmacia AB, Helsingborg, Sweden.)Volunteers' blood samples were withdrawn at 0, 15, 30, 40 min, concentration of nicotine in blood were measured by HPLC. The 199 subjects were openly recruited under the project of "The smoking cessation for Phor Laung" (5-December). All of them received Nicomild-2 (nicotine polyestex gum) between November 2007 and December 2007. Results: The absorption rate of nicotine in volunteers' blood Nicomild-2 and Nicorette at 0, 15, 30,40 minutes were 0, 51.84, 26.73, 21.012 and 0, 56.603, 21.83, 15.183 (ng / min). Both of them were found to have maximum absorption rate at 15 minutes. When comparing the maximum absorption rate at 15 minute of Nicomild-2 (sugar free) with Nicorette (sugar free) didn't have significant differences detected. Treatment with nicotine polyestex gum were reported 65.3% (130/199) at 4 weeks compared with failure 30.15% (60/199)[ 65.3% vs 30.15%; p = 0.005]. The authors found 9 (4.5%) subjects successfully quit smoking free nicotine replacement therapy (NRT).
dc.subjectnicotine gum
dc.subjectadult
dc.subjectanalytic method
dc.subjectarticle
dc.subjectbioequivalence
dc.subjectcalibration
dc.subjectclinical trial
dc.subjectcontrolled clinical trial
dc.subjectcontrolled study
dc.subjectdizziness
dc.subjectdrug absorption
dc.subjectdrug blood level
dc.subjectdrug formulation
dc.subjectdyspepsia
dc.subjectdyspnea
dc.subjecthigh performance liquid chromatography
dc.subjecthuman
dc.subjecthuman experiment
dc.subjectmouth pain
dc.subjectnicotine replacement therapy
dc.subjectnormal human
dc.subjectrandomized controlled trial
dc.subjectsmoking cessation
dc.subjecttobacco dependence
dc.subjectAdult
dc.subjectChewing Gum
dc.subjectChromatography, High Pressure Liquid
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNicotine
dc.subjectNicotinic Agonists
dc.subjectPolymethacrylic Acids
dc.subjectPolyvinyls
dc.subjectSmoking
dc.subjectSmoking Cessation
dc.subjectTherapeutic Equivalency
dc.titleThe bioequivalent and effect of nicotine formulation gum on smoking cessation
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 93, No.5 (2010), p.574-579
Appears in Collections:Scopus 1983-2021

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