• 제목/요약/키워드: Theophylline concentration

검색결과 30건 처리시간 0.021초

소아 호출기 환자에서 경구 투여된 Formoterol이 Theophylline의 혈중농도에 미치는 영향의 연구 (Effect of Formoterol on the Plasma Levels of Theophylline after the Oral Administration to the Children with Respiratory Diseases)

  • 장진경;정낙균;이숙향;조혜경
    • 한국임상약학회지
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    • 제10권3호
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    • pp.107-110
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    • 2000
  • Theophylline and $\beta$-adrenergic agonists are frequently used together in patients with respiratory diseases. However the clinical impact of $\beta_2$-adrenergic agonists on the blood concentration of theophylline is not fully evaluated. Formoterol, a newly available oral ${\beta}_2$-adrenergic agonist is frequently used in pediatric respiratory patients. The objective of this study was to investigate the effect of oral formoterol on theophylline's blood concentration. Randomized prospective study was conducted. Twenty-four children were enrolled on the study. Their age ranged 2 to 73 months (mean 35.8 months). Theophylline group (12 patients) received 10 mg/kg/day of for theophylline orally. Theophylline/formoterol group (12 patients) received 10 mg/kg/day of theophylline and $4\;{\mu}g/kg/day$ of formoterol orally. All medications were administered at least for 5 days starting on admission day. Theophylline's trough concentrations were obtained on days 3 and day 5. Pulse rates were recorded before the study medications were given on admission, and days 3 and day 5. Statistical significance was calculated by two-tailed Student's t-test. Theophylline's levels in children given theophylline and formoterol together were lower an those given theophylline alone ($6.38\pm0.90\;{\mu}g/ml\;vs\;7.43\pm0.77\;{\mu}g/ml$ on day 3(p<0.05), $5.62\pm0.56\;{\mu}g/ml\;vs.\;6.78\pm0.61\;{\mu}g/ml$ on day 5 (p<0.05)). In both groups, theophylline's trough concentration on day 5 were lower than day 3. There was no significant side effects in both groups. In conclusion, the new ${\beta}_2$ selective adrenergic agonist formoterol reduced serum theophylline levels in children with respiratory diseases. Further investigation is needed to clarify the long term effect of this drug interaction.

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간장장해에서 Theophylline의 체내동태 (Pharmacokinetics of Theophylline in Rabbits with Hepatic Failure)

  • 문흥섭;이종기;최준식
    • 한국임상약학회지
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    • 제2권1호
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    • pp.23-28
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    • 1992
  • This study was attempted to investigate the pharmacokinetics of theophylline(4mg/kg) in the rabbits of carbon tetrachloride induced hepatic Cailure, The plasma concentration and relative bioavailability of theophylline were increased significantly in hepatic railure rabbits compared with those of normal rabbits. There was significant relationship between SGOT value and bioavailability parameters of theophylline. From the results of this experiments, dosage regimen of theophylline is considered to be adjusted in dose size and dosing interval using SGOT values.

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습식 상 전이법으로 제조된 Theophylline 각인 대칭 막의 선택적 흡착 (Selective Adsorption of a Symmetrie Theophylline Imprinted Membrane Prepare by a Wet Phase Inversion Method)

  • 박중곤;오창엽;서정일
    • KSBB Journal
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    • 제17권2호
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    • pp.207-211
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    • 2002
  • 습식 상 전환법으로 theophylline이 각인된 poly(acryloni-trile-co-acrylic acid) 막을 제조하였다. theophylline은 고분자가 공중합되는 과정에 각인시키거나(in-situ implanting) 제자리 동시 각인) 공중합된 고분자를 DMSO 용액에 녹이면서 template를 섞어 각인시켰다(post implanting, 후 각인). 막의 template molecule에 대한 흡착 선택도는 응고시키는 물의 온도가 높을수록, 혼합물의 초기 농도가 높을수록 크게 나타났다. 후 각인법으로 제조된 막의 흡착선택도가 제자리 동시각인 제작법으로 제조된 막보다 흡착선택도가 우수하였다.

Effect of Smoking on Theophylline Pharmacokinetics in Normal Korean Volunteers

  • Park, Kyoung-Ho;Shin, Hyun-Teak;Kim, Nak-Doo
    • Toxicological Research
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    • 제4권1호
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    • pp.1-12
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    • 1988
  • In order to evaluate the effect of cigarette smoking on the pharmacokinetics of theophylline in Koreans, doses of 4.5 to 5.0 mg/kg of theophylline, as injectable aminophylline, were administered to 12 normal young volunteers (male, 22 to 35 yrs;mean, 26 yrs) through intravenous infusion over 30 minutes, and pharmacokinetics of theophylline were tested. Among subjects, six were nonsmokers and the other were smokers (range 1 to 2 packs/day). Also the correlations between plasma and saliva theophylline concentrations were investigated by determining the concentrations of theophylline in saliva simultaneously at each plasma sampling time. The total body clearances of theophylline in smokers (Mean${\pm}$SD, 0.0578${\pm}$0.0092 L/hr/kg)were appreciably higher than thoxe of nonsmokers (Mean${\pm}$SD, 0.0359${\pm}$0.0063 L/hr/kg), and the half-lives of theophylline in smokers averaged 5.36${\pm}$1.22hr, and significantly shorter than those of nonsmokers which averaged 9.14${\pm}$1.73hrs(p<0.005). But the apparent volumes of distribution of theophylline did not show any significant difference between smokers (Mean${\pm}$SD,0.44 ${\pm}$0.05L/kg) and nonsmokers (Mean${\pm}$SD, 0.46${\pm}$0.05L/kg). The average concentration ratios in saliva and plasma were 0.61 in smokers and 0.56 in nonsmokers after 2 hrs following drug administrations, and the smoker group had a slightly higher value of ratio(S/P) than the nonsmoker group (p<0.05). The correlations between saliva and plasma theophylline concentration in smokers were r=0.852(p<0.0005) within 2 hr and r=0.985(p<0.0005) after 2 hrs and also those of nonsmokers were r=0.729(p<0.0005) within 2 hrs and r=0.957(p<0.0005) after 2 hrs starting the infusion. From the results, it was found that smoking cigarettes had significantly increased the clearance of theophylline and that the relationships between saliva and plasma theophylline concentrations in all subjects were better after 2 hrs than within 2 hrs starting the infusion of aminophlline.

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푸로푸라놀롤 전처리 가토에서 테오필린의 동태학적 연구 (Pharmacokinetics of Theophylline in Rabbits Pretreated with Propranolol)

  • 고숙영;이진환;최준식;범진필
    • 약학회지
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    • 제35권5호
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    • pp.379-383
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    • 1991
  • This study was attempted to investgate the pharmacokinetics of theophylline (4 mg/kg i.v) in the rabbits pretreated with propranolol (1 and 2.5 mg/kg/hr, infusion) for four hours. The plasma concentration and AUC of theophylline were increased in rabbits pretreated with propranolol as compared with those of normal rabbits. The amount of cumulative urinary excretion and renal clearance and total body clearance were decreased in rabbits pretreated with propranolol as compared with those of normal rabbits. The apparent volume of distribution was slightly affected by change of the clearance of theophylline. From the results of this experiment, it is desirable that dosage regimen of theophylline should be adjusted when theophylline combined with propranolol in clinical pharmacy practice.

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혈중 Theophylline 농도 및 청소율에 대한 Erythromycin과 New Macrolides 항생제의 영향 (Effects of Erythromycin and New Macrolides on the Serum Theophylline Level and Clearance)

  • 이흥범;이용철;이양근
    • Tuberculosis and Respiratory Diseases
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    • 제45권3호
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    • pp.546-552
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    • 1998
  • 연구배경: Macrolide란 구조식에 14-number macrocyclic lactone ring을 갖는 항생제를 총칭한다. 최근 개발된 clarythromycin, azythromycin, roxithromycin 등은 기존의 erythromycin에 비하여 소화관 흡수가 용이하고, 반감기가 길며, 위장관 부작용은 덜하면서 몇몇 세균속에 대해서는 더욱 강력한 항균 효과가 있다고 알려져 있다. Erythromycin은 간장의 cytochrome P-450 효소계에 의해 불활성화 되기 때문에, 특히 호흡기 질환 환자에서 사용되는 theophylline의 혈중농도를 증가시켜 theophylline toxicity를 초래할 수 있다고 알려져 있다. 그러나 현재까지 new macrolide에 있어서는 이러한 효과에 대해서는 임상 연구가 미미한 실정이다. 방 법: 기관지 천식환자에서 erythromycin (1000mg/day), clarithromycin(500mg/day), azithromycin(500mg/day), roxithromycin(300mg/day) 등을 theophylline(400mg/day)과 경구 복합 투여하여, 투여전, 투여 후 1주 및 4주(azythyromycin은 1주)에 각각 theophylline 혈중 농도와 청소율을 측정하여 혈중 theophylline 농도 및 청소율에 대한 erythromycin과 new macrolides 항생제의 영향을 평가하고자 하였다. 결 과: Erythromycin과 roxithromycin 투여군에서는 투여 1주 후부터 유의한 theophylline 혈중농도의 상승을 보였으며 특히, erythromycin 투여군에서는 2예에서 병합 투여를 중지하였다. 이러한 소견은 theophylline 청소율에서도 유사하였으나 1주 및 4주간에는 유의한 상승소견을 보이지 않았다. Clarithromycin, azithromycin 투여군에서는 병합 투여중 유의한 혈중 농도의 상승이나 청소율의 감소 소견은 관찰되지 않았다. 결 론: 이상의 결과로 erythromycin 혹은 roxithromycin 투여 환자에 대하여 theophylline을 동시에 복합 투여하는 경우 혈중 theophylline 농도가 예상보다 증가될 수 있으므로 적절한 주기적 관리가 요할 것으로 사료된다.

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타액 시료를 이용한 지속성 테오필린 제제의 생물할적 동등성 시험 (Bioequivalence Test of Slow-Release Theophylline Dosage Forms Using Saliva Samples)

  • 심창구;권혁노;이창기;한익수;최광식
    • Journal of Pharmaceutical Investigation
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    • 제19권4호
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    • pp.191-194
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    • 1989
  • Bioequivalence test of $Asthcontin^{\circledR}$ tablet, a commercial slow-release theophylline (TP) dosage form, was performed using $Slo-bid^{\circledR}$ capsule as the reference. Since it has been confirmed that the saliva concentration of TP is closely correlated with the plasma concentration in man, the area under the saliva concentration-time curve was used as a bioavailability parameter. The statistical analysis showed that the two dosage forms are equivalent in bioavailability estimating from the saliva concentration. The results supported that the use of soliva as a test sample provides simple and easy techniques for bioequivalence tests of TP-containing dosage forms.

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흰쥐에서 사염화탄소 또는 N,N-Dimethylnitrosamine에 의한 간경화시 Theophylline의 생체내변환 (Biotransformation of Theophylline in Cirrhotic Rats Induced by Carbon Tetrachloride or N,N-Dimethylnitrosamine)

  • 박은전;김재백;손동환;고건일
    • 한국임상약학회지
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    • 제9권1호
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    • pp.55-61
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    • 1999
  • The object of this work was to study the pharmacokinetic differences and the cause of these differences in cirrhotic rats induced by N,N-dimethylnitrosamine or carbon tetrachloride treatment when aminophylline (8 mg/kg as theophylline, i.v.) was injected. The concentrations of theophylline and its major metabolite (1,3-dimethyluric acid) in plasma were determined by HPLC. In addition, formation of 1,3-dimethyluric acid from theophylline in microsomes was determined. In cirrhotic rats, the systemic clearance of theophylline was reduced to $17\%$ of the control value while AUC (area under the plasma concentration-time curve) and $(t_{1/2})_{\beta}$ were increased to about 6 fold and 10 fold, respectively. The formation of 1,3-dimethyluric acid was decreased to $33-41\%$ of the control value in microsomes of cirrhotic rat liver. From these results, it can be concluded that in cirrhotic rats induced by N,N-dimethylnitrosamine or carbon tetrachloride the total body clearance of theophylline is markedly reduced due to a reduced hepatic metabolism.

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테오필린과 페플록사신과의 상호작용 (Interaction of Theophylline and Pefloxacin)

  • 장일효;최준식;이진환
    • 약학회지
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    • 제36권4호
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    • pp.321-325
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    • 1992
  • Pharmacokinetic interaction of theophylline with pefloxacin following i.v. administrations was investigated in rabbits. Pefloxacin was coadministrated at doses of 10 and 20 mg/kg or previously administered for 6 days 10 and 20 mg/kg. Plasma concentration and AUC of theophylline were increased significantly (p<0.05) and the renal clearance $(CL_r)$, total body clearance $(CL_r)$ and the volume of distribution $(Vd_{ss})$ were decreased significantly (p<0.005) by the pretreatment. It demonstrates that adjustment of dosage regimen of theophylline should be considered when concomitant administration of pefloxacin is prescribed.

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PCL 기반 생분해성 분자 날인 고분자의 광중합 및 물성 (Photopolymerization and Properties of PCL-Based Biodegradable Molecularly Imprinted Polymers)

  • 김선희;이경수;김용훈;최우진;김범수;김응국;김대수
    • 폴리머
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    • 제31권2호
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    • pp.153-159
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    • 2007
  • 생분해성 분자 날인 고분자는 바이오센서 약물 전달 등의 생의학적 분야에 적응이 가능하다. 그러므로, 본 연구에서는 생분해성 고분자인 $poly(\varepsilon-caprolactone)$ (PCL) 매크로머를 가교제로 사용하여 theophylline 분자 날인 고분자를 광중합을 통해 제조하고 물성을 조사하였다. PCL 매크로머는 말단에 아크릴기를 갖도록 합성하였으며 FT-IR과 $^1H-NMR$로 확인하였다. PCL 매크로머의 합성수율은 약 78 mol%였다. Theophylline의 제거 및 재결합 실험은 UV/Vis분광기를 이용하여 용액 내 theophylline의 농도를 확인함으로써 이루어졌다. Theophylline분자 날인 고분자의 생분해성 실험을 $37^{\circ}C$의 PBS 용액 내에서 진행한 결과 우수한 생분해성을 보였다.