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Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea
OBJECTIVES: Despite extensive caffeine use in preterm infants, the pharmacokinetics (PKs) data are limited because of the studies are complicated to do in these patients. This research was investigated the PK profile of two various dosages of caffeine in premature neonates. MATERIALS AND METHODS: Th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265417/ https://www.ncbi.nlm.nih.gov/pubmed/34100394 http://dx.doi.org/10.4103/ijp.IJP_504_19 |
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author | Faramarzi, Fatemeh Shiran, Mohammadreza Rafati, Mohammadreza Farhadi, Roya Salehifar, Ebrahim Nakhshab, Maryam |
author_facet | Faramarzi, Fatemeh Shiran, Mohammadreza Rafati, Mohammadreza Farhadi, Roya Salehifar, Ebrahim Nakhshab, Maryam |
author_sort | Faramarzi, Fatemeh |
collection | PubMed |
description | OBJECTIVES: Despite extensive caffeine use in preterm infants, the pharmacokinetics (PKs) data are limited because of the studies are complicated to do in these patients. This research was investigated the PK profile of two various dosages of caffeine in premature neonates. MATERIALS AND METHODS: The PK values of caffeine in premature neonates with Apnea were predicted by using all of computer-based simulation (Simcyp(®)), population-based PK, and modeling (P-Pharm(®)). We assayed the plasma levels of caffeine in two groups. The information was analyzed utilizing nonlinear mixed-effects modeling approach. The PK parameters were assessed simulating virtual clinical considers with subjects got 20 mg. kg(−1) of caffeine in both groups, which was followed by a 5 mg. kg(−1) once daily in Group 1 or 2.5 mg. kg(−1) twice daily in Group 2. All statistical analysis was executed utilizing SSPS issue 19 and a P value of 0.05 was chosen significance. RESULTS: In the present study, the means CL, volume of distribution, and T1/2 of caffeine in preterm infants were 0.0476 L. h(−1), 1.1081 L, 16.2284 h, respectively. Whereas our simulated means by Simcyp were 0.090 L. h(−1), 1.841 L, and 14.653 h in Group 1 and 16.223 h in Group 2, respectively. CONCLUSIONS: There was overall good agreement between predicted and measured PK values in our study. This study provides an initial demonstration of Simcyp simulation advantage on anticipating of PK parameters. |
format | Online Article Text |
id | pubmed-8265417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-82654172021-07-16 Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea Faramarzi, Fatemeh Shiran, Mohammadreza Rafati, Mohammadreza Farhadi, Roya Salehifar, Ebrahim Nakhshab, Maryam Indian J Pharmacol Research Article OBJECTIVES: Despite extensive caffeine use in preterm infants, the pharmacokinetics (PKs) data are limited because of the studies are complicated to do in these patients. This research was investigated the PK profile of two various dosages of caffeine in premature neonates. MATERIALS AND METHODS: The PK values of caffeine in premature neonates with Apnea were predicted by using all of computer-based simulation (Simcyp(®)), population-based PK, and modeling (P-Pharm(®)). We assayed the plasma levels of caffeine in two groups. The information was analyzed utilizing nonlinear mixed-effects modeling approach. The PK parameters were assessed simulating virtual clinical considers with subjects got 20 mg. kg(−1) of caffeine in both groups, which was followed by a 5 mg. kg(−1) once daily in Group 1 or 2.5 mg. kg(−1) twice daily in Group 2. All statistical analysis was executed utilizing SSPS issue 19 and a P value of 0.05 was chosen significance. RESULTS: In the present study, the means CL, volume of distribution, and T1/2 of caffeine in preterm infants were 0.0476 L. h(−1), 1.1081 L, 16.2284 h, respectively. Whereas our simulated means by Simcyp were 0.090 L. h(−1), 1.841 L, and 14.653 h in Group 1 and 16.223 h in Group 2, respectively. CONCLUSIONS: There was overall good agreement between predicted and measured PK values in our study. This study provides an initial demonstration of Simcyp simulation advantage on anticipating of PK parameters. Wolters Kluwer - Medknow 2021 2021-05-26 /pmc/articles/PMC8265417/ /pubmed/34100394 http://dx.doi.org/10.4103/ijp.IJP_504_19 Text en Copyright: © 2021 Indian Journal of Pharmacology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Faramarzi, Fatemeh Shiran, Mohammadreza Rafati, Mohammadreza Farhadi, Roya Salehifar, Ebrahim Nakhshab, Maryam Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title | Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title_full | Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title_fullStr | Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title_full_unstemmed | Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title_short | Prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
title_sort | prediction of pharmacokinetic values of two various dosages of caffeine in premature neonates with apnea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265417/ https://www.ncbi.nlm.nih.gov/pubmed/34100394 http://dx.doi.org/10.4103/ijp.IJP_504_19 |
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