The significance of a new parameter – plasma protein binding – in therapeutic drug monitoring and its application to carbamazepine in epileptic patients. Issue 45 (26th May 2017)
- Record Type:
- Journal Article
- Title:
- The significance of a new parameter – plasma protein binding – in therapeutic drug monitoring and its application to carbamazepine in epileptic patients. Issue 45 (26th May 2017)
- Main Title:
- The significance of a new parameter – plasma protein binding – in therapeutic drug monitoring and its application to carbamazepine in epileptic patients
- Authors:
- Gao, Jing-lin
Wang, Xin-yu
An, Jing
Du, Chao-hui
Li, Meng-jiao
Ma, Hai-yan
Zhang, Li-na
Bian, Jing
Jiang, Ye - Abstract:
- Abstract : The primary cause of the variability of C f in pharmacology is the change in plasma protein binding (PPB), thus PPB monitoring should be applied to a better individualization of drug dosage regimens in clinical patients. Abstract : Free drug concentration ( C f ) is instantaneous and susceptible to sampling time, which can confuse clinicians and cause them to adjust the dosage regimen. In the present work, we indicated a new parameter, the plasma protein binding (PPB) of clinical plasma samples, and discussed its application in TDM (Therapeutic Drug Monitoring). Furthermore, carbamazepine was selected as a model drug to develop a simple pretreatment method for the determination of PPB, in which C f and C t can be simultaneously analyzed in one plasma sample using a single device. Our results demonstrated that this proposed method exhibited some advantages, including perfect recovery (approximately 100%) and high precision (CV% < 3.0%). Furthermore, it achieved successful application in real plasma samples. Individual differences in PPB (from 10.1–68.9%) were among patients, and in additon, between the patients and healthy people ( p < 0.05). Moreover, there was a weak correlation between C t and C f ( r 2 = 0.470 and p < 0.05), so the C f of CBZ cannot be estimated from C t . However, the primary cause of the variability of C f is the change in PPB. As a consequence, applying PPB to guide individual dose adjustment is more accurate and more scientific than using CAbstract : The primary cause of the variability of C f in pharmacology is the change in plasma protein binding (PPB), thus PPB monitoring should be applied to a better individualization of drug dosage regimens in clinical patients. Abstract : Free drug concentration ( C f ) is instantaneous and susceptible to sampling time, which can confuse clinicians and cause them to adjust the dosage regimen. In the present work, we indicated a new parameter, the plasma protein binding (PPB) of clinical plasma samples, and discussed its application in TDM (Therapeutic Drug Monitoring). Furthermore, carbamazepine was selected as a model drug to develop a simple pretreatment method for the determination of PPB, in which C f and C t can be simultaneously analyzed in one plasma sample using a single device. Our results demonstrated that this proposed method exhibited some advantages, including perfect recovery (approximately 100%) and high precision (CV% < 3.0%). Furthermore, it achieved successful application in real plasma samples. Individual differences in PPB (from 10.1–68.9%) were among patients, and in additon, between the patients and healthy people ( p < 0.05). Moreover, there was a weak correlation between C t and C f ( r 2 = 0.470 and p < 0.05), so the C f of CBZ cannot be estimated from C t . However, the primary cause of the variability of C f is the change in PPB. As a consequence, applying PPB to guide individual dose adjustment is more accurate and more scientific than using C f or C t . … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 45(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 45(2017)
- Issue Display:
- Volume 7, Issue 45 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 45
- Issue Sort Value:
- 2017-0007-0045-0000
- Page Start:
- 28048
- Page End:
- 28055
- Publication Date:
- 2017-05-26
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra02991h ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2050.xml