Abstract
Diazepam is highly sorbed to the plastic materials of administration sets for intravenous infusion. This can be detrimental as it should be delivered to the patient at the administered amount for efficacy and safety. We report here the sorption levels of diazepam onto various types of tubes in administration sets. The tube materials of the administration sets included polyvinylchloride (PVC) and the non-PVC materials such as polyurethane (PU) and polyolefin (PO) were used. Two conditions of diazepam administered in preclinical and clinical settings were tested using an infusion pump. Injections were prepared by diluting diazepam to 20 mg/500 mL and 10 mg/100 mL in 5% dextrose. Diluted diazepam solutions at the concentrations of 10 mg/100 mL and 20 mg/500 mL were separately delivered through 1 m of tubing at 1 mL/min for 1.05 and 4.05 h. Samples were analyzed using a high-performance liquid chromatography with UV detection. PVC- and PU-based tubes showed higher sorption of diazepam than did PO-based tubes. PO-based tubes delivered more than 90% of the administered diazepam. The results showed that PO-based tubes of administration sets have a promising potential to deliver hydrophobic drugs like diazepam with minimal sorption levels. In addition, the tube materials in administration sets may be one of the critical factors to ensure drug efficacy and safety.
Original language | English |
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Pages (from-to) | 414-419 |
Number of pages | 6 |
Journal | International Journal of Pharmaceutics |
Volume | 506 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 2016 Jun 15 |
Bibliographical note
Funding Information:This work was supported by the Korea Ministry of Environment (MOE) as “The advancement of scientific research and technological development in environmental science program” (E315-00015-0414-2). This work was partially supported by the Mid-career Researcher Program through a National Research Foundation grant funded by the Ministry of Science , ICT and Future Planning, Republic of Korea (NRF-2014R1A2A2A01005059).
Publisher Copyright:
© 2016 Elsevier B.V. All rights reserved.
All Science Journal Classification (ASJC) codes
- Pharmaceutical Science