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Pharmacokinetics and Biodistribution of Thymoquinone-loaded Nanostructured Lipid Carrier After Oral and Intravenous Administration into Rats.
- Source :
-
International journal of nanomedicine [Int J Nanomedicine] 2020 Oct 09; Vol. 15, pp. 7703-7717. Date of Electronic Publication: 2020 Oct 09 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Background: Thymoquinone (TQ), an active compound isolated from Nigella sativa , has been proven to exhibit various biological properties such as antioxidant. Although oral delivery of TQ is valuable, it is limited by poor oral bioavailability and low solubility. Recently, TQ-loaded nanostructured lipid carrier (TQ-NLC) was formulated with the aim of overcoming the limitations. TQ-NLC was successfully synthesized by the high-pressure homogenization method with remarkable physiochemical properties whereby the particle size is less than 100 nm, improved encapsulation efficiency and is stable up to 24 months of storage. Nevertheless, the pharmacokinetics and biodistribution of TQ-NLC have not been studied. This study determined the bioavailability of oral and intravenous administration of thymoquinone-loaded nanostructured lipid carrier (TQ-NLC) in rats and its distribution to organs.<br />Materials and Methods: TQ-NLC was radiolabeled with technetium-99m before the administration to the rats. The biodistribution and pharmacokinetics parameters were then evaluated at various time points. The rats were imaged at time intervals and the percentage of the injected dose/gram (%ID/g) in blood and each organ was analyzed.<br />Results: Oral administration of TQ-NLC exhibited greater relative bioavailability compared to intravenous administration. It is postulated that the movement of TQ-NLC through the intestinal lymphatic system bypasses the first metabolism and therefore enhances the relative bioavailability. However, oral administration has a slower absorption rate compared to intravenous administration where the AUC <subscript>0-∞</subscript> was 4.539 times lower than the latter.<br />Conclusion: TQ-NLC had better absorption when administered intravenously compared to oral administration. However, oral administration showed greater bioavailability compared to the intravenous route. This study provides the pharmacokinetics and biodistribution profile of TQ-NLC in vivo which is useful to assist researchers in clinical use.<br />Competing Interests: Prof. Dr Rasedee Abdullah reports a pending patent: Thymoquinone-loaded nanostructured lipid carriers (TQ-NLC) and uses thereof, Malaysian Patent No. P12012001818. The authors report no other potential conflicts of interest in this work.<br /> (© 2020 Zakarial Ansar et al.)
- Subjects :
- Administration, Intravenous
Administration, Oral
Animals
Biological Availability
Drug Carriers administration & dosage
Drug Carriers pharmacokinetics
Drug Delivery Systems methods
Drug Liberation
Drug Stability
Lipids chemistry
Male
Nanostructures administration & dosage
Particle Size
Rats, Sprague-Dawley
Solubility
Tissue Distribution
Benzoquinones administration & dosage
Benzoquinones pharmacokinetics
Drug Carriers chemistry
Nanostructures chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1178-2013
- Volume :
- 15
- Database :
- MEDLINE
- Journal :
- International journal of nanomedicine
- Publication Type :
- Academic Journal
- Accession number :
- 33116496
- Full Text :
- https://doi.org/10.2147/IJN.S262395