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Pharmacokinetics and Biodistribution of Thymoquinone-loaded Nanostructured Lipid Carrier After Oral and Intravenous Administration into Rats.

Authors :
Zakarial Ansar FH
Latifah SY
Wan Kamal WHB
Khong KC
Ng Y
Foong JN
Gopalsamy B
Ng WK
How CW
Ong YS
Abdullah R
Aziz MY
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.)

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