- Title
- Liposomes are poorly absorbed via lung lymph after inhaled administration in sheep
- Creator
- Ibrahim, Jibriil; Haque, Shadabul; Bischof, Robert; Whittaker, Andrew; Whittaker, Michael; Kaminskas, Lisa
- Date
- 2022
- Type
- Text; Journal article
- Identifier
- http://researchonline.federation.edu.au/vital/access/HandleResolver/1959.17/199277
- Identifier
- vital:19187
- Identifier
-
https://doi.org/10.3389/fphar.2022.880448
- Identifier
- ISSN:1663-9812
- Abstract
- Enhancing the delivery of therapeutic agents to the lung lymph, including drugs, transfection agents, vaccine antigens and vectors, has the potential to significantly improve the treatment and prevention of a range of lung-related illnesses. One way in which lymphatic delivery can be optimized is via the use of nanomaterial-based carriers, such as liposomes. After inhaled delivery however, there is conflicting information in the literature regarding whether nanomaterials can sufficiently access the lung lymphatics to have a therapeutic benefit, in large part due to a lack of reliable quantitative pharmacokinetic data. The aim of this work was to quantitatively evaluate the pulmonary lymphatic pharmacokinetics of a model nanomaterial-based drug delivery system (HSPC liposomes) in caudal mediastinal lymph duct cannulated sheep after nebulized administration to the lungs. Liposomes were labelled with 3 H-phosphatidylcholine to facilitate evaluation of pharmacokinetics and biodistribution in biological samples. While nanomaterials administered to the lungs may access the lymphatics via direct absorption from the airways or after initial uptake by alveolar macrophages, only 0.3 and 0.001% of the 3 H-lipid dose was recovered in lung lymph fluid and lymph cell pellets (containing immune cells) respectively over 5 days. This suggests limited lymphatic access of liposomes, despite apparent pulmonary bioavailability of the 3 H-lipid being approximately 17%, likely a result of absorption of liberated 3 H-lipid after breakdown of the liposome in the presence of lung surfactant. Similarly, biodistribution of 3 H in the mediastinal lymph node was insignificant after 5 days. These data suggest that liposomes, that are normally absorbed via the lymphatics after interstitial administration, do not access the lung lymphatics after inhaled administration. Alternate approaches to maximize the lung lymphatic delivery of drugs and other therapeutics need to be identified.
- Publisher
- Frontiers Media SA
- Relation
- Frontiers in pharmacology Vol. 13, no. (2022), p. 880448-880448
- Rights
- All metadata describing materials held in, or linked to, the repository is freely available under a CC0 licence
- Rights
- http://creativecommons.org/licenses/by/4.0/
- Rights
- Copyright © 2022 Ibrahim, Haque, Bischof, Whittaker, Whittaker and Kaminskas
- Rights
- Open Access
- Subject
- Pharmacology; Nanoparticles; Pharmacokinetics; Aspiration and aspirators; Sheep; 3214 Pharmacology and pharmaceutical sciences
- Full Text
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