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Biodistribution of the cationic host defense peptide LL-37 using SPECT/CT.
Esposito, Tullio V F; Rodríguez-Rodríguez, Cristina; Blackadar, Colin; Klodzinska, Sylvia; Mørck Nielsen, Hanne; Saatchi, Katayoun; Häfeli, Urs O.
Affiliation
  • Esposito TVF; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada. Electronic address: esposit@mskcc.org.
  • Rodríguez-Rodríguez C; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada; Department of Physics and Astronomy, Faculty of Science, University of British Columbia, Vancouver, Canada.
  • Blackadar C; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.
  • Klodzinska S; Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Mørck Nielsen H; Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Saatchi K; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada. Electronic address: kathy.saatchi@ubc.ca.
  • Häfeli UO; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada; Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address: urs.hafeli@ubc.ca.
Eur J Pharm Biopharm ; : 114398, 2024 Jul 05.
Article in En | MEDLINE | ID: mdl-38972467
ABSTRACT
Human cathelicidin LL-37, a cationic host defense peptide (CHDP), has several important physiological roles, including antimicrobial activity, immune modulation, and wound healing, and is a being investigated as a therapeutic candidate for several indications. While the effects of endogenously produced LL-37 are well studied, the biodistribution of exogenously administered LL-37 are less known. Here we assess the biodistribution of a gallium-67 labeled variant of LL-37 using nuclear imaging techniques over a 48 h period in healthy mice. When administered as an intravenous bolus just over 20 µg, the LL-37-based radiotracer was rapidly cleared from the blood, largely by the liver, while an appreciable fraction of the dose temporarily distributed to the lungs. When administered subcutaneously at the same dose level, the radiotracer was absorbed systemically following a two-phase kinetic model and was predominately cleared renally. Uptake into sites rich in immune cells, such as the lymph nodes and the spleen, was observed for both routes of administration. Scans of free gallium-67 were also performed as controls. Important preclinical insights into the biodistribution of exogenously administered LL-37 were gained from this study, which can aid in the understanding of this and related cationic host-defense peptides.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2024 Document type: Article