4.8 Article

Comparison of three remote radiolabelling methods for long-circulating liposomes

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 220, Issue -, Pages 239-244

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jconrel.2015.10.043

Keywords

DTPA-DSPE-PEG liposomes; DTPA-PEG liposomes; Staphylococcus aureus; Targeting; MicroSPECT/CT imaging

Funding

  1. NanoNextNL Drug Delivery Programme (3D) [03D.06]

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Long-circulating liposomes (LCL) are often used as a drug carrier system to improve the therapeutic index of water-soluble drugs. To track these LCL in vivo, they can be radiolabelled with In-111-oxine. For this labelling-method, generally DTPA is encapsulated in the aqueous phase of LCL (DTPA-LCL). Alternatively, LCL can be labelled with (InCl3)-In-111 after incorporation of DTPA-conjugated DSPE in the lipid bilayer (DTPA-DSPE LCL). Here, we compared the in vitro properties of DTPA-DSPE LCL with those of DTPA LCL and empty LCL. Additionally, we compared the in vivo performance of DTPA-DSPE LCL with those of DTPA LCL in mice. DTPA LCL (88 nm) and empty LCL (84 nm) were labelled with In-111-oxine, and DTPA-DSPE LCL (83 nm) were labelled with (InCl3)-In-111. Labelling efficiency at increasing specific activity was determined. In vitro stability of In-111-labelled LCL was determined in human serumat 37 degrees C. The in vivo properties of In-111-labelled LCL were determined in mice with a Staphylococcus aureus infection in the thigh muscle. Image acquisition, blood sampling and biodistribution studies were performed 1, 4 (blood sampling only), 24, 48 and 72 h p.i. of In-111-labelled LCL. DTPA-DSPE LCL could be labelled efficiently at a much higher specific activity compared to DTPA LCL and empty LCL: >90% at 15 GBq/mmol, >90% at 150 MBq/mmol and 60-65% at 150 MBq/mmol, respectively. In-111-labelled DTPA-DSPE LCL and DTPA LCL were stable in human serum, regarding label retention, for at least 48 h at 37 degrees C (>98% retention of the radiolabel). In contrast, only 68% radiolabel was retained in empty LCL after 48 h. In vivo targeting of In-111-DTPA-DSPE LCL to the abscess was comparable to targeting of In-111-DTPA LCL (3.5 +/- 0.9% ID/g and 3.4 +/- 0.9% ID/g abscess uptake respectively, 48 h p.i.). In conclusion, labelling of DTPA-DSPE LCL with (InCl3)-In-111 represents a robust, easy and fast procedure which is preferred over the more laborious conventional labelling of DTPA-LCL with In-111-oxine. (C) 2015 Elsevier B.V. All rights reserved.

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