Copper-64 labeled liposomes for imaging bone marrow
Creators
- 1. Molecular Pharmacology and Chemistry Program, Memorial Sloan Kettering Cancer Center, New York, NY (United States)
- 2. Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY (United States)
- 3. Ph. D program in Chemistry, The Graduate Center, The City University of New York, New York, NY (United States)
- 4. Department of Chemistry, Hunter College, The Graduate Center, The City University of New York, New York, NY (United States)
- 5. Department of Radiology, Weill Cornell Medical College, New York, NY (United States)
- 6. Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY (United States)
Description
Introduction: Bone marrow is the soft tissue compartment inside the bones made up of hematopoietic cells, adipocytes, stromal cells, phagocytic cells, stem cells, and sinusoids. While [18F]-FLT has been utilized to image proliferative marrow, to date, there are no reports of particle based positron emission tomography (PET) imaging agents for imaging bone marrow. We have developed copper-64 labeled liposomal formulation that selectively targets bone marrow and therefore serves as an efficient PET probe for imaging bone marrow. Methods: Optimized liposomal formulations were prepared with succinyl PE, DSPC, cholesterol, and mPEG-DSPE (69:39:1:10:0.1) with diameters of 90 and 140 nm, and were doped with DOTA-Bn-DSPE for stable 64Cu incorporation into liposomes. Results: PET imaging and biodistribution studies with 64Cu-labeled liposomes indicate that accumulation in bone marrow was as high as 15.18 ± 3.69%ID/g for 90 nm liposomes and 7.01 ± 0.92%ID/g for 140 nm liposomes at 24 h post-administration. In vivo biodistribution studies in tumor-bearing mice indicate that the uptake of 90 nm particles is approximately 0.89 ± 0.48%ID/g in tumor and 14.22 ± 8.07%ID/g in bone marrow, but respective values for Doxil® like liposomes are 0.83 ± 0.49%ID/g and 2.23 ± 1.00%ID/g. Conclusion: Our results indicate that our novel PET labeled liposomes target bone marrow with very high efficiency and therefore can function as efficient bone marrow imaging agents.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.nucmedbio.2016.08.011Additional details
Identifiers
- DOI
- 10.1016/j.nucmedbio.2016.08.011;
- PII
- S0969-8051(16)30221-9;
Publishing Information
- Journal Title
- Nuclear Medicine and Biology
- Journal Volume
- 43
- Journal Issue
- 12
- Journal Page Range
- p. 781-787
- ISSN
- 0969-8051
- CODEN
- NMBIEO
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49030687
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BONE MARROW; BORON NITRIDES; CHOLESTEROL; COPPER; COPPER 64; DOPED MATERIALS; FLUORINE 18; FUNCTIONS; IMAGES; IN VIVO; LIPOSOMES; MICE; NEOPLASMS; POSITRON COMPUTED TOMOGRAPHY; POSITRONS; SKELETON; STEM CELLS; UPTAKE
- Descriptors DEC
- ANIMAL CELLS; ANIMAL TISSUES; ANIMALS; ANTILEPTONS; ANTIMATTER; ANTIPARTICLES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; BORON COMPOUNDS; COMPUTERIZED TOMOGRAPHY; COPPER ISOTOPES; DIAGNOSTIC TECHNIQUES; DISEASES; ELECTRON CAPTURE RADIOISOTOPES; ELEMENTARY PARTICLES; ELEMENTS; EMISSION COMPUTED TOMOGRAPHY; FERMIONS; FLUORINE ISOTOPES; HEMATOPOIETIC SYSTEM; HOURS LIVING RADIOISOTOPES; HYDROXY COMPOUNDS; INTERMEDIATE MASS NUCLEI; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LEPTONS; LIGHT NUCLEI; MAMMALS; MATERIALS; MATTER; METALS; NANOSECONDS LIVING RADIOISOTOPES; NITRIDES; NITROGEN COMPOUNDS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PNICTIDES; RADIOISOTOPES; RODENTS; SOMATIC CELLS; STEROIDS; STEROLS; TOMOGRAPHY; TRANSITION ELEMENTS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.