Hydroxyapatite Binding Peptide Lipid Nanoparticles for Biomimetic mRNA Delivery to Bone

Abstract Development of strategies for non‐viral gene delivery targeted to bone can be used for bone pathologies. Applications include rheumatologic disease, metastatic disease to the bone, pathologies with deficits in hematopoiesis, osteomyelitis, and regenerative medicine. However, specific delivery to tissues like bone is challenging. Here mRNA LNPs (lipid nanoparticles) decorated with a biomimetic hydroxyapatite‐binding peptide (HABP‐LNP) are described, which show improved binding to bone minerals compared to sham peptide conjugated mRNA LNPs (Sham‐LNP). The HABP‐LNPs also increase transfection when associated with bone mineral. Furthermore, HABP mRNA LNPs improve intraosseous transfection and reduce hepatic uptake in vivo. The continued development of these mRNA LNPs can result in non‐viral therapies for bone pathologies.

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Publication Details

Journal
Advanced Therapeutics
Published
2025-04-17
DOI
https://doi.org/10.1002/adtp.202400505
Citations
2
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
1.61

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Hydroxyapatite Binding Peptide Lipid Nanoparticles for Biomimetic mRNA Delivery to Bone

Douglas G. McNeel, Ashley M. Weichmann, Joshua A. Choe, Jamie Jones et al.
2 citations
Advanced Therapeutics
RNA Interference and Gene Delivery
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article

Hydroxyapatite Binding Peptide Lipid Nanoparticles for Biomimetic mRNA Delivery to Bone

Douglas G. McNeel, Ashley M. Weichmann, Joshua A. Choe, Jamie Jones, Jacobus C. Burger, William L. Murphy, Jena E. Moseman
article en
2 citations

Abstract

Abstract Development of strategies for non‐viral gene delivery targeted to bone can be used for bone pathologies. Applications include rheumatologic disease, metastatic disease to the bone, pathologies with deficits in hematopoiesis, osteomyelitis, and regenerative medicine. However, specific delivery to tissues like bone is challenging. Here mRNA LNPs (lipid nanoparticles) decorated with a biomimetic hydroxyapatite‐binding peptide (HABP‐LNP) are described, which show improved binding to bone minerals compared to sham peptide conjugated mRNA LNPs (Sham‐LNP). The HABP‐LNPs also increase transfection when associated with bone mineral. Furthermore, HABP mRNA LNPs improve intraosseous transfection and reduce hepatic uptake in vivo. The continued development of these mRNA LNPs can result in non‐viral therapies for bone pathologies.

Advanced TherapeuticsVol. 8(5)
University of Wisconsin–Madison (US)
Foundation for the National Institutes of Health, University of Wisconsin Carbone Cancer Center, National Institutes of Health, National Cancer Institute
Openalex Percentile: Top 18%
RNA Interference and Gene Delivery
1.61
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