Development of Optimized Tissue Factor-Targeted Peptide Amphiphile Nanofibers to Slow Non-Compressible Torso Hemorrhage

Non-compressible torso hemorrhage accounts for a significant portion of preventable trauma deaths. We report here on the development of injectable, targeted supramolecular nanotherapeutics based on peptide amphiphile (PA) molecules that are designed to target tissue factor (TF) and, therefore, selec...

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Bibliographic Details
Published inACS nano Vol. 14; no. 6; pp. 6649 - 6662
Main Authors Klein, Mia K., Kassam, Hussein Aziz, Lee, Robert H., Bergmeier, Wolfgang, Peters, Erica B., Gillis, David C., Dandurand, Brooke R., Rouan, Jessica R., Karver, Mark R., Struble, Mark D., Clemons, Tristan D., Palmer, Liam C., Gavitt, Brian, Pritts, Timothy A., Tsihlis, Nick D., Stupp, Samuel I., Kibbe, Melina R.
Format Journal Article
LanguageEnglish
Published 03.06.2020
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Summary:Non-compressible torso hemorrhage accounts for a significant portion of preventable trauma deaths. We report here on the development of injectable, targeted supramolecular nanotherapeutics based on peptide amphiphile (PA) molecules that are designed to target tissue factor (TF) and, therefore, selectively localize to sites of injury to slow hemorrhage. Eight TF-targeting sequences were identified, synthesized into PA molecules, co-assembled with non-targeted backbone PA at various weight percentages, and characterized via circular dichroism spectroscopy, transmission electron microscopy, and X-ray scattering. Following intravenous injection in a rat liver hemorrhage model, two of these PA nanofiber co-assemblies exhibited the most specific localization to the site of injury compared to controls (p<0.05), as quantified using immunofluorescence imaging of injured liver and uninjured organs. To determine if the nanofibers were targeting to TF in vivo , a mouse saphenous vein laser injury model was performed and showed that TF-targeted nanofibers co-localized with fibrin, demonstrating increased levels of nanofiber at TF-rich sites. Thromboelastograms obtained using samples of heparinized rat whole blood containing TF demonstrated that no clots were formed in the absence of TF-targeted nanofibers. Lastly, both PA nanofiber co-assemblies decreased blood loss in comparison to sham and backbone nanofiber controls by 35% to 59% (p<0.05). These data demonstrate an optimal TF-targeted nanofiber that localizes selectively to sites of injury and TF exposure, and, interestingly, reduces blood loss. This research represents a promising initial phase in the development of a TF-targeted injectable therapeutic to reduce preventable deaths from hemorrhage.
Bibliography:The manuscript was written through contributions of all authors. NDT, LCP, MRK1 (Karver), and MDS designed TF-targeted peptide sequences. MKK performed all conventional TEM. MKK conceived and designed the rat experiments and performed the surgeries. HAK assisted with the rat hemorrhage model. MKK and RHL conceived and designed the mouse experiments, with laser injury performed by RHL. DCG and BRD provided assistance with tissue processing and handling. MKK conceived, designed, and performed the TEG experiments. DCG provided additional assistance with TEGs. MDS and TDC performed CD spectroscopy. TDC performed cryo-TEM, SAXS, and WAXS. MRK1 synthesized all PAs. WB, EBP, LCP, NDT, TAP, SIS, MRK2 (Kibbe) helped guide the research. MKK, NDT, MRK2 interpreted all results. EBP assisted with statistical analysis. EBP and JRR performed CAC measurements. MKK prepared the initial draft of the manuscript. NDT and MRK2 critically revised the manuscript. MRK2, SIS, and BG provided oversight and funding of the entire project. All authors have given approval to the final version of the manuscript.
Author Contributions
ISSN:1936-0851
1936-086X
DOI:10.1021/acsnano.9b09243