journal article·2026-07

Improved localization to sites of hemorrhage via peptide amphiphile nanofibers containing a factor VII-mimetic epitope

Trevor P. Stone, Sophia L. Maragos, James D. Greenwood, Gabrielle K. Steinl, Simon A. Egner, Benjamin T. Ledford, David C. Gillis, Mark R. Karver, Liam C. Palmer, Timothy A. Pritts, Nick D. Tsihlis, Samuel I. Stupp, Melina R. Kibbe

Publisher page

Abstract

Hemorrhage is a leading cause of potentially preventable deaths in pre-hospital settings. Hence, there is a great need to develop a therapeutic that can be administered in the field to slow or stop hemorrhage before definitive treatment can be sought. The aim of this work was to develop a nanoscale delivery vehicle that could successfully localize to sites of active hemorrhage in the vasculature. We first synthesized four peptides derived from Factor VII as putative targeting epitopes for tissue factor (TF). The peptide sequence ERTFSERT was chosen after microscale thermophoresis revealed a micromolar dissociation constant for TF. The ERTFSERT peptide was covalently linked to a peptide amphiphile (PA) molecule and co-assembled to form supramolecular nanofibers, which were found to have a parallelepiped shape with a width of ∼12 nm and β-sheet secondary structure. Using a microfluidic channel with cultured human umbilical vein endothelial cells, we found that co-assemblies of the targeted nanofibers preferentially localized to endothelial cells activated with tumor necrosis factor alpha, validating the targeting capability of ERTFSERT in a physiologically relevant in vitro model. When administered intravenously in a rat model of liver hemorrhage, biodistribution assessed using ex vivo imaging revealed an increased concentration of targeted nanofibers near the site of liver injury with no adverse effect on mean arterial pressure or blood loss. Overall, these data suggest that TF-targeted PA nanofiber co-assemblies can be used in future studies to deliver therapeutic agents to the site of injury to treat hemorrhage. STATEMENT OF SIGNIFICANCE: We developed and validated a peptide amphiphile with a targeting moiety derived from Factor VII that can localize to tissue factor at the site of hemorrhage. This can be used in future studies to deliver hemostatic agents to the site of injury to treat hemorrhage or to treat other conditions where tissue factor is upregulated.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · RNA Interference and Gene Delivery · Nanoparticle-Based Drug Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (65)

Show source-provided references
1. Death on the battlefield (2001-2011): implications for the future of combat casualty care10.1097/TA.0b013e3182755dcc ↗
2. Died of wounds on the battlefield: causation and implications for improving combat casualty care
3. Analysis of the causes of death of casualties in field military setting10.7205/MILMED-D-12-00161 ↗
4. Outcomes of traumatic hemorrhagic shock and the epidemiology of preventable death from injury10.1111/trf.15161 ↗
5. Epidemiology and outcomes of non-compressible torso hemorrhage10.1016/j.jss.2013.05.099 ↗
6. Abdominal insufflation for prevention of exsanguination10.1097/01.TA.0000056162.86054.00 ↗
7. Abdominal insufflation decreases blood loss and mortality after porcine liver injury10.1097/01.ta.0000198374.16218.ca ↗
8. Abdominal insufflation for control of bleeding after severe splenic injury
9. Optimal pressure of abdominal gas insufflation for bleeding control in a severe swine splenic injury model10.1016/j.jss.2013.03.016 ↗
10. Use of resuscitative endovascular balloon occlusion of the aorta for proximal aortic control in patients with severe hemorrhage and arrest10.1001/jamasurg.2017.3549 ↗
11. Self-expanding polyurethane polymer improves survival in a model of noncompressible massive abdominal hemorrhage10.1097/TA.0b013e31828da937 ↗
12. Self-expanding foam for prehospital treatment of intra-abdominal hemorrhage: 28-day survival and safety10.1097/TA.0000000000000380 ↗
13. Self-expanding foam improves survival following a lethal, exsanguinating iliac artery injury10.1097/TA.0000000000000263 ↗
14. Chronic safety assessment of hemostatic self-expanding foam: 90-day survival study and intramuscular biocompatibility10.1097/TA.0000000000000571 ↗
15. Efficacy of a prehospital self-expanding polyurethane foam for noncompressible hemorrhage under extreme operational conditions10.1097/TA.0000000000000507 ↗
16. Adenosine, lidocaine, and Mg2+ (ALM): from cardiac surgery to combat casualty care–teaching old drugs new tricks10.1097/TA.0000000000000881 ↗
17. Correction of acute traumatic coagulopathy with small-volume 7.5% NaCl adenosine, lidocaine, and Mg2+ occurs within 5 minutes: a ROTEM analysis10.1097/TA.0000000000000587 ↗
18. 3.0% NaCl adenosine, Lidocaine, Mg 2+ (ALM) bolus and 4 hours 'drip' infusion reduces non-compressible hemorrhage by 60% in a rat model
19. Lyophilized platelets: fifty years in the making10.1080/10731190600974962 ↗
20. Evaluation of lyophilized platelets as an infusible hemostatic agent in experimental non-compressible hemorrhage in swine10.1111/j.1538-7836.2009.03562.x ↗
21. Dried platelets in a swine model of liver injury10.1097/SHK.0000000000000141 ↗
22. Control of severe intra-abdominal hemorrhage with an infusible platelet-derived hemostatic agent in a nonhuman primate (rhesus macaque) model10.1097/TA.0000000000000964 ↗
23. Thrombosomes: a platelet-derived hemostatic agent for control of noncompressible hemorrhage
24. In vitro characterization of SynthoPlate (synthetic platelet) technology and its in vivo evaluation in severely thrombocytopenic mice10.1111/jth.13579 ↗
25. Intravenous synthetic platelet (SynthoPlate) nanoconstructs reduce bleeding and improve 'golden hour' survival in a porcine model of traumatic arterial hemorrhage10.1038/s41598-018-21384-z ↗
26. Uncontrolled hemorrhagic shock modeled via liver laceration in mice with real time hemodynamic monitoring10.3791/55554 ↗
27. Intravenous administration of synthetic platelets (SynthoPlate) in a mouse liver injury model of uncontrolled hemorrhage improves hemostasis10.1097/TA.0000000000001893 ↗
28. Arginyl-glycyl-aspartic acid sequences and fibrinogen binding to platelets10.1182/blood.V70.1.110.110 ↗
29. Intravenous hemostat: nanotechnology to halt bleeding10.1126/scitranslmed.3000397 ↗
30. Tuning ligand density on intravenous hemostatic nanoparticles dramatically increases survival following blunt trauma10.1021/bm400619v ↗
31. Facile assembly of cost-effective and locally applicable or injectable nanohemostats for hemorrhage control10.1021/acsnano.6b04124 ↗
32. Engineering a two-component hemostat for the treatment of internal bleeding through wound-targeted crosslinking10.1002/adhm.202202756 ↗
33. Independent effect of polymeric nanoparticle zeta potential/surface charge on their cytotoxicity and affinity to cells10.1111/cpr.12192 ↗
34. Supramolecular nanofibers of peptide amphiphiles for medicine10.1002/ijch.201300046 ↗
35. Self-assembly and mineralization of peptide-amphiphile nanofibers10.1126/science.1063187 ↗
36. Self-assembly of peptide amphiphiles: from molecules to nanostructures to biomaterials10.1002/bip.21328 ↗
37. Self-assembling amphiphilic peptides10.1002/psc.2633 ↗
38. Shape-dependent targeting of injured blood vessels by peptide amphiphile supramolecular nanostructures10.1002/smll.201403429 ↗
39. Evaluation of a targeted drug-eluting intravascular nanotherapy to prevent neointimal hyperplasia in an atherosclerotic rat model10.1002/anbr.202000093 ↗
40. Peptide amphiphile supramolecular nanofibers designed to target abdominal aortic aneurysms10.1021/acsnano.1c06258 ↗
41. Peptide amphiphile nanostructures for targeting of atherosclerotic plaque and drug delivery10.1002/adbi.201700123 ↗
42. Tissue factor: an essential mediator of hemostasis and trigger of thrombosis10.1161/ATVBAHA.117.309846 ↗
43. Tissue factor in coagulation: which? Where? When?10.1161/ATVBAHA.108.177402 ↗
44. Structure of the complex of blood coagulation Factor VIIa with soluble tissue factor10.1038/380041a0 ↗
45. Tissue-factor targeted peptide amphiphile nanofibers as an injectable therapy to control hemorrhage10.1021/acsnano.5b06025 ↗
46. Development of optimized tissue-factor-targeted peptide amphiphile nanofibers to slow noncompressible torso hemorrhage10.1021/acsnano.9b09243 ↗
47. Identification of surface residues mediating tissue factor binding and catalytic function of the serine protease factor VIIa10.1073/pnas.93.25.14379 ↗
48. Key residues regulating von Willebrand factor A1/A2 interactions: insights from molecular dynamics simulations and experimental validation10.1016/j.rpth.2025.103267 ↗
49. DND-CAT's new triple area detector system for simultaneous data collection at multiple length scales10.1016/j.nima.2010.12.045 ↗
50. GSAS-II: the genesis of a modern open-source all purpose crystallography software package10.1107/S0021889813003531 ↗
51. Systemic peptide amphiphile nanofiber delivery following subcutaneous injection10.1016/j.biomaterials.2023.122401 ↗
52. Tuning nanostructure dimensions with supramolecular twisting10.1021/jp3087978 ↗
53. Supramolecular interactions and morphology of self-assembling peptide amphiphile nanostructures10.1021/acs.nanolett.1c01737 ↗
54. ibidi, Human endothelial cells cultivated under shear stress on the glass membrane of the µ-slide ibiPore SiN: application note 59, 2024, pp. 1-3.
55. Blood flow rate and wall shear stress in seven major cephalic arteries of humans10.1111/joa.13119 ↗
56. Von Willebrand disease: advances in pathogenetic understanding, diagnosis, and therapy10.1182/asheducation-2013.1.254 ↗
57. Collagen synthesis in atherosclerosis: too much and not enough10.1016/S0008-6363(98)00321-6 ↗
58. Bos · 2015
59. Self-assembled peptide amphiphile nanofibers for controlled therapeutic delivery to the atherosclerotic niche10.1002/adtp.202100103 ↗
60. Microscale thermophoresis quantifies biomolecular interactions under previously challenging conditions10.1016/j.ymeth.2012.12.005 ↗
61. MicroScale thermophoresis as a tool to study protein-peptide interactions in the context of large eukaryotic protein complexes10.21769/BioProtoc.2632 ↗
62. Peptide amphiphile supramolecular nanostructures as a targeted therapy for atherosclerosis10.1002/mabi.201970016 ↗
63. Development of fractalkine-targeted nanofibers that localize to sites of arterial injury10.3390/nano10030420 ↗
64. Pharmacokinetics and biodistribution of a collagen-targeted peptide amphiphile for cardiovascular applications10.1002/prp2.672 ↗
65. Effects of particle size, charge, shape, animal disease state, and sex on the biodistribution of intravenously administered nanoparticles10.1002/ppsc.202300001 ↗