Wound‐triggered shape change microgels for the development of enhanced biomimetic function platelet‐like particles

Author:

Chee Eunice12,Mihalko Emily3,Nellenbach Kimberly12,Sollinger Jennifer1,Huang Ke4,Hon Mason1,Pandit Sanika12,Cheng Ke4,Brown Ashley12ORCID

Affiliation:

1. Joint Department of Biomedical Engineering North Carolina State University and University of North Carolina–Chapel Hill Raleigh North Carolina USA

2. Comparative Medicine Institute North Carolina State University Raleigh North Carolina USA

3. Trauma and Transfusion Medicine Research Center University of Pittsburgh Pittsburgh Pennsylvania USA

4. Department of Molecular Biomedical Sciences North Carolina State University Raleigh North Carolina USA

Abstract

AbstractPlatelets play a pivotal role in hemostasis and wound healing and conditional shape change is an important component of platelet functionality. In normal circumstances, platelets travel through the circulatory system in an inactive rounded state, which enables platelets to easily move to vessel walls for attachment. When an injury occurs, platelets are prompted by molecules, such as thrombin, to shift into a stellate shape and increase exposure of fibrin‐binding receptors. When active, platelets promote hemostasis and clot retraction, which enhances clot stability and promotes healing. However, in conditions where platelets are depleted or hyporeactive, these functions are diminished and lead to inhibited hemostasis and healing. To treat platelet depletion, our group developed platelet‐like particles (PLPs) which consist of highly deformable microgels coupled to fibrin binding motif. However, first generation PLPs do not exhibit wound‐triggered shape change like native platelets. Thus, the objective of these studies was to develop a PLP formulation that changes shape when prompted by thrombin. To create thrombin‐sensitive PLPs (TS‐PLPs), we incorporated a thrombin‐cleavable peptide into the microgel body and then evaluated PLP properties before and after exposure to thrombin including morphology, size, and in vitro clot retraction. Once thrombin‐prompted shape change ability was confirmed, the TS‐PLPs were tested in vivo for hemostatic ability and subsequent wound healing outcomes in a murine liver trauma model. We found that TS‐PLPs exhibit a wound‐triggered shape change, induce significant clot retraction following exposure to thrombin and promote hemostasis and healing in vivo after trauma.

Funder

National Science Foundation

Publisher

Wiley

Subject

Metals and Alloys,Biomedical Engineering,Biomaterials,Ceramics and Composites

Reference26 articles.

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