4.5 Article

Reduction of fibrous encapsulation by polyethylene glycol-grafted liposomes containing phosphatidylserine

Journal

BIOMEDICAL MATERIALS
Volume 15, Issue 6, Pages -

Publisher

IOP Publishing Ltd
DOI: 10.1088/1748-605X/aba238

Keywords

phosphatidylserine; polyethylene glycol; liposome; fibrous encapsulation; TGF-beta 1

Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MIST) [2019R1F1A1041075]
  2. Korea Health Industry Development Institute (KHIDI) - Ministry of Health AMP
  3. Welfare, Republic of Korea [HI15C1535]
  4. National Research Foundation of Korea [2019R1F1A1041075] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Biomedical implants tend to induce fibrous encapsulation which can cause malfunction of devices and local discomfort of patients. The purpose of this study was to reduce foreign body-induced fibrous capsule formation by immunomodulation of macrophages. Polyethylene-glycol-grafted liposomes containing phosphatidylserine (PEG-PSLs) were used to modulate macrophages. Mixed cellulose ester (MCE) membranes coated with a PEG-PSLs-entrapped alginate-gelatin matrix were subcutaneously implanted into rats, and the thickness of the fibrous capsule around each MCE membrane was analyzed after four weeks. PEG-PSLs significantly reduced fibrous capsule thickness, while liposomes containing phosphatidylserine (PSLs) did not affect fibrosis. Inin vitroassays, PEG-PSLs suppressed TGF-beta 1 secretion and multinucleated giant cell (MGC) formation in IL-4-treated RAW 264.7, a murine macrophage cell line. Although PSLs inhibited MGC formation, they exerted no effect on the secretion of TGF- beta 1, which is known to be an important factor in tissue fibrosis. Therefore, our results suggest that PEG-PSLs reduce fibrous capsule formation by mediating the suppression of TGF-beta 1 secretion from macrophages.

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