Cited by 19Intestinal and Peritoneal AdhesionsElectrospun Nanofibers in Biomedical ApplicationsSilk-based biomaterials and applications

Prevention of peritoneal adhesions formation by core-shell electrospun ibuprofen-loaded PEG/silk fibrous membrane

Open access
Nadri, Samad, Rahmani, Ali, Hosseini, Seyed Hojjat, Habibizadeh, Mina, Araghi, Mahmood, Mostafavi, Hossein·2022·Artificial Cells, Nanomedicine, and Biotechnology

Abstract

Adhesion bands are pathological fibrous tissues that create in the middle of tissues and organs, often reasons of intestinal obstruction, and female infertility. Here, we explored the anti-adhesive and inflammatory capacities of PEG/silk and Ibuprofen-loaded PEG/Silk core-shell nanofibrous membranes, respectively. The ibuprofen-loaded Silk Fibroin-Poly ethylene Glycol (SF-PEG) core-shell membrane was fabricated by electrospinning and considered in terms of morphology, surface wettability, drug release, and degradation. To reveal the membrane capability for adhesion bands inhibition, the membrane was stitched among the abdominal partition and peritoneum and then evaluated using two scoring adhesion systems. According to results, the fibrous membrane hindered cell proliferation, and the scoring systems and pathology showed that in a rat model, Ibuprofen-loaded PEG/Silk core-shell membrane caused a lightening in post-operative adhesion bands and the low-grade inflammatory reaction in animal models. Collectively, we fabricated new ibuprofen-loaded PEG/SF membranes with anti-adhesion and anti-inflammation properties. Moreover, this core-shell electrospun fibrous membrane has not even now been used to prevent peritendinous adhesion generation.

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Crossref · 10.1080/21691401.2021.1883043

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  • Electrospun anti-adhesion films can be made from biodegradable polymers and can incorporate drugs by techniques like coaxial (core-shell) electrospinning.

    “Electrospun anti-adhesion films can be made from biodegradable polymers and even incorporate drugs by techniques like coaxial (core–shell) electrospinning [12,271].”
  • An ibuprofen-loaded PEG/silk fibroin core-shell nanofiber membrane placed between injured peritoneal surfaces lightened adhesion bands and caused only a low-grade inflammatory reaction in rats.

    “Similarly, an ibuprofen-loaded PEG/silk fibroin core–shell nanofiber membrane, placed between injured peritoneal surfaces, lightened adhesion bands and caused only a low-grade inflammatory reaction in rats [271].”

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Research works printed but not linked: 54

  1. Cheong YC, Laird SM, Li TC, et al. Peritoneal healing and adhesion formation/reformation. Hum Reprod Update. 2001;7(6):556–566. diZerega GS, Campeau JD. Peritoneal repair and post-surgical adhesion formation. Hum Reprod Update. 2001;7(6):547–555.
  2. Taras JS, Lamb MJ. Treatment of flexor tendon injuries: surgeons' perspective. J Hand Ther. 1999;12(2):141–148.
  3. Kamel RM. Prevention of postoperative peritoneal adhesions. Eur J Obstet Gynecol Reprod Biol. 2010;150(2):111–118.
  4. James R, Kesturu G, Balian G, et al. Tendon: biology, biomechanics, repair, growth factors, and evolving treatment options. J Hand Surg Am. 2008;33(1):102–112.
  5. Pagidas K, Tulandi T. Effects of ringer's lactate, interceed(TC7) and Gore-Tex surgical membrane on postsurgical adhesion formation. Fertil Steril. 1992;57(1):199–201.
  6. March CM, Boyers S, Franklin R, et al. Prevention of adhesion formation/reformation with the Gore-Tex surgical membrane. Prog Clin Biol Res. 1993;381:253–259.
  7. Rice VM, Shanti A, Moghissi KS, et al. A comparative evaluation of poloxamer 407 and oxidized regenerated cellulose (interceed [TC7]) to reduce postoperative adhesion formation in the rat uterine horn model. Fertil Steril. 1993;59(4):901–906. diZerega GS, Verco SJ, Young P, et al. A randomized, controlled pilot study of the safety and efficacy of 4% icodextrin solution in the reduction of adhesions following laparoscopic gynaecological surgery. Hum Reprod. 2002;17(4):1031–1038.
  8. Drollette CM, Badawy SZ. Pathophysiology of pelvic adhesions. Modern trends in preventing infertility. J Reprod Med. 1992;37(2):107–121. discussion 21–2.
  9. Becker JM, Dayton MT, Fazio VW, et al. Prevention of postoperative abdominal adhesions by a sodium hyaluronate-based bioresorbable membrane: a prospective, randomized, double-blind multicenter study. J Am Coll Surg. 1996;183:297–306.
  10. Chen SH, Chen CH, Fong YT, et al. Prevention of peritendinous adhesions with electrospun chitosan-grafted polycaprolactone nanofibrous membranes. Acta Biomater. 2014;10(12):4971–4982.
  11. Yang DJ, Chen F, Xiong ZC, et al. Tissue anti-adhesion potential of biodegradable PELA electrospun membranes. Acta Biomater. 2009;5(7):2467–2474.
  12. Dinarvand P, Hashemi SM, Seyedjafari E, et al. Function of poly (lactic-co-glycolic acid) nanofiber in reduction of adhesion bands. J Surg Res. 2012;172(1):e1–e9.
  13. Zong X, Li S, Chen E, et al. Prevention of postsurgery-induced abdominal adhesions by electrospun bioabsorbable nanofibrous poly(lactide-co-glycolide)-based membranes. Ann Surg. 2004;240(5):910–915.
  14. Min BM, Lee G, Kim SH, et al. Electrospinning of silk fibroin nanofibers and its effect on the adhesion and spreading of normal human keratinocytes and fibroblasts in vitro. Biomaterials. 2004;25(7–8):1289–1297.
  15. Vollrath F, Knight DP. Liquid crystalline spinning of spider silk. Nature. 2001;410(6828):541–548.
  16. Melke J, Midha S, Ghosh S, et al. Silk fibroin as biomaterial for bone tissue engineering. Acta Biomater. 2016;31:1–16.
  17. Harris JM, Chess RB. Effect of pegylation on pharmaceuticals. Nat Rev Drug Discov. 2003;2(3):214–221.
  18. Pasut G, Veronese FM. State of the art in PEGylation: the great versatility achieved after forty years of research. J Controlled Release. 2012;161(2):461–472.
  19. Xiao X-F, Jiang X-Q, Zhou L-J. Surface modification of poly ethylene glycol to resist nonspecific adsorption of proteins. Chin J Anal Chem. 2013;3:445–453.
  20. D'souza AA, Shegokar R. Polyethylene glycol (PEG): a versatile polymer for pharmaceutical applications. Expert Opin Drug Deliv. 2016;13(9):1257–1275.
  21. Lee JH, Kim KO, Ju YM. Polyethylene oxide additive-entrapped polyvinyl chloride as a new blood bag material. J Biomed Mater Res. 1999;48(3):328–334.
  22. Lee JH, Go AK, Oh SH, et al. Tissue anti-adhesion potential of ibuprofen-loaded PLLA-PEG diblock copolymer films. Biomaterials. 2005;26(6):671–678.
  23. Bhavsar D, Shettko D, Tenenhaus M. Encircling the tendon repair site with collagen-GAG reduces the formation of postoperative tendon adhesions in a chicken flexor tendon model. J Surg Res. 2010;159(2):765–771.
  24. Tan V, Nourbakhsh A, Capo J, et al. Effects of nonsteroidal anti-inflammatory drugs on flexor tendon adhesion. J Hand Surg Am. 2010;35(6):941–947.
  25. Rahmani A, Nadri S, Kazemi HS, et al. Conductive electrospun scaffolds with electrical stimulation for neural differentiation of conjunctiva mesenchymal stem cells. Artif Organs. 2019;43(8):780–790.
  26. Li JJ, Gil ES, Hayden RS, et al. Multiple silk coatings on biphasic calcium phosphate scaffolds: effect on physical and mechanical properties and in vitro osteogenic response of human mesenchymal stem cells. Biomacromolecules. 2013;14(7):2179–2188.
  27. Zuhlke HV, Lorenz EM, Straub EM, et al. Pathophysiology and classification of adhesions. Langenbecks Archiv Fur Chirurgie Supplement II, Verhandlungen Der Deutschen Gesellschaft Fur Chirurgie Deutsche Gesellschaft Fur Chirurgie Kongress. 1990;1:1009–1016.
  28. Duran B, Ak D, Cetin A, et al. Reduction of postoperative adhesions by N,O-carboxymethylchitosan and spermine NONOate in rats. Exp Anim. 2003;52(4):267–272.
  29. Hooker GD, Taylor BM, Driman DK. Prevention of adhesion formation with use of sodium hyaluronate-based bioresorbable membrane in a rat model of ventral hernia repair with polypropylene mesh–a randomized, controlled study. Surgery. 1999;125(2):211–216.
  30. Janse van Rensburg A, Davies NH, Oosthuysen A, et al. Improved vascularization of porous scaffolds through growth factor delivery from heparinized polyethylene glycol hydrogels. Acta Biomater. 2017;49:89–100.
  31. Wang W. Instability, stabilization, and formulation of liquid protein pharmaceuticals. Int J Pharm. 1999;185(2):129–188.
  32. Yin H-M, Qian J, Zhang J, et al. Engineering porous poly (lactic acid) scaffolds with high mechanical performance via a solid state extrusion/porogen leaching approach. Polymers. 2016;8(6):213.
  33. Karageorgiou V, Kaplan D. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials. 2005;26(27):5474–5491.
  34. Jing X, Mi H-Y, Cordie T, et al. Fabrication of porous poly (ε-caprolactone) scaffolds containing chitosan nanofibers by combining extrusion foaming, leaching, and freeze-drying methods. Ind Eng Chem Res. 2014;53(46):17909–17918.
  35. Liu S, Hu C, Li F, et al. Prevention of peritendinous adhesions with electrospun ibuprofen-loaded poly(L-lactic acid)-polyethylene glycol fibrous membranes. Tissue Eng Part A. 2013;19(3–4):529–537.
  36. Zhu Y, Gao C, Liu X, et al. Surface modification of polycaprolactone membrane via aminolysis and biomacromolecule immobilization for promoting cytocompatibility of human endothelial cells. Biomacromolecules. 2002;3(6):1312–1319.
  37. Wang Y, Ji Y, Zhao Y, et al. Effects of surface functional groups on proliferation and biofunction of schwann cells. J Biomater Appl. 2016;30(10):1494–1504.
  38. Zhu X, Cui W, Li X, et al. Electrospun fibrous mats with high porosity as potential scaffolds for skin tissue engineering. Biomacromolecules. 2008;9(7):1795–1801.
  39. Kundu SC, Kundu B, Talukdar S, et al. Invited review nonmulberry silk biopolymers. Biopolymers. 2012;97(6):455–467.
  40. Yeo Y, Kohane DS. Polymers in the prevention of peritoneal adhesions. Eur J Pharm Biopharm. 2008;68(1):57–66.
  41. Yeo A, Rai B, Sju E, et al. The degradation profile of novel, bioresorbable PCL-TCP scaffolds: an in vitro and in vivo study. J Biomed Mater Res A. 2008;84:208–218.
  42. Sagnella A, Pistone A, Bonetti S, et al. Effect of different fabrication methods on the chemo-physical properties of silk fibroin films and on their interaction with neural cells. RSC Adv. 2016;6(11):9304–9314.
  43. Drummy LF, Phillips DM, Stone MO, et al. Thermally induced α-Helix to β-Sheet transition in regenerated silk fibers and films. Biomacromolecules. 2005;6(6):3328–3333.
  44. Qi Y, Wang H, Wei K, et al. A review of structure construction of silk fibroin biomaterials from single structures to multi-level structures. IJMS. 2017;18(3):237.
  45. Tsukada M, Gotoh Y, Nagura M, et al. Structural changes of silk fibroin membranes induced by immersion in methanol aqueous solutions. J Polym Sci B Polym Phys. 1994;32(5):961–968.
  46. Jackson EK. Intraperitoneal administration of adenosine inhibits formation of abdominal adhesions. Dis Colon Rectum. 2004;47(8):1390–1396.
  47. Wiseman DM, Gottlick-Iarkowski L, Kamp L. Effect of different barriers of oxidized regenerated cellulose (ORC) on cecal and sidewall adhesions in the presence and absence of bleeding. J Invest Surg. 1999;12:141–146.
  48. Kusunoki M, Ikeuchi H, Yanagi H, et al. Bioresorbable hyaluronate-carboxymethylcellulose membrane (seprafilm) in surgery for rectal carcinoma: a prospective randomized clinical trial. Surg Today. 2005;35(11):940–945.
  49. Hellebrekers BW, Trimbos-Kemper GC, van Blitterswijk CA, et al. Effects of five different barrier materials on postsurgical adhesion formation in the rat. Hum Reprod. 2000;15(6):1358–1363.
  50. Zeng J, Xu X, Chen X, et al. Biodegradable electrospun fibers for drug delivery. J Controlled Release. 2003;92(3):227–231.
  51. Verreck G, Chun I, Rosenblatt J, et al. Incorporation of drugs in an amorphous state into electrospun nanofibers composed of a water-insoluble, nonbiodegradable polymer. J Controlled Release. 2003;92(3):349–360.
  52. Strick MJ, Filan SL, Hile M, et al. Adhesion formation after flexor tendon repair: a histologic and biomechanical comparison of 2- and 4-strand repairs in a chicken model. J Hand Surg Am. 2004;29(1):15–21.
  53. Oh SH, Kim JK, Song KS, et al. Prevention of postsurgical tissue adhesion by anti-inflammatory drug-loaded pluronic mixtures with sol-gel transition behavior. J Biomed Mater Res A. 2005;72(3):306–316.
  54. Miller JA, Ferguson RL, Powers DL, et al. Efficacy of hyaluronic acid/nonsteroidal anti-inflammatory drug systems in preventing postsurgical tendon adhesions. J Biomed Mater Res. 1997;38(1):25–33.

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Authors
Nadri, S., Rahmani, A., Hosseini, S. H., Habibizadeh, M., Araghi, M., & Mostafavi, H.
Affiliations
  • Zanjan University of Medical Sciences (IR)
  • Department of Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
Corresponding author
Nadri, Samad
Venue
Artificial Cells, Nanomedicine, and Biotechnology
Published
2022-03-17
Volume
50
Issue
1
Pages
40-48
ISSN
  • 2169-1401 (ISSN-L)
  • 2169-141X
OpenAlex
W4220666443
Cited by
19
References
0
Citations by year
2026: 3 · 2025: 3 · 2024: 9 · 2023: 4
FWCI
3.73
Type
journal article
Language
en
Open access
Locations
  • Artificial Cells Nanomedicine and Biotechnology (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
National Institute for Medical Research and Development (957687)
Topics
  • Health Sciences › Medicine › Surgery › Intestinal and Peritoneal Adhesions
  • Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
  • Physical Sciences › Materials Science › Biomaterials › Silk-based biomaterials and applications
Keywords
peritoneal adhesions, postoperative adhesion prevention, ibuprofen, silk fibroin, polyethylene glycol, electrospinning, adhesion prevention, anti-inflammatory agents, drug release, membrane degradation, rat model, abdominal wall closure
MeSH terms
Tissue Adhesions, Animals, Female, Ibuprofen, Membranes, Artificial, Silk, Rats, Nanofibers

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