Modification of mesh endoprostheses for hernioplasty by electrospinning method


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Objecties. The improvement of biocompatibility of polypropylene mesh endoprostheses for hernioplasty. Materials and methods. The endoprostheses based on tricot polypropylene meshes of standard and low density are investigated. The solution of polycaprolactone in chloroform and electrospinning method were used for the surface modification. The specimens were sterilized in low-temperature hydrogen peroxide plasma. Structural analysis of modified surface was performed by scanning electron microscopy, the strain-strength parameters of endoprostheses were determined in mechanical tests on uniaxial tension. Results. Micro-sized spatial fibrous structure of polycaprolactone as a modiftiator was formed on the surface of polypropylene mesh by electrospinning that allowing to increase the biocompatibility of reticular endoprostheses for hernioplasty on retention of strain-strength properties of issues. Conclusion. In order to increase the biocompatibility of polypropylene mesh endoprostheses for hernioplasty, the parameters of the technological mode of modifying the surface of a knitted prosthetic mesh by forming an adhesively bonded microstructured fibrous polymer modifier are optimized. The required porosity of the endoprosthesis structure, uniformity of distribution and adhesion of the modifier to the knitted base are provided during the modification process. To obtain a fibrous structure from a 7.5% polycaprolactone solution on by electrospinning, the optimal mode parameters are: voltage 30 kV, distance between electrodes 10 cm and application rate 14 cm/min.

全文:

受限制的访问

作者简介

V. Bereschenko

Gomel State Medical University

Email: val_71@inbox.nu
Associate Professor, Candidate of Medical Science Gomel, Republic of Belarus

A. Lyzikov

Gomel State Medical University

Email: val_71@inbox.nu
Professor, MD; Associate Professor Gomel, Republic of Belarus

S. Shil’ko

V.A. Belyi Metal-Polymer Research Institute of NASB

Email: val_71@inbox.nu
Candidate of Engineering Sciences Gomel, Republic of Belarus

T. Drobysh

V.A. Belyi Metal-Polymer Research Institute of NASB

Email: val_71@inbox.nu
Gomel, Republic of Belarus

参考

  1. Верещагина Г.Н. Системная дисплазия соединительной ткани. Клинические синдромы, диагностика, подходы к лечению. Метод. пособ. для врачей. Новосибирск: НГМУ, 2008; 37 с.
  2. Radu P., Brätucu M., Garofil D. et al. The Role of Collagen Metabolism in the Formation and Relapse of Incisional Hernia. Chirurgie (Bucur). 2015; 110 (3): 224-30.
  3. Дисплазия соединительной ткани: тактика ведения пациентов в условиях общей врачебной практики. Проект клинических рекомендаций. М., 2013; 20 с.
  4. Cano-Valderrama O., Porrero J.L., Quirös E. et al. Is Onlay Polypropylene Mesh Repair an Available Option for Incisional Hernia Repair? A Retrospective Cohort Study. Am Surg. 2019; 85 (2): 183-7.
  5. Azevedo M.C., Reis R.L., Claase M.B. et al. Development and Properties of Polycaprolactone/Hydroxyapatite Composite Biomaterials. J Mater Sci Mat Med. 2003; 14: 103-7. doi: 10.1023/A:1022051326282
  6. A Polycaprolactone-Based Collagen Stimulator. Safety data report. Mode of access: https://ellanse.com/wp-content/uploads/sites/2/2017/04/1605-Ellanse%CC%81-eSafety-report.pdf
  7. Galadari H., van Abel D., Al Nuami K. et al. A Randomized, Prospective, Blinded, Split-Face, Single-Center Study Comparing Polycaprolactone to Hyaluronic Acid for Treatment of Nasolabial Folds. J Cosmet Dermatol. 2015; 14 (1): 27-32. doi: 10.1111/jocd.12126
  8. Moers-Carpi M.M., Sherwood S. Polycaprolactone for the Correction of Nasolabial Folds: A 24-Month, Prospective, Randomized, Controlled Clinical Trial. Dermatol Surg. 2013; 39 (3 Pt 1): 457-63. doi: 10.1111/dsu.12054
  9. Лызиков А.Н., Берещенко В.В., Петренев Д.Р. и др. Метод подготовки сетчатого эндопротеза для герниопластики. Гомель: ГомГМУ, 2014; 11 с.

补充文件

附件文件
动作
1. JATS XML

版权所有 © Russkiy Vrach Publishing House, 2021
##common.cookie##