email   Email Us: info@lupinepublishers.com phone   Call Us: +1 (914) 407-6109   57 West 57th Street, 3rd floor, New York - NY 10019, USA

Lupine Publishers Group

Lupine Publishers

  Submit Manuscript

ISSN: 2644-1209

Trends in Ophthalmology: Open Access Journal

Review Article(ISSN: 2644-1209)

Advances in Antibacterial Textile Sutures Volume 1 - Issue 3

N Gokarneshan*

  • Professor and Head, Department of Textile Technology, Park college of engineering and technology, Coimbatore, India

Received: May 12, 2018;   Published: May 22, 2018

Corresponding author: N Gokarneshan, Department of Textile Technology, Park college of engineering and technology, India

DOI: 10.32474/TOOAJ.2018.01.000114

 

Abstract PDF

Abstract

The article highlights some significant research trends in the development in antibacterial textile sutures. Braided polyamide sutures are frequently used in dermatologic surgery for wound closure. However, braided sutures promote bacteria proliferation. In order to prevent wound complications due to this effect, antibacterial sutures should be used. The major focus has been the development of new non-absorbable antibacterial polyamide braided suture. A new coating process has been proposed that leads to obtain suture uniformly covered by antibacterial film enclosing chitosan, which is known for its antibacterial benefit. Silk sutures have been treated with natural fungal pigment in varying concentrations. Also, the influence on the silk suture properties like tenacity, knot strength, friction and antimicrobial activity has been studied. Attempts have been made to systematically study the randomized, controlled trials that compare the use of antibacterial sutures (ABS) for skin closure in controlling surgical site infections.

Keywords: Braided Polyamide Suture; Antibacterial Effect; Chitosan; Wound Closure; Pigment; Fungal

Introduction

Today sutures are the most implanted biomaterials in human body because they are used in almost all wound closure [1]. They are either multifilaments (twisted or braided) or monofilament [2]. They have physical and chemical properties quite different from each other. In the last century, synthetic materials, both absorbable and non-absorbable, have been introduced in the making of surgical sutures. Wound closure using suture materials is an integral part of the surgical process. Sutures are natural or synthetic textile biomaterials widely used in wound closure, to ligate blood vessels and to draw tissues together [3]. Sutures consist of a fibre or fibrous structure with a metallic needle attached at one of the fibre ends and they can be classified into two broad categories namely absorbable and non-absorbable sutures. Surgical site infection (SSI) is an immense burden on healthcare resources even in the modern era of immaculate sterilization approaches and highly effective antibiotics. An estimated 234 million various surgical procedures, involving skin incisions requiring various types of wound closure techniques, are performed in the world, with the majority resulting in a wound healing by primary intention [4].

Braided Polyamide Suture Coated with Chitosan- Citric Acid Biopolymer

In the last few years there has been a growing interest in the improvement of absorbable sutures. Quite recently, considerable attention has been paid to marketed non-absorbable sutures, which have undergone some improvements in their mechanical properties. However, there have been no new significant improvements in their physiological properties since their first use. Several researches have appeared in recent years verifying that the presence of suture significantly enhances the susceptibility of surrounding tissues to infection [5,6]. Indeed, many distressing complications such as infection, wound disruption and chronic sinus formation occur in sutured wound. Previous studies indicate that suture materials vary in their propensity to produce bacterial infection in surgical wounds. The physical configuration of the suture thread has been suggested to be an important factor in determining its susceptibility to surgical infection.4 Thus, multifilament suture have been known for their compliance leading to secure and compact knots. However, their intrinsic surface roughness and capillarity increase the potential of wound infection [7]. Thus, sutures in multifilament form result in higher wound infection than the same sutures in monofilament form. To solve this problem, many researchers have proposed various methods to develop antimicrobial non-absorbable multifilament sutures by using antimicrobial agents, compounds that have the ability to kill or inhibit the growth of microbes, thus preventing infection [8-10]. These include: antibiotics that are capable of inhibiting life processes of all foreign organisms and antibacteria that kill and prevent the growth of bacteria.

Several publications have appeared in recent years, documenting several approaches to the development of antimicrobial sutures [11,12]. For several years, great effort has been devoted to the study of the incorporation of silver metal on the surface of suture and conventional antibiotics, such as neomycin palmitate, penicillin and sulfonamide, onto suture surface by impregnation. Previous research have shown that the antimicrobial activity in sutures can be achieved by blending or incorporating volatile or non-volatile antimicrobial agent while processing, coating or graft polymerization followed by immobilization of antimicrobial agents onto the suture surface [13-15]. Coating has been the most common technique used for applying the antibacterial agents on the textile surface. The antibacterial agents have been connected to the surface by physical bonds or fixed to the molecular chains of the fiber by using crosslinking agents. Focus on polyamide suture, antibiotic sutures have been developed by grafting acrylic acid onto suture surface followed by antibiotic fixation [16]. Antibiotic monofilament suture was prepared by doping with iodine and antimicrobial properties against E coli and S aureus were tested by zone of inhibition method. Drug doxycycline has been also used to obtain antibiotic suture. However, all of the previous studies do not take into account to produce commercial sutures because the frequent use of antibiotics can avoid long-term, ineffective, systemic antibiotics and reduce the risk of microbial resistant generation [17]. Based on this approach, only antibacterial compounds are recommended and used for producing suture that inhibit bacterial proliferation.

In 2004, Ethicon Inc. developed and marketed the first antibacterial sutures on the market called Vicryl Plus, Monocryl Plus and PDS II Plus. These absorbable sutures have been coated with Triclosan and have an antibacterial effect against S Aureus, S Epidermidis, Meticillin, E coli and K pneumoniae. Following the commercialization of Vicryl plus suture by Ethicon Inc, several works have been conducted and confirmed the effectiveness of this suture. Alonso et al. [18] and Rothenburger et al. [19] have also proved the antibacterial effect of this suture against S aureus and S epidermidis and Marzo et al. [20] have shown a decrease of infection with P aeruginosa germs. The success of these sutures has been also confirmed by statistical survey, proving that the use of antibacterial sutures leads to reduction in the infection frequency [21-23]. Furthermore, the use of this suture contributes to budgetary gain of $ 1.5 million in a medical center [24].

Despite the efficiency of Triclosan, which is the most and only used antibacterial product for marketed sutures, this product has several limitations, which can cause complications. In fact, Clayton et al. have shown that Triclosan can negatively affect immune functions and the reproducibility of the cells [25]. For this reason, many attempts are recommended new antibacterial products to be used for the development of antimicrobial sutures. With this goal, in recent years, research on new antibacterial biomaterials has become very popular. Recent research reports the development of new antibacterial suture threads that show better results than Vicryl Plus [26]. Referring to the sources in general, chitosan is a biomaterial well used in biomedical field because of beneficial properties for wound healing and particularly for its antibacterial effect [27]. Several studies have confirmed the effect of chitosan as an antibacterial agent [28-33]. It is one of many antibacterial products widely present in nature. It is not affected by sterilization with ethylene oxide (EO), and keeps its antibacterial property after this treatment [34,35]. That is why chitosan is ideal for use on the development of antibacterial suture, which is subjected to sterilization by EO in the last step of manufacturing process such as polyamide suture.

The literature shows a variety of approaches permitting to apply chitosan on suture surface. Antibacterial polyester sutures have been prepared by grafting chitosan to the suture surface using acrylic acid. Much research has been done to develop chitosan coated polylactic acid (PLA) and silk sutures. Viju and Thilagavathi [36] have studied the effect of this treatment on the mechanical properties and the surface state of the braided antibacterial silk sutures. They reported a slight improvement in the suture mechanical and antibacterial properties. Nonetheless, the used dipping process does not make it possible to have a uniform treatment on the suture surface and sutures can stick between them in the bath. Although several studies have been conducted in order to develop antibacterial non-absorbable suture, today, no antibacterial non-absorbable sutures are presented in market and only antibacterial absorbable sutures are produced and marketed by Ethicon Inc. With this goal, in this study we explore the possibility of use of chitosan for the development of new antibacterial nonabsorbable polyamide suture [37]. Thus, the aim of the present study was to determine optimal manufacturing conditions permitting to attain this purpose. Biopolymer compounds and non-toxic products suitable for implantation in human body will be used. Appropriate method of applying biopolymers compounds on suture surface will be presented. Chemical reactions between different biopolymer compounds and polyamides will be investigated. Mechanical, antibacterial and surface properties of sutures will be investigated in order to determine best manufacturing conditions to obtain the best antibacterial suture.

This paper is a modest contribution to the ongoing discussions on the development of antibacterial non absorbable sutures, particularly the possibility of use of chitosan for the development of antibacterial sutures. The main purpose of this paper is the development of new process for producing antibacterial PA 6-6 braided sutures. PAD-dry process was used in order to apply uniform multilayers of chitosan-CA biopolymer on suture surface. This paper has clearly presented an investigation of chemicals and mechanical properties of suture. For study purpose, chemical characteristics of applied biopolymer coating on suture surface are determined by using ATR-IF. It has been demonstrated that many eventual bonds between compounds present in coating solutions and PA-66 may occur. The existence of these bonds implies the fixation of biopolymer coating on suture surface. Suture surface has been investigated by using image analysis (SEM image) and friction difference test (FCD-mean). These experiments have demonstrated that uniform surface may be obtained by progressively applying coating solution containing little amount of chitosan on suture surface. We have also found that the developed coating process has not affected tensile properties of suture. In fact, TS and KPS still meet USP requirement. Antibacterial activity of developed sutures has been also tested against four colonies and the optimal conditions permitting to have an antibacterial effect and a smooth surface have been determined. From the research that has been carried out, it is possible to conclude that the best suture may be obtained by applying three layers of chitosan-CA biopolymer containing 1% of chitosan and polymerized at a temperature equal to 160oC. Indeed, these sutures have shown remarkable antibacterial effect against E coli (gram-negative) and P aeruginosa (gram-negative). Based on these results, it can be concluded that research conducted into development of antibacterial suture in vitro has been very successful. However, the main limit of the experimental results is that suture performance efficiency has not been conducted in vivo. Clearly, further research will be desirable to validate the obtained result in vivo. In an effort to prove coating film stability against friction, realized test is presented in the Supplementary

Silk sutures treated with natural fungal extract

The most crucial requirements of suture materials are physical and mechanical properties, handling properties, biocompatibility, and antimicrobial nature [38]. Till date, there is no single suture material which can fulfill all the crucial requirements of sutures [39]. The present surgeon has several choices of suture material available and he may choose them based on availability and his familiarity. Silk, a natural non-absorbable suture material has been used as biomedical suture for centuries due to its advantageous characteristics. However, one of the major problems associated with the silk is its poor microbe resistance characteristics. Several researchers have used different antimicrobial agents onto silk sutures to impart microbe resistance characteristics. Researchers have also used silver doped bioactive glass powder to coat silk surgical suture [40]. Recently, studies on the effect of chitosan coating on the characteristics of silk sutures. Another study on tetracycline coating on silk sutures was carried out and they investigated the effect of tetracycline treatment on silk suture properties [41].

Recently, antimicrobial finishing of textiles using microbial dyes have received greater attention as they require less labour, land, and cost effective solvents for extraction as opposed to higher plant materials. In this study, silk sutures are treated with Thermomyces, a natural fungal extract and its effect on the properties of silk sutures such as antimicrobial activity, friction, tenacity and knot strength are studied.

Silk suture produced was treated with natural fungal extract at optimum concentration and the effects of natural fungal treatment on the suture properties were studied. The result showed that the tenacity and knot strength of silk braided sutures increased compared to the untreated silk suture. The frictional properties of both the fungal treated silk suture and the untreated silk suture were determined by the dynamic coefficient of friction and there is a slight reduction in frictional value found in the treated silk suture compared to the untreated silk suture [42]. The uniform deposition of natural fungal pigment on to the surface of the silk braided suture was confirmed by Scanning Electron Microscopy. The antibacterial activity of fungal treated silk braided suture at optimum concentration against S. aureus and E. coli is found to be good compared to the untreated silk suture. The result suggests that the silk suture treated with optimum concentration of the natural fungal pigment is appropriate to retard the exponential growth of S. aureus, a gram-positive bacterium and E. coli a gramnegative bacterium and hence silk sutures can be developed with the required characteristics for healthcare applications.

Sutures for skin closure in controlling surgical site infections

Skin wounds are at risk of SSI and therefore may lead to increased morbidity, delayed recovery and prolonged hospital stay [43]. The prevalence of SSI in the developed world is variable but reported figures are estimated at around 5% [44,45]. The development of SSI is a multifactorial phenomenon, which requires a multimodal approach to prevent and treat it in a timely manner to avoid financial, psychological and health-related quality of life consequences. Various predisposing aetiopathological factors for SSI include immune supression, nutritional deficiencies, hypoproteinemias, congestive cardiac failure, hepatic failure, renal failure, use of steroids, chemotherapy agents, steroids and diabetes mellitus [46-49]. In additions to these factors, wound contamination, contaminated instruments, surgical technique and sutures used to close skin have also been reported to be responsible for SSI and cosmetic outcomes [50-52]. The prevention of the SSI by various invasive and non-invasive interventions is the most common measure surgeons and other healthcare professional advocate to tackle the problem of SSI. This includes use of prophylactic antibiotics and various other multimodal approaches already reported in the medical literature [53-56]. Triclosan [5-chloro-2- (2,4-dichlorophenoxy)phenol] is a broad-spectrum bacteriocidal agent that has been used for more than 40 years in various products, such as toothpaste and soaps. Higher concentrations of triclosan work as a bactericide by attacking different structures in the bacterial cytoplasm and cell membrane [57].

At lower concentrations, triclosan acts as bacteriostatic agent, binding to enoyl-acyl reductase (ENR), a product of the Fab I gene and thus inhibiting fatty acid synthesis [58,59]. Use of triclosancoated sutures should theoretically result in the reduction of SSI. Several studies have shown a reduction in the number of bacteria in vitro and also of wound infections in animals [60-62]. The objective of this article is to systematically analyse the randomized, controlled trials comparing the use of triclosan-coated antibacterial sutures (ABS) versus simple sutures (SS) for skin closure in controlling the SSIs. We aimed to include only those trials in which the SSI was investigated as a primary outcome regardless the surgical specialty. The SSI was the primary outcome of this study, whereas postoperative complications, duration of the operation and length of the hospital stay (if reported) were analysed as secondary outcome measures. Although our conclusion is based on the summated outcome of seven randomized, controlled trials, it should be considered cautiously because the quality of the majority of included trials was poor [63]. There is still a lack of stronger evidence to support the routine use of ABS but it can be considered an alternative and may initially be applied in selected groups of patients. A major, multicentre, randomized, controlled trial of high quality according to CONSORT guidelines is mandatory to validate these findings.

Conclusion

Antibacterial sutures should be used. The main objective of this study is the development of new non-absorbable antibacterial polyamide braided suture. This paper suggests new coating process that leads to obtain suture uniformly covered by antibacterial film enclosing chitosan, which is known for its antibacterial benefit. Mechanical properties and surface morphology of developed sutures were investigated by using mechanical tests. Sutures surfaces were also examined by scanning electron microscope, to perceive spreading of coating product on suture surface. In order to identify potential reactions between chemical compounds present in coating solution and suture material, sutures were analyzed by ATR-IF spectroscopy. It has been demonstrated that many eventual bonds between compounds present in coating solutions and polyamide macromolecular chain may occur. The existence of these bonds implies the fixation of biopolymer coating on suture surface. It has been demonstrated that uniform surface may be obtained by progressively applying coating solution containing little amount of chitosan on suture surface. We have also found that developed coating process has not affected mechanical properties of suture, which still meet United States Pharmacopeia requirement. Finally, antibacterial effects against four colonies, very widespread in hospitals, were studied. Prominent antibacterial effects of braided polyamide suture against two gram-positive (S Aureus, S epidermidis) and two gram-negative (E coli and P aeruginosa) colonies are presented. Optimal result of best properties is obtained by applying three layers of biopolymer coating comprising 1% chitosan and 10% citric acid. The new developed suture coating process appears as a promising method for obtaining important antibacterial effect with smooth suture surface.

The result showed that the pigment concentration in the selected range has no significant effect on friction, tenacity and knot strength of silk sutures. Antimicrobial test results showed that as the pigment concentration increases the antimicrobial activity also increases against both E. coli and S. aureus bacteria. At 2.5% concentration, a zone of inhibition of 10 mm and 14 mm are observed against E. coli and S. aureus respectively. Silk suture treated with optimum concentration of the natural fungal pigment is appropriate to retard the exponential growth of S. aureus, a grampositive bacterium and E. coli a gram-negative bacterium and hence silk sutures can be developed with the required characteristics for healthcare applications. Randomized, controlled trials on surgical patients comparing the use of ABS for skin closure in controlling the surgical site infections were analysed systematically using RevMan and combined outcomes were expressed as odds ratios (OR) and standardized mean differences (SMD). Seven randomized, controlled trials evaluating 1631 patients were retrieved from electronic databases. There were 760 patients in the ABS group and 871 patients in the simple suture group. There was moderate heterogeneity among trials (Tau2= 0.12; chi2= 8.40, df = 6 [P<0.01]; I2= 29%). Therefore in the random-effects model, the use of ABS for skin closure in surgical patients was associated with a reduced risk of developing surgical site infections (OR, 0.16; 95% CI, 0.37, 0.99; z = 2.02; P<0.04) and postoperative complications (OR, 0.56; 95% CI, 0.32, 0.98 z = 2.04; P=0.04). The durations of operation and lengths of hospital stay were similar following the use of ABS and SS for skin closure in patients undergoing various surgical procedures. Use of ABS for skin closure in surgical patients is effective in reducing the risk of surgical site infection and postoperative complications. ABS is comparable with SS in terms of length of hospital stay and duration of operation.

References

  1. Chu CC, Greisler HP, JAv Fraunhofer (1997) Wound closure biomaterials and devices. 1st Ed. New York: United States of America: CRC Press, USA p.416.
  2. Patel KA, Thomas WEG (2008) Sutures, ligatures and staples. Surg (Oxford) 26(2): 48-53.
  3. Chu CC, Fraunhofer JAV, Greisle HP (1997) Wound closure biomaterials and devices. 1: 35-49. CRC Press New York, USA.
  4. Walter CJ, Dumville JC, Sharp CA, Page T (2012) Systematic review and meta analysis of wound dressings in the prevention of surgical site infections in surgical wounds healing by primary intention. Br J Surg 99(9): 1185-1194.
  5. Mingmalairak C (2011) Antimicrobial sutures: new strategy in surgical site infections. In: A. Me`ndez-Vilas (ed.) Formatex Spain pp. 311-323.
  6. Hoshino S, Yoshida Y, Tanimura S, Yamauchi Y, Noritomi T, et al. (2013) A study of the efficacy of antibacterial sutures for surgical site ınfection: a retrospective controlled trial. Int Surg 98(2): 129-132.
  7. Federov MB, Vikhoreva GA, Kil deeva NR, Yu K Borisova, TI Vinokurova, et al. (2006) Structure and strength properties of surgical sutures modified with a polyhydroxybutyrate coating. Fibre Chem 38(6): 471-475.
  8. Enescu D (2008) Use of chitosan in surface modification of textile materials. Roumanian Biotechnol Lett 13(6): 4037-4048.
  9. Shigemasa Y, Minami S (1996) Application of chitin and chitosan for biomaterials. Bio technol Genet Eng Rev 13: 383-420.
  10. Rinaudo M (2006) Chitin and chitosan: Properties and applications. Progr Polym Sci 31(7): 603-632.
  11. Khulbe KC, Feng C, Matsuura T (2010) The art of surface modification of synthetic polymeric membranes. J Appl Polym Sci 115(2): 855-895.
  12. Werner C, Maitz MF, Sperling C (2007) Current strategies towards hemocompatible coatings. J Mater Chem 17(32): 3376-3384.
  13. Deopura BL, Alagirusamy R, Joshi M, et al. (2008) Polyester and polyamide. Cambridge, England: Woodhead publishing limited and CRC Press LLC, USA pp.608.
  14. Dumitriu S (2001) Polymeric biomaterials. New York, USA: Marcel Dekker Inc pp.1183.
  15. Gao Y, Robin C (2008) Recent advances in antimicrobial treatments of textiles. Text Res J 78(1): 60-72.
  16. Bucheńska J (1996) Polyamide fibers (PA6) with antibacterial properties. J Appl Polym Sci 61(3): 567-576.
  17. Michel M, Gutmann L (1997) Methicillin resistant Staphylococus aureus and vancomycin resistant enterococci: therapeutic realities and possibilities. The Lancet 349(9069): 1901-1906.
  18. Alonso AG, García Criado FJ, Parreno F, García Sánchez JE, García Sánchez E, et al. (2007) Study of the efficacy of coated VICRYL plus antibacterial suture (coated Polyglactin 910 suture with Triclosan) in two animal models of general surgery. J Infect 54(1): 82-88.
  19. Rothenburger S, Spangler D, Bhende S, Burkley D (2002) In vitro antimicrobial evaluation of coated VICRYL* plus antibacterial suture (coated Polyglactin 910 with Triclosan) using zone of ınhibition assays. Surg Infect 3(supp 1): 79-87.
  20. Marzo G, Loffredi R, Marchetti E, S Di Martino, C Di Pietro, et al. (2008) In vitro antibacterial efficacy of Vicryl Plus suture (coated Polyglactin 910 with triclosan) using zone of inibition assays. Oral Implant 1(1): 43-48.
  21. Rozzelle CJ, Leonardo J, Li V (2008) Antimicrobial suture wound closure for cerebrospinal fluid shunt surgery: a prospective, double-blinded, randomized controlled trial. J Neurosurg Pediatr 2(2): 111-117.
  22. Justinger C, Moussavian MR, Schlueter C, Kopp B, Kollmar O, et al. (2009) Antibiotic coating of abdominal closure sutures and wound infection. Surgery 145(3): 330-334.
  23. Rasić Z, Schwarz D, Adam VN, Sever M, Lojo N, et al. (2011) Efficacy of antimicrobial triclosan coated polyglactin 910 (Vicryl* Plus) suture for closure of the abdominal wall after colorectal surgery. Colleg Antropolog 35(2): 439-443.
  24. Galal I, El Hindawy K (2011) Impact of using triclosan antibacterial sutures on incidence of surgical site infection. Am J Surg 202(2): 133- 138.
  25. Clayton EMR, Todd M, Dowd JB, Aiello AE (2011) The ımpact of bisphenol A and triclosan on ımmune parameters in the US population, Nhanes 2003-2006. Environ Health Perspect 119(3): 390-396.
  26. Li Y, Kumar KN, Dabkowski JM, Meagan Corrigan§, Richard W Scott§, et al. (2012) New bactericidal surgical suture coating. Langmuir 28(33): 12134-12139.
  27. Alvarenga ESd (2011) Characterization and properties of chitosan. In: Elnashar M (ed.) Biotechnology of Biopolymers. Rijeka, Croatia: Intech pp. 1200.
  28. Kenawy ER, Abdel Hay FI, El Magd AA, Yehia AG Mahmoud (2005) Biologically active polymers: modification and antimicrobial activity of chitosan derivatives. J Bioactive Compatible Polym 20(1): 95-111.
  29. Huang KS, Wu WJ, Chen JB, Huey Shan Lian (2008) Application of low molecular weight chitosan in durable press finishing. Carbohydr Polym 73(2): 254-260.
  30. Yunli M, Tao Z, Changsheng Z (2008) Preparation of chitosan nylon-6 blended membranes containing silver ions as antibacterial materials. Carbohydr Res 343(2): 230-237.
  31. Strnad S, Sauper O, Jazbec A, Karin Stana Kleinschek (2008) Influence of chemical modification on sorption and mechanical properties of cotton fibers treated with chitosan. Text Res J 78(5): 390-398.
  32. Shin Y, Yoo DI, Jang J (2001) Molecular weight effect on antimicrobial activity of chitosan treated cotton fabrics. J Appl Polym Sci 80(13): 2495- 2501.
  33. Weijun Y, Fai LM, John X, Tsz Leung Kwong, Daniel Kam Len Lee, et al. (2005) Novel core shell particles with poly (n-butyl acrylate) cores and chitosan shells as an antibacterial coating for textiles. Polymer 46(23): 10538-10543.
  34. Juan AS, Montembault A, Gillet D, J P Say, S Rouif, et al. (2012) Degradation of chitosan based materials after different sterilization treatments. IOP Conference Series: Mater Sci Eng 31: 012007.
  35. Marreco PR, Da Luz Moreira P, Genari SC, Moraes AM (2004) Effects of different sterilization methods on the morphology, mechanical properties, and cytotoxicity of chitosan membranes used as wound dressings. J Biomed Mater Res Part B Appl Biomater 71: 268-277.
  36. Viju S, Thilagavathi G (2013) Effect of chitosan coating on the characteristics of silk braided sutures. J Industr Text 42(3): 256-268.
  37. Faten D, Sondes G, Mohamed AHA, Saber BA (2017) Development and characterization of antibacterial braided polyamide suture coated with chitosan citric acid biopolymer. Journal of Biomaterials Applications 32(3): 384-398.
  38. Saxena S, Ray AR, Kapil A, Pavon Djavid G, Letourneur D, et al. (2011) Development of a New Polypropylene Based Suture: Plasma Grafting, Surface Treatment, Characterization, and Biocompatibility Studies. Mol Biosci 11(3): 373-382.
  39. Pillai CKS, Sharma CP (2010) Absorbable Polymeric Surgical Sutures: Chemistry, Production, Properties, Biodegradability, and Performance. J Biomater Appl 25(4): 291-366.
  40. Blacker JJ, Nazat SN, Bocc AR (2004) Development and characterisation of silver doped bioactive glass coated sutures for tissue engineering and wound healing applications. Biomaterials 25(7,8): 1319-1329.
  41. H Liu H, Ge Z, Wang Y, Toh SL, Sutthikhum V, et al. (2007) Modification of sericin free silk fibers for ligament tissue engineering application. J Biomed Mat Res App Bio 82(1): 129-138.
  42. Parthiban M, Thilagavathi G, Viju S (2016) Development of Antibacterial Silk Sutures Using Natural Fungal Extract for Healthcare Applications. J Textile Sci Eng 6(2): 249.
  43. (2002) Health Protection Agency. Surveillance of surgical site infection in English hospitals 1997-2002. A national surveillance and quality improvement programme. Health Protection Agency: London.
  44. Wick EC, Vogel JD, Church JM, Remzi F, Fazio VW (2009) Surgical site infections in a ‘high outlier’ institution: are colorectal surgeons to blame? Dis Colon Rectum 52(3): 374-379.
  45. Boltz MM, Hollenbeak CS, Julian KG Ortenzi G, Dillon PW (2011) Hospital costs associated with surgical site infections in general and vascular patients. Surgery 150(5): 934-42.
  46. Berard F, Gandon J (1964) Postoperative wound infections: the influence of ultraviolet irradiation of the operating room and of various other factors. Ann Surg 160(Suppl 2): 1-192.
  47. McLaws ML, Murphy C, Whitby M (2000) Standardising surveillance of nosocomial infections: the HISS program. Hospital Infection Standardised Surveillance. J Qual Clin Pract 20(1): 6-11.
  48. (2008) National Institute for Health and Clinical Excellence (NICE). Surgical Site Infection: Prevention and Treatment of Surgical Site Infection. NICE Clinical Guideline 74.
  49. Horan TC, Andrus M, Dudeck MA (2008) DC/HNSN surveillance definition of healthcare associated infection and criteria for specific types of infection in the acute care setting. Am J Infect Control 36(5): 309-332.
  50. Poandl TM (2008) A 21day exploratory pilot study comparing the cosmetic result of sub cutuicular MONOCRYL Plus* versus transcutaneous Chinese silk for incisional wound closure in a pig model. Report, PSE Accession No. 07-0118, Project No. 67506.
  51. Nandi PL, Soundara Rajan S, Mak KC, SC Chan, YP So (1999) Surgical wound infection. Hong Kong Med J 5: 82-86.
  52. Dancer SJ, Stewart M, Coulombe C, A Gregori, M Virdi (2012) Surgical site infections linked to contaminated surgical instruments. J Hosp Infect 81(4): 231-238.
  53. Lin GL, Qiu HZ, Xiao Y, Wu B, Niu BZ (2012) Safety and efficacy of prophylactic single antibiotics administration in selective open colorectal surgery. Zhonghua Wei Chang Wai Ke Za Zhi 15(10): 1040- 1043.
  54. Cannon JA, Altom LK, Deierhoi RJ, Morris M, Richman JS, et al. (2012) Preoperative oral antibiotics reduce surgical site infection following elective colorectal resections. Dis Colon Rectum 55: 1160-1166.
  55. Junker T, Mujagic E, Hoffmann H, Rosenthal R, Misteli H, et al. (2012) Prevention and control of surgical site infections: review of the Basel Cohort Study. Swiss Med Wkly 142: 13616.
  56. Phatak UR, Pedroza C, Millas SG, Chang GJ, Lally KP, et al. (2012) Revisiting the effectiveness of interventions to decrease surgical site infections in colorectal surgery: A Bayesian perspective. Surgery 152(2): 202-211.
  57. Russell AD (2004) Whither triclosan? J Antimicrob Chemother 53(5): 693-695.
  58. McMurry LM, Levy SB (1998) Triclosan targets lipid synthesis. Nature 394(6693): 531-532.
  59. Levy CW, Roujeinikova A, Sedelnikova S, Baker PJ, Stuitje AR, et al. (1999) Molecular basis of triclosan activity. Nature 398(6726): 383-384.
  60. Marco F, Vallez R, Gonzalez P, Ortega L, De La Lama J, et al. (2007) Study of the efficacy of coated Vicryl plus antibacterial suture in an animal model of orthopedic surgery. Surg Infect (Larchmt) 8(3): 359-365.
  61. Storch ML, Rothenburger SJ, Jacinto G (2004) Experimental efficacy study of coated VICRYL plus antibacterial suture in guinea pigs challenged with Staphylococcus aureus. Surg Infect (Larchmt) 5(3): 281-288.
  62. Higgins JPT, Green S (2008) Cochrane Handbook for Systematic Reviews of Interventions Version 5.0.0 (updated February 2008).
  63. Muhammad S Sajid, L Craciunas, P Sains, KK Singh, MK Baig (2013) Use of antibacterial sutures for skin closure in controlling surgical site infections: a systematic review of published randomized, controlled trials. Gastroenterology Report 1(1): 42-50.