具有緩釋效果的抗菌真絲縫合線的研發(fā)

Pethile Sibanda，陳曉潔，王 璐

東華大學(xué)紡織學(xué)院 紡織面料技術(shù)教育部重點(diǎn)實(shí)驗(yàn)室(上海,201620)

具有緩釋效果的抗菌真絲縫合線的研發(fā)

Pethile Sibanda，陳曉潔，王 璐*

東華大學(xué)紡織學(xué)院 紡織面料技術(shù)教育部重點(diǎn)實(shí)驗(yàn)室(上海,201620)

近年來，經(jīng)臨床證實(shí)手術(shù)部位感染(SSIs)與實(shí)縫合線密切有關(guān)，因而，具有抗菌效果的縫合線已被開發(fā)，試圖減少細(xì)菌在縫合線表面的粘附和定植。該文以磺胺甲惡唑(SMZ)為抗菌劑，通過對真絲編織縫合線表面涂層的方法賦予其抗菌性能，并以聚己內(nèi)酯(PCL)為抗菌劑涂層處理的載體，以確保其具有長效緩釋的抗菌效果。選取大腸桿菌(ATCC25922)和金黃色葡萄球菌(ATCC25923)，分別對經(jīng)SMZ和SMZ+PCL處理的真絲縫合線進(jìn)行抑菌帶寬度、抗菌持久性和藥物釋放試驗(yàn)。結(jié)果表明，經(jīng)SMZ和SMZ+PCL處理的真絲縫合線均具有抗菌性，經(jīng)SMZ+PCL處理的真絲縫合線長效緩釋抗菌效果更優(yōu)異。

手術(shù)部位感染(SSIs)；真絲編織縫合線；抗菌涂層劑；抑菌帶寬度試驗(yàn)；抗菌持久性

0 INTRODUCTION

The development of infection at the incision site following suturing is among the main concerns that surgeons, physicians and patients have in the medical field[1]. The role of suture material in the development of wound surgical site infections has been the subject of speculation among surgeons since the 1960s[2]. A numerous number of bacteria may contaminate not only the tissue material but also the suture material. Once the sutures become contaminated it is difficult for local tissue defense or antibiotics to eliminate the bacteria and prevent infection[3-4]. Therefore it is very important to take note of the antimicrobial properties of a suture before using it in the wound litigation.

Silk fibers in the form of sutures have been used for centuries due to its ability to offer a wide range of properties. They are well known for their impressive mechanical properties, biocompatibility, environmental morphologic flexibility and stability[5].

Poly Epsilon-Caprolactone (PCL) is a widely used polymer in the field of medical research due to its appealing properties as linear aliphatic polyester that is biodegradable whose biocompatibility, low melting and elastomeric properties[6].

A number of studies showed a considerable decrease in the bacterial adherence to triclosan and chitosan coated sutures in vitro[7-9]. Therefore the main aim of this study is to try to explore the use of Sulfamethoxazole Trimethoprim as a suitable antibacterial coating agent on braided silk sutures in order to produce antimicrobial coated silk sutures which can posses the properties that match the current ones used in the medical field today.

1 MATERIALS AND METHODS

1.1Suturematerial

The silk suture that was used was procured from, Jiangsu Medical Supplies Ltd Co. in China. It was a size 2-0 silk suture of 0.320-0.331 mm diameter.

1.2Preparationoftheantimicrobialcoatingagent

Compound Sulfamethoxazole (SMZ) tablets a synergic drug made from a combination of Sulfamethoxazole and Trimethoprim where used as the antibacterial agent. A biodegradable polymer, Polycaprolactone (PCL) of 80 000 molecular weight was chosen to act as the drug carrier polymer add on for the suture.

2500 μg/mL of antibacterial agent was first suspended in acetic acid and homogenized at high speed (250 rev/min) for 10 minutes to reduce the gathering of particles. Then the coating agent, PCL was added into the resulting suspension and stirred for 1 hr at high speed (350 rev/min) to build up the drug concentration of 10% under sterile conditions using the same method[10].

1.3Testorganisms

Staphylococcus aureus (ATCC25923) and Escherichia coli (ATCC25922) were used for in vitro tests. All the strains were cultured to late logarithmic growth phase on agar plates at 37℃ for 18 hrs before conducting tests under aseptic conditions in a laminar airflow. The colonies where touched with a loop and then transferred to a tryptone soy broth (TSB) and incubated at 37℃ until the growth reached turbidity equal to or greater than that of 0.5 McFarland standard. The culture was then diluted using broth to give a turbidity of 1×10^8 (CFU)/mL bacterium concentration.

1.4Coatingprocess

The sterile sutures were first coated with SMZ solution only and then another set of sutures were coated with SMZ+PCL in solution using a dip coating method[11]. A uniform distribution of the polymer coating along the length of the suture was done through the use of a roller drying system as shown in the following figure (Fig. 1).

圖1 涂裝設(shè)備示意圖Fig.1 The schematic diagram of the coating equipment

1.Uncoatedbraidedsilksuture,2.Dipcoatingtank,3.Dippingrollers,4.Rubberpressrollers,5.Coatedbraidedsilksuture

1.5Evaluationofantibacterialsuture

After coating the silk suture with antibacterial agent, then an in vitro performance evaluation on antimicrobial properties of suture was done. This included the zone of inhibition assay,sustained efficacy assay,scanning electron microscopy tests, and drug release evaluation whereby the suture without coating acted as the control

1.5.1 Zone of inhibition Assay

A qualitative agar diffusion test was carried out on the coated silk sutures of 5 cm in length. It was done according to the antimicrobial performance evaluation (Zone of inhibition assay) standard (ISO 20645:2004) Determination of antibacterial properties - Part 1: agar diffusion method[12]. The zone of inhibition diameter was measured using an electronic Venire Calipers measuring instrument. Pieces of braided silk sutures (5 cm each) with and without antibacterial agent were challenged in vitro with indicator strains of selected test organisms and incubated at 37°C for 24 h and examined for zones of inhibition.

1.5.2 Sustained efficacy Assay

Five-centimeter sections of braided silk sutures with antibacterial agent were evaluated by zone of inhibition assays, as described above. After 24 hrs of incubation at 37°C, suture samples were transferred daily onto new Petri plates growing a similar number of bacteria[13]. The assay was terminated when the sutures ceased to inhibit bacterial growth.

The inhibition zone diameter was calculated according to the following formula[14]:

H= (D-d)/2

WhereHis inhibition zone (mm)

Dis the total diameter of specimen and inhibition zone (mm)

dis the total diameter of specimen (mm)

1.5.3 Drug release study under static conditions

The study of drug release was done using a UV VIS Spectrophotometer (TU-1901, Beijing, China) to compare the drug release of sutures coated with SMZ only and those coated with SMZ+PCL. The sutures where divided into two sets whereby each set had four 5 cm samples of coated sutures. They where immersed in 4 mL PBS Solution (pH 7.4) and left under static conditions for 1 day[15]. The supernatant was replaced with fresh PBS Solution every day until it showed no traces of SMZ in the UV VIS spectrophotometer. The amount of drug released in the supernatant was determined by observing the absorbance of the supernatant solution at 259 nm using the UV VIS Spectrophotometer. The value of absorbance was then used in the equation y=mx (standard absorbance curve)to calculate the concentration of compound SMZ in the solution.

圖2 SMZ標(biāo)準(zhǔn)吸收曲線Fig.2 The standard absorbance curve for SMZ

1.6Surfacemorphologicalanalysis

The scanning electron microscope (SEM, HITACHI/SU8010, JEOL, Japan) was used to observe the effect of antimicrobial coating on the suture. SEM images of sutures coated with SMZ only where obtained and then compared with SEM images of sutures coated with both PCL and SMZ.

2 RESULTS AND DISCUSSION

2.1Zoneofinhibitionassay

The sutures coated with SMZ demonstrated antibacterial efficacy against both test strains. The antibacterial treated sutures prevented both the test strains from colonizing and growing on the suture surface and inhibited both gram positive and gram negative bacteria. However the zone of inhibition results for sutures first coated with SMZ only showed larger zone diameters compared to the ones coated with both PCL and SMZ. As shown in figure 3 it is seen that picture (b)has a larger zone diameter than (a) against both test strains. This shows that the introduction of PCL into the antibacterial coating solution helped enhance the viscosity of the coating agent solution, thus improving the better binding of coating agent onto the silk fibres. The larger zone diameters of sutures coated with SMZ only, show that there was an outburst of drug release from the surface of the sutures. The polymetric structure of PCL helps retain the antibacterial particles on the braided structure so that they are not released at once but are released at slow controlled rate. This is good for the production of longlasting antibacterial sutures.

圖3 抑菌試驗(yàn)區(qū)Fig.3 Zone of inhibition assay, (a) SMZ+PCL coated suture (b) SMZ only coated suture

表1 抑菌試驗(yàn)區(qū)Tab.1 Zone of inhibition assay

2.2Sustained efficacy assay

Sustained efficacy against S. aureus and E. coli was observed for the sutures coated with SMZ+PCL coating agent. As shown in Table 2, a zone of inhibition that is greater 1mm was observed for up to 4 days compared to only 2 days for sutures coated with SMZ only. SMZ was continually released from the SMZ+PCL coated suture and therefore antibacterial efficacy continued for up to 4 days. The sutures coated with SMZ alone, show that the antibacterial agent was released at once and therefore antibacterial efficacy stopped after 2 days.

表2 抑菌效果 Tab.2 Sustained efficacy assay

2.3Drugreleasestudy

The SMZ+PCL combination on the silk suture showed best results. Traits of SMZ drug where observed for up to 4 days as compared to only 2 days for sutures coated with SMZ only. The graph in figure 4 below show that, the drug embedded on the surface of the suture is released faster initially and the remaining residual drug inside the structure of the suture is released slowly when the suture is coated with PCL+SMZ. This indicates that there is a possibility of drug release from suture even after a day or so when the suture is used on the patients' wound litigation.

圖4 藥物釋放動(dòng)力學(xué)Fig.4 Drug release kinetics

2.4Surfacemorphologicalanalysis

Figure 5 shows a smoother surface on the suture treated with PCL+SMZ as compared to suture only treated with SMZ only. The SEM images show that a stable and regular coating was applied on the surface of the suture after the addition of PCL into the coating agent. This shows relatively good properties for sutures as it prevents friction during suturing process.

圖5 SEM纖維紡織顯微圖Fig.5 SEM micrographs of braided silk suture (a)SMZ treated suture (b)SMZ+PCL treated suture

3 CONCLUSION

Sulfamethoxazole Trimethoprim is a suitable anti-bacterial agent for braided silk sutures. However a biodegradable polymer like PCL has to be applied with it for it to provide stable and sustainable antibacterial efficacy. Therefore it can be concluded that PCL+SMZ can be used as a coating agent for silk sutures in order for them to provide sustained antibacterial efficacy.

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TheDevelopmentofSustainedReleaseAntimicrobialSilkSutures

Pethile Sibanda, Chen Xiaojie, Wang Lu*

Key Laboratory of Textile Science and Technology of Ministry of Education, College of Textiles, Donghua University( Shanghai, 201620)

In recent years, surgical site infections (SSIs) has been confirmed to be closely relative to sutures, and sutures possessing antibacterial effect are being developed in attempt to reduce bacterial adherence and colonization of on the surface of suture materials. This study was done in a bid to develop a braided silk suture with antibacterial properties by coating the surface of the suture with an antibacterial agent, Sulfamethoxazole Trimethoprim (SMZ). For the sake of sustained antibacterial efficacy, a drug carrier polymer, Polycaprolactone (PCL) was introduced as the coating agent. Antimicrobial tests against gram negative bacteria Escherichia coli (ATCC25922) and gram positive bacteria Staphylococcus aureus (ATCC25923) were then carried out to compare the effects of coating the silk suture with SMZ and SMZ+PCL, which included zone of inhibition, sustained efficacy and drug release assay. The results revealed that both sutures with SMZ alone and with SMZ+PCL showed zone of bacterial inhibition, indicating certain antibacterial property.The sutures coated with SMZ+PCL demonstrateda better sustained antibacterial efficacy.

surgical site infections (SSIs), silk braided suture, antimicrobial coating agent, zone of inhibition assay, sustained antibacterial efficacy

10.3969/j.issn.1674-1242.2014.01.003

王璐，教授，E-mail:wanglu@dhu.edu.cn

TS 101.4

A

1674-1242(2014)01-0013-05

2014-01-27)