• Users Online: 405
  • Print this page
  • Email this page


 
 Table of Contents  
ORIGINAL ARTICLE
Year : 2019  |  Volume : 9  |  Issue : 3  |  Page : 179-184

Prevalence of microbial contamination in donor corneas


1 Department of Ophthalmology, Chang Gung Memorial Hospital, Chiayi, Taiwan
2 Department of Medicine, Chang Gung University College of Medicine, Taoyuan; Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou, Taiwan
3 Department of Infection, Chang Gung Memorial Hospital, Chiayi, Taiwan
4 Department of Ophthalmology, Chang Gung Memorial Hospital, Chiayi; Department of Medicine, Chang Gung University College of Medicine, Taoyuan, Taiwan

Date of Submission11-Jun-2018
Date of Acceptance29-Sep-2018
Date of Web Publication12-Sep-2019

Correspondence Address:
Dr. Li-Ju Lai
Department of Ophthalmology, Chiayi Chang Gung Memorial Hospital, No. 6, West Section, Chia-Pu Road, Pu-Zih City, Chia-Yi County 61363
Taiwan
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/tjo.tjo_60_18

Rights and Permissions
  Abstract 


BACKGROUND/PURPOSE: Postoperative infection is the most disastrous complication of penetrating keratoplasty (PK). Corneoscleral rim culture provided information regarding subsequent infections. Our aims were to identify the incidence of microbial contamination in donor corneas and to report the recovery of bacteria with two culture methods, i.e., conventional culture media after aerobic/anaerobic cotton swabs and blood culture media (Fastidious Antibiotic Neutralization [FAN]).
MATERIALS AND METHODS: A total of 118 patients underwent PK. Corneoscleral rim cultures were performed using aerobic/anaerobic culture cotton swabs (Transystem™, COPAN, Italia) with subsequent convention media and blood culture media (FAN bottle, BD BACTEC™, USA). The results of the different methods were reported and analyzed.
RESULTS: Microorganisms were recovered from 24 in total 118 cases (20.3%, n = 118), 14 from blood culture media (FAN) (11.8%, n = 118), 9 from conventional culture media after aerobic/anaerobic cotton swabs (7.63%, n = 118), and 2 from fungus culture (1.69%, n = 118). The most commonly identified pathogen was coagulase-negative Staphylococcus (CoNS) (n = 13, 54.2%), and more isolates of CoNS and staphylococcus aureus were recovered from blood culture media (FAN) than those from conventional culture media after aerobic/anaerobic cotton swabs (13 vs. 4,P= 0.05). Conversely, more nonfermentative Gram-negative bacilli were recovered from conventional culture media after aerobic/anaerobic cotton swabs. None of the 24 cases with positive corneoscleral rim cultures reported ocular infection for the recipients in at least 6 months' follow-up.
CONCLUSION: The conventional culture media after aerobic/anaerobic cotton swabs and blood culture media (FAN) did not yield identical isolates of bacteria. The blood culture media (FAN) could further yield Gram-positive bacteria in addition to those recovered from convention media. It seemed adding gentamicin and streptomycin could achieve bacteriostatic effect instead of the bactericidal effect. The administration of postoperative antibiotic in the recipient was suggested.

Keywords: Corneoscleral rim cultures, penetrating keratoplasty, postpenetrating keratoplasty infection


How to cite this article:
Chen NN, Wu PL, Chen HC, Huang TY, Lai LJ. Prevalence of microbial contamination in donor corneas. Taiwan J Ophthalmol 2019;9:179-84

How to cite this URL:
Chen NN, Wu PL, Chen HC, Huang TY, Lai LJ. Prevalence of microbial contamination in donor corneas. Taiwan J Ophthalmol [serial online] 2019 [cited 2023 Apr 2];9:179-84. Available from: https://www.e-tjo.org/text.asp?2019/9/3/179/251056

Nan-Ni Chen, and Pei-Lun Wu had equal contribution to this work.





  Introduction Top


Keratoplasty (corneal transplantation) is a surgical procedure where a damaged or diseased cornea is replaced by donated corneal tissue (the graft). Infections, following penetrating keratoplasty (PK), including microbial keratitis and endophthalmitis, are devastating complications and the incidence has been reported to be approximately 0.2%–0.77% for endophthalmitis [1] and 6.5%–10.5% for microbial keratitis.[2],[3],[4] It resultsin further surgery, including therapeutic PK with an incidence ranging from 9.5% to 30.7%; and evisceration from 7.1% to 9% in those infected eyes [2],[3],[4] Recently, it is debated for routine culture involving corneoscleral rim during implantation on the basis of cost-effectiveness.[5],[6],[7],[8],[9],[10] However, microbiological testing of media and/or remaining scleral rim postoperatively is still recommended by the Eye Bank Association of America and the European Eye Bank Association.[11],[12] Since the corneoscleral rim cultures could benefit in earlier infection detection, and the better detection rate for aerobic and anaerobic microbes becomes a crucial issue.

In literature, these were inconsistent methods in obtaining microbial culture at cornea transplantation, involving conventional culture media after aerobic/anaerobic cotton swabs or blood culture media. In fact, complex issues including different antibiotic supplementations of the preservation medium and types of culture medium to increase positive detection rate from aerobic and anaerobic microbes were involved in corneoscleral rim cultures. Conventional culture media after aerobic/anaerobic cotton swabs usually were composed of blood agar, chocolate agar, and thioglycolate broth in cultures of the corneoscleral rim [2],[3],[7],[10],[13],[14],[15],[16] Recently, blood culture media (Fastidious Antibiotic Neutralization [FAN]) which contains agents for neutralization of antibiotic were developed to alleviate the influence of added antibiotics.[17],[18],[19] Indeed, the modern cornea storage media such as Optisol GS, which contained gentamicin and streptomycin could possible result in a higher false-negative recovery rate. The current study aimed to report the culture result of corneoscleral rim at transplantation surgery from conventional culture media after aerobic/anaerobic cotton swabs and blood culture media (FAN).


  Materials and Methods Top


The medical charts of 142 patients receiving PK from January 2000 to January 2017 in Chiayi Chang Gung Memorial Hospital were reviewed. All patients receiving PK were prescribed wide spectrum topical antibiotics after surgery. Twenty-four patients were excluded because of lack of both culture methods. One hundred and eighteen (n = 118) cases were collected for aerobic/anaerobic culture results by conventional culture media after aerobic/anaerobic cotton swabs (Transystem™, COPAN, Italia) and blood culture media (FAN) (BD BACTEC™, America) [Figure 1]. Convention media included chocolate agar, sheep blood agar, and thioglycolate broth at 37°C. Sabouraud agar plates were also obtained and maintained at 25°C to enhance fungal growth. Positive microbial cultures were defined as growth of the same pathogen on 2 or more culture media. The positive fungal culture was defined on morphology.
Figure 1: Flowchart of study design

Click here to view


The medical charts of patients receiving PK were reviewed.

All the donor corneas were obtained from the National Eye Bank of Taiwan and American Eye Bank. Our study was approved by the Ethics Committee of the Chang Gung Memorial Hospital (IRB: 201600959B0). Clinical information including recipient characteristics, surgical details, and postoperative outcomes were collected and analyzed. Microbiological studies in corneoscleral rim were carried out during operation, using conventional culture media after aerobic/anaerobic cotton swabs and blood culture media (FAN), which were shown in [Figure 2]. The preserving solution of donor cornea (5 ml) was added to the Blood culture media (FAN). On the other hand, aerobic/anaerobic culture cotton swabs scraped donor corneoscleral rim surface and were soaked in the preserving solution of donor cornea, which further inoculated in conventional culture media. The remaining donor corneoscleral rim tissue was sent for fungus culture afterward.
Figure 2: Culture media used in corneoscleral rim culture: (a) Aerobic blood culture media, (b) anaerobic blood culture media, (c) aerobic culture cotton swab, (d) anaerobic culture cotton swab

Click here to view


Contingency tables and mean values of recipient characteristics were analyzed between cases and controls using Chi-square test as described by McNemar for categorical variables. P < 0.05 is considered statistically significant.


  Results Top


The mean age of our patients was 68 years old (range 7–89 years), and of them, 74 were male (62.7%), 44 were female (37.3%). The laterality was equally distributed with 61 right eyes (51.7%) and 57 left eyes (48.3%). The leading indication for PK in our patients were postinfectious corneal scarring (n = 58, 49.2%), refractory corneal ulcers (n = 20, 16.9%), regraft (n = 16, 13.6%), aphakic or pseudophakic bullous keratopathy (n = 11, 9.3%), and traumatic corneal scarring (n = 7, 5.9%). The patient's characteristics of age, gender, diagnosis, and source of cornea are identified as shown in [Table 1].
Table 1: Characteristics of recipient and indications for penetrating keratoplasty

Click here to view


Microorganisms were recovered from 24 in total 118 cases (20.3%, n = 118), 14 by blood culture media (FAN) (11.8%, n = 118), 9 by conventional culture media after aerobic/anaerobic cotton swabs (7.63%, n = 118), and 2 in fungus culture (1.69%, n = 118). Pathogens identified and the culture methods used are shown in [Table 2]. Interestingly, pathogen recovered from blood culture system (FAN) was not identical to those recovered from swab culture system.
Table 2: Comparative yields of bacteria in Fastidious Antibiotic Neutralization blood culture bottles and in conventional culture media (Swabs methods

Click here to view


Among 24 positive corneoscleral rim cultures, the most common pathogen identified was coagulase-negative Staphylococcus (CoNS) (n = 13, 54.2%), with decreasing frequency as follows: Staphylococcus epidermidis (n = 2, 8.3%), Stenotrophomonas maltophilia (n = 2, 8.3%), Staphylococcus aureus (n = 1, 4.2%), Viridans streptococcus (n = 1, 4.2%), Staphylococcus haemolyticus (n = 1, 4.2%), Nocardia spp. (n = 1, 4.2%), Gram-positive bacilli (n = 1, 4.2%), Acremonium (n = 1, 4.2%), and Candida spp. (n = 1, 4.2%). The microorganisms identified in our study were shown in [Table 3].
Table 3: Microorganisms identified in corneoscleral rim culture

Click here to view


One case isolated two pathogens, CoNS in blood culture media (FAN) and Nocardia spp. in conventional culture media after aerobic/anaerobic cotton swabs, respectively. Otherwise, there was no pathogen identified in both methods. There was no correlation between these two methods using Chi-square test (χ2 = 0.005, P= 0.648).

As compared with conventional culture media after aerobic/anaerobic cotton swabs, more isolates of CoNS and S. aureus (13 vs. 4, P= 0.052, Odds Ratio: 3.25) and V. streptococcus (1 vs. 0) were recovered from blood culture media (FAN). Conversely, more nonfermentative Gram-negative bacilli S. maltophilia (2 vs. 0) and Gram-positive bacilli (1 vs. 0) were recovered from conventional culture media after aerobic/anaerobic cotton swabs. None of the 24 cases with positive corneoscleral rim cultures resulted in ocular infection of the recipient for at least 6 months' follow-up.


  Discussion Top


The most significant finding of the present study was that conventional culture media after aerobic/anaerobic cotton swabs and blood culture media (FAN) did not yield identical isolates of bacteria. That was, either culture system had its own advantages and limitations in yielding the bacteria residing the corneoscleral rim. This issue became complex since evolving techniques, such as adding effective spectrum antibiotics in preservation mediums, were developed. It was reported that the combination of gentamicin and streptomycin in 4°C significantly improve anti-microbial activity against S. aureus, S. epidermidis, Propionibacterium acnes,  Escherichia More Details coli, and Pseudomonas aeruginosa, which were common pathogens leading to postoperative endophthalmitis.[20] The present study included cases after the year 2000 to meet the current standards as storage media, culture techniques, and transplantation technique.[21] We found that the conventional medium only yield 7.6%, while blood culture media (FAN) recovered 11.8%. With the advances in disinfection techniques such as better iodine sterilization of donor, and adding antibiotics in preservation medium, a lower rate of 7.6% for positive corneoscleral rim culture by conventional media was shown as compared to literature that ranged from 11% to 39%.[22] However, the blood culture media (FAN) could further yield bacterial isolates that were not recovered by convention media. It seemed adding gentamycin could achieve bacteriostatic effect instead of the bactericidal effect. These results supported the continuity of antibiotic usage in the donor until the local immunity was completely recovered.

In literature, direct inoculation and swab with subsequent convention medium have been employed for corneoscleral rim culture.[4],[7],[10],[13],[16],[23] However, it seemed the positive rate would be underestimated if there were antibiotics in the preservation medium. Blood culture media (FAN), which contains agents for neutralization of antibiotic, seemed more logical for corneoscleral rim culture because of the antibiotics in the preservation medium.[17],[18],[19] We did find a further detection of Gram-positive pathogen in this method. More isolates of CoNS and S. aureus were recovered in blood culture media (FAN) as compared to conventional culture media after aerobic/anaerobic cotton swabs (13 vs. 4) in the present study. It has been reported that the medium contained in FAN bottles have been shown superior recovery for Staphylococci.[17] In spite of the limited case number, it was noteworthy that using blood culture media (FAN) could recover more CoNS and S. aureus in corneoscleral rim cultures which was reported clinically significant species following keratoplasty. Besides, discrepancies of recovered microbial pattern between these two methods were probably partially explained by lower oxygen content in FAN bottles. For example, S. maltophilia, which is strictly dependent on the oxygen concentration of the medium was only recovered in conventional culture media in the present study, could be associated with the lower oxygen content in FAN bottles. Similarly, it was also possible that more nonfermentative Gram-negative bacilli were recovered in conventional culture media because of higher oxygen tension.

Controversy in prevailing pathogens existed in microbial keratitis following PK in Taiwan.[2],[3] Chen et al. have demonstrated the most frequently isolated microbes were Gram-negative microbes (50%), fungus (26%), and Gram-positive microbes (24%), which is contrasted by Sun et al. as Gram-positive microbes (58%), Gram-negative microbes (22%), and fungus (20%).[2],[3] In Germany, the contamination rate and spectrum of microbes in 3306 organ-cultured donor corneas were shown that the most frequently isolated microbes were Enterococci (19%), Staphylococci (10.8%), and Candida (37.4%).[24] While in the National Eye Bank of Taiwan,[25] 39 out of 232 collected donor corneas isolated microbes (16.8%), with Staphylococcus species (57%) predominant. Because of the changing microbial environment in different region across time, the methods to recover the truly existed microbes seemed important. In the current study, we have shown that combination of blood culture media (FAN) and conventional culture media after aerobic/anaerobic cotton swabs could recover the wide spectrums of microbes existing in the corneoscleral rim.

Even though several recent studies challenged the cost-effectiveness of corneoscleral rim culture, it was evident that a positive corneoscleral culture was associated with 5 times more frequent among recipients developing endophthalmitis than among negative culture.[15],[26] Postoperative infection is the most disastrous complication of PK.[27],[28],[29] Several studies emphasized on early diagnosis and treatment based on culturing of the preservation medium.[5],[6],[30] If local medical therapy for infection succeeded, early removal of the infected corneal graft may be prevented.[31] Therefore, the corneoscleral rim culture at transplantation did provide important clinical information for the ophthalmologist.

The current study was limited by small number of patients. However, it revealed different patterns of bacterial isolate from the two culture system. Longer term follow-up is suggested.


  Conclusion Top


The aerobic/anaerobic cotton swabs system with convention media and blood culture media (FAN) did not yield identical isolates of bacteria. The blood culture media (FAN) bottle could further recover Gram-positive bacteria in addition to those recovered from convention media. It seemed adding gentamycin and streptomycin could achieve bacteriostatic effect instead of bactericidal effect. The administration of postoperative antibiotics in the recipient was suggested.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

The authors declare that there are no conflicts of interests of this paper.



 
  References Top

1.
Krachmer JH, Holland EJ, Mannis MJ. In: Cornea, 2nd ed. Vol. 2. Surgery of the Cornea and Conjunctiva, Corneal Surgery: Elsevier; 2005.  Back to cited text no. 1
    
2.
Chen HC, Lee CY, Lin HY, Ma DH, Chen PY, Hsiao CH, et al. Shifting trends in microbial keratitis following penetrating keratoplasty in Taiwan. Medicine (Baltimore) 2017;96:e5864.  Back to cited text no. 2
    
3.
Sun JP, Chen WL, Huang JY, Hou YC, Wang IJ, Hu FR, et al. Microbial keratitis after penetrating keratoplasty. Am J Ophthalmol 2017;178:150-6.  Back to cited text no. 3
    
4.
Sung MS, Choi W, You IC, Yoon KC. Factors affecting treatment outcome of graft infection following penetrating keratoplasty. Korean J Ophthalmol 2015;29:301-8.  Back to cited text no. 4
    
5.
Antonios SR, Cameron JA, Badr IA, Habash NR, Cotter JB. Contamination of donor cornea: Postpenetrating keratoplasty endophthalmitis. Cornea 1991;10:217-20.  Back to cited text no. 5
    
6.
Cameron JA, Antonios SR, Cotter JB, Habash NR. Endophthalmitis from contaminated donor corneas following penetrating keratoplasty. Arch Ophthalmol 1991;109:54-9.  Back to cited text no. 6
    
7.
Cornish KS, Ramamurthi S, Butcher I, Ramaesh K. Is microbiological analysis of donor cornea transport culture media necessary? Eur J Ophthalmol 2009;19:137-8.  Back to cited text no. 7
    
8.
Everts RJ, Fowler WC, Chang DH, Reller LB. Corneoscleral rim cultures: Lack of utility and implications for clinical decision-making and infection prevention in the care of patients undergoing corneal transplantation. Cornea 2001;20:586-9.  Back to cited text no. 8
    
9.
Matsumoto M, Suzuma K, Miyamura N, Imamura N, Kitaoka T. Conjunctival swabs and corneoscleral rim cultures from corneal transplantation donors as possible early indicators for posttransplant endopthalmitis. Jpn J Ophthalmol 2011;55:321-6.  Back to cited text no. 9
    
10.
Wilhelmus KR, Hassan SS. The prognostic role of donor corneoscleral rim cultures in corneal transplantation. Ophthalmology 2007;114:440-5.  Back to cited text no. 10
    
11.
European Business Aviation Association (EBAA). America EBAo: Medical Standards. Washington: EBAA; 2015.  Back to cited text no. 11
    
12.
Association EEB. Technical Guidelines for Ocular Tissue, Prague, Czech Republic: Association EEB; 2017.  Back to cited text no. 12
    
13.
Al-Assiri A, Al-Jastaneiah S, Al-Khalaf A, Al-Fraikh H, Wagoner MD. Late-onset donor-to-host transmission of Candida glabrata following corneal transplantation. Cornea 2006;25:123-5.  Back to cited text no. 13
    
14.
Alharbi SS, Alrajhi A, Alkahtani E. Endophthalmitis following keratoplasty: Incidence, microbial profile, visual and structural outcomes. Ocul Immunol Inflamm 2014;22:218-23.  Back to cited text no. 14
    
15.
Chen JY, Jones MN, Srinivasan S, Neal TJ, Armitage WJ, Kaye SB, et al. Endophthalmitis after penetrating keratoplasty. Ophthalmology 2015;122:25-30.  Back to cited text no. 15
    
16.
Ritterband DC, Shah MK, Meskin SW, Shapiro DE, Seedor JA, Koplin RS, et al. Efficacy and safety of moxifloxacin as an additive in optisol-GS a preservation medium for corneal donor tissue. Cornea 2006;25:1084-9.  Back to cited text no. 16
    
17.
Wilson ML, Weinstein MP, Mirrett S, Reimer LG, Feldman RJ, Chuard CR, et al. Controlled evaluation of BacT/alert standard anaerobic and FAN anaerobic blood culture bottles for the detection of bacteremia and fungemia. J Clin Microbiol 1995;33:2265-70.  Back to cited text no. 17
    
18.
Portillo ME, Salvadó M, Trampuz A, Siverio A, Alier A, Sorli L, et al. Improved diagnosis of orthopedic implant-associated infection by inoculation of sonication fluid into blood culture bottles. J Clin Microbiol 2015;53:1622-7.  Back to cited text no. 18
    
19.
Bourbeau P, Riley J, Heiter BJ, Master R, Young C, Pierson C, et al. Use of the bacT/Alert blood culture system for culture of sterile body fluids other than blood. J Clin Microbiol 1998;36:3273-7.  Back to cited text no. 19
    
20.
Smith TM, Popplewell J, Nakamura T, Trousdale MD. Efficacy and safety of gentamicin and streptomycin in optisol-GS, a preservation medium for donor corneas. Cornea 1995;14:49-55.  Back to cited text no. 20
    
21.
Kiatos E, Armstrong JJ, Hutnik CM, Tsioros SM, Malvankar-Mehta MS, Hodge WG, et al. The value of corneoscleral rim cultures in keratoplasty: A systematic review and cost-effectiveness analysis. Clinicoecon Outcomes Res 2017;9:459-74.  Back to cited text no. 21
    
22.
Inomata T, Ono K, Matsuba T, Shiang T, Di Zazzo A, Nakatani S, et al. Pre-banking microbial contamination of donor conjunctiva and storage medium for penetrating keratoplasty. Jpn J Ophthalmol 2017;61:369-77.  Back to cited text no. 22
    
23.
Melo GB, Bispo PJ, Yu MC, Pignatari AC, Höfling-Lima AL. Microbial profile and antibiotic susceptibility of culture-positive bacterial endophthalmitis. Eye (Lond) 2011;25:382-7.  Back to cited text no. 23
    
24.
Gruenert AK, Rosenbaum K, Geerling G, Fuchsluger TA. The influence of donor factors on corneal organ culture contamination. Acta Ophthalmol 2017;95:733-40.  Back to cited text no. 24
    
25.
National Eye Bank of Taiwan, editor. National Eye Bank of Taiwan, Annual report. Taipei: National Eye Bank of Taiwan; 2015.  Back to cited text no. 25
    
26.
Röck D, Wude J, Bartz-Schmidt KU, Yoeruek E, Thaler S, Röck T, et al. Factors influencing the contamination rate of human organ-cultured corneas. Acta Ophthalmol 2017;95:e706-12.  Back to cited text no. 26
    
27.
Ple-plakon PA, Shtein RM, Musch DC, Blachley T, Saponara F, Woodward MA, et al. Tissue characteristics and reported adverse events after corneal transplantation. Cornea 2013;32:1339-43.  Back to cited text no. 27
    
28.
Fasolo A, Capuzzo C, Fornea M, Franch A, Birattari F, Carito G, et al. Risk factors for graft failure after penetrating keratoplasty: 5-year follow-up from the corneal transplant epidemiological study. Cornea 2011;30:1328-35.  Back to cited text no. 28
    
29.
Jambulingam M, Parameswaran SK, Lysa S, Selvaraj M, Madhavan HN. A study on the incidence, microbiological analysis and investigations on the source of infection of postoperative infectious endophthalmitis in a tertiary care ophthalmic hospital: An 8-year study. Indian J Ophthalmol 2010;58:297-302.  Back to cited text no. 29
[PUBMED]  [Full text]  
30.
Pinna A, Zanetti S, Sotgiu M, Sechi LA, Fadda G, Carta F, et al. Identification and antibiotic susceptibility of coagulase negative staphylococci isolated in corneal/external infections. Br J Ophthalmol 1999;83:771-3.  Back to cited text no. 30
    
31.
Schotveld JH, Raijmakers AJ, Henry Y, Zaal MJ. Donor-to-host transmitted candida endophthalmitis after penetrating keratoplasty. Cornea 2005;24:887-9.  Back to cited text no. 31
    


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]


This article has been cited by
1 Donor related corneal graft infection: a review of literature and preventive strategies
Ketan Deogaonkar, Aravind Roy
Seminars in Ophthalmology. 2022; : 1
[Pubmed] | [DOI]
2 Eye bank and theatre factors for positive microbiological culture of corneoscleral rim and cornea storage medium in the real-world
Noelia Sabater-Cruz,Nausica Otero,Marina Dotti-Boada,José Ríos,Oscar Gris,José L. Güell,Ana Vilarrodona,Ricardo P. Casaroli-Marano
Eye. 2021;
[Pubmed] | [DOI]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Materials and Me...
Results
Discussion
Conclusion
References
Article Figures
Article Tables

 Article Access Statistics
    Viewed3444    
    Printed135    
    Emailed0    
    PDF Downloaded330    
    Comments [Add]    
    Cited by others 2    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]