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Dive into the research topics where Eugene Sherry is active.

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Featured researches published by Eugene Sherry.


Journal of Biomedical Materials Research Part B | 2010

Ceramic scaffolds produced by computer-assisted 3D printing and sintering: Characterization and biocompatibility investigations

Patrick H. Warnke; Hermann Seitz; Frauke Warnke; Stephan T. Becker; Sureshan Sivananthan; Eugene Sherry; Qin Liu; Jörg Wiltfang; Timothy Douglas

Hydroxyapatite (HAP) and tricalcium phosphate (TCP) are two very common ceramic materials for bone replacement. However, in general HAP and TCP scaffolds are not tailored to the exact dimensions of the defect site and are mainly used as granules or beads. Some scaffolds are available as ordinary blocks, but cannot be customized for individual perfect fit. Using computer-assisted 3D printing, an emerging rapid prototyping technique, individual three-dimensional ceramic scaffolds can be built up from TCP or HAP powder layer by layer with subsequent sintering. These scaffolds have precise dimensions and highly defined and regular internal characteristics such as pore size. External shape and internal characteristics such as pore size can be fabricated using Computer Assisted Design (CAD) based on individual patient data. Thus, these scaffolds could be designed as perfect fit replacements to reconstruct the patients skeleton. Before their use as bone replacement materials in vivo, in vitro testing of these scaffolds is necessary. In this study, the behavior of human osteoblasts on HAP and TCP scaffolds was investigated. The commonly used bone replacement material BioOss(R) served as control. Biocompatibility was assessed by scanning electron microscopy (SEM), fluorescence microscopy after staining for cell vitality with fluorescin diacetate (FDA) and propidium iodide (PI) and the MTT, LDH, and WST biocompatibility tests. Both versions were colonised by human osteoblasts, however more cells were seen on HAP scaffolds than TCP scaffolds. Cell vitality staining and MTT, LDH, and WST tests showed superior biocompatibility of HAP scaffolds to BioOss, while BioOss was more compatible than TCP. Further experiments are necessary to determine biocompatibility in vivo. Future modifications of 3D printed scaffolds offer advantageous features for Tissue Engineering. The integration of channels could allow for vascular and nerve ingrowth into the scaffold. Also the complex shapes of convex and concave articulating joint surfaces maybe realized with these rapid prototyping techniques.


Journal of Cranio-maxillofacial Surgery | 2009

The battle against multi-resistant strains: Renaissance of antimicrobial essential oils as a promising force to fight hospital-acquired infections

Patrick H. Warnke; Stephan T. Becker; Rainer Podschun; Sureshan Sivananthan; Ingo N. Springer; Paul A.J. Russo; Joerg Wiltfang; Helmut Fickenscher; Eugene Sherry

Hospital-acquired infections and antibiotic-resistant bacteria continue to be major health concerns worldwide. Particularly problematic is methicillin-resistant Staphylococcus aureus (MRSA) and its ability to cause severe soft tissue, bone or implant infections. First used by the Australian Aborigines, Tea tree oil and Eucalyptus oil (and several other essential oils) have each demonstrated promising efficacy against several bacteria and have been used clinically against multi-resistant strains. Several common and hospital-acquired bacterial and yeast isolates (6 Staphylococcus strains including MRSA, 4 Streptococcus strains and 3 Candida strains including Candida krusei) were tested for their susceptibility for Eucalyptus, Tea tree, Thyme white, Lavender, Lemon, Lemongrass, Cinnamon, Grapefruit, Clove Bud, Sandalwood, Peppermint, Kunzea and Sage oil with the agar diffusion test. Olive oil, Paraffin oil, Ethanol (70%), Povidone iodine, Chlorhexidine and hydrogen peroxide (H(2)O(2)) served as controls. Large prevailing effective zones of inhibition were observed for Thyme white, Lemon, Lemongrass and Cinnamon oil. The other oils also showed considerable efficacy. Remarkably, almost all tested oils demonstrated efficacy against hospital-acquired isolates and reference strains, whereas Olive and Paraffin oil from the control group produced no inhibition. As proven in vitro, essential oils represent a cheap and effective antiseptic topical treatment option even for antibiotic-resistant strains as MRSA and antimycotic-resistant Candida species.


Oral Oncology | 2009

Endocultivation: 3D printed customized porous scaffolds for heterotopic bone induction

Stephan T. Becker; H. Bolte; Oliver Krapf; Hermann Seitz; Timothy Douglas; Sureshan Sivananthan; Jörg Wiltfang; Eugene Sherry; Patrick H. Warnke

The aim of this study was to evaluate the ability of computer assisted designed (CAD) synthetic hydroxyapatite and tricalciumphosphate blocks to serve as precise scaffolds for intramuscular bone induction in a rat model. A central channel to allow for vessel pedicle or nerve integration was added. Natural bovine hydroxyapatite blocks served as controls to evaluate and compare biocompatibility of the new matrices. Individually designed 3D-printed rounded and porous hydroxyapatite (HA) and tricalcium phosphate (TCP) blocks were placed in pouches in the Musculus latissimus dorsi in 12 Lewis rats bilaterally. Bovine hydroxyapatite blocks with and without a central channel served as controls. Simultaneously, 200 microg rhBMP-2 in 1 ml sodium chloride was injected on both sides. For 8 weeks, bone generation was monitored by computer tomography and fluorescence labeling. The increase rates of bone density in CT examinations were higher in the HA groups (184-220 HU 8 weeks after implantation) compared to the TCP group (18 HU; p<0.0001). Microradiography and fluorescence microscopy 8 weeks after implantation showed new bone formation for all materials tested. For all scaffolds, toluidine staining revealed vital bone directly on the scaffold materials but also in the gaps between. It can be concluded from our data that the specially shaped hydroxyapatite and tricalcium phosphate blocks tested against the bovine hydroxyapatite blocks showed good biocompatibility and osteoinductivity in vivo. Further studies should explore if the stability of the individually designed blocks is sufficient to cultivate larger replacements without an external matrix for support.


Anz Journal of Surgery | 2003

Minimal invasive surgery for hip replacement: a new technique using the NILNAV hip system

Eugene Sherry; Michael Egan; Patrick H. Warnke; Antony Henderson

Background:  Minimal invasive surgical techniques are used for cruciate ligament reconstructions, unicondylar knee replacements and, more recently, for fixation of fractures. This is a report of the first instrumented technique for hip replacement using a 5‐cm incision without the need for a navigation system or X‐rays.


Journal of Materials Science: Materials in Medicine | 2009

Porous polymer/hydroxyapatite scaffolds: characterization and biocompatibility investigations

Timothy Douglas; Elżbieta Pamuła; Dominik Hauk; Jörg Wiltfang; Sureshan Sivananthan; Eugene Sherry; Patrick H. Warnke

Poly-lactic-glycolic acid (PLGA) has been widely used as a scaffold material for bone tissue engineering applications. 3D sponge-like porous scaffolds have previously been generated through a solvent casting and salt leaching technique. In this study, polymer–ceramic composite scaffolds were created by immersing PLGA scaffolds in simulated body fluid, leading to the formation of a hydroxyapatite (HAP) coating. The presence of a HAP layer was confirmed using scanning electron microscopy, energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy in attenuated total reflection mode. HAP-coated PLGA scaffolds were tested for their biocompatibility in vitro using human osteoblast cell cultures. Biocompatibility was assessed by standard tests for cell proliferation (MTT, WST), as well as fluorescence microscopy after standard cell vitality staining procedures. It was shown that PLGA–HAP composites support osteoblast growth and vitality, paving the way for applications as bone tissue engineering scaffolds.


Clinical Oral Implants Research | 2011

Comparison of in vitro biocompatibility of NanoBone(®) and BioOss(®) for human osteoblasts.

Qin Liu; Timothy Douglas; Christiane Zamponi; Stephan T. Becker; Eugene Sherry; Sureshan Sivananthan; Frauke Warnke; Jörg Wiltfang; Patrick H. Warnke

INTRODUCTION Scaffolds for bone tissue engineering seeded with the patients own cells might be used as a preferable method to repair bone defects in the future. With the emerging new technologies of nanostructure design, new synthetic biomaterials are appearing on the market. Such scaffolds must be tested in vitro for their biocompatibility before clinical application. However, the choice between a natural or a synthetic biomaterial might be challenging for the doctor and the patient. In this study, we compared the biocompatibility of a synthetic bone substitute, NanoBone(®) , to the widely used natural bovine bone replacement material BioOss(®) . MATERIAL AND METHODS The in vitro behaviour of human osteoblasts on both materials was investigated. Cell performance was determined using scanning electron microscopy (SEM), cell vitality staining and four biocompatibility tests (LDH, MTT, WST, BrdU). RESULTS We found that both materials showed low cytotoxicity and good biocompatibility. The MTT proliferation test was superior for Nanobone(®) . DISCUSSION Both scaffolds caused only little damage to human osteoblasts and justify their clinical application. However, NanoBone(®) was able to support and promote proliferation of human osteoblasts slightly better than BioOss(®) in our chosen test set-up. The results may guide doctors and patients when being challenged with the choice between a natural or a synthetic biomaterial. Further experiments are necessary to determine the comparison of biocompatibility in vivo.


Journal of Cranio-maxillofacial Surgery | 2010

Endocultivation: Does delayed application of BMP improve intramuscular heterotopic bone formation?

Patrick H. Warnke; H. Bolte; Kristina Schünemann; Tobias Nitsche; Sureshan Sivananthan; Eugene Sherry; Timothy Douglas; Jörg Wiltfang; Stephan T. Becker

INTRODUCTION The time point of Bone morphogenetic protein (BMP) delivery on matrices in vivo may play an important role. Delayed application could be advantageous as this would allow soft tissue (ST) ingrowth and vascularisation of scaffolds prior to BMP-loading. The aim of this study was to compare the application of BMP injected simultaneously during matrix implantation with delayed application four weeks after matrix implantation for endocultivation in a rat model. MATERIAL AND METHODS Bovine hydroxyapatite blocks were placed in pouches in the Musculus latissimus dorsi in 6 Lewis rats unilaterally to allow for soft tissue ingrowth. Four weeks later, a second block was inserted on the contralateral side of each rat. At that time point, 100microg rhBMP-2 in 2ml sodium chloride was injected on both sides to induce bone formation. For eight weeks, bone regeneration was monitored by computed tomography (CT) and fluorescent labelling. RESULTS The simultaneous and delayed BMP application groups were significantly different (p=0.01). Slightly lower bone densities were seen for the delayed BMP application with a mean of 588 Hounsfield Units (HU) (standard deviation (SD) 30HU). Simultaneous BMP application revealed slightly higher densities with a mean of 633HU (SD 30HU). The largest differences were observed when comparing bone density directly after implantation or at the end of the observation period (p<0.0001). CONCLUSION Bone density was slightly lower in the case of delayed application of BMP-2. The increase of bone density after application of BMP-2 was similar for both groups. Thus, delayed application of BMP had no advantageous effect in this particular study design. Further studies are needed to explore if varying delays, different material designs or special BMP application devices may alter these results.


Journal of Craniofacial Surgery | 2010

Antimicrobial peptide immunity protects human nasal and auricular cartilage against infection

Patrick H. Warnke; Paul Russo; Martin Hopfenziz; Bodo Kurz; Stephan T. Becker; Eugene Sherry; Ingo N. Springer; Sureshan Sivananthan

Background: Despite being impervious to surveillance by the adaptive immune system because of its lack of vascularity, infection of the nasal and auricular cartilage after surgery such as rhinoplasty or otoplasty is rare. Why is this so? Our goal was to determine whether the expression of antimicrobial peptides provides a previously unrecognized nonepithelial layer of innate immune defense within the nasal and auricular cartilage. Materials and Methods: Seven samples of nasal septum cartilage and 2 biopsies from auricular cartilage grafts were harvested during rhinoplasty and otoplasty procedures. Ten cadaveric samples of auricular and 9 samples of nasal cartilage were also obtained. Immunohistochemical staining was directed against the human &bgr;-defensin antimicrobial peptides (hBD) 1, 2, and 3. A semiquantitative analysis was performed to measure immunoreactivity. Results: All 3 human &bgr;-defensins were detected along the perichondral line and within the cartilage matrix in the nasal and auricular samples. Areas with positive immunohistochemical staining were also detected within chondrocyte cytoplasm. Conclusions: We provide the first evidence of antimicrobial peptide expression (hBD-1, -2 and -3) within the perichondrium and cartilage matrix layers of the nasal and auricular cartilage. This previously unrecognized innate immune function of perichondrocytes and chondrocytes may explain the resistance of the nasal and auricular cartilage to infection after surgical procedures despite the absence of a vascular system.


Surgery Today | 2006

Development of a new surgical gown : A multicenter study

Eugene Sherry; G. Deirmendjian; Patrick H. Warnke; Antony Henderson

found it remained closed during surgery, 91% (n = 81) found derobing easier, 65.3% (n = 47) agreed that it improved infection control, and 69.8% (n = 60) preferred it to other surgical gowns. This new surgical gown eliminates violations of sterile technique related to gown robing through its final flap closure. Surgeons no longer need to spin to secure the final flap of the gown. Almost half of the hospitals found that the new gown was faster to don than other gowns. However, the spread of responses to the difficulty of final closure of the gown was fairly even among the hospitals. One of the most important questions addressed its contribution to infection. Responses from three of the five hospitals indicated that the gown improved infection control, and most of the responses from the other two hospitals indicated that it may not affect the current status of infection control. The S-gown may be particularly useful in small, crowded operating rooms, especially in emergency disaster relief situations or other conditions where severe trauma or infectious disease may require strict adherence to sterile techniques for the safety of patients and surgical staff.


Biomaterials | 2006

Man as living bioreactor : Fate of an exogenously prepared customized tissue-engineered mandible

Patrick H. Warnke; Jörg Wiltfang; Ingo N. Springer; Yahya Açil; H. Bolte; Markus Kosmahl; Paul A.J. Russo; Eugene Sherry; Ulf Lutzen; Stefan Wolfart; Hendrik Terheyden

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Sureshan Sivananthan

Robert Jones and Agnes Hunt Orthopaedic Hospital

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Antony Henderson

University of New South Wales

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Paul A.J. Russo

Australian National University

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