Alastair J Sloan

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Professor Alastair J Sloan is an applied bioscientist and expert in the broad field of mineralised connective tissues, and since January 2020 current head of the Melbourne Dental School, University of Melbourne.

Contents

Biography

Following primary and secondary education in Poulton-Le-Fylde, Lancashire in the UK, Alastair obtained his BSc in Biomedical Sciences from the University of Wales in 1993 and his PhD in Oral Biology and Pathology from Faculty of Medicine and Dentistry at The University of Birmingham, UK in 1997. He is currently Head of School of the Melbourne Dental School, holding that position from 2020. Before that, in 2005, he developed his own lab at Cardiff University, and was awarded his personal chair in 2012. He was Head of Oral and Biomedical Sciences at the School of Dentistry between 2010 and 2015, Director of International (2012-2015) and Director of Research (2015-2017). He was Director of the Cardiff Institute for Tissue Engineering and Repair at Cardiff University and appointed Head of School at Cardiff University School of Dentistry in 2017 before moving to Melbourne.

Alastair Sloan's research is multi-disciplinary and in the broad field of mineralised connective tissues. He is interested in the reparative potential and behaviour of the dentine-pulp complex and bone, specifically the potential therapeutic manipulation of the dental pulp stem cells  : (DPSCs). This includes understanding the heterogeneity within dental pulp progenitor populations and potential therapeutic roles of these DPSCs in the wider context of regenerative medicine. His lab is also focused on development of 'smart' materials and drug delivery systems for use in oral and dental medicine.

Alastair has authored several books and book chapters in his field, as well as having his research widely published in leading medical, dental, tissue engineering and health policy journals including the Journal of Dental Research, The International Journal of Nanomedicine, BioMed Research International and The European Journal of Dental Education.

He has been interviewed by and written articles for Newspaper and TV media including the BBC, [1] the Wall Street Journal, [2] the Irish Daily Mail, [3] The Daily Mail [4] and The Times of India [5]

He is currently a research funding panel member for the EU and Research Foundation, Flanders, having previously been a member of the UK NC3Rs grant assessment panel. He sits on the Nominations Committee of the International Association for Dental Research (IADR) and is a member of both the British Society for Oral and Dental Research and Australian and New Zealand Division of the IADR.

Selected publications

Sloan has published more than 100 articles and book chapters in a large number of journals on dentistry, bone repair and general health, including:

Source [6]

Awards

Professor Sloan has received multiple international awards including:

Related Research Articles

<span class="mw-page-title-main">Dentin</span> Calcified tissue of the body; one of the four major components of teeth

Dentin or dentine is a calcified tissue of the body and, along with enamel, cementum, and pulp, is one of the four major components of teeth. It is usually covered by enamel on the crown and cementum on the root and surrounds the entire pulp. By volume, 45% of dentin consists of the mineral hydroxyapatite, 33% is organic material, and 22% is water. Yellow in appearance, it greatly affects the color of a tooth due to the translucency of enamel. Dentin, which is less mineralized and less brittle than enamel, is necessary for the support of enamel. Dentin rates approximately 3 on the Mohs scale of mineral hardness. There are two main characteristics which distinguish dentin from enamel: firstly, dentin forms throughout life; secondly, dentin is sensitive and can become hypersensitive to changes in temperature due to the sensory function of odontoblasts, especially when enamel recedes and dentin channels become exposed.

Tooth whitening or tooth bleaching is the process of lightening the color of human teeth. Whitening is often desirable when teeth become yellowed over time for a number of reasons, and can be achieved by changing the intrinsic or extrinsic color of the tooth enamel. The chemical degradation of the chromogens within or on the tooth is termed as bleaching.

<span class="mw-page-title-main">Pulp (tooth)</span> Part in the center of a tooth made up of living connective tissue and cells called odontoblasts

The pulp is the connective tissue, nerves, blood vessels, and odontoblasts that comprise the innermost layer of a tooth. The pulp's activity and signalling processes regulate its behaviour.

<span class="mw-page-title-main">Epidermal growth factor</span> Protein that stimulates cell division and differentiation

Epidermal growth factor (EGF) is a protein that stimulates cell growth and differentiation by binding to its receptor, EGFR. Human EGF is 6-kDa and has 53 amino acid residues and three intramolecular disulfide bonds.

<span class="mw-page-title-main">Dental abrasion</span> Medical condition

Abrasion is the non-carious, mechanical wear of tooth from interaction with objects other than tooth-tooth contact. It most commonly affects the premolars and canines, usually along the cervical margins. Based on clinical surveys, studies have shown that abrasion is the most common but not the sole aetiological factor for development of non-carious cervical lesions (NCCL) and is most frequently caused by incorrect toothbrushing technique.

<span class="mw-page-title-main">Enamel organ</span> Aggregate of cells involved in tooth development

The enamel organ, also known as the dental organ, is a cellular aggregation seen in a developing tooth and it lies above the dental papilla. The enamel organ which is differentiated from the primitive oral epithelium lining the stomodeum. The enamel organ is responsible for the formation of enamel, initiation of dentine formation, establishment of the shape of a tooth's crown, and establishment of the dentoenamel junction.

Pulpitis is inflammation of dental pulp tissue. The pulp contains the blood vessels, the nerves, and connective tissue inside a tooth and provides the tooth's blood and nutrients. Pulpitis is mainly caused by bacterial infection which itself is a secondary development of caries. It manifests itself in the form of a toothache.

<span class="mw-page-title-main">Dentinogenesis imperfecta</span> Medical condition

Dentinogenesis imperfecta (DI) is a genetic disorder of tooth development. It is inherited in an autosomal dominant pattern, as a result of mutations on chromosome 4q21, in the dentine sialophosphoprotein gene (DSPP). It is one of the most frequently occurring autosomal dominant features in humans. Dentinogenesis imperfecta affects an estimated 1 in 6,000-8,000 people.

Dentin hypersensitivity is dental pain which is sharp in character and of short duration, arising from exposed dentin surfaces in response to stimuli, typically thermal, evaporative, tactile, osmotic, chemical or electrical; and which cannot be ascribed to any other dental disease.

<span class="mw-page-title-main">Odontoma</span> Benign tumour of dental tissue

An odontoma, also known as an odontome, is a benign tumour linked to tooth development. Specifically, it is a dental hamartoma, meaning that it is composed of normal dental tissue that has grown in an irregular way. It includes both odontogenic hard and soft tissues. As with normal tooth development, odontomas stop growing once mature which makes them benign.

In dentistry, the hydrodynamic or fluid movement theory is one of three main theories developed to explain dentine hypersensitivity, which is a sharp, transient pain arising from stimuli exposure. It states that different types of stimuli act on exposed dentine, causing increased fluid flow through the dentinal tubules. In response to this movement, mechanoreceptors on the pulp nerves trigger the acute, temporary pain of dentine hypersensitivity.

<span class="mw-page-title-main">Pulpotomy</span>

Pulpotomy is a minimally invasive procedure performed in children on a primary tooth with extensive caries but without evidence of root pathology. The minimally invasive endodontic techniques of vital pulp therapy (VPT) are based on improved understanding of the capacity of pulp (nerve) tissues to heal and regenerate plus the availability of advanced endodontic materials. During the caries removal, this results in a carious or mechanical pulp exposure (bleeding) from the cavity. During pulpotomy, the inflamed/diseased pulp tissue is removed from the coronal pulp chamber of the tooth leaving healthy pulp tissue which is dressed with a long-term clinically successful medicament that maintains the survival of the pulp and promotes repair. There are various types of medicament placed above the vital pulp such as Buckley's Solution of formocresol, ferric sulfate, calcium hydroxide or mineral trioxide aggregate (MTA). MTA is a more recent material used for pulpotomies with a high rate of success, better than formocresol or ferric sulfate. It is also recommended to be the preferred pulpotomy agent in the future. After the coronal pulp chamber is filled, the tooth is restored with a filling material that seals the tooth from microleakage, such as a stainless steel crown which is the most effective long-term restoration. However, if there is sufficient remaining supporting tooth structure, other filling materials such as amalgam or composite resin can provide a functional alternative when the primary tooth has a life span of two years or less. The medium- to long-term treatment outcomes of pulpotomy in symptomatic permanent teeth with caries, especially in young people, indicate that pulpotomy can be a potential alternative to root canal therapy (RCT).

Dental pulp stem cells (DPSCs) are stem cells present in the dental pulp, which is the soft living tissue within teeth. DPSCs can be collected from dental pulp by means of a non-invasive practice. It can be performed with an adult after simple extraction or to the young after surgical extraction of wisdom teeth. They are pluripotent, as they can form embryoid body-like structures (EBs) in vitro and teratoma-like structures that contained tissues derived from all three embryonic germ layers when injected in nude mice. DPSCs can differentiate in vitro into tissues that have similar characteristics to mesoderm, endoderm and ectoderm layers. They can differentiate into many cell types, such as odontoblasts, neural progenitors, osteoblasts, chondrocytes, and adipocytes. DPSCs were found to be able to differentiate into adipocytes and neural-like cells. These cells can be obtained from postnatal teeth, wisdom teeth, and deciduous teeth, providing researchers with a non-invasive method of extracting stem cells. The different cell populations, however, differ in certain aspects of their growth rate in culture, marker gene expression and cell differentiation, although the extent to which these differences can be attributed to tissue of origin, function or culture conditions remains unclear. As a result, DPSCs have been thought of as an extremely promising source of cells used in endogenous tissue engineering.

Pulp necrosis is a clinical diagnostic category indicating the death of cells and tissues in the pulp chamber of a tooth with or without bacterial invasion. It is often the end result of many cases of dental trauma, caries and irreversible pulpitis.

Dental pulpal testing is a clinical and diagnostic aid used in dentistry to help establish the health of the dental pulp within the pulp chamber and root canals of a tooth. Such investigations are important in aiding dentists in devising a treatment plan for the tooth being tested.

<span class="mw-page-title-main">Dental trauma</span> Medical condition

Dental trauma refers to trauma (injury) to the teeth and/or periodontium, and nearby soft tissues such as the lips, tongue, etc. The study of dental trauma is called dental traumatology.

<span class="mw-page-title-main">Pulp stone</span>

Pulp stones are nodular, calcified masses appearing in either or both the coronal and root portion of the pulp organ in teeth. Pulp stones are not painful unless they impinge on nerves.

<span class="mw-page-title-main">Regenerative endodontics</span> Dental specialty

Regenerative endodontic procedures is defined as biologically based procedures designed to replace damaged structures such as dentin, root structures, and cells of the pulp-dentin complex. This new treatment modality aims to promote normal function of the pulp. It has become an alternative to heal apical periodontitis. Regenerative endodontics is the extension of root canal therapy. Conventional root canal therapy cleans and fills the pulp chamber with biologically inert material after destruction of the pulp due to dental caries, congenital deformity or trauma. Regenerative endodontics instead seeks to replace live tissue in the pulp chamber. The ultimate goal of regenerative endodontic procedures is to regenerate the tissues and the normal function of the dentin-pulp complex.

<span class="mw-page-title-main">Pulp capping</span>

Pulp capping is a technique used in dental restorations to prevent the dental pulp from necrosis, after being exposed, or nearly exposed during a cavity preparation, from a traumatic injury, or by a deep cavity that reaches the center of the tooth causing the pulp to die. When dental caries is removed from a tooth, all or most of the infected and softened enamel and dentin are removed. This can lead to the pulp of the tooth either being exposed or nearly exposed which causes pulpitis (inflammation). Pulpitis, in turn, can become irreversible, leading to pain and pulp necrosis, and necessitating either root canal treatment or extraction. The ultimate goal of pulp capping or stepwise caries removal is to protect a healthy dental pulp and avoid the need for root canal therapy.

Atraumatic restorative treatment (ART) is a method for cleaning out tooth decay from teeth using only hand instruments and placing a filling. It does not use rotary dental instruments to prepare the tooth and can be performed in settings with no access to dental equipment. No drilling or local anaesthetic injections are required. ART is considered a conservative approach, not only because it removes the decayed tissue with hand instruments, avoiding removing more tissue necessary which preserves as much tooth structure as possible, but also because it avoids pulp irritation and minimises patient discomfort. ART can be used for small, medium and deep cavities caused by dental caries.

References

  1. "Researchers grow teeth from gum cells". BBC News. 3 September 2013. Retrieved 17 September 2021.
  2. Wang, Shirley (5 July 2013). "To Avoid Root Canals, Teeth That Replace Themselves; Stem-Cell Research Makes Progress in Quest to Avoid the Dreaded Drill". The Wall Street Journal.
  3. Sloane, Alastair (23 April 2013). "We could Grow Bone, cartilage or fat, but there's still much we don't know". Irish Daily Mail.
  4. COUNIHAN, DR NEIL (17 September 2021). "Don't leave that tooth under the pillow - it might save your child's life: The 12-year-old pioneer storing stem cells that might cure him in the future". The Daily Mail.
  5. "Tooth Regeneration: Teeth grown from mice cells offer hope for tooth replacement - Times of India". The Times of India. 9 March 2013. Retrieved 2021-09-17.
  6. "- University of Birmingham research gateway". research.birmingham.ac.uk. Retrieved 2021-08-10.
  7. Alraies, Amr; Waddington, Rachel J.; Sloan, Alastair J.; Moseley, Ryan (2020-09-10). "Evaluation of Dental Pulp Stem Cell Heterogeneity and Behaviour in 3D Type I Collagen Gels". BioMed Research International. 2020: 1–12. doi: 10.1155/2020/3034727 . ISSN   2314-6133. PMC   7501571 . PMID   32964026.
  8. Teoh, Leanne; Sloan, Alastair J; McCullough, Michael J; Thompson, Wendy (2020-09-16). "Measuring Antibiotic Stewardship Programmes and Initiatives: An Umbrella Review in Primary Care Medicine and a Systematic Review of Dentistry". Antibiotics. 9 (9): 607. doi: 10.3390/antibiotics9090607 . ISSN   2079-6382. PMC   7558917 . PMID   32947838.
  9. Bennett, Jon H.; Beeley, Josie A.; Anderson, Paul; Belfield, Louise; Brand, Henk S.; Didilescu, Andreea C.; Dymock, David; Guven, Yegane; Hector, Mark P.; Holbrook, Peter; Jayasinghe, Jaya A. P. (August 2020). "A core curriculum in the biological and biomedical sciences for dentistry". European Journal of Dental Education. 24 (3): 433–441. doi:10.1111/eje.12518. hdl:11343/273477. ISSN   1396-5883. PMID   32078216. S2CID   211215067.
  10. Avery, Steven James; Ayre, Wayne Nishio; Sloan, Alastair James; Waddington, Rachel Jane (2020-06-01). "Interrogating the Osteogenic Potential of Implant Surfaces In Vitro : A Review of Current Assays". Tissue Engineering Part B: Reviews. 26 (3): 217–229. doi:10.1089/ten.teb.2019.0312. hdl:11343/273452. ISSN   1937-3368. PMID   31952457. S2CID   210710096.
  11. Serra, Elisa; Saubade, Fabien; Ligorio, Cosimo; Whitehead, Kathryn; Sloan, Alastair; Williams, David W.; Hidalgo-Bastida, Araida; Verran, Joanna; Malic, Sladjana (2020-02-06). "Methylcellulose Hydrogel with Melissa officinalis Essential Oil as a Potential Treatment for Oral Candidiasis". Microorganisms. 8 (2): 215. doi: 10.3390/microorganisms8020215 . ISSN   2076-2607. PMC   7074814 . PMID   32041100.
  12. Bender, Lena; Boostrom, Hannah M.; Varricchio, Carmine; Zuanon, Marika; Celiksoy, Vildan; Sloan, Alastair; Cowpe, Jonathan; Heard, Charles M. (April 2020). "A novel dual action monolithic thermosetting hydrogel loaded with lidocaine and metronidazole as a potential treatment for alveolar osteitis". European Journal of Pharmaceutics and Biopharmaceutics. 149: 85–94. doi:10.1016/j.ejpb.2020.01.007. hdl:11343/273439. PMID   32001314. S2CID   210982657.
  13. Lim, Sim Yee; Dafydd, Mali; Ong, JieJi; Ord-McDermott, Launa A.; Board-Davies, Emma; Sands, Kirsty; Williams, David; Sloan, Alastair J.; Heard, Charles M. (January 2020). "Mucoadhesive thin films for the simultaneous delivery of microbicide and anti-inflammatory drugs in the treatment of periodontal diseases". International Journal of Pharmaceutics. 573: 118860. doi:10.1016/j.ijpharm.2019.118860. hdl:11343/273484. PMID   31759104. S2CID   208254193.
  14. Alraies, Amr; Canetta, Elisabetta; Waddington, Rachel J.; Moseley, Ryan; Sloan, Alastair J. (August 2019). "Discrimination of Dental Pulp Stem Cell Regenerative Heterogeneity by Single-Cell Raman Spectroscopy". Tissue Engineering Part C: Methods. 25 (8): 489–499. doi:10.1089/ten.tec.2019.0129. ISSN   1937-3384. PMID   31337281. S2CID   198194170.
  15. Jiang, Wenkai; Wang, Diya; Alraies, Amr; Liu, Qian; Zhu, Bangfu; Sloan, Alastair J.; Ni, Longxing; Song, Bing (2019-01-28). "Wnt-GSK3 β / β -Catenin Regulates the Differentiation of Dental Pulp Stem Cells into Bladder Smooth Muscle Cells". Stem Cells International. 2019: 1–13. doi: 10.1155/2019/8907570 . ISSN   1687-966X. PMC   6369468 . PMID   30809265.
  16. Rivera, Melissa C.; Perni, Stefano; Sloan, Alastair; Prokopovich, Polina (February 2019). "

    Anti-inflammatory drug-eluting implant model system to prevent wear particle-induced periprosthetic osteolysis

    "
    . International Journal of Nanomedicine. 14: 1069–1084. doi: 10.2147/ijn.s188193 . ISSN   1178-2013. PMC   6371946 . PMID   30804671.
  17. Aziz, T (2003-04-04). "Surface modification of an experimental silicone rubber maxillofacial material to improve wettability". Journal of Dentistry. 31 (3): 213–216. doi:10.1016/s0300-5712(02)00131-8. ISSN   0300-5712. PMID   12726706.
  18. Alraies, Amr; Cole, David K.; Rees, Jeremy S.; Glasse, Carl; Young, Nigel; Waddington, Rachel J.; Sloan, Alastair J. (January 2019). "Real-time binding kinetic analyses of the interaction of the dietary stain orange II with dentin matrix". Journal of Dentistry. 80: 80–88. doi:10.1016/j.jdent.2018.06.001. PMID   29894765. S2CID   48360274.
  19. Yusop, Norhayati; Battersby, Paul; Alraies, Amr; Sloan, Alastair J.; Moseley, Ryan; Waddington, Rachel J. (2018). "Isolation and Characterisation of Mesenchymal Stem Cells from Rat Bone Marrow and the Endosteal Niche: A Comparative Study". Stem Cells International. 2018: 1–14. doi: 10.1155/2018/6869128 . ISSN   1687-966X. PMC   5885338 . PMID   29765418.
  20. Nishio Ayre, Wayne; Melling, Genevieve; Cuveillier, Camille; Natarajan, Madhan; Roberts, Jessica L.; Marsh, Lucy L.; Lynch, Christopher D.; Maillard, Jean-Yves; Denyer, Stephen P.; Sloan, Alastair J. (May 2018). Freitag, Nancy E. (ed.). "Enterococcus faecalis Demonstrates Pathogenicity through Increased Attachment in an Ex Vivo Polymicrobial Pulpal Infection". Infection and Immunity. 86 (5). doi:10.1128/IAI.00871-17. ISSN   0019-9567. PMC   5913860 . PMID   29483293.
  21. Melling, Genevieve E.; Colombo, John S.; Avery, Steven J.; Ayre, Wayne Nishio; Evans, Samuel L.; Waddington, Rachel J.; Sloan, Alastair J. (July 2018). "Liposomal Delivery of Demineralized Dentin Matrix for Dental Tissue Regeneration". Tissue Engineering Part A. 24 (13–14): 1057–1065. doi:10.1089/ten.tea.2017.0419. ISSN   1937-3341. PMC   6033301 . PMID   29316874.
  22. Sadaghiani, L.; Gleeson, H.B.; Youde, S.; Waddington, R.J.; Lynch, C.D.; Sloan, A.J. (2016-07-21). "Growth Factor Liberation and DPSC Response Following Dentine Conditioning". Journal of Dental Research. 95 (11): 1298–1307. doi: 10.1177/0022034516653568 . ISSN   0022-0345. PMID   27307049. S2CID   23659445.
  23. "Above and Beyond". Journal of Public Health Dentistry. 53 (1): 64. March 1993. doi:10.1111/j.1752-7325.1993.tb02676.x. ISSN   0022-4006.
  24. Carrotte, P (January 2005). "Surgical endodontics". British Dental Journal. 198 (2): 71–79. doi: 10.1038/sj.bdj.4811970 . ISSN   0007-0610. PMID   15702099. S2CID   27504925.
  25. Journal of Pharmaceutical and Biopharmaceutical Research. Syncsci Publishing Pte., Ltd. doi:10.25082/jpbr.
  26. Bender, Lena; Boostrom, Hannah M.; Varricchio, Carmine; Zuanon, Marika; Celiksoy, Vildan; Sloan, Alastair; Cowpe, Jonathan; Heard, Charles M. (April 2020). "A novel dual action monolithic thermosetting hydrogel loaded with lidocaine and metronidazole as a potential treatment for alveolar osteitis". European Journal of Pharmaceutics and Biopharmaceutics. 149: 85–94. doi:10.1016/j.ejpb.2020.01.007. hdl:11343/273439. PMID   32001314. S2CID   210982657.
  27. Lim, Sim Yee; Dafydd, Mali; Ong, JieJi; Ord-McDermott, Launa A.; Board-Davies, Emma; Sands, Kirsty; Williams, David; Sloan, Alastair J.; Heard, Charles M. (January 2020). "Mucoadhesive thin films for the simultaneous delivery of microbicide and anti-inflammatory drugs in the treatment of periodontal diseases". International Journal of Pharmaceutics. 573: 118860. doi:10.1016/j.ijpharm.2019.118860. hdl:11343/273484. PMID   31759104. S2CID   208254193.
  28. Rivera, Melissa C.; Perni, Stefano; Sloan, Alastair; Prokopovich, Polina (February 2019). "

    Anti-inflammatory drug-eluting implant model system to prevent wear particle-induced periprosthetic osteolysis

    "
    . International Journal of Nanomedicine. 14: 1069–1084. doi: 10.2147/ijn.s188193 . ISSN   1178-2013. PMC   6371946 . PMID   30804671.
  29. Nishio Ayre, Wayne; Melling, Genevieve; Cuveillier, Camille; Natarajan, Madhan; Roberts, Jessica L.; Marsh, Lucy L.; Lynch, Christopher D.; Maillard, Jean-Yves; Denyer, Stephen P.; Sloan, Alastair J. (May 2018). Freitag, Nancy E. (ed.). "Enterococcus faecalis Demonstrates Pathogenicity through Increased Attachment in an Ex Vivo Polymicrobial Pulpal Infection". Infection and Immunity. 86 (5). doi:10.1128/IAI.00871-17. ISSN   0019-9567. PMC   5913860 . PMID   29483293.
  30. Sadaghiani, L.; Gleeson, H.B.; Youde, S.; Waddington, R.J.; Lynch, C.D.; Sloan, A.J. (2016-07-21). "Growth Factor Liberation and DPSC Response Following Dentine Conditioning". Journal of Dental Research. 95 (11): 1298–1307. doi: 10.1177/0022034516653568 . ISSN   0022-0345. PMID   27307049. S2CID   23659445.
  31. "Top Award for University Researcher". South Wales Echo. 12 April 2011.
  32. "Head of School awarded for outstanding contribution to dentistry". 8 April 2021.