BUKU ABSTRAK - Universiti Putra Malaysia
BUKU ABSTRAK - Universiti Putra Malaysia
BUKU ABSTRAK - Universiti Putra Malaysia
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Bonigen: A Potential Anti-biofilm Bone Substitute<br />
Prof. Dr. Fauziah Othman<br />
Au Lee Fong, Sharmili Vidyadaran, Asmah Rahmat, Rusnah Mustaffa, Idris Besar, Azfar Rizal Ahmad, Fuzina<br />
Nor Hussein, Mohd. Azam Khan Goriman Khan, Abdah Md. Akim, Saidi Moin and Che Nor Zarida Che Seman<br />
Faculty of Medicine and Health Sciences, University <strong>Putra</strong> <strong>Malaysia</strong>,<br />
43400 UPM Serdang, Selangor, <strong>Malaysia</strong>.<br />
+603-8947 2315; fauziah@putra.upm.edu.my<br />
Biomaterials have been widely used in the tissue engineering of bone as medical devices. It plays important<br />
role in treating diseases and improving healthcare, which are commonly used in dental, surgery and drug delivery<br />
applications. Hydroxyapatite (HA) is the major inorganic component of hard tissue in human body and is also<br />
known to have superior biocompatibility and can be reabsorbed and replaced by bone to repair the bone damage<br />
zone. Therefore, HA loaded with suitable antibiotics can be used as a carrier to limit biofilm formation. Biofilms<br />
are multi-layered colonies of bacteria that are typically more resistant to the host immune response and routine<br />
antibiotic therapy. Biofilm has negatively impacted in health and medicine. Thus, this study was aimed to<br />
assess the biocompatibility of locally produced HA coated with gentamicin on osteoblasts and to determine the<br />
efficacy of gentamicin-coated HA on Staphylococcus aureus biofilm. For in vitro, S. aureus strain and normal<br />
human osteoblast cell line were used. MTT assays were performed to determine the effects of various doses of<br />
gentamicin-coated HA (from 0.02 mg/ml to 10 mg/ml) on biofilm viability and also used to determine IC50<br />
value of gentamicin-coated HA on osteoblasts to assess the cytotoxicity level of this coated HA. For in vivo, the<br />
tissue immediately surrounding the implanted catheter was determined by using H&E staining post-implantation.<br />
Gentamicin-coated HA is biocompatible with bone tissue (osteoblasts) in vitro. It showed no detectable IC50 and<br />
the percentage of osteoblasts viability was high (75%) via MTT assay. It was also able to reduce the viability of<br />
S. aureus biofilm. After seven days of post-implantation, results also showed no post-implantation inflammatory<br />
reaction in rats. In conclusion, gentamicin-coated HA proved to be biocompatible with human osteoblasts and<br />
effective in reducing the number of bacteria both in vitro and in vivo.<br />
Keywords: Hydroxyapatite, staphylococcus aureus biofilm, MTT assays, gentamicin<br />
A Rapid Dipstick Immunoassay based on Recombinant SAG1 for Detection of<br />
Immunoglobulin G (Igg) and M (Igm) Antibodies in Human Toxoplasmosis<br />
Prof. Dr. Hj. Wan Omar Abdullah<br />
Ngah Zasmy Unyah, Hairul Bazli Hairuddin, Malina Osman, Rukman Awang Hamat and Khairul Anuar<br />
Faculty of Medicine and Health Sciences, University <strong>Putra</strong> <strong>Malaysia</strong>,<br />
43400 UPM Serdang, Selangor, <strong>Malaysia</strong>.<br />
+603-8947 2365; wanomar@medic.upm.edu.my<br />
A dipstick immunoassay (DIA) has been successfully developed to detect specific immunoglobulin G<br />
(IgG) or IgM antibodies to human toxoplasmosis. These assays employ nitrocellulose membrane (NCP) as a<br />
test matrix, peroxidase conjugated to sheep anti-human IgG and rabbit anti-human IgM as detecting antibodies<br />
and a Toxoplasma gondii recombinant SAG1 as the detective antigen. The assays are rapid (the whole test can<br />
be completed within 15 min), simple, and cheap, and they do not require any equipment. They are sensitive and<br />
specific for the detection of anti-Toxoplasma IgG or IgM antibodies and generally agree closely with the results<br />
from the enzyme-linked immunosorbent assay. The assays are especially suitable for field applications.<br />
Keywords: Dipstick, immunoassay, recombinant SAG1<br />
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