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| Mahidol
University Annual Research Abstracts, Vol.28, 2001 |
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EXAMINE THE PIT AND FISSURE SEALANT RETENT ON RATE OF
FIRST
PERMANENT MOLARS IN PRATOM 2 AND 3 STUDENTS AFTER
APPLICATION PROGRAM FOR 1 AND 2 YEARS IN
SOMITTRAPAPH 140th ,
SCHOOL OF PUBLIC, SOPISAI DISTRICT, NONG
KAI PROVINCE. (NO. 001) |
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| Salunya
Tancharoen1, Pornsirin Chaicharothornkul2,
Kaidsirin Charoensangsuriya3, Pornpimol Chiamvongsa3
, Kamolrat Hiranrat 3 |
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| 1
Department of Pharmacology, Faculty of Dentistry,
Mahidol University.2 Department of Hospital
Dentistry, Faculty of Dentistry, Khonkaen University. 3
Public Hospital, Ministry of Public Health. |
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| Key
words : Fissure sealant, Caries
prevention |
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A descriptive study has been done to evaluate the sealant
application program in Somittrapaph 140th, School of public,
Sopisai District, Nong Kai Province. The Ministry of Public
Health advocated this sealant application program to prevent
occlusal caries. Dental sealant was placed by dental nurses on
first permanent molars of Pratom 1 (first grade) students in
1996 and 1997 under the mobile clinic setting. Forty Pratom 2
(second grade) students (160 teeth) and thirty-four Pratom 3
(third graded) students (136 teeth) whose teeth had sealant
placed for 1 and 2 years respectively were examined for the
sealant retention rates. 39.17% and 29.31% of all teeth had
sealant retained in good condition after 1 and 2 years
respectively. 41.53% of teeth required sealant replacement and
24.15% had caries associated with sealant. This finding
suggested that the sealant program in this school had low 1
and 2 years success rates; and the program, therefore, should
be further evaluate for the cost-effectiveness.
Mahidol Dental Journal 2000 Vol.20(1) ;47-54. |
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IMMUNOHISTOCHEMICAL LOCALLIZATION OF CYTOKERATIN AND PCNA
DESMOPLASTIC AMELOBLASTOMA. ( NO. 002) |
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| H. Nagatsuka 1, E.
Fujii 1, R. Tamamuta 1, K. Hibi 1,
Y. Ishiwari 1, S. Tancharoen 2 ,
P. Thunyakitpisal 3, S.G. Rao 4, Q.
Jin-ping5 , L. Sun 6, 6), N. Nagai 1 |
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| 1Oral Pathology,
Okayama Univ. Dent. Sch., Japan, 2Department of
Pharmacolgy, Mahidol University, Thailand, 3Chulalongkorn
University, Thailand, 4 Rajiv Univ. of Health Sci.,
India, 1Harbin medical Univ., China, 6Dalian
medical Univ., China. |
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| Key words :
Desmoplastic ameloblastoma, Immunohistochemistry. |
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Desmoplastic ameloblastoma is histologically characterized by
extensive stromal collagenization or desmoplasia. In this
study, anti-cytokeratin as well as anti-PCNA, were used to
detect the expression of these proteins in the desmoplastic
ameloblastoma. Six cases of desmoplastic ameloblastoma were
used. All specimens were obtained from Okayama University
Dental Hospital. The monoclonal anti-cytokeratin No.8, and 19,
anti-cytokeratin squamous epithelium (SE-K), anti-PCNA were
used in this study. The tumor islands varied in shape and size
and in some areas they were compressed by the desmoplastic
stroma resulting in narrow strands or cords which appeared as
sheets. The tumor islands lacked the peripheral palisading of
columnar cells and were rimmed with cuboidal or flattened
cells. Central parts of the nests often showed squamous
metaplasia and scattered foci of keratinazation. The tumor
nests showed the different patterns of response to
anti-cytokeratin antibodies. In some of the tumor nests, all
tumor cells were positive to antibodies of CK-8, and 19, but
had the limited area of staining in the central area with the
SE-K antibodies. However, some of the tumor nests show the
positive staining in the localized, periphery area with CK 8,
19 antibodies. The staining periphery tumor cells are cuboidal
and columnar cell shape while the non-positive staining tumor
cells are stellate-shape. Some of peripheral cells of tumor
nest were positively detected while the stroma part of
connective tissue were strongly stained with PCNA. We noted
the intense of PCNA staining of the stroma around the tumor
nest. These results suggests
desmoplastic ameloblastoma composed many different tumor cell
types, and have high proliferating activity in the
desmoplastic stroma. |
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| (Oral Presentation at
Frontier of Molecular Biology in Biological Reconstructive
Dentistr and Medicine, August 27th- September 6th,2000.
Department of Pathology, Okayama University Dental School,
Japan) |
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| In print: Special issue of
Journal of Hard Tissue Biology |
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IN VITRO ANTIBACTERIAL EFFECT OF
DENTAL VARNISHES (NO. 003) |
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| Warungkana Chidchuangchai1,
Sroisiri Thaweboon2, and Boonyanit Thaweboon2 |
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| 1 Department of
Pharmacology, 2 Department of Microbiology, Faculty
of Dentistry, Mahidol University. |
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| Key words :
Antibacterial effect, Dental varnishes |
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The purpose of the present study was to evaluate and compare
the antibacterial properties of different concentrations of a
chlorhexidine varnish prepared at Faculty of Dentistry,
Mahidol University (range 5-40%), 1% chlorhexidine/thymol
varnish (Cervitec®), 0.1%
fluoride varnish (Fluor Protector®)
and 2.26% fluoride varnish (Duraphat®).
Agar diffusion method was used to test the antibacterial
effect against clinical strain of Streptococcus mutans including
KPSK2 reference strain. After 48 hours incubation, zones of
bacterial inhibition of these varnishes were measured in
millimeters and compared with the negative control (alcohol).
The chlorhexidine varnish demonstrated excellent activity
against the bacterial tested (p<0.01) and revealed
bacterial inhibition in a dose-response manner. No significant
difference was found between the concentrations (p>0.05).
The antibacterial effects of 1% chlorhexidine/thymol varnish
and 2.26% fluoride varnish were comparable, however, less than
that noted with chlorhexidine varnish. While 0.1% fluoride
varnish slightly inhibited the growth of Streptococcus
mutans but no significant difference was found when
compared with the control (p>0.05). The reference strain
and clinical strains (tested bacterial strains) were similarly
inhibited. These in vitro results indicated that 5-40%
chlorhexidine varnish, 1% chlorhexidine/thymol varnish and
2.26% fluoride varnish were effective in inhibiting the growth
of Streptococcus mutans while 0.1% fluoride varnish was not. |
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