Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Adicionar filtros








Intervalo de ano
1.
Chinese Journal of Stomatology ; (12): 180-183, 2014.
Artigo em Chinês | WPRIM | ID: wpr-274113

RESUMO

<p><b>OBJECTIVE</b>To investigate the feasibility of extraction site preservation using injectable calcium phosphate cement (CPC) combine with poly (lactic-co-glycolic acid) (PLGA) microspheres.</p><p><b>METHODS</b>Immediate extraction defects models were created in canine mandibles, and the defects were filled with CPC/PLGA (experimental group, E) , Bio-Oss (positive control, P), non-treatment (blank control, B) respectively. Dogs were sacrificed after 4, 8, 12 weeks post operation. Statistical analysis were conducted using SPSS 19.</p><p><b>RESULTS RESULTS</b>of radiological observation showed that there were not significantly different between groups in 4 and 8 week (P > 0.05). After 12 week,E (114.9 ± 8.4) were not significantly different compared with P (117.4 ± 12.1) (P > 0.05) , both were significantly higher than B (95.0 ± 12.6) (P < 0.05) . Histology examination showed that at 4 week following surgery, the result of newly formed bone was as follow, P[ (87.5 ± 1.5) %] > B[(78.7 ± 2.7)%] > E[(69.2 ± 1.8)%] (P < 0.05). At 8, 12 week, results of P[(94.0 ± 2.3)% and (93.5 ± 1.9) %] and E[ (94.7 ± 1.1) % and (96.0 ± 0.9) %] were better than those of B[ (76.8 ± 3.0)% and (87.0 ± 2.4)%] (P < 0.05).</p><p><b>CONCLUSIONS</b>The effect of CPC/PLGA repair immediate alveolar ridge defects is the same as that of Bio-Oss, and CPC/PLGA can be used as a material in extraction site preservation.</p>


Assuntos
Animais , Cães , Fosfatos de Cálcio , Cimentos Dentários , Modelos Dentários , Glicolatos , Ácido Láctico , Microesferas , Minerais , Poliésteres , Ácido Poliglicólico , Polímeros , Extração Dentária
2.
China Pharmacy ; (12)2007.
Artigo em Chinês | WPRIM | ID: wpr-533215

RESUMO

OBJECTIVE:To prepare granisetron hydrochloride nasal spray and establish a method for its quality control. METHODS: Granisetron hydrochloride nasal spray was prepared using granisetron hydrochloride as chief ingredient and its content was determined by UV spectrophotometry. RESULTS: Spray appeared as colorless or yellowish supernatant liquid and it was up to the standard specified in Chinese Pharmacopeia (2005 edition). The linear range of granisetron hydrochloride was 105.9~635.4 ?g?mL-1 (r=0.999) and its average recovery rate was 100.1% (RSD=0.4%). CONCLUSION: The preparation is simple and feasible in preparation process and its quality is controllable.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA