000 03090cam a2200349 a 4500
003 EG-GiCUC
005 20250223031159.0
008 150322s2014 ua dh f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aPh.D
099 _aCai01.09.02.Ph.D.2014.Ne.A
100 0 _aNehal Nabil Abdelaziz Roshdy
245 1 0 _aAssessment of the biocompatibility and antimicrobial activity of prepared specified standardized phytopharmaceuticals extracts used as intracanal medicaments :
_bComparative in vivo study /
_cNehal Nabil Abdelaziz Roshdy ; Supervised Jealan Mohammed Elshafei , Hesham Ibrahim Elaskary , Tamer Mohammed Essam
246 1 5 _a تقييم التوافق الحيوى ونشاط تضاد الميكروبات لمستخلصات معايرة محددة المحضرة من الأدوية الصيدلانية النباتية و المستخدمة كادوية موضوعه داخل القناة :
_bدراسة مقارنة حية
260 _aCairo :
_bNehal Nabil Abdelaziz Roshdy ,
_c2014
300 _a159 Leaves :
_bcharts , facsimiles ;
_c30cm
502 _aThesis (Ph.D.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Endodontics
520 _aObjectives: The aim of this in-vivo study was to prepare specified standardized extracts from certain natural plants: (Green tea leaves, Cinnamon bark and Olive leaves) and to compare them with calcium hydroxide intra-canal medicament regarding: The biocompatibility of these drugs and their antimicrobial activity. Materials and methods: In the first part of the study, the selected drugs were air dried, cut into pieces and ground into powder form. The extracts were prepared using different solvents, fractionated using solvents of different polarity .Then, screened against different bacteria and the most potent extracts were chosen for the study. In the second part of the study, the subcutaneous implantation technique was carried out on forty male albino Sprague-Dawley rats. The rats were classified into four groups, ten rats each, according to the tested material and the experimental period: Group I: Green tea extract, cinnamon bark extract and negative control. (14 days observation period), Group II: Olive leaves extract, Meta paste and negative control (14 days observation period), Group III: same as Group I (30 days observation period) and Group IV: same as Group II (30 days observation period). In the third part of the study, thirty two patients free of systemic diseases were selected. All the selected upper anterior teeth were diagnosed as having pulpal necrosis
530 _aIssued also as CD
653 4 _aBiocompatibility
653 4 _aIntracanal medicaments
653 4 _aPhytopharmaceuticals
700 0 _aHesham Ibrahim Elaskary ,
_eSupervisor
700 0 _aJealan Mohammed Elshafei ,
_eSupervisor
700 0 _aTamer Mohammed Essam ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aAml
_eCataloger
905 _aNazla
_eRevisor
942 _2ddc
_cTH
999 _c49980
_d49980