000 | 01949nam a2200361 a 4500 | ||
---|---|---|---|
003 | EG-GiCUC | ||
005 | 20250223025917.0 | ||
008 | 090819s2009 ua d f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
||
041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aM.Sc | ||
099 | _aCai01.08.08.M.Sc.2009.Ta.P | ||
100 | 0 | _aTayseer Mohamed Abdelrazek Elnawawy | |
245 | 1 | 2 |
_aA pharmaceutical study on formulation of an antihypertensive drug in controlled release systems / _cTayseer Mohamed Abdelrazek Elnawawy ; Supervised Samia Abdelkader Nour , Dalia M. Ghorab , Abdelmonaem Swailam |
246 | 1 | 5 | _aدراسة صيدلية على صياغة احد عقاقير ضغط الدم المرتفع على هيئة انظمة ممتدة المفعول |
260 |
_aCairo : _bTayseer Mohamed Abdelrazek Elnawawy , _c2009 |
||
300 |
_a147 P. : _bcharts ; _c25cm |
||
502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutics | ||
520 | _aFormulation of gastroretentive dosage forms is a step toward improving the bioavailability of the drug tested. In order to control its release, diltiazem hydrochloride (highly soluble drug) was formulated as effervescent floating granules prepared using different polymers like eudragit S100, L100, RS100,RL100, in D/P ratio 1:3, 1:5 and 1:7, Also 1:1 1:3, 1:5 and 1:7 were the D/P ratios used for granules prepared using ethylcellulose and lipophilic matrices as: beeswax and carnauba wax | ||
530 | _aIssued also as CD | ||
653 | 4 | _aDiltiazem hydrochloride | |
653 | 4 | _aEffervescent floating granules | |
653 | 4 | _aGastroretentive dosage forms | |
700 | 0 |
_aAbdelmonaem Swailam , _eSupervisor |
|
700 | 0 |
_aDalia Mahmoud Ghorab , _eSupervisor |
|
700 | 0 |
_aSamia Abdelkader Nour , _eSupervisor |
|
856 | _uhttp://172.23.153.220/th.pdf | ||
902 | _a1 | ||
905 |
_aMustafa _eRevisor |
||
905 |
_aSamia _eCataloger |
||
942 |
_2ddc _cTH |
||
999 |
_c23365 _d23365 |