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003 | EG-GiCUC | ||
005 | 20250223032334.0 | ||
008 | 190727s2019 ua d f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aM.Sc | ||
099 | _aCai01.08.10.M.Sc.2019.Re.P | ||
100 | 0 | _aReham Waheed Mahmoud Hammad | |
245 | 1 | 2 |
_aA pharmaceutical study on mosapride for intranasal administration / _cReham Waheed Mahmoud Hammad ; Supervised Nevine Shawky Abdelmalak , Randa Latif Aziz , Rania Abdelbaset Sanad |
246 | 1 | 5 | _aدراسة صيدلية علي عقار الموزابريد لاستخدامة عن طريق الانف |
260 |
_aCairo : _bReham Waheed Mahmoud Hammad , _c2019 |
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300 |
_a229 P. : _bcharts ; _c25cm |
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502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Industrial Pharmacy | ||
520 | _aMosapride citrate (MOS) is a potent gastroprokinetic agent, used in the treatment of various gastrointestinal disorders caused by reduced gastrointestinal motility including gastroesophageal reflux disease (GERD). MOS would neither result in cardiac nor nervous adverse reactions due to selective stimulation of serotonin 5-HT4 receptors, without any considerable affinity for dopamine D2, 5-HT1, 5-HT2, or adrenergic receptors. Presently, available tablet dosage formulation of MOS is incapable to achieve the required clinical efficacy. Its short half-life (t1/2), intensive first-pass metabolism, poor solubility, and poor wettability lower its oral bioavailability to be 8-14%.This very low oral bioavailability restricts its use. So, the aim of this study was to improve the bioavailability MOS through intranasal administration | ||
530 | _aIssued also as CD | ||
653 | 4 | _aMosapride citrate | |
653 | 4 | _aNasal | |
653 | 4 | _aXyloglucan | |
700 | 0 |
_aNevine Shawky Abdelmalak , _eSupervisor |
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700 | 0 |
_aRanda Latif Aziz , _eSupervisor |
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700 | 0 |
_aRania Abdelbaset Sanad , _eSupervisor |
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856 | _uhttp://172.23.153.220/th.pdf | ||
905 |
_aAsmaa _eCataloger |
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905 |
_aNazla _eRevisor |
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942 |
_2ddc _cTH |
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999 |
_c73081 _d73081 |