A pharmaceutical study on improving the solubility & bioavailability of an antihistaminic drug / Nolwa Gamal Ahmed Elsherif ; Supervised Soad Ali Yehia , Mohamed Shafik Elridy , Mina Ibrahim Tadros
Material type:
- دراسة صيدلية لتحسين الذوبان والاتاحة الحيوية لعقار مضاد للحساسية [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.08.M.Sc.2014.No.P (Browse shelf(Opens below)) | Not for loan | 01010110063858000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.08.M.Sc.2014.No.P (Browse shelf(Opens below)) | 63858.CD | Not for loan | 01020110063858000 |
Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutics
Fexofenadine, the active metabolite of the well-known and effective H1 receptor antagonist, terfenadine, is administered as the hydrochloride salt. Fexofenadine hydrochloride (FXD) is a non-sedating antihistamine that provides rapid, long-acting, and highly selective peripheral H1 receptor antagonist activity. It is used for allergic rhinitis and urticarial at a recommended oral dose of 30 to 180 mg. But it has a bitter taste, slightly soluble in water and having an oral bioavailability of 35%. The maximum plasma concentration is reached 2.6 hours (Tmax) post-dose. Various approaches have been applied to mask the taste and improve its solubility and bioavailability. Solid oral dosage forms represent the preferred class of products of the drugs that are administered orally. The tablets dosage form has a number of advantages. Tablets are unit dosage form that offers the greatest dose precision and the least content variability. Tablets are also the lowest in their cost, the easiest and cheapest to package
Issued also as CD
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