نتایج جستجو برای: in vitro release studies

تعداد نتایج: 17166397  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید مدنی آذربایجان - دانشکده زبانهای خارجی 1391

since esp received universal attention to smooth the path for academic studies and productions, a great deal of research and studies have been directed towards this area. swales’ (1990) model of ra introduction move analysis has served a pioneering role of guiding many relevant studies and has proven to be productive in terms of helpful guidelines that are the outcome of voluminous productions ...

H Rahman MS Islam S Reza

Extended-release matrix tablets of diltiazem hydrochloride (DTZ) were prepared using waxy materials alone or in combination with Kollidon SR. Matrix waxy materials were carnauba wax (CW), bees wax (BW), cetyl alcohol (CA) and glyceryl monostearate (GMS). Dissolution studies were carried out by using a six stations USP XXII type 1 apparatus. The in vitro drug release study was done in 1000 ml ph...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی مشهد - دانشکده دندانپزشکی 1390

objective: the objective of this study was to investigate the invitro fluoride release of four new self-adhesive resin cements; set (sdi, australia), breeze (pentron, usa), embrace wetbond (pulpdent, usa), g-cem (gc, japan) and to assess the bonding performance of these self-adhesive resin cements for bonding of orthodontic brackets. materials and methods: for fluoride release experiment, six ...

Journal: :iranian journal of pharmaceutical sciences 0
indranil ganguly department of pharmaceutics,m.s. ramaiah college of pharmacy, m.s.r. nagar, m.s.r.i.t post, bangalore-560054 sindhu abraham department of pharmaceutics,m.s. ramaiah college of pharmacy, m.s.r. nagar, m.s.r.i.t post, bangalore-560054 srinivasan bharath department of pharmaceutics,m.s. ramaiah college of pharmacy, m.s.r. nagar, m.s.r.i.t post, bangalore-560054 varadharajan madhavan department of pharmacognosy, m.s. ramaiah college of pharmacy, m.s.r. nagar, m.s.r.i.t post, bangalore-560054

promethazine hydrochloride, a 5-ht3 antagonist is a powerful antiemetic drug with an oral bioavailability of 25% due to extensive hepatic first pass metabolism and is extremely bitter in taste. to overcome the above draw backs, the present study was carried out to formulate and evaluate fast dissolving taste masked wafers of promethazine hydrochloride for sublingual administration. taste maskin...

Journal: :iranian journal of pharmaceutical sciences 0
veerendra s. rajpurohit rajendra institute of technology and sciences, hisar road, sirsa-125055, india pankaj rakha rajendra institute of technology and sciences, hisar road, sirsa-125055, india surender goyal rajendra institute of technology and sciences, hisar road, sirsa-125055, india harish durejab department of pharmaceutical sciences, m. d. university, rohtak- 124001, india gitika arorac ncrd’s sterling institute of pharmacy, navi mumbai- 400706, india manju nagpal school of pharmaceutical sciences, chitkara university, solan-174103, india

in order to enhance in vitro dissolution and content uniformity of poorly soluble drug glimepiride by preparing solid dispersions using modified solvent fusion method, solid dispersions of drug were prepared by modified fusion solvent method using peg 6000 and pvp k25 (as carrier). eight batches (f1-f8) were prepared by factorial design (23) by taking three factors i.e. the concentration of: dr...

Journal: :iranian journal of pharmaceutical research 0
ms islam s reza h rahman

extended-release matrix tablets of diltiazem hydrochloride (dtz) were prepared using waxy materials alone or in combination with kollidon sr. matrix waxy materials were carnauba wax (cw), bees wax (bw), cetyl alcohol (ca) and glyceryl monostearate (gms). dissolution studies were carried out by using a six stations usp xxii type 1 apparatus. the in vitro drug release study was done in 1000 ml ph...

Journal: :iranian journal of pharmaceutical research 0
a rezaei mokarram

preparation of chitosan (cs) microspheres as a novel drug delivery vehicle for intranasal immunization using high, medium and low cs molecular weight (mw) was investigated in this study. diphtheria toxoid (dt) was used as a model antigen. the emulsion-solidification method was adopted for microencapsulation of dt.  in the first step, following the purification of semi-crude dt by the ion-exchan...

A Gadad A Kulkarni P Dandagi S Kerur V Mastiholimath

The aim of this study is to formulate a novel ophthalmic nanosuspension (ONS), an alternative carrier system to traditional colloidal carriers for controlled release (CR) of acyclovir (ACV). In the present study, ONS is employed to avoid some of major disadvantages of colloidal carriers systems such as instability in cul de sac and short half life by increasing efficiency of drug encapsulation ...

Indranil Ganguly, Sindhu Abraham, Srinivasan Bharath Varadharajan Madhavan

Promethazine hydrochloride, a 5-HT3 antagonist is a powerful antiemetic drug with an oral bioavailability of 25% due to extensive hepatic first pass metabolism and is extremely bitter in taste. To overcome the above draw backs, the present study was carried out to formulate and evaluate fast dissolving taste masked wafers of Promethazine hydrochloride for sublingual administration. Taste maskin...

A Gadad A Kulkarni P Dandagi S Kerur V Mastiholimath

The aim of this study is to formulate a novel ophthalmic nanosuspension (ONS), an alternative carrier system to traditional colloidal carriers for controlled release (CR) of acyclovir (ACV). In the present study, ONS is employed to avoid some of major disadvantages of colloidal carriers systems such as instability in cul de sac and short half life by increasing efficiency of drug encapsulation ...

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