Formulation and Evaluation of Orodispersible Tablets of an Antiulcer Agent

2017 ◽  
Vol 10 (3) ◽  
pp. 747
Author(s):  
Srinivasa D Sastry ◽  
Narayana R Charyulu ◽  
D S Satyanarayana ◽  
D Srilakshmi
2017 ◽  
Vol 26 (4) ◽  
pp. 1025-1035 ◽  
Author(s):  
Neveen A. Salem ◽  
Mohammed A. Wahba ◽  
Wael H. Eisa ◽  
Marwa El-Shamarka ◽  
Wagdy Khalil

2018 ◽  
Vol 154 (6) ◽  
pp. S-256-S-257 ◽  
Author(s):  
Alex Straumann ◽  
Stephan Miehlke ◽  
Michael Vieth ◽  
Christoph Schlag ◽  
Ulrike von Arnim ◽  
...  

INDIAN DRUGS ◽  
2016 ◽  
Vol 53 (06) ◽  
pp. 32-39
Author(s):  
A. K Mahapatra ◽  
◽  
P. N. Murthy

The aim of the study was to enhance the dissolution rate of atovaquone by preparing inclusion complexes with cyclodextrins (β-CD/ HP β-CD) and formulating their orodispersible tablets. Phase solubility studies were conducted by adding 0.5, 1, 2 and 4% of cyclodextrins in water. The values of Gibb’s free energy were found increased. Inclusion complexes of atovaquone were prepared using β -CD/ HP β -CD by kneading method. Tablets were formulated using superdisintegrants i.e., sodium starch glycolate, crospovidone and Ac-Di sol at concentrations of 4, 8 and 12% of tablet weight by direct compression technique. The interaction studies were made by Fourier transform infrared spectroscopy and differential scanning calorimetry, and no significant interaction was observed. Inclusion complexes showed better dissolution than pure atovaquone and HP-β-CD established better than β-CD. Inclusion complexes of atovaquone at 1:0.25 w/w (drug: HP β -CD) in the tablets with 12% of crospovidone showed satisfactory results.


Author(s):  
Sarika S. Malode ◽  
Milind P. Wagh

The objective of present work was to develop taste masked orodispersible tablets of mirabegron. Mirabegron is beta 3 adrenoceptor agonist used to treat overactive bladder. Overactive bladder (OAB) is defined as a symptom syndrome showing feeling of urgency to urinate, typically accompanied by frequent daytime and nocturnal urination, in the absence of proven infection or other obvious pathology. Over active bladders are generally common in geriatrics. Moreover, this drug has a very strong bitter taste. Frequent dosing requires frequent water intake, which further aggregates the condition of over active bladder and bitter taste of drug affects patient compliance. Hence a need arises to mask the bitter taste for development of an ODT which does not require consuming water with every dosage. In this work, the bitter taste of mirabegron was masked by forming a complex with an ion exchange resin tulsion 344. The drug resin complexation process was optimized for resin activation, drug: resin ratio, soaking time and stirring time. In –vitro release studies revealed complete drug elution from the complex within 10 minutes in pH 1.2 buffer. The taste-masked complex was then formulated into palatable orodispersible tablets using a direct compression approach by use of superdisintegrants to achieve a rapid disintegration. The tablets were evaluated for weight variation, hardness, friability, drug content, wetting time, In- vivo disintegration time and in-vitro dissolution time.


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