scholarly journals Evaluation of a new coprocessed compound based on lactose and maize starch for tablet formulation

AAPS PharmSci ◽  
2004 ◽  
Vol 6 (2) ◽  
pp. 27-38 ◽  
Author(s):  
Karsten Hauschild ◽  
Katharina M. Picker
Keyword(s):  
Tablet Formulation ◽  
Maize Starch

scholarly journals Production and Evaluation of Disintegrant Properties of Microcrystalline Cellulose Derived from SaccharumofficinarumL (Poaceae) in Metronidazole Based Formulation

2021 ◽  
Vol 6 (4) ◽  
pp. 42-51
Author(s):  
Oraeluno J.N. ◽  
Obasi J.C ◽  
Bamigbola E.A ◽  
Joseph B.A
Keyword(s):  
Microcrystalline Cellulose ◽  
Release Profile ◽  
Tablet Formulation ◽  
Maize Starch ◽  
Flow Properties ◽  
British Pharmacopoeia ◽  
Comparative Characterization ◽  
High Release ◽  
Dissolution Properties

The aim of the study was to produce microcrystalline cellulose from Saccharumofficinarum and to evaluate its use as a disintegrant in metronidazole tablet formulation. Cellulose was produced and characterized. This was followed by a comparative characterization of the tablets formulated by using Saccharumofficinarummicrocrystalline cellulose (SO-MCC), maize starch and crosscarmellose sodium (Ac-di-sol®) as disintegrants. The granules were evaluated for flow properties and the tablet evaluated for hardness, friability, disintegration and dissolution properties. For disintegration studies, the disintegrants disintegrated within 10 minutes in this order: Ac-di-sol® >SO-MCC>Maize starch. All the tablets exhibited high release profile which conformed to British Pharmacopoeia standards. Hence, SO-MCC can be used as an alternative disintegrant in terms of cost and availability.

Preparation and Characterization of Phytosomal-Phospholipid Complex of P. Amarus and its Tablet Formulation

2013 ◽  
Vol 1 (1) ◽  
pp. 1-18
Author(s):  
Sandeep Arora ◽  
Arvind Sharma ◽  
Parneet Kaur
Keyword(s):  
Tablet Formulation ◽  
Phospholipid Complex

A comparison of the effect of native and sonicated Maize starch on batter rheology and nugget quality

2017 ◽  
Vol 10 (4) ◽  
pp. 448-459
Author(s):  
Sepideh Yosefzadeh Sani* ◽  
◽  
Ali Mortazavi** ◽  
Zahra Sheikholeslami*** ◽  
Amir Hosesein Elhamirad***** ◽  
...  
Keyword(s):  
Maize Starch

Exploration of Neem Gum, Acrylamide Grafted Neem Gum and Carboxymethylated Neem Gum as Retardant in Tablet Formulation

2020 ◽  
Vol 16 (9) ◽  
pp. 1404-1410
Author(s):  
Rishabha Malviya
Keyword(s):  
Diclofenac Sodium ◽  
Tablet Formulation ◽  
Angle Of Repose ◽  
Wet Granulation ◽  
Binding Agent ◽  
Grafted Polymer ◽  
Model Drug ◽  
Tablet Dosage ◽  
Tapped Density ◽  
Derivatives Of

Background: In the previous study, investigators have synthesized acrylamide grafted and carboxymethylated derivatives of neem gum and evaluated their potential in the formulation of nanoparticles. In continuation of previous work, authors have evaluated neem gum polysaccharide (NGP), acrylamide grafted neem gum polysaccharide (NGP-g-Am) and carboxymethylated neem gum polysaccharide (CMNGP) as binding agent in the tablet dosage form. Methods: Diclofenac sodium was used as a model drug while microcrystalline cellulose and talc were used as excipient in the preparation of granules employing wet granulation technique. NGP, NGP-g-Am and CMNGP were utilized as binding agent in the preparation of granules. Prepared granules were characterized for various pre-compression and post-compression parameters. Results and Discussion: Binding agents were used in the concentration of 4-24%w/w. NGP incorporated granules showed more bulk density and lower values of tapped density, Carr’s index, bulkiness, Hausner’s ratio and angle of repose as compared to NGP-g-Am consisting granules. NGP-g-Am consisting tablets showed more hardness and zero friability as compared to NGP based tablets. Drug content was found lower for the tablets having grafted polymer in place of NGP. CMNGP were also utilized to prepare granules but granules were not be able to compress keeping all the compacting parameters same as used in the case of NGP and NGP-g-Am consisting granules. NGP and NGP-g-Am were able to sustain drug release up to 6 and 8 h, respectively. Conclusion: It can be concluded that NGP-g-Am induces better properties when used as a binder in the tablet formulation than native polymer, while CMNGP cannot be utilized as a binding agent in the preparation of a tablet.

Preparation and characterization of chemically modified high amylose maize starch-ascorbyl palmitate inclusion complexes in mild reaction condition

LWT ◽  
2021 ◽  
Vol 142 ◽  
pp. 110983
Author(s):  
Dingpeng Zhou ◽  
Shaowei Liu ◽  
Haoyu Song ◽  
Xue Liu ◽  
Xiaozhi Tang
Keyword(s):  
Inclusion Complexes ◽  
Ascorbyl Palmitate ◽  
Maize Starch ◽  
Chemically Modified ◽  
Reaction Condition ◽  
High Amylose

scholarly journals Development of effervescent tablet formulation for rapid control of mosquito problem in early stages from different breeding sites

2021 ◽  
Vol 14 (4) ◽  
pp. 103082
Author(s):  
Nusrat Iqbal ◽  
Amrish Agrawal ◽  
Jitendra Kumar
Keyword(s):  
Tablet Formulation ◽  
Breeding Sites ◽  
Early Stages ◽  
Rapid Control ◽  
Effervescent Tablet
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