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Chandigarh, India

Chitkara University is a private university in India with its campus in Punjab and Himachal Pradesh, India. Chitkara University is a UGC recognized university with the right to confer degrees as per the sections 2 and 22 of the UGC Act, 1956. The university offers full courses in undergraduate and postgraduate degree programs in the fields of Engineering, Information Technology, Management, Hospitality, Hotel Administration Architecture, Pharmacy, Mass Communication & Journalism, Architecture, Pharmacy, and Teacher Training. The university has over 10,000 students and more than 600 tenured faculty members. Wikipedia.


Fast melt tablets, also known as fast dissolving tablets, disintegrate instantaneously within the mouth and thus can be consumed without water. The present study was aimed to formulate fast melt tablets of nimesulide by using Ocimum Sanctum seeds as a natural tablet superdisintegrant. Powdered Ocimum seeds were characterized for powder flow properties (bulk density, tapped density, Carr's consolidation index, Hausner ratio, angle of repose), swelling index, viscosity, pH, loss on drying and microbial load. The prepared tablets were evaluated for different tablet parametric tests, wetting time, water absorption ratio, effective pore radius, porosity, packing fraction, in vitro and in vivo disintegration time, in-vitro dissolution and stability studies. The swelling index was evaluated to be 1600. An appreciable effect of the natural material was seen on tablet hardness and friability. The water absorption ratio increased from 56.15 +/- 0.85 to 80.76 +/- 0.70 (A1-A4). Water uptake coupled natural polymer swelling could be the most probable mechanism for concentration dependent reduction in disintegration time by the Ocimum Sanctum seeds. Porosity of the formulated tablets was found to increase from batch A1-A4. The in vitro disintegration results were in line with in vivo disintegration results. The f2 values (in comparison with Nimulid MD) of 95.90 and 93.65 were obtained with A3 and A4 batches respectively. It could be concluded that Ocimum Sanctum seeds could be used as a natural superdisintegrant in the formulation of fast melt tablets. Source


Kumar S.,Chitkara University
Physical Review C - Nuclear Physics | Year: 2012

The Q values of α decay and the half-lives [log 10T1/ 2α(s)] are calculated for the α-decay chains of 293 ,294117 nuclei, within the framework of the isospin cluster model (ICM). In the ICM model the proximity energy is improved by using the isospin dependent radius of parent, daughter, and α particle. For the Q values the binding energy B(A i,Z i) (i=1,2) of any nucleus of mass number A and atomic number Z was obtained from a phenomenological and more generalized BW mass formula given by Samanta and Adhikari. The calculated results in ICM using different Q values, are compared with the experimental data and the other theoretical macro-microscopic (MM) Relativistic Mean Field (RMF) (with NL3 and FSU gold force parameters) model calculations. The estimated values of α-decay half-lives are in good agreement with the recent experimental data. The ICM calculation is in favor of the presence of neutron magic number at N=172. © 2012 American Physical Society. Source


Dutt I.,Chitkara University
AIP Conference Proceedings | Year: 2013

Using twelve different parametrized pocket formulae fusion barrier heights and positions are calculated and confronted with available experimental data. All different parametrized pocket formulae are able to reproduce fusion barrier heights and positions within ±10% and ±20%, respectively. Our detailed study investigate that the parametrized pocket formulae based on models such as Bass 1980, Winther 1995, Prox 1988, and Royer 2001 reproduce the barrier heights nicely as compared to other formulae available in the literature. © 2013 AIP Publishing LLC. Source


The present study was aimed to formulate and evaluate oral controlled release mucoadhesive matrix tablets of taro gum incorporating domperidone as model drug. Tablets were prepared by direct compression and were evaluated for bioadhesive strength and in vitro dissolution parameters. A central composite design for 2 factors, at 3 levels each, was employed to evaluate the effect of criti cal formulation variables, namely the amount of taro gum (X1) and PVP K 30 (X2), on mucoadhesive strength, tensile strength, release exponent (n) and t50 (time for 50% drug release). The mucoadhesive detachment force (evaluated using texture analyzer) was found to be 18.266, 54.684 and 65.904 N for A4, A5 and A6 batches of the formulated tablets. The polynomial equation indicates that taro gum has dominating effect on mucoadhesive strength and both X1 and X2 have almost equal and comparable effect on tensile strength. The drug release follows first order kinetics (release of drug depends on remaining concentration of drug) and shows best linearity (r2 = 0.983) with higuchi model. The release exponent (n) lies between 0.339 and 0.543 indicating drug release from the matrix tablets may be fickian or non fickian (anamolous) depending upon the concentration of natural polymer. T50 was 58, 140 and 220 minutes for A7, A8 and A9 batches showing overriding potential of taro gum but still the effect of PVP K 30 is noteworthy. PVP K 30 has indirect effect on all the factors by increasing tensile strength and making the tablet firm and intact. Source


Orodispersible tablets disperse instantaneously in the mouth so that they can be swallowed without the aid of water. The aim of the present study was to formulate nimesulide orodispersible tablets using locust bean gum as a natural superdisintegrant. The gum was evaluated for powder flow properties, swelling index and loss on drying. Excellent powder flow properties were observed, swelling index was found to be 20 which indicated appreciable capability of locust bean gum to be used as superdisintegrant. The prepared tablets were evaluated against standard superdisintegrant i.e. cross-carmellose sodium. Disintegration time of tablets containing 10 % locust bean gum was found to be 13 seconds. The prepared batches were also evaluated for wetting time, water absorption ratio, effective pore radius, porosity, in vitro and in vivo disintegration time, in vitro release and stability studies. Wetting time was found to reduce from 19 +/- 2 to 11 +/- 3 sec (A1-A4) and 51 +/- 2 to 36 +/- 3 sec (B1-B4). Effective pore radius and porosity were found to be increase with increase in polymer concentration. The superdisintegrant property of locust bean gum may be due to concentration dependent wicking action leading to formation of porous structure which disintegrates the tablet within seconds. In-vivo results were complementary to in-vitro disintegration time results. The in-vitro release studies were compared against marketed nimesulide fast dissolving tablets (Nimulid MD). Stability studies showed that there was no significant change in hardness, friability, tensile strength and assay of the prepared formulations. The f2 values (in comparison with Nimulid MD) of 92.27 and 98.19 were obtained with A3 and A4 batches respectively. Source

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