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American Journal of PharmTech Research

V. Madhavan

Author Profile
Department of Pharmacognosy, M. S. Ramaiah College of Pharmacy, M.S.R.I.T., Bangalore – 560054,India.
2
Publications
1
Years Active
8
Collaborators
29
Citations

Publications by V. Madhavan

2 publications found • Active 2012-2012

2012

2 publications

Synthesis and Biological Evaluation of 2-(1h-Benzotriazol-1-Yl) Acetohydrazide Containing Isatin Derivatives

with B. V. Suma, Surendra Kumar, C. H. S. Venkataramana, Judy Jays
6/1/2012

Benzotriazole was condensed stoichiometrically with ethyl chloro acetate in presence of potassium carbonate. The resulting ethyl-1H-benzotriazole-1yl-acetate was reacted with hydrazine hydrate in ethanolic solution. The resulting 2-(1H-benzotriazole-1-yl) aceto hydrazide was characterized by physical data and spectral studies and further it was condensed with 1H-indole-2,3-dione derivatives to form 2-(1H-benzotriazole-1-yl)-N'-[(3Z)-2-oxo-1,2-dihydro-3H-indol-3-ylidene] aceto hydrazide derivatives. These derivatives were characterized by melting point, TLC, IR, 1H-NMR and Mass spectrum. From the biological activity profile it was revealed that they have considerable anti-inflammatory activity & antimicrobial activity against S. aureus, B. subtilis, Klebsiella and E. Coli.

Plantago Ovata Mucilage: A Natural Release Rate Retardant In Aceclofenac Tablet Formulation

with B. V. Basavaraj, P. Anusha, S. Bharath, R. Deveswaran
4/1/2012

In the present work, an attempt has been made to study the sustaining release property of isolated mucilage powder of Plantago ovata by formulating the sustained release tablets of aceclofenac and comparing its efficiency with hydrophilic matrix polymer HPMC K4 M. The drug compatibility with mucilage was checked by FTIR studies and found to be intact and stable. The results of pre-compression studies revealed that they were within prescribed limits that indicate good flowing property. All the formulations were found to be within the acceptable limits of official weight variation test. In all the formulations, friability was less than 1 % indicating good mechanical resistance of tablets. Drug content was found to be within acceptable limits. The formulations were also evaluated for hardness, thickness and dissolution profile. The data of drug dissolution was fitted into kinetic models which revealed that all the formulations followed Peppas release kinetics. The results revealed that the formulation F4 showed sustained drug release up to 12 hours. It also revealed that the isolated mucilage powder of Plantago ovata showed better sustained release over HPMC K4 M. In conclusion, Plantago ovata mucilage, obtained from natural source could be used as a reliable alternative over the synthetic polymers used for sustained release formulations. Key words: Aceclofenac, Plantago ovata mucilage, HPMC K4 M, Release retardant

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