mail
editor@ajptr.com
whatsapp
9409046853
logo

American Journal of PharmTech Research

Devprakash

Author Profile
Department of Pharmaceutical Chemistry, Bharathi College of Pharmacy, Bharthinagara- 571422, Bangalore, India
5
Publications
2
Years Active
15
Collaborators
109
Citations

Publications by Devprakash

5 publications found • Active 2011-2012

2012

3 publications

In vitro Antioxidant Potential of Ethanol Extract and Different Fractions of whole plant of Tephrosia Purpurea (Linn.) Pers.

with B.V. Sumalatha, Senthil Kumar G.P, Tamizh Mani
6/1/2012

The Antioxidant potential of ethanol extract as well as petroleum ether, chloroform, ethyl acetate and aqueous soluble fractions of Tephrosia purpurea (Linn.) Pers., which is widely used in indigenous system of medicine for different purposes. The ethanol extract as well as petroleum ether, chloroform, ethyl acetate and aqueous soluble fraction were analysed for total phenolics content, total flavonoid content and free radical scavenging activity using DPPH (1,1- diphenyl- 2- picryl hydrazyl) radical. The ethanol extract was found more effective than four different fractions of ethanol extract of Tephrosia purpurea. Total phenolics content and total flavonoid content are found to be highest in ethyl acetate fraction and least in petroleum ether and more or less similar in aqueous and chloroform fractions. In general, the results indicate that the ethanol extract and ethyl acetate fraction are rich in phenolic content and flavonoid content with potent free radical scavenging activity implying their importance to human health. Key Words: Antioxidant, Tephrosia purpurea, DPPH.

METHOD DEVELOPMENT AND VALIDATION OF METFORMIN IN BULK AND PHARMACEUTICAL DOSAGE FORMS BY USING SPECTROPHOTOMETRIC METHOD

with Parag. S. Mahadik, Senthilkumar. G. P, Devprakash Dahia, T. Tamiz mani, Priyanka. K. Gaikwad, Sulbha. A. Gavali
2/1/2012

  In the present research a simple, accurate, precise and cost effective UV-Vis spectrophotometric method for the estimation of Metformin, in bulk and pharmaceutical dosage form was illustrated. The absorption maxima of the drug was found to be 233 nm in 0.1 N HCl: Distilled water (27:75). A linear response was observed in the range of 5-10 µg/ml with a regression coefficient of 0.999. Validation parameters were carried out as per the guidelines of International Conference for Harmonization. This method can be used in the industries for determination of Metformin to analyze the quality of formulation without interference of the excipients.

METHOD DEVELOPMENT AND VALIDATION OF GLIBENCLAMIDE IN BULK AND PHARMACEUTICAL DOSAGE FORMS BY USING UV-VIS SPECTROPHOTOMETRIC METHOD

with Rohan Tembare, Suhas Gurav, Sachin Singh
2/1/2012

  A simple, sensitive and accurate spectrophotometric method was developed in ultraviolet region for the estimation of Glibenclamide in pure drug, pharmaceutical formulation. Linear response obtained was in the concentration range of 5-30µg/ml with correlation coefficient of 0.999 in acetronitrile: 0.2M NaOH (20:80). Excellent recovery proved that the method was sufficiently accurate. There is no interference from any common pharmaceutical additives and diluents. Results of the analysis were validated by recovery studies according to ICH Q2B guidelines. Key words: Glibenclamide, UV- Spectrophotometry, recovery, accuracy.

2011

2 publications

SPECTROPHOTOMETRIC DETERMINATION OF CLOPIDOGREL BISULFATE IN PHARMACEUTICAL FORMULATIONS

with Suhas Gurav, Rohan Tembare, Vishali Salunkhe, Senthilkumar G.P
12/1/2011

  A simple, sensitive and accurate spectrophotometric method was developed in ultraviolet region for the estimation of Clopidogrel bisulfate in pure drug, pharmaceutical formulation. Linear response obtained was in the concentration range of 25-50 µg/ml with correlation coefficient of 0.999 in 0.1 N HCl. Excellent recovery proved that the method was sufficiently accurate. There is no interference from any common pharmaceutical additives and diluents. Results of the analysis were validated by recovery studies according to ICH Q2B guidelines.  

METHOD DEVELOPMENT AND VALIDATION OF CLOBAZAM IN BULK AND PHARMACEUTICAL DOSAGE FORMS BY USING SPECTROPHOTOMETRIC METHOD

with Parag. S. Mahadik, Senthilkumar. G. P, Devprakash Dahia, T. Tamizh Mani, Priyanka. K. Gaikwad
12/1/2011

  In the present research a simple, accurate, precise and cost effective UV-Vis spectrophotometric method for the estimation of Clobazam, in bulk and pharmaceutical dosage form was illustrated. The absorption maxima of the drug was found to be 230 nm in methanol: water (1:1). A linear response was observed in the range of 6- 16 µg/ml with a regression coefficient of 0.999. Validation parameters were carried out as per the guidelines of International Conference for Harmonization. This method can be used in the industries for determination of Clobazam to analyze the quality of formulation without interference of the excipients.   Key words: Clobazam, Anti-epileptic, λmax, ICH, UV-Vis spectroscopy.

Whatsapp