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American Journal of Pharmacy and Health Research

Preeti Kothiyal

Author Profile
2
Publications
2
Years Active
4
Collaborators
88
Citations

Publications by Preeti Kothiyal

2 publications found • Active 2016-2017

2017

1 publication

A Review on Chia Seeds: Salvia hispanica

with Nidhi Gairola, Prof. (Dr.) Preeti Kothiyal
12/1/2017

ABSTRACTChia seeds (obtained from plant Salvia hispanica; Lamiaceae family.) are referred to be the superfoods in the health community. These seeds are rich in protein, dietary fibers, omega 3 fatty acid, flavonoids, polyphenolic compound, Vitamin C&K. Minerals like potassium, manganese, copper, calcium, magnesium also contribute toward its nutritional profiling. It’s oil is rich in several bioactive compounds namely quercetin, kaempferol, myricetin, cholorgenic acid & 3,4-dihydroxyphenyl ethanol- elenolic acid di-aldehyde (DHPEA-EDA) .Study showed that chia seeds exhibited anti-inflammatory, anti-cancer, anti-hyperglycemic, anti-oxidant properties. Keywords: Chia seeds, Salvia hispanica, Super food, Omega 3-fatty acid, polyphenolic compound, antioxidant.

2016

1 publication

Preparation and Evaluation of Donepezil Loaded Nanoparticles

with Renu Tiruwa, Sayantan Mukhopadhyay
7/1/2016

The purpose of the present study was to formulate and evaluate donepezill loaded nanoparticles for effective treatment of Alzheimer’s disease. Drug loaded nanoparticles was prepared by using modified nanoprecipitation technique, for this Ethyl Cellulose was selected as polymer in different ration with drug. The prepared nanoparticles were then subjected to several evaluation parameters like measurement of particles size, zeta potential, surface morphology, surface entrapment and drug content, in vitro dissolution study and stability study. Experimental results revealed that % yield was in range of 33.5% to 40.83% and drug entrapment was 70.003% to 86.8%. Particle size evaluation clearly state that prepared formulation within nano range (61.21 to 265.6 nm). Zeta potential value was find in the range of -32.9 to -17.4 mv and surface morphology study indicate smooth surface without fracture. In vitro release study shows that drug was released at a control rate and release rate depends on polymeric concentration. By kinekic study it was observed that zero order model is dominant for all five formulations and in all cases a super case II transport mechanism is dominant. After comparing all the evaluation parameter, formulation F4 was selected as optimized formulation and subjected for stability study which indicate that optimized formulation was stable. From this experiment it was clearly concluded that Donepezil Hydrochloride (model drug) can be successfully delivered to brain by preparing the nanoformulation at a control rate.

Author Statistics
Total Publications:2
Years Active:2
First Publication:2016
Latest Publication:2017
Collaborators:4
Citations:88