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Page 51

Mater Sci Nanotechnol 2017 | Volume 1 Issue 2

allied

academies

Nanomaterials and Nanochemistry

November 29-30, 2017 | Atlanta, USA

International Conference on

T

enoxicam (TX) is NSAID indicated to treat rheumatoid

arthritis but possess poor solubility, GI irritation and first

pass effect. Hence in the present work it was initially made

as nanoparticles to facilitate absorption and at later stage

nanoparticles loaded transdermal patches were developed

using promising nanoparticles of tenoxicam. Nanoparticles

were prepared with chitosan by ionic-gelation technique Trail

formulations such as F1 to F5 were prepared by using 0.25%

w/v sodium TPP and different concentrations of chitosan

(0.5%,1%, 1.5%,2% and 2.5%,w/v). These formulations were

evaluated for percent drug content, and % drug release

and mean particle size by zeta sizer. They were evaluated

by percentage drug content, in-vitro release, particle size,

zeta potential, DSC and FTIR analysis. Percentage drug

content values were in acceptable range of 99.1 -99.8%. All

formulations were produced in nanosizes and the sizes are

101.10nm, 108.7nm, 178.30nm, 314.3nm, and 923.2nm for

F1, to F5 in sequence. DSC and FTIR analysis indicated there is

no interaction between the drug and polymers. Among them

F4 having mean particle size 178.30nm and zeta potencial

of 35.5 mV45 was considered as pomising formulation.

Transdermal patches of TX were prepared by solvent casting

method using different ratios of polymers HPMC, E.C, and

PVP. Chloroform: methanol (1:1) was used as solvent. Dibutyl

phthalate and propylene glycol were added as plasticizer and

permeation enhancer respectively. Three formulations were

obtained with optimum properties in terms of percentage

drug content (98.56%-99.88%), thickness (1.7mm±0.03 to

1.3mm±0.021 surface pH (6.5 to 6.9), folding endurance

(191 to 200). Ex- vivo permeation studies of a patch (TT6)

containing HPMC K400M 880 mg EC, 270 mg and PVP 260

mg exhibited optimum drug release of 99.51% in 60 min.

e:

jeevanajyothi@yahoo.com

Development of nanoparticles loaded transdermal patches of tenoxicam

B Jeevana Jyothi

Sri Padmavati Mahila Visvavidyalayam, India