Synthesis, Characterization and Evaluation of antioxidant properties of Catechin Hydrate nanoparticles

Authors

  • Ramneek Kaur Department of Biotechnology, Jaypee Institute of Information Technology, Noida - 201307, India.
  • Rashi Rajput Department of Biotechnology, Jaypee Institute of Information Technology, Noida - 201307, India.
  • Payal Nag Department of Biotechnology, Jaypee Institute of Information Technology, Noida - 201307, India
  • Rachana Department of Biotechnology, Jaypee Institute of Information Technology, Noida - 201307, India
  • Manisha Singh Department of Biotechnology, Jaypee Institute of Information Technology, A-10, sector 62, Noida, Uttar Pradesh., India-201307

Keywords:

Ionic gelation, encapsulation efficiency, statistical modelling, release kinetics, antioxidant activity

Abstract

Catechin hydrate (CH), is an important phyto compound, reported to have potential therapeutic activity for prevention and treatment of various central nervous system (CNS) disorders. However, its therapeutic action is limited by their low oral bioavailability, poor stability and intestinal absorption, therefore, development of a targeted nanoparticle based carrier system which can overcome its physicochemical limitations and can enhance its biological activity is required. The objective of the present study was to formulate nanoparticle based formulation by ionic gelation method for catechin hydrate. Result and conclusion: After optimising the formulation by statistical tool, further, characterization results showed zeta average particle size of 68.76 ± 1.72 nm along with polydispersibility index of 0.174 ± 0.81 and zeta potential of -5.32 mV. Moreover, TEM analysis also confirmed its nanometric size range (range of 61. 8- 128nm) and FT – IR scan showed no bond formation between polymers and loaded extract (CH). The in vitro compound release kinetics showed a typical linear diffusion profile and cytotoxicity analysis done on NB41A3 cell lines results exhibited the cell viability of 89.5 ± 0.25% in catechin loaded nanoparticles (CH NP’s) whereas, it is 82.7 ± 0.34% in CH indicating negligible toxicity in nanoparticle based formulation. The stability testing was done for CH NP’s after 8 weeks, and results revealed minimal degradation of catechin. Lastly, the antioxidant activities estimated through DPPH (2, 2 – Diphenyl-1-picrylhydrazyl-hydrate), Nitric oxide (NO) and Hydrogen peroxide (H2O2) scavenging assays revealed that CH NP’s have higher and prolonged antioxidant activity in comparison with CH.

References

. Carlini EA. Plants and the central

nervous system. Pharmacol Biochem

Behav, 2003;75(3): 501-12.

. Farver D. The use of "natural products"

in clinical medicine. S D J Med.

;49(4): 129-30.

. Dube A, Nicolazzo JA, and Larson I.

Chitosan nanoparticles enhance the

intestinal absorption of the green tea

catechins (+)-catechin and (-)-

epigallocatechin gallate. Eur J Pharm

Sci. 2010;41(2): 219-25.

. Munin A and Edwards-Levy F.

Encapsulation of natural polyphenolic

compounds; a review. Pharmaceutics.

; 3(4): 793-829.

. Gomes NG. Plants with neurobiological

activity as potential targets for drug

discovery. Prog

Neuropsychopharmacol Biol

Psychiatry. 2009;33(8): 1372-89.

. Fang Z , Bhandari B. Encapsulation of

polyphenols – a review. Trends in Food

Science & Technology. 2010;21(10):

-523.

. Liu Z. Polysaccharides-based

nanoparticles as drug delivery systems.

Adv Drug Deliv Rev. 2008;60(15):

-62.

. Agnihotri SA, Mallikarjuna NN and

Aminabhavi TM. Recent advances on

chitosan-based micro- and

nanoparticles in drug delivery. J

Control Release. 2004;100(1): 5-28.

. Dodane V, Vilivalam VD.

Pharmaceutical applications of

chitosan. Pharmaceutical Science &

Technology Today. 1998;1(6): 246-

. Fan W. Formation mechanism of

monodisperse, low molecular weight

chitosan nanoparticles by ionic gelation

technique. Colloids Surf B

Biointerfaces. 2012; 90: 21-7.

. Shu XZ and Zhu KJ. A novel approach

to prepare tripolyphosphate/chitosan

complex beads for controlled release

drug delivery. Int J Pharm. 2000;

(1): 51-8.

. Hooda A. Optimization and evaluation

of gastroretentive ranitidine HCl

microspheres by using design expert

software. Int J Biol Macromol.

;51(5): 691-700.

. Padhye SG, Nagarsenker MS.

Simvastatin Solid Lipid Nanoparticles

for Oral Delivery: Formulation

Development and In vivo Evaluation.

Indian J Pharm Sci. 2013; 75(5): 591-8.

. Nagpal K, Singh SK and Mishra DN.

Optimization of brain targeted chitosan

nanoparticles of Rivastigmine for

improved efficacy and safety. Int J Biol

Macromol, 2013;59: 72-83.

. Gan Q , Wang T. Chitosan nanoparticle

as protein delivery carrier--systematic

examination of fabrication conditions

for efficient loading and release.

Colloids Surf B Biointerfaces. 2007;

(1): 24-34.

. Ramos-Tejada MM. Investigation of

alumina/(+)-catechin system properties.

Part I: a study of the system by FTIRUV–Vis spectroscopy. Colloids and

Surfaces B: Biointerfaces. 2002; 24(3–

: 297-308.

. Lee DW, Powers K, Baney R.

Physicochemical properties and blood

compatibility of acylated chitosan

nanoparticles. Carbohydrate Polymers.

; 58(4): 371-377.

. Xu BJ, Chang SK. A comparative study

on phenolic profiles and antioxidant

activities of legumes as affected by

extraction solvents. J Food Sci.

;72(2): 159-66.

. CHEN CW, HO CT. Antioxidant

properties of polyphenols extracted

rom green and black teas. Journal of

food lipids. 1995;2(1): 35-46.

. Re R. Antioxidant activity applying an

improved ABTS radical cation

decolorization assay. Free Radical

Biology and Medicine. 1999; 26(9–10):

-1237.

. Verma V, Ram A. Preparation,

characterization and in-vitro release of

piroxicam–loaded solid lipid

nanoparticles. Int. J. Pharm. Sci

Nanotech. 2010;3: 1136-1146.

. Jenning V, Schafer-Korting M, Gohla S.

Vitamin A-loaded solid lipid

nanoparticles for topical use: drug

release properties. J Control Release.

;66(2-3): 115-26.

. Gerlier D, Thomasset N. Use of MTT

colorimetric assay to measure cell

activation. Journal of Immunological

Methods. 1986;94(1): 57-63.

. Freitas C, Müller RH. Effect of light and

temperature on zeta potential and

physical stability in solid lipid

nanoparticle (SLN™) dispersions.

International Journal of Pharmaceutics.

;168(2): 221-229.

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Published

06/30/2017

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Original Research Articles