Reversible Cholinesterase Inhibitor Loaed Chitosan Based Nanoparticle

Main Article Content

Dr. Subhasri Mohapatra

Abstract

Memantine hydrochloride is a is a reversible cholinesterase inhibitor used in the treatment of Alzheimer’s disease, low-moderate affinity, uncompetitive n-methyl-d-aspartate (NMDA) receptor antagonist, with strong voltage dependency and rapid blocking/unblocking kineticsThe present study was explore the potential of mamentine loaded nanoparticle.with varying quantity of chitosan byionotropic gelation method.The effect of chitosan quantity on the particle size was studied by varying stirring time and stirring speed. The particle morphology can be modulated by selecting the agitation speed as well as drug polymer ratio In the present study.The evaluation parameters like Zeta potential, Entrapment efficiency and Poly dispersity index,of optimized formulation CN15 was found to be 364.2±3.37, -8.46, 79.9±0.2 sand 0.283± 0.048 respectively Determination of percentage yield and loading  efficiency,in vitro drug release was also found optimum en 99-100%.

Article Details

How to Cite
Mohapatra, D. S. . (2023). Reversible Cholinesterase Inhibitor Loaed Chitosan Based Nanoparticle. International Journal of Pharmaceutical and Bio Medical Science, 3(3), 130–136. https://doi.org/10.47191/ijpbms/v3-i3-07
Section
Articles

References

I. Venkateswara Rao S, Md. Meherunnisa, K. Padmalatha. Formulation, characterisation and in-vitro evaluation of novel ionically cross linked casein nanoparticles for memantine hydrochloride delivery. IJPSR. 2018; 9(8): 3307-3316.

II. Muzzarelli RAA, ed. Natural Chelating Polymers. New York: Pergamon Press, 1973; 83–227.

III. Zikakis JP, ed. Chitin, Chitosan and Related Enzymes. New York: Academic Press, 1974.

IV. Kumar MNVR. A review of chitin and chitosan applications. React Funct Polym 2000; Paul JA, Borm and Wolfgang Kreyling., Toxicological Hazards of Inhaled Nanoparticles- Potential Implications for Drug Delivery. J Nanosci Nanotech. 2004; 4(6):1- 11.

V. Kost J, Horbett TA, Ratner BD, Singh MJ. Biomed. Mater. Res. 1985; 19: 1117.

VI. Cristina Buzea, Ivan Pacheco, Kevin Robbie., Nanomaterials and Nanoparticles:Sources and Toxicity., Biointerphases. 2007; 2: MR17– MR7146: 1–27

VII. Calvo, et al. Journal of Applied Polymer Science. 1997;63:125-132.

VIII. Yesim A, Karine Andrieux B, Maria Jose Alonso C, et al. Int J Pharm. 2005;298:378-383.

IX. Rawat M, Singh D, Saraf S, Nanocarriers: Promising Vehicle for Bioactive Drugs. Biol. Pharm. Bull.2006; 29(9):1790-1798.

X. Zengshuan M, Tit Meng L, Lee-Yong L, et al. Int J Pharm. 2005;293:271-280.

XI. Nandgude T, Thube R, Jaiswal N, Deshmukh P, Chatap V, Hire N. Int J Pharm Sci Nanotechnol. 2008;1:177-182.

XII. Miller SC, Donovan MD. Int J Pharm. 1982;12:142-152.

XIII. Douglas SJ, Davis SS, Illum L. Nanoparticles in drug delivery. Rev, Ther, Drug Carr, Syst.1987; 3(3): 233.

XIV. Cherian AK, Rana AC, Jain SK. Drug Dev. Ind. Pharm.2000; 26(4): 459.

XV. Taylor R, Coulombe, S, Otanicar T, Phelan P, Gunawan, A, Lv, W, Rosengarten G.Small particles, big impacts: A review of the diverse applications of nanofluids. Journal of Applied Physics. 2013; 113: 011301.