UGC Approved Journal no 63975(19)

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Published in:

Volume 9 Issue 12
December-2022
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

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Published Paper ID:
JETIR2212051


Registration ID:
505369

Page Number

a443-a450

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Title

preparation and evalution of aspirin

Abstract

Aspirin is a nonsteroidal anti-inflammatory medication (NSAID). . Easily absorbed from the digestive system is aspirin. Aspirin functions in a manner similar to other NSAIDs but also inhibits platelet activity normally. To create acetylsalicylic acid for the first time, scientist Charles Frédéric Gerhardt combined sodium salicylate with acetyl chloride in 1853. Formulations with improved physicochemical qualities is a difficult issue for pharmaceutical researchers and industry. Acetylsalicylic Acid, better known as aspirin, In solutions of ammonium acetate or the acetates, carbonates, citrates, or hydroxides of the alkali metals, aspirin decomposes very quickly. We constructed two-phase enteric-coated granules of aspirin and L-glutamate compound by extrusion spheronization method and fluidized bed coating. Aspirin is classified as a bcs classification ii tablet, which are solid dosage forms manufactured by compression and containing one or more medicines with or without excipients. It offers the least content fluctuation and good dosage accuracy. Tablet additives refer to inert substances used in addition to active components.This aspirin product is collected, refined by recrystallization, and its purity is assessed by measuring its melting temperature. Utilizing a Büchner filtration device, separate the crystals from the liquid while completely removing the aspirin from the flask using tiny amounts of the ice-cold deionized water. The monsanto hardness test equipment was used to measure the hardness of the tablets. Instead, we switched to another piece of equipment and discovered that salicylic acid, which has a molecular weight of 0.330 g, was synthesised by reacting excessively with acetic amhydride. The amount of aspirin product that is theoretically feasible is determined by the amount of salicylic acid utilised because too much aceticanhydride was used. The molecular weight of aspirin is 0.635 g.

Key Words

ASPIRIN, ACETYLSALICYCLIC ACID, NON INFLAMMATORY DRUG, ACETIC ACID.

Cite This Article

"preparation and evalution of aspirin ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 12, page no.a443-a450, December-2022, Available :http://www.jetir.org/papers/JETIR2212051.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"preparation and evalution of aspirin ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 12, page no. ppa443-a450, December-2022, Available at : http://www.jetir.org/papers/JETIR2212051.pdf

Publication Details

Published Paper ID: JETIR2212051
Registration ID: 505369
Published In: Volume 9 | Issue 12 | Year December-2022
DOI (Digital Object Identifier):
Page No: a443-a450
Country: DEHRADUN, UTTARAKHAND, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


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