Formulation of quercetin tablet : (Record no. 105219)

MARC details
000 -LEADER
fixed length control field 04145ntm a2200349 i 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260714173657.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field t|||||r|||| 000 0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field ta
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 260714t20252025my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0010733 (Local)
Qualifying information Hardback
040 ## - CATALOGING SOURCE
Original cataloging agency UMPSA
Language of cataloging eng
Transcribing agency UMPSA
Description conventions rda
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) FTKKP .M395 2025 r Bc.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Maziah Binti Zakaria, , ,
Relator term author.
245 10 - TITLE STATEMENT
Title Formulation of quercetin tablet :
Remainder of title enhancing solubility with microcrstalline cellulose /
Statement of responsibility, etc. Maziah Binti Zakaria
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Kuantan, Pahang :
Name of producer, publisher, distributor, manufacturer UMPSA,
Date of production, publication, distribution, manufacture, or copyright notice 2025
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice © 2025
300 ## - PHYSICAL DESCRIPTION
Extent xiii, 44 pages :
Other physical details illustrations ;
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
347 ## - DIGITAL FILE CHARACTERISTICS
Source rda
File type text file
Encoding format PDF
500 ## - GENERAL NOTE
General note Faculty of Chemical and Process Engineering Technology
502 ## - DISSERTATION NOTE
Dissertation note Final Year Report (Bachelor of Manufacturing Engineering Technology (Pharmaceuticals) with Hons ) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Include bibliographical reference
520 3# - SUMMARY, ETC.
Summary, etc. This thesis presents the formulation and evaluation of quercetin supplement tablets utilizing microcrystalline cellulose (MCC) as a primary excipient. Quercetin, a flavonoid with significant antioxidant properties, has garnered attention for its potential health benefits, including anti-inflammatory and anti-cancer effects. The objective of this study was to investigate the effect of microcrystalline cellulose on the formulation of quercetin tablets on the physical and mechanical properties of quercetin tablets. The formulation process involved the selection of appropriate excipients, with MCC chosen for its excellent binding and compressibility properties. Various formulations were prepared and subjected to rigorous testing, including pre-formulation studies, tablet compression, and post-compression evaluations. The methodology involved several key steps, beginning with the preparation of raw materials, where quercetin powder, MCC, starch, and magnesium stearate were carefully weighed and prepared to ensure uniformity and compatibility. Pre-formulation experiments were conducted to assess the physical characteristics of quercetin and its compatibility with excipients, leading to the creation of a mixture of quercetin, starch, and varying concentrations of MCC (7%, 10%, 13%, 17%, and 20%), followed by the addition of magnesium stearate as a lubricant. The mixture underwent wet granulation, sieving, and drying to form granules, which were then compressed into tablets using a tablet press machine. Rigorous quality control tests were performed on the tablets, including friability, hardness, weight variation, disintegration, and dissolution tests. The results indicated that varying concentrations of MCC significantly influenced the mechanical properties and dissolution profiles of the quercetin tablets. In friability testing, an increase in MCC content generally improved tablet strength, although a peak was observed at 13% MCC, where friability exceeded acceptable limits. Hardness testing revealed that the hardness of tablets increased with MCC concentration up to 10%, after which it declined, suggesting an optimal range for MCC to enhance tablet integrity. Weight variation analysis showed that the weight of the tablets varied with MCC concentration, indicating that higher MCC levels contributed to better compaction and uniformity. Disintegration times decreased with increasing MCC concentrations, particularly at 17%, which also exhibited the fastest dissolution rate, indicating improved bioavailability of quercetin. Overall, the study successfully demonstrated that MCC plays a crucial role in optimizing the formulation of querceti tablets, balancing mechanical strength and dissolution properties to enhance the therapeutic efficacy of the supplement.
610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Faculty of Chemical and Process Engineering Technology
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Universities and colleges
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Theses
General subdivision Dissertations
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://umpir.ump.edu.my/id/eprint/47617
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Final Year Report
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
  Not lost Library of Congress Classification     UMPLIB GAMBANG UMPLIB GAMBANG 14/07/2026   FTKKP .M395 2025 r Bc. T000004326 14/07/2026 14/07/2026 Final Year Report

Perpustakaan Universiti Malaysia Pahang Al-Sultan Abdullah
26600 Pekan, Pahang Darul Makmur
Phone: +609 431 5063 (Gambang) / +609 431 5035 (Pekan)
Email: umplibrary@umpsa.edu.my

Connect With Us