The influence of stirring position on the product properties of carbamazepine-saccharin co-crystal / (Record no. 105305)

MARC details
000 -LEADER
fixed length control field 03651ntm a2200349 i 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260727101813.0
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 260727t20252025my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0010763 (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 .U45 2025 r Bc.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Umie Umaira, , ,
Relator term author.
245 10 - TITLE STATEMENT
Title The influence of stirring position on the product properties of carbamazepine-saccharin co-crystal /
Statement of responsibility, etc. Umie Umaira
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 xii, 32 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 (Pharmaceutical) 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. Carbamazepine (CBZ) is a widely used drug for the treatment of epilepsy and neuropathic pain; however, its poor solubility and polymorphic behavior limit its therapeutic effectiveness. One promising strategy to enhance its solubility and stability is through co-crystallization with saccharin (SAC). This study investigates the impact of stirrer position on the crystallization and quality of CBZ-SAC co-crystals using a batch cooling crystallization method. The stirrer height was varied at 10 mm, 20 mm, and 30 mm from the bottom of the crystallizer to evaluate its effect on nucleation, crystal morphology, and overall co-crystal formation. The synthesized co-crystals were analyzed using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Differential Scanning Calorimetry (DSC), and particle size analysis to determine their structural integrity and thermal stability. The results revealed that stirrer position significantly influenced crystal formation and quality. A stirrer height of 10 mm resulted in irregular crystal morphology due to inadequate mixing and localized supersaturation, while a height of 30 mm caused excessive turbulence, leading to fragmented and mechanically stressed crystals. The optimal stirrer height was found to be 20 mm, producing uniform, well-defined crystals with enhanced thermal and structural stability. FTIR analysis confirmed the formation of strong hydrogen bonding interactions between CBZ and SAC, while XRD validated the crystalline nature of the co-crystals. Additionally, DSC analysis demonstrated improved thermal stability, reinforcing the pharmaceutical viability of the optimized co-crystals. These findings underscore the importance of optimizing stirring conditions in pharmaceutical crystallization to enhance drug solubility, stability, and overall performance. The results provide valuable insights into improving the co-crystallization process for pharmaceutical applications. Further research is recommended to explore additional process parameters such as solvent selection, cooling rates, and stirring speeds, as well as to evaluate the scalability of this approach for industrial applications. By refining crystallization techniques, this study contributes to the development of more effective and reliable drug formulations.
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/47705
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 27/07/2026   FTKKP .U45 2025 r Bc. T000004357 27/07/2026 27/07/2026 Final Year Report

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