MARC details
| 000 -LEADER |
| fixed length control field |
04628ntm a2200373 i 4500 |
| 003 - CONTROL NUMBER IDENTIFIER |
| control field |
MY-KuUP |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
| control field |
20251125105738.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS |
| fixed length control field |
t||||fr|||| 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 |
201016t20192 M a|||fram|| 000 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
| International Standard Book Number |
THE0008919(Local) |
| Qualifying information |
hardback |
| 040 ## - CATALOGING SOURCE |
| Original cataloging agency |
UMP |
| Language of cataloging |
eng |
| Transcribing agency |
UMP |
| 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 .A45 2019 r Thesis |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
| Personal name |
Aljbour, Nawzat Deeb, |
| Relator term |
author. |
| 245 10 - TITLE STATEMENT |
| Title |
Preparation and characterization of chitosan/poly lactic acid nanofibers using electrospinning process for drug delivery applications / |
| Statement of responsibility, etc. |
Nawzat Deeb Aljbour |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
| Place of production, publication, distribution, manufacture |
Kuantan, Pahang : |
| Name of producer, publisher, distributor, manufacturer |
UMP, |
| Date of production, publication, distribution, manufacture, or copyright notice |
2019 |
| 264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
| Date of production, publication, distribution, manufacture, or copyright notice |
© 2019 |
| 300 ## - PHYSICAL DESCRIPTION |
| Extent |
xxi, 177 pages : |
| Other physical details |
illustrations (some color) ; |
| Dimensions |
30 cm. + |
| Accompanying material |
1 CD-ROM |
| 336 ## - CONTENT TYPE |
| Content type term |
text |
| Source |
rdacontent |
| 336 ## - CONTENT TYPE |
| Content type term |
text |
| Source |
rdacontent |
| 337 ## - MEDIA TYPE |
| Media type term |
unmediated |
| Source |
rdamedia |
| 337 ## - MEDIA TYPE |
| Media type term |
computer |
| Source |
rdamedia |
| 338 ## - CARRIER TYPE |
| Carrier type term |
volume |
| Source |
rdacarrier |
| 338 ## - CARRIER TYPE |
| Carrier type term |
computer disc |
| Source |
rdacarrier |
| 347 ## - DIGITAL FILE CHARACTERISTICS |
| File type |
text file |
| Encoding format |
PDF |
| Source |
rda |
| 500 ## - GENERAL NOTE |
| General note |
Faculty of Chemical and Process Engineering Technology |
| 502 ## - DISSERTATION NOTE |
| Dissertation note |
Thesis (Doctor of Philosophy in Chemical Engineering) -- Universiti Malaysia Pahang – 2019 |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE |
| Bibliography, etc. note |
Includes bibliographical references |
| 520 3# - SUMMARY, ETC. |
| Summary, etc. |
Nanofibers are considered as a new class of highly important materials in the biomedical field, whereas free surface wire electrospinning system is one of the most versatile technologies for the continuous and mass production of nanofibrous layers. On the other hand, chitosan is a bio-derived, biodegradable and biocompatible polymer. However, the production of chitosan nanofibers is considered difficult because the application of high electric field during electrospinning triggers the repulsive forces between the ionic groups within the polymer backbone, resulting into formation of beads instead of continuous fibers. In addition, the low solubility of chitosan is another major limitation for the production of chitosan nanofibers. In this study high molecular weight chitosan was converted to low molecular weight chitosan with subsequent deacetylation, to produce low molecular weight chitosan with different degrees of deacetylation. These were further blended with a solution of poly(lactic) acid (PLA) in dichloromethane to facilitate the spinning process. The chitosan-PLA blend was electrospun using the free surface wire electrospinning process and the produced nanofibers were characterized for their surface properties using scanning electron miscroscopy (SEM) and contact angle analysis. In addition, the structural properties were determined through fourier transforms infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). Furthermore, mechanical and physicochemical characterizations were conducted using different techniques. Fibers with the best performance were then modified for drug delivery applications by loading a model drug, Diclofenac Sodium (DNa), into the nanofibers, after which it was characterized accordingly using different elemental and physicochemical techniques. Then, the potential of the fabricated nanofibers for drug delivery applications was verified through in vitro release studies as well as drug release kinetic studies. Results showed that 25% fully deacetylated chitosan of 15 kDa and 7.5 kDa produces better quality nanofibers compared with the higher molecular weight (30 kDa) chitosan. Significantly, the produced nanofibers showed improved mechanical properties compared with the previously reported chitosan nanofibers prepared using the high molecular weight chitosan. In fact, the tensile strength (3 MPa), Young’s modulus (1.5 MPa), and %Elongation (10%) are comparable to the previously reported values of nanofibrous mats produced using different polymers and used for drug delivery applications. On the other hand, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results reveal that the incorporated DNa is distributed within the nanofibers. Notably, release results showed that chitosan-PLA nanofibers prepared using 25% chitosan (15 kDa) could be used to deliver the model drug (DNa) in a controlled release manner for 96 h with burst release of about 25%, and release kinetics follow the Fickian Diffusion kinetics. Therefore, the nanofibers produced herein can open up a new type of nanofibers with both hydrophilic and hydrophobic properties which are highly desirable for the delivery of drugs with various degrees of polarity. |
| 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 |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
| Source of classification or shelving scheme |
Library of Congress Classification |
| Koha item type |
Thesis |