Formulation of pangasianodon hypophthalmus (ikan patin) collagen/pva hydrogel loaded with curcumin nanoparticles for wound healing / (Record no. 104219)

MARC details
000 -LEADER
fixed length control field 04307nam a22003377a 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260223103731.0
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 260223t20252025my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0010366 (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 .S53 2025 r Thesis
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Md Shaekh Forid,
Relator term author.
245 10 - TITLE STATEMENT
Title Formulation of pangasianodon hypophthalmus (ikan patin) collagen/pva hydrogel loaded with curcumin nanoparticles for wound healing /
Statement of responsibility, etc. Md Shaekh Forid
260 #1 - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Kuantan, Pahang :
Name of publisher, distributor, etc. UMPSA,
Date of publication, distribution, etc. 2025
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice © 2025
300 ## - PHYSICAL DESCRIPTION
Extent xiv, 126 pages :
Other physical details illustrations ;
Dimensions 30 cm. +
Accompanying material 1 CD-ROM.
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 Thesis (Master of Science) -- Universiti Malaysia Pahang - 2025
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographical references
520 3# - SUMMARY, ETC.
Summary, etc. Effective wound healing remains a critical challenge in global healthcare, as conventional dressings often fail to provide optimal healing conditions and can cause discomfort, irritation, and delayed recovery. Hydrogels have emerged as a promising agent for wound care but commercial availability of bioactive drug-loaded hydrogels remains limited. Curcumin, known for its multifaceted pharmacological properties, faces challenges in topical applications due to poor solubility and limited skin permeability. Additionally, concerns regarding the use of collagen in hydrogel fabrication, such as disease transmission from bovine and porcine sources and issues of religious acceptability have prompted the exploration of alternative collagen sources. To address these limitations, curcumin nanoparticles (CNPs) were prepared using antisolvent precipitation method and incorporated into a hydrogel composed of collagen extracted from Pangasianodon hypophthalmus fish skin and polyvinyl alcohol (PVA). The prepared CNPs had a size of 118.20 nm and cell viability assays revealed that a dose of 500 μg/mL was the safest dose. The swelling behavior of the hydrogels was pH-dependent, with the highest observed 1304-1337% at pH 5.4. In vitro biodegradation studies showed 50-60% degradation at different pH over 14 days, confirming their degradability. Water vapor transmission rate (WVTR) measurements of the CNPs-loaded hydrogel (2216.68 ± 65.37 g/m²/day) aligned with the ideal range of 2000 to 2500 g/m²/day for wound dressings. The CNPs-loaded hydrogel exhibited 59.32 ± 3.34% porosity and demonstrated good mechanical properties. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analyses confirmed the purity of the CNPs-loaded hydrogel. Field emission scanning electron microscopy (FESEM) revealed a porous and interconnected structure in the collagen/PVA hydrogel, with a heterogenous structure observed after the incorporation of CNPs. Cell viability assays on 3T3-L1 cells showed that hydrogels containing CNPs at concentration of 15.62 μg/ml, 31.25 μg/ml and 62.5 μg/ml exhibited over 85% cell viability, indicating good biocompatibility. In vitro wound healing assessments via wound scratch assay on 3T3-L1 cell line demonstrated 95% wound closure at a concentration of 62.5 μg/ml CNPs-loaded hydrogel, significantly higher compared to native collagen/PVA hydrogel of 79%. Ex-vivo skin penetration studies revealed that 49.78±1.37% of the drug penetrated within 72 hours. Drug release kinetics followed the Korsmeyer Peppas model (R² = 0.944). Furthermore, CNPs-loaded hydrogel at a concentration of 62.5 μg/ml significantly increased TGF-β1 expression and decreased MMP-9 expression, suggesting a favorable effect on the wound healing process. These findings indicate that the developed CNPs-loaded hydrogel holds significant potential as an advanced wound dressing by promoting a favorable biological response for effective wound healing. However, further in vivo studies are required to validate its efficacy.
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
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Thesis
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Use restrictions 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   Restricted access   UMPLIB GAMBANG UMPLIB GAMBANG 23/02/2026   FTKKP .S53 2025 r Thesis T000004018 23/02/2026 23/02/2026 Restricted Collection
  Not lost Library of Congress Classification   Restricted access In Transit UMPLIB GAMBANG UMPLIB GAMBANG 23/02/2026   CD13921 T000004019 23/02/2026 23/02/2026 Restricted Collection

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