pH-Responsive Aloe Vera Hydrogels Loaded with Imatinib for Targeting Drug Resistance in Cancer / (Record no. 611346)

000 -LEADER
fixed length control field 02296nam a22001697a 4500
003 - CONTROL NUMBER IDENTIFIER
control field NUST
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Hasan Khan ,Aroob
245 ## - TITLE STATEMENT
Title pH-Responsive Aloe Vera Hydrogels Loaded with Imatinib for Targeting Drug Resistance in Cancer /
Statement of responsibility, etc. Aroob Hasan Khan
264 ## - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Islamabad,
Name of producer, publisher, distributor, manufacturer SMME-NUST ;
Date of production, publication, distribution, manufacture, or copyright notice 2024.
300 ## - PHYSICAL DESCRIPTION
Extent 77p. ;
Other physical details softcopy
Dimensions 30cm.
500 ## - GENERAL NOTE
General note Cancer and its reoccurrence have become a major health problem affecting the<br/>quality of life for millions of individuals every year. The currently available strategies,<br/>radiotherapy, and chemotherapy have non-specific targets, lower solubility, and severe<br/>side effects. Hydrogels are crosslinked polymeric networks with higher swelling<br/>properties, degradation, biocompatibility, and flexibility which can be manipulated based<br/>on the desired application. Incorporating AV can elevate the antioxidant, and anticancer<br/>properties of the hydrogel based drug delivery system (DDS) also warranting enhanced<br/>swelling, drug release, and environmental degradability of the system. Acrylic acid (AA)<br/>induces pH-responsive properties in the hydrogels. The PVA/SA and PVA/SA/AV<br/>hydrogels were synthesized with a pH responsive behavior and investigated at different<br/>pH conditions. The unloaded and loaded PVA/SA and PVA/SA/AV hydrogels with<br/>imatinib (IM) were characterized for their structural morphology, physiochemical<br/>characteristics, and antioxidant and anticancer activity. The IM loaded PVA/SA/AV<br/>hydrogels showed increased pore size in SEM micrographs, enhanced swelling abilities<br/>up to 400%, 100% degradation, 56% encapsulation efficiency, and drug release profiles<br/>of up to 94% in 24 h, compared to PVA/SA hydrogels loaded with IM. Dpph radical<br/>scavenging activity was also observed to be enhanced in PVA/SA/AV hydrogels. Finally,<br/>the cell viability analysis in resistant MCF-7 breast cancer cell lines exhibited 41% cell<br/>viability of the PVA/SA/AV hydrogels loaded with IM implying a promising potential of<br/>AV to be incorporated in a hydrogel based drug delivery system for targeting drug<br/>resistance in cancer.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element MS Biomedical Sciences (BMS)
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Supervisor: Dr. Adeeb Shehzad
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/45792">http://10.250.8.41:8080/xmlui/handle/123456789/45792</a>
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Thesis
Holdings
Withdrawn status Permanent Location Current Location Shelving location Date acquired Full call number Barcode Koha item type
  School of Mechanical & Manufacturing Engineering (SMME) School of Mechanical & Manufacturing Engineering (SMME) E-Books 09/03/2024 610 SMME-TH-1052 Thesis
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