Metal Nanoparticles Enhances Sorafenib Activity against Cancerous Cell Lines / (Record no. 610779)

000 -LEADER
fixed length control field 02647nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Jamil, Muhammad Ammad
245 ## - TITLE STATEMENT
Title Metal Nanoparticles Enhances Sorafenib Activity against Cancerous Cell Lines /
Statement of responsibility, etc. Muhammad Ammad Jamil
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 108p.
Other physical details Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Globally, cancer prevalence is increasing rapidly, requiring urgent development of effective<br/>therapeutics strategies. Cancer is characterized by uncontrolled cell growth and is categorized into<br/>various stages and types, each with different epidemiology. Cancer cell lines are derived from<br/>many tumor types, then cultured in vitro, and are essential for studying cancer genetic and drug<br/>testing. Sorafenib is a multi-kinase inhibitor drug, widely used in treatment of hepatocellular<br/>carcinoma and renal cell carcinoma, but has limitations such as low bioavailability and solubility.<br/>This study deals with the use of bacopa monnieri for the synthesis of copper formulated and zinc<br/>formulated nano-coated drugs; and investigates their effect of on cancer cell line (MCF-7). Both<br/>nano-coated drugs were characterized by various techniques; UV-Vis spectrometry confirmed the<br/>drug absorbance at 262nm and 263nm, Fourier transform infrared spectroscopy (FTIR) confirmed<br/>the presence of interaction between the sorafenib drug and nanoparticles, X-ray diffraction (XRD)<br/>confirmed their crystallinity nature, Scanning electron microscopy (SEM) revealed that copper<br/>formulated nano-coated drug was stable with good coating and surface morphology and zinc<br/>formulated nano-coated drug was less stable due to irregular shape morphology, Dynamic light<br/>scattering (DSL) confirmed that copper formulated nano-coated drug size ranged from 12nm to<br/>13nm and zinc formulated nano-coated drug size ranged from 9nm to 10nm, Zeta potential<br/>confirmed that copper formulated nano-coated drug was stable (fit values ranged between (-21mV ̶<br/>-18mV)) and zinc formulated nano-coated drug was slightly less stable (fit values ranges -7.12mV ̶<br/>+12.35mV). MTT assay showed that copper formulated nano-coated drug has the cell viability of<br/>64.8% with IC50 value of 4.599µM and zinc formulated nano-coated drug has the cell viability of<br/>68.5% with IC50 value of 34.50µM. Both nano-coated drugs exhibited less cell viability than the<br/>actual drug and are stable, thus, making them suitable for the cancer treatment.
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/123456789/45204">http://10.250.8.41:8080/xmlui/handle/123456789/45204</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 08/06/2024 610 SMME-TH-1036 Thesis
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