Analyzing The Hepatoprotective Effects Of Silymarin Encapsulated Pegylated Liposomal Nanoparticles And Vitamin D & E For Targeted Nafld Treatment In Wistar Rats / (Record no. 608372)

000 -LEADER
fixed length control field 02836nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Batool, Farhat
245 ## - TITLE STATEMENT
Title Analyzing The Hepatoprotective Effects Of Silymarin Encapsulated Pegylated Liposomal Nanoparticles And Vitamin D & E For Targeted Nafld Treatment In Wistar Rats /
Statement of responsibility, etc. Farhat Batool
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 2022.
300 ## - PHYSICAL DESCRIPTION
Extent 78p.
Other physical details Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Nanotechnology-based therapeutics have recently emerged as an inventive and optimistic<br/>replacement for traditional therapy. Currently, biocompatible materials are used to create<br/>nanoparticles and they have the potential to deliver drugs more precisely, either inactively by<br/>enhancing the drug nanocarriers' physicochemical characteristics or actively by applying<br/>homing technologies tailored to particular tissues or cells that enable disease site targeting<br/>while minimising side effects. Because of their ability to overcome a wide range of<br/>biomedical, biological or biophysical constraints, NPs can be developed as nanoplatforms for<br/>efficient drug delivery.<br/>Silymarin has a diverse set of in vitro and in vivo actions, including antioxidant, antiinflammatory, dose-dependent anti-apoptotic, and cell transporter altering properties. As a<br/>result, it has the potential to be a promising medication in alternative medicine. However,<br/>oral silymarin has a low bioavailability, which restricts its medical applications. But the<br/>bioavailability of silymarin can be increased by using liposomes as drug delivery systems. In<br/>the current study, the silymarin-loaded pegylated liposomal nanoparticle was successfully<br/>created and employed as a treatment for NAFLD. Liposomal NPs can be created as<br/>nanoplatforms for the effective and targeted delivery of drugs due to their ability to pass<br/>through a number of biological, biophysical, and biomedical barriers<br/>To overcome the drawbacks, silymarin encapsulated liposome nanoparticles were synthesized<br/>utilizing DPPE by the ‘thin film hydration method’ and used against liver cirrhosis for the<br/>first time. To enhance the stability, Polyethylene glycol (PEG) was used to enhance stability<br/>and for inducing the stealth effect, by coating the liposomes nanoparticles. Pegylation<br/>enhances the steric repulsion and is hence known a as better stabilizer for different types of<br/>nanoparticles. PEG follows the erosion-controlled release mechanisthe m of drug that resulta<br/>ed in sustained release. Hence, it is noteworthy that encapsulating the silymarin drug within<br/>liposomes and tailoring these liposome nanoparticles by PEG, is a substantial strategy to<br/>combat NAFLD.
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. Nosheen Fatima Rana
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/31456">http://10.250.8.41:8080/xmlui/handle/123456789/31456</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 02/27/2024 610 SMME-TH-794 Thesis
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