Polycaprolactone Nanoparticle Encapsulating Antifouling Ceftaroline for Enhanced In-vitro Controlled Drug Release / (Record no. 607829)

000 -LEADER
fixed length control field 02451nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Hanif, Naeema
245 ## - TITLE STATEMENT
Title Polycaprolactone Nanoparticle Encapsulating Antifouling Ceftaroline for Enhanced In-vitro Controlled Drug Release /
Statement of responsibility, etc. Naeema Hanif
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 79p.
Other physical details Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Globally, infectious diseases are among the top ten significant contributors to large number of fatalities<br/>affecting both developed and developing countries evenly. It has been challenging to treat infections<br/>like skin infections due to the global trend of developing antibiotic resistance. In context of this,<br/>antibiotics that are effective against both gram-positive and gram-negative organisms and have a long<br/>half-life as well as high tissue permeability are needed. Cefepime, a member of the fourth generation<br/>intravenous cephalosporins, is one such antibiotic. However, the intravenous administration of drug has<br/>restricted the supply of drug to the intended area i.e., skin, instead reaches directly to the blood.<br/>This draws attention to the significance of developing a drug delivery system that stays at the skin surface<br/>while regulating drug absorption, boosts the drug's bioavailability, and lessens the requirement for<br/>frequent drug usage. The current research focuses on developing a chitosan nano-carrier using the ionic<br/>gelation method, subsequently transformed into carbopol gel for more effective, longer-lasting skin drug<br/>release. SEM analysis shows the spherical morphology of chitosan/alginate nanoparticles with sizes of<br/>156±12.75nm and 222±56nm for both blank and drug-loaded nanoparticles, respectively. Positive<br/>zetapotential i.e., 18.2mV indicates polycationic chitosan matrix of the nano-capsules. Finally, the in-vitro<br/>drug release study manifested controlled drug release at two different pH (5.5 and 7.4) for a period of<br/>24h. Furthermore, antibacterial activity of nano-formulation as well as the gel was observed against both<br/>+Ve and -Ve bacterial strains with better zones of inhibition. The obtained data significantly pointed out<br/>that the cefepime nanoparticles loaded carbopol gel would be an encouraging choice for skin infections.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element MS Biomedical Science (BMS)
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Supervisor : Dr. Nabeel Anwar
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/42140">http://10.250.8.41:8080/xmlui/handle/123456789/42140</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 02/16/2024 610 SMME-TH-984 Thesis
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