Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/15530
Title: | Novel functionalised polymer for nanoparticle formulaton with anti cancer drug |
Researcher: | Shaik.Md.Zakir Hussain |
Guide(s): | G.VIDYA SAGAR |
Keywords: | Pharmaceutical sciences |
Upload Date: | 3-Feb-2014 |
University: | Shri Jagdishprasad Jhabarmal Tibarewala University |
Completed Date: | 01-02-2013 |
Abstract: | The aim of this study was to investigate whether various polymers and drugs interacts in a specific manner and whether the nature of these interactions I influences the physicochemical characteristic of the particles and their drug loading and release profile. By investigating drugs belonging to various classes and with different properties it has been possible to correlate properties associated with drug and pendent functional group of the polymer which are ultimately responsible for the drug loading and release characteristic. The chemistry and structure of poly (glycerol adipate) facilitate its substitution with various pendent functional groups leading to modification of the physicochemical properties of the polymer. Modified backbone then can be selected based upon the properties of the compound to be incorporated. Thus, this could be explored as a drug delivery system without many of the limitations of commercially available polymer. For some drug polymer formulations, good loading and controlled release rates have been achieved. Compared to various conventional polymer systems reported for nanoparticle formulations, poly (glycerol adipate) polymer have also demonstrated the ability to control rate of release of highly water soluble drugs, even from the most hydrophilic polymer backbone in its unsubustituted form. From the various drug loading and release profile it has been demonstrated that, unlike reported literature, particle size is not the primary factor influencing drug release over the relatively small range of particle size seen in this study. Neither is the water solubility of either the drug or the polymer alone responsible for the rapid and uncontrolled release profile from nanoparticles. Thus, Drug polymer interactions are more likely to influence drug loading and release and unlikely common reports in the literature, hydrophilicity, molecular weight or concentration of polymer / drug are less likely to affect these parameters in isolation. Recently, biodegradable polyesters such as poly |
Pagination: | |
URI: | http://hdl.handle.net/10603/15530 |
Appears in Departments: | Faculty of Pharmacy |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 13.83 kB | Adobe PDF | View/Open |
02_decleration.pdf | 5.09 kB | Adobe PDF | View/Open | |
03_certificate.pdf | 11.71 kB | Adobe PDF | View/Open | |
04_acknowledment.pdf | 5.84 kB | Adobe PDF | View/Open | |
05_contents.pdf | 10.98 kB | Adobe PDF | View/Open | |
06_list of tables.pdf | 18.96 kB | Adobe PDF | View/Open | |
07_list of figures.pdf | 22.35 kB | Adobe PDF | View/Open | |
08_abstract.pdf | 14 kB | Adobe PDF | View/Open | |
09_chapter -1 introduction 1-11.pdf | 173.04 kB | Adobe PDF | View/Open | |
10_chapter-2 material and methods 12-15.pdf | 36.33 kB | Adobe PDF | View/Open | |
11_chapter-3 results and discussion 16-51.pdf | 642.86 kB | Adobe PDF | View/Open | |
12_chapter-4 summary and conclusion 52-53.pdf | 16.98 kB | Adobe PDF | View/Open | |
13_ refferences 54-56.pdf | 31.59 kB | Adobe PDF | View/Open | |
14_ annexure 57-74.pdf | 199.77 kB | Adobe PDF | View/Open |
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