Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/424302
Title: Formulation Development And Evaluation Of Nanosponges For Topical Application
Researcher: Shaikh Nasheer Shadulla
Guide(s): Nagoba Shivappa N.
Keywords: Clinical Pre Clinical and Health
Pharmacology and Pharmacy
Pharmacology and Toxicology
University: Swami Ramanand Teerth Marathwada University
Completed Date: 2022
Abstract: Atopic dermatitis is a hyperproliferative, autoimmune skin disorder. Regardless of the newlineavailability of drugs and advances in therapies, no fast cure is seen in atopic dermatitis newlinepatients. Drugs available for atopic dermatitis treatment have several disadvantages. To newlineovercome this, Nanotechnologically prepared (nanosponges) drug therapy has been practiced newlinewhich has several advantages in atopic dermatitis treatment. newlineNanosponges are nanosized microscopic particles with wide cavities, during which an newlineoversized sort of substances may be encapsulated. These particles possess the flexibility to newlinehold each lipotropic and deliquescent substance and thereby raising the solubility of poorly newlinewater-soluble molecules. Medicine encapsulated inside the nanosponges pores secures newlinepremature destruction and stability of the drug is increased. newlinePresent study aims to formulate Crisaborole-loaded nanosponges utilizing a variety of newlinepolymers for anti-inflammatory research and to ensure a consistent and predictable release of newlinethe medication. The negative effects of this formulation were decreased, as were the newlinefrequency of dosage and the dose. newlineObjective newlineTo formulate nanosponges (NS) and nanosponges based topical hydrogel gels of for newlinefacilitated treatment of atopic dermatitis newlineMethod newlineNS were prepared using polymers ethyl cellulose and HPMC K35 by emulsion solvent newlinediffusion method. Full Factorial design (32) (FFD) was constructed in a fully randomized newlinemanner to formulate and evaluate all nine possible experimental runs. Detailed evaluation newlinestudies for NS and optimized NS were conducted. Optimized nanosponges were incorporated newlinein topical hydrogels. Also, factorial design (32) in a fully randomized manner was constructed newlineto formulate hydrogels and evaluate all nine possible experimental runs. Detailed evaluation newlinestudies for nanosponges based hydrogel and optimized NS based hydrogels were conducted. newlineIn vivo animal studies were also done for optimized formulation. newlineResults newlineThe physical and chemical characteristics displayed by the prepared NS (CF1-C
Pagination: 207p
URI: http://hdl.handle.net/10603/424302
Appears in Departments:Department of Pharmacy

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01_title.pdfAttached File64.59 kBAdobe PDFView/Open
02_certificate.pdf116.77 kBAdobe PDFView/Open
03_abstract.pdf17.71 kBAdobe PDFView/Open
04_declaration.pdf113.69 kBAdobe PDFView/Open
05-acknowledement.pdf246.24 kBAdobe PDFView/Open
06_contents.pdf14.79 kBAdobe PDFView/Open
07_list_of_tables.pdf21.09 kBAdobe PDFView/Open
08_list_of_figures.pdf96.86 kBAdobe PDFView/Open
09_list_of_abbreviations.pdf91.33 kBAdobe PDFView/Open
10_chapter 1.pdf777.78 kBAdobe PDFView/Open
11_chapter 2.pdf171.7 kBAdobe PDFView/Open
12_chapter 3.pdf35.17 kBAdobe PDFView/Open
13_chapter 4.pdf99.92 kBAdobe PDFView/Open
14_chapter 5.pdf43.65 kBAdobe PDFView/Open
15_chapter 6.pdf411.19 kBAdobe PDFView/Open
16_chapter 7.pdf258.8 kBAdobe PDFView/Open
17_chapter 8.pdf2.27 MBAdobe PDFView/Open
18_summary and conclusion.pdf174.07 kBAdobe PDFView/Open
19_bibliography.pdf175.01 kBAdobe PDFView/Open
80_recommendation.pdf153.05 kBAdobe PDFView/Open
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