Title : Evaluation of polymeric systems for buccal drug delivery of Rasagiline mesylate

Type of Material: Thesis
Title: Evaluation of polymeric systems for buccal drug delivery of Rasagiline mesylate
Researcher: Rama, Bukka
Guide: Kalyani, Prakasam
Department: Faculty of Pharmaceutical Sciences
Publisher: Jawaharlal Nehru Technological University, Hyderabad
Place: Hyderabad
Year: 2016
Language: English
Subject: Immunology
Life Sciences
Pharmacology and Pharmacy
Polymeric systems
Rasagiline mesylate
Medical Sciences
Medical and Health Sciences
Dissertation/Thesis Note: PhD; Faculty of Pharmaceutical Sciences, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad; 2016
Fulltext: Shodhganga

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035__|a(IN-AhILN)th_454251
040__|aJNTU_500028|dIN-AhILN
041__|aeng
100__|aRama, Bukka|eResearcher
110__|aFaculty of Pharmaceutical Sciences|bJawaharlal Nehru Technological University, Hyderabad|dHyderabad|ein|0U-0017
245__|aEvaluation of polymeric systems for buccal drug delivery of Rasagiline mesylate
260__|aHyderabad|bJawaharlal Nehru Technological University, Hyderabad|c2016
300__|a163p.|dDVD
502__|cFaculty of Pharmaceutical Sciences, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad|d2016|bPhD
518__|dFebruary 2016|oDate of Award
518__|oDate of Registration|d2008-01-01
520__|aThe present work is planned to evaluate various polymeric systems for buccal drug delivery of Rasagiline Mesylate. Because the route avoids first pass metabolism and improve the bioavailability; in addition to its ease of administration, termination and high patient compliance; the buccal route became very important among other mucosal routes. The various forms of drug delivery systems like tablets, gels, patches and films were administered by buccal route. Because of small size, reduced thickness, flexibility and comfortness, films were selected as the formulation for the evaluation. Rasagiline Mesylate is a selective MAO type B inhibitor, indicated for the treatment of Parkinson s disease either as mono therapy or as an adjuvant to other drugs depending on the severity. The low dose of 1 mg and low oral bioavailability of 36% because of intestinal and first pass hepatic metabolism made the drug suitable for the study. In addition, hypertensive crisis, the major disadvantage of MAO inhibitors, can be overc
650__|aMedical Sciences|2UGC
650__|aMedical and Health Sciences|2AIU
653__|aImmunology
653__|aLife Sciences
653__|aPharmacology and Pharmacy
653__|aPolymeric systems
653__|aRasagiline mesylate
700__|eGuide|aKalyani, Prakasam
856__|uhttp://shodhganga.inflibnet.ac.in/handle/10603/292960|yShodhganga
905__|afromsg

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