Design and fabrication of different nano formulation for in corporation of selected poorly soluble phytochemicals
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newlineABSTRACT
newlinePhytochemicals are a rich source of medicines that are helpful in treating wide
newlinerange of chronic inflammatory diseases such as rheumatoid arthritis (RA),
newlineneurodegenerative diseases, and ocular inflammation/ocular distress conditions. Treating
newlinethese classes of diseases still poses a major challenge globally. Not many drugs are
newlineavailable for treating this class of diseases. Naringin (NAR), Sulforaphane (SFN), and
newlinePhenethyl isothiocyanate (PEITC) are phytochemicals with promising anti-inflammatory
newlineproperties. However, their clinical effectiveness gets hindered due to their non-
newlinecomplying pharmacokinetic parameters, such as poor solubility and stability. To address
newlinethese limitations, we used novel drug delivery systems to improve the pharmacokinetics
newlineof poorly soluble phytochemicals which can treat these abovementioned disease
newlineconditions effectively.
newlineFor the current thesis, I have chosen to study different formulations of
newlinephytochemicals (NAR, SFN and PEITC), either alone or as their combinations as
newlinenanoformulations. The therapeutic efficacy of prepared nano-formulations was assessed
newlinein suitable animal models.
newlineThe objective of this thesis is, therefore, to prepare either combinations or single
newlinenanoformulations. Study the preparations thoroughly in different in vivo models of acute
newlineand chronic inflammation, such as Acute inflammation rat model (Carrageenan
newline/Histamine/Egg-albumin), Sub-chronic rat model (Cotton-pellet induced granuloma) and
newlineChronic inflammatory (FCA induced rat model); Neurodegenerative diseases (Catalepsy
newlinerat model); and in rabbit eye model (Carrageenan inflammation and IOP studies).
newlineThe results from ELISA, histopathology, and radiology studies of FCA induced
newlinearthritic rat model showed that these pure phytochemicals via the oral route of
newlineadministration exhibited better therapeutic efficacy at their higher doses. (NAR at dose
newline20mg/kg, SFN at dose 5mg/kg, and PEITC at 5mg/kg , respectively.)
newlineThe polymeric nanoparticles (NPs) of NAR (NAR-PLGA-NPs) were prepared b
newline