Chapter I: preformulation studies on piperlongumine Piperlongumine is a natural alkaloid extracted from piper plant which has been used traditionally for the treatment of certain diseases. This compound shows interesting in-vitro pharmacological activity such as selective anticancer activity and higher cytotoxicity than methotrexate, cyclophosphamide and adriamycin on breast, colon, and osteosarcoma cancers, respectively. However, the physicochemical properties of this compound have not been well characterized. In this research, preformulation studies for piperlongumine have been performed to determine factors which influence solubility and stability which, in turn, can be used to assist future formulation development. The solubility of piperlongumine in water was found to be approximately 26 μg/ml. Using 10% polysorbate 80 as a surfactant resulted in a 27 fold increase in solubility. Cosolvents and cyclodextrins afforded concentrations of 1 mg/ml and higher. The pH degradation rate profile for piperlongumine at various temperatures shows significant instability of the drug at pH values 7 and 3, and maximum stability around pH 4. It was estimated that it would take approximately 17 weeks for piperlongumine to degrade by 10% at 25°C, pH 4. Additionally, piperlongumine showed marked photo-degradation upon exposure to an ultraviolet light source, especially in aqueous media. Chapter II: preformulation and evaluation of resatorvid topical delivery Resatorvid is a small molecule shows interesting anti- inflammatory biological activity. The clinical trial was conducted for sepsis-induced cardiovascular and respiratory failure, but it was terminated due to low efficacy. Further researches show a different biological activity of resatorvid such as its activity against UV-induced skin cancer. The goal of this study is to determine some important physiochemical properties of resatorvid, as well as intrinsic penetration criteria through the murine skin, either ex-vivo or in-vivo. Intrinsic water solubility of resatorvid was found to be 95.32± 1.75 ug/ml and could be duplicated by using 10 % ethanol as cosolvent. The pH solubility profile shows the acidic pka value of resatorvid is around 8-8.1. Photo-stability results indicate more stability in non-aqueous more than aqueous medium. Resatorvid pH degradation rate profiles indicate the maximum stability between pH3 -5 and maximum instability at pH 8 and 9 at all experimental temperatures over 26 days. T90 at 25 °C was 648 days in pH 3 versus 11 days in pH 9. Ex-vivo penetration evaluation for resatorvid through hairless murine skin was evaluated using acetone and phosphate buffer formulations. The flux values were 0.82 and 0.36 for acetone and phosphate buffer formulation respectively. The percent of drug retention in the dermis layer of skin were also evaluated and found to be 37.99% for the acetone formulation and 21.13 % for phosphate buffer formulation. The in-vivo penetration evaluation study was performed by topically applying of resatorvid in acetone solution. Skin biopsy from the site of application was analyzed one, three, eight and 24 hours post-application. The analysis was performed by tape stripping of the stratum corneum of the skin segment. It was found that percent of resatorvid at the dermis layers 5.92, 1.47, 0.45 and 0.23 % for 1, 3, 8 and 24 hours post-application respectively. The percent of resatorvid retention in dermis layer from the in-vivo study are not in compliance with the result of the ex-vivo study, which could refer to possible enzymatic degradation of resatorvid in the live animal skins. Chapter III: correlation of drug penetration between Strat-MTM membranes and murine skin for various drugs. Strat-MTM is a synthetic model for transdermal diffusion testing made by EMD Millipore and was marketed as a new skin mimetic membrane. It has been reported to be predictive of diffusion in human skin. Independent researchers had evaluated this membrane and compared it with animal and human skin and other polymeric membranes. Yet, there are not a published research to correlate the animal skin and Strat-MTM based on the amount of drug retained after topical application, which is one of the critical criteria for dermal drug delivery system. In this research, five compounds, with various physiochemical properties, were selected to perform this correlation. Resatorvid, Methyl Para aminobenzoate (M-PABA), Diclofenac sodium, Salicylic acid and hydrocortisone, each one was dissolved in phosphate buffer saline (pH 7.4) in concentrations of 60 ug/ml for resatorvid and 100-120 ug/ ml for others. All experiments were uniform in the setting and made in triplicate. As a conclusion from the results, the number of tested compounds were shorted to reflect the correlation in flux or permeability coefficient between murine skin and Strat-MTM membrane. With exception of M-PABA, there is a trend of correlation with the percentage of drug retained in dermis layers; however, the number of compounds still low to reflect a real correlation.

Diploma thesis deals with the experimental study of transdermal transport of individual hydroxyacids and their combination with water-soluble vitamins. During this work the literature review was prepared, which was focused on the use of hydroxyacids in the cosmetic and pharmaceutical industries. At the same time the current state of use of water-soluble vitamins for topical applications was studied. Series of experiments was performed using Franz diffusion cells to simulate transdermal transport in vitro across cutaneous, synthetic and artificial Strat M ® membranes. The methodology of sample preparation and analysis of their transport properties was invented and optimized. The optimized methodology was subsequently used in a series of diffusion experiments in which the penetrated amount of hydroxyacids was analyzed by ion chromatography. The concentration of water-soluble vitamins was determined by HPLC. All examined active substances demonstrate positive penetration properties. The best results were obtained with combination of glycolic acid with pyridoxine.