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Download the complete chemistry project topic and material (chapter 1-5) titled ISOLATION AND CHARACTERIZATION OF BIOACTIVE COMPOUNDS FROM STEMBARK EXTRACT OF Uapaca pilosa Hutch here on PROJECTS.ng. See below for the abstract, table of contents, list of figures, list of tables, list of appendices, list of abbreviations and chapter one. Click the DOWNLOAD NOW button to get the complete project work instantly.

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Download the complete chemistry project topic and material (chapter 1-5) titled ISOLATION AND CHARACTERIZATION OF BIOACTIVE COMPOUNDS FROM STEMBARK EXTRACT OF Uapaca pilosa Hutch here on PROJECTS.ng. See below for the abstract, table of contents, list of figures, list of tables, list of appendices, list of abbreviations and chapter one. Click the DOWNLOAD NOW button to get the complete project work instantly.

 

PROJECT TOPIC AND MATERIAL ON ISOLATION AND CHARACTERIZATION OF BIOACTIVE COMPOUNDS FROM STEMBARK EXTRACT OF Uapaca pilosa Hutch

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  • Name: ISOLATION AND CHARACTERIZATION OF BIOACTIVE COMPOUNDS FROM STEMBARK EXTRACT OF Uapaca pilosa Hutch
  • Type: PDF and MS Word (DOC)
  • Size: [1,092kb]
  • Length: [92] Pages

 

ABSTRACT

Uapaca pilosa (Hutch.) a plant used in some parts of Africa in the treatment of dysentery, menstrual pain, fever, constipation, erectile dysfunction, skin infections, female sterility, pile, rheumatism, emetic, tooth-troubles and fatigue. The dried plant was extracted, the extract was subjected tophytochemical investigation using standard method revealed the presence of alkaloids, flavonoids, anthraquinones, tannins, saponins, steroids, terpenoids and glycocides. Extensive silica gel column chromatography of the ethylacetate fraction of the stem bark extract, the most active of all the fractions, led to the isolation of two compounds GF1 and GF2. Their identities were determined by analysis of their spectral data using FTIR, 1D and 2D NMR. The structures of the compounds were supported by comparing their spectral data with the literature. GF1 was found to be betulin while GF2 was found to be beta-sitosterol. The antimicrobial screening of the crude extract and fractions using agar well diffusion methodshowed activity against Staphylococcus aureus, Shigella dysenteriae, Salmonella typhii, Bacillus subtilis and Escherichia coli. The Zone of Inhibition of the plant extract against selected microorganisms ranges from 13mm to 17mm against Staphylococcus aureus, 10mm to 14mm against Bacillus subtilis, 12mm to 15mm against Shigella dysenteriae, 15mm to 18mm against Escherichia coliand 10mm to 11mm againstSalmonella typhii. The MIC and MBC for the extract, fractions and isolated compounds were also determined. The range of Minimum Inhibitory concentration is between 6.25 mg/mL to 25 mg/mL for Staphylococcus aureus, 25 mg/mL for Shigella dysenteriae, 6.25 mg/mL for Bacillus subtilisand 12.50 mg/mL for Escherichia coli while the Minimum Bactericidal Concentration range between 12.50 mg/mL for Staphylococcus aureus, 50 mg/mL for Shigella dysenteriae, 12.50 mg/mL for Bacillus subtilis and 25 mg/mL for Escherichia coli. This study on the stem bark extract from Uapaca pilosa, used traditionally in some parts of Africa as a medicinal plant for the treatment of various ailments has confirmed that it has antimicrobial activity against the microbes that cause some of these diseases.

TABLE OF CONTENTS

Title Pagei
Declarationii
Certificationiii
Dedicationiv
Acknowledgements v
Abstractvi
Table of Contentsviii
List of Figuresxii
List of Tables x
List of Platesxiii
CHAPTER ONE
1.0 INTRODUCTION1
1.1 Statement of the Research Problem3
1.2 Aim of the Research4
1.3 Objectives of the Research4
1.4 Justification of the Research4
CHAPTER TWO
2.0 LITERATURE REVIEW5
2.1 The Euphorbiaceae Family5
2.2 The Uapaca genus6
2.3 Uapaca pilosa6
2.4 Taxonomy of the Plant7
2.5 Traditional Uses of Uapaca pilosa9
2.6 Medicinal Importance of Other Uapaca Species9
2.7 Some Compounds Isolated from Uapaca Species9
2.8 Some Compounds Isolated from Euphorbeceae Family14
CHAPTER THREE
3.0 MATERIALS AND METHODS 21
3.1.0 MaterialsError! Bookmark not defined.
3.1.1 Equipment Error! Bookmark not defined.
3.1.2Thin Layer Chromatography (TLC)Error! Bookmark not defined.
3.2.0 Methods21
3.2.1 Extraction of Plant Material.23
3.2.2Preliminary Phytochemical Screening23
3.2.2.1. Test for Reducing Sugars (Molischs test)24
3.2.2.2 Test for Tannins (Ferric Chloride test)24
3.2.2.3 Test for Flavonoids (Shinoda test).24
3.2.2.3.1 Magnessium Chips test24
3.2.2.3.2 Sodium Hydroxide test25
3.2.2.4 Test for Anthraquinones25
3.2.2.4.1 Free Anthraquinones25
3.2.2.4.2 Combined Anthraquinones25
3.2.2.5Test for Saponins (Frothing test)25
3.2.2.6 Test for Glycoside (FeCl3 test)26
3.2.2.7 Test for cardiac glycoside (kella-killani test)26
3.2.2.8 Test for Steroids/Triterpenes26
3.2.2.8.1 Liebermann-Buchard test26
3.2.2.8.2 Salkowski test26
3.2.2.9. Test for Alkaloids27
3.2.3.0Antimicrobial Studies of Extracts and Isolated components27
3.2.3.1 Preparation of the Plants Extracts for antimicrobial screening27
3.2.3.2Preparation of culture media28
3.2.3.3Susceptibility Test28
3.2.3.4Minimum Inhibitory Concentration (MIC)28
3.2.3.5 Minimum bactericidal concentration (MBC)29
3.2.3.6 Minimum fungicidal concentration (MFC)30
3.3.0Column Chromatography30
3.3.1Chromatographic Separation31
3.3.1.1Column Chromatography of ethyl acetate Fraction of Uapaca pilosa31
3.3.1.2Preparative Thin Layer Chromatography of the Sub-fractions (SF1 and SF2)31
3.4Melting Point Determination32
3.5 Spectral Analysis32
CHAPTER FOUR
4.0RESULTS33
4.1Result of Extraction of the Stembark of Uapaca pilosa33
4.2. Result of Phytochemical screening33
4.3 Result of antimicrobial activity of the plant extracts33
4.4 Result of Chromatographic Separation33
4.5 Column Chromatography of Ethyl acetate fraction33
4.6 Thin Layer Chromatography Analysis of Isolated CompoundsError! Bookmark not defined.
4.7 Result of Thin layer Chromatography analyses of GF1 and GF241
4.9 Spectroscopic Analyses of GF1 and GF241
4.10 Antibacterial Activity of Isolated Compounds60
4.10.1 Antimicrobial Activity of GF1 and GF260
CHAPTER FIVE
5.0 DISCUSSION64
5.1 Extraction of the stem bark of Uapaca pilosa64
5.2 Phytochemical Screening of the Stem bark of Uapaca pilosa64
5.3 Antimicrobial Screening of Stem bark of Uapaca pilosa65
5.4 Isolation, Purification and Characterisation of Isolates from Uapaca pilosa65
5.4.1 Isolation and Characterisation of GF166
5.4.2 Isolation and Characterisation of GF267
CHAPTER SIX
6.0 SUMMARY, CONCLUSION AND RECOMMENDATIONS70
6.1 Summary70
6.2 Conclusion71
6.3 Recommendation71
References72

CHAPTER ONE

INTRODUCTION
Over the years the world traditional medicine has been known to take its source from higher plants and their extracts in the treatment of diseases and infections (Sofowora, 1983). Until 19th century, when the development of chemistry and synthetic organic chemistry started, medicinal plants were the sources of active materials used in healing and curing human diseases. Before the advent of modern methods of producing drugs, medicinal plants such as Allium sativum, Azadirchata indica and Citrus limonum were used in treating both malaria and typhoid fever. Also some plant leaves were used in treating skin rashes and to heal wounds. Likewise, modern pharmaceuticals rely heavily on these medicinal plants for their raw materials such as cocoa leaves and opium plant from papaver species for analgesics. The active principles of plants differ from one plant to another due to the diversity in biological activities (Sofowora, 1983; Kubmarawa et al., 2007; Krishnaiah et al., 2009).
Traditional medicinal practice has been established for centuries in many parts of the world. Numerous plants and herbs are used globally by traditional medicine practitioners. The practice is known to vary from one country to another (Sofowora, 1984). Extracts from the various plant parts (leaves, stem bark and roots) of various higher plants are used in herbal medicine production (Sofowora, 1983, 1984, 1993). Plants` extracts are given singly or as concoctions for the treatment of various ailments. In actual sense more than 75% of the world population depend on these various forms of concoctions and herbal decoctions for the treatment of infections (Robenson and Zhang, 2011). Phytochemical constituents are the basic raw materials source for the establishment of pharmaceutical industries (Mothana and Lindequist, 2005; Wojdylo et al., 2007). The constituents present in the plant play vital roles in the crude drugs identity. Phytochemical screening is very important in identifying new sources of therapeutically and pharmacologically important compounds like alkaloids, anthraquinones, flavonoids, phenolic compounds, saponins, steroids, tannins and terpenoids (Akindele and Adeyemi, 2007).
Some plants such as Aloe vera, Alliium sativum, Maranta arundinacea, Pimpinella anisum and Arnica montana widely distributed in Africa, Asia and Southern part of North America have been reported to be the basis of treatment in human diseases and also as useful components in the development of new active components (Boudreau and Beland, 2006; Bunyapraphatsaraet al., 1996; Alan et al., 1995). The World Health Organization (WHO) estimates that 80 % of the world‟s population relies mainly on herbal medicine for primary healthcare (Hong et al., 2010). In China, traditional medicine is largely based on around 5000 plants which were used in treating 40 % of urban patients and 90 % of rural patients (Abdel-Azim et al., 2011). In industrialized countries, plants have contributed more than 7000 compounds used in the pharmaceutical industries including ingredients in heart drugs, laxatives, anti-cancer agents, hormones, contraceptives, diuretics, antibiotics, decongestants, analgesics, ulcer treatments and anti-parasitic compounds (Simo, 2012). About 25 % of all prescription drugs dispensed by Western pharmacists is likely to contain ingredients derived from plants (Simo, 2012). These include: Laevodopamine from tropical legume Mucuna deeringiana, used for treating Parkinson disease (dos Santos et al., 2012). Picrotoxin derived from Anaminta cocculus, a tropical climbing plant from south East Asia, is used as a nervous system stimulant and in cases of barbiturate poisoning (Abebe and Haramaya, 2013). Reserpine, extracted from the root of the serpent-root, Rauwolfia
serpentine, is used for lowering blood pressure, as a tranquilizer and in India as a remedy for snake bites (Unnikrishnan, 2004). Eucalyptol obtained from species of eucalyptus, is a well-known antiseptic used in throat medicines, cough syrups, ointments, liniments, as inhalant for bronchitis and asthma. Eucalyptus is used throughout the world and is regarded as a universally available product (Eschler et al., 2000). Cultivation has replaced wild collection for the supply of some essential drugs used in modern medicine. The Madagascar rosy periwinkle (Cathrathus roseus) is widely cultivated in Spain and Texas for its alkaloids vinblastine and vinscristine, which are used for treating childhood leukaemia and hoolgkin disease (Bauer et al., 1996). The best known example is probably aspirin, chemically related to a compound that was first extracted from the leaves and bark of willow tree, Salix alba and a herb meadow sweet, Filipino dula malaria. The anti-malarial drug quinine, extracted from the bark of a South American tree, Cinchona ledgeriana, was first brought to Europe (where malaria was widespread) in early 17th century by Jesuit priests (Fruhstorfer et al, 2001). It was once remarked that Oliver Cromwell died of malaria because he refused to be treated with a “Jesuit” medicine. Synthetic guanine has now been developed for drug use, but the bark is still in use to treat certain heart arrhythmias and commercially sold as a bitter flavouring agent well known in tonic water (Fruhstorfer et al, 2001). Also, the bark of yohimbe, Pausinnystalia yohimbe is used extensively in traditional healthcare system in West Africa (Robber and Tyler, 1999).
1.1 Statement of the Research Problem
About half of the number of death recorded in the tropical countries are largely due to infectious diseases (Iwu et al., 1999). This can be linked to the increasing bacterial

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