- Title page Declaration Certification Dedication Acknowledgment Table of content Abstract
Chapter ONE
INTRODUCTION
-
- 1.1 INTRODUCTION LITERATURE REVIEW
- 1.2 TYPES OF OIL 1.
- 2.1Drying oil 1.
- 2.2Semi-Drying Oil NON- DRYING OIL
- 1.3 COMPOSITION OF OIL
- 1.4 PIGMENT VITAMINS ANTIOXIDANTS
- 1.7 BOTANIC DESCRIPTION
- 1.8 FUNCTIONAL USES
Chapter TWO
LITERATURE REVIEW
- MATERIALS AND METHODS
- 2.0 SAMPLE COLLECTION
- 2.1 OIL EXTRACTION
- 2.2 DETERMINATION OF SPECIFIC GRAVITY
- 2.3 DETERMINATION OF DENSITY
- 2.4 DETERMINATION OF FREE FATTY ACID CONTENT DETERMINATION OF SAPONIFICATION VALUE DETERMINATION OF IODINE VALUE DETERMINATION OF PEROXIDE VALUE ANTI-MICROBIAL ACTIVITY SCREENING REAGENTS AND MEDIA PREPARATION OF FUNGAL TEST ORGANISM PREPARATION OF THE SENSITIVE TEST AGAR PREPARATION OF THE NUTRIENT DEXTROSEAGAR 2.
- 8.5THE PUNCHED AGAR DIFFUSION METHOD AS RECOMMENDED BY BRYANT (1972) 2.
- 7.6BACTERIAL INOCULATION AND INCUBATION 2.
- 8.7FUNGAL INOCULATION AND INCUBATION READING INHIBITION ZONES OF THE OIL
Chapter THREE
RESEARCH METHODOLOGY
- TABLE
- 3.1ORGANOLEPTIC CHARACTERISTICS OF Crysophylum albidum SEED OIL
- 3.2 CHARACTERIZATION OF THE SAMPLE TABLE
- 3.3RESULT OF ANTI-BACTERIAL ACTIVITY OF C. albidum OIL ON TWO GRAM POSITIVE BACTERIA TABLE
- 3.4RESULT OF ANTI-BACTERIAL ACTIVITY OF C. albidum OIL ON TWO GRAM NEGATIVE BACTERIA TABLE
- 3.5RESULT OF ANTI-FUNGAL ACTIVITY OF C. albidum OIL ON TWO TEST FUNGI
- 3.6 RESULT OF MINIMUM INHIBITORY CONCENTRATION (MIC) OF C. albidum OIL ON SIX TEST ORGANISM
Chapter FOUR
DATA PRESENTATION AND ANALYSIS
-
- 4.0 DISCUSSION
- 4.1 CONCLUSION RECOMMENDATION REFERENCES APPENDIX I
Thesis Abstract
Crysophylum albidum oil was extracted from its seed. The percentage yield was 2.56%. The characterization of the oil showed showed that the refractive index is 1.487, peroxide value is 45.4mg/kg, iodine value is 50.76g, saponification value is 105.188, free fatty acids 47.46 and acid value is 94.92. The Punched Ager Diffusion Method was used to assay for the antimicrobial and anti fungal properties of the oil in the test isolate. The antimicrobial and anti fungal activity showed some inhibitory effects against test organisms; Staphylococcus aureus, E. coli, B. subfilis, C. albican and A. flavons, but non for S. pyogens. The minimum inhibitory concentration of these test organisms are as follows; Staphylococcus aureus 0.16, E. coli 0.06, B. subfilis 0.14, C. albican 2.50 and A. flavons 0.40. The pharmacological screening confirmed the medical value of this plant oil and it established a good support for the sample in herbal medicine and as a base for the development of new drugs and phytomedicine.