TABLE OF CONTENT
CONTENT
Title page
Declaration
Certification
Dedication
Acknowledgment
Table of content
Abstract
CHAPTER ONE
1.1 INTRODUCTION
LITERATURE REVIEW
1.2 TYPES OF OIL
1.2.1 Drying oil
1.2.2 Semi-Drying Oil
1.3 COMPOSITION OF OIL
1.4 PIGMENT
1.7 BOTANIC DESCRIPTION
1.8 FUNCTIONAL USES
CHAPTER TWO
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 DEXTROSE
AGAR
2.8.5 THE PUNCHED AGAR DIFFUSION METHOD AS
RECOMMENDED BY BRYANT (1972)
2.7.6 BACTERIAL INOCULATION AND INCUBATION
2.8.7 FUNGAL INOCULATION AND INCUBATION
CHAPTER THREE
TABLE 3.1 ORGANOLEPTIC CHARACTERISTICS OF
Crysophylum albidum SEED OIL
3.2 CHARACTERIZATION OF THE SAMPLE
TABLE 3.3 RESULT OF ANTI-BACTERIAL ACTIVITY OF C.
albidum OIL ON TWO GRAM POSITIVE BACTERIA
TABLE 3.4 RESULT OF ANTI-BACTERIAL ACTIVITY OF C.
albidum OIL ON TWO GRAM NEGATIVE BACTERIA
TABLE 3.5 RESULT 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
4.0 DISCUSSION
4.1 CONCLUSION
- RECOMMENDATION
REFERENCES
APPENDIX I
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.
