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UNIVERSITI PUTRA MALAYSIA EXTRACTION OF -ORYZANOL AND TOCOPHEROLS FROM RICE (Oryza sativa) BRAN ROSNIZAM ISMAIL FSTM 2008 19

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  • UNIVERSITI PUTRA MALAYSIA

    EXTRACTION OF -ORYZANOL AND TOCOPHEROLS FROM RICE (Oryza sativa) BRAN

    ROSNIZAM ISMAIL FSTM 2008 19

  • EXTRACTION OF -ORYZANOL AND TOCOPHEROLS

    FROM RICE (Oryza sativa) BRAN

    By

    ROSNIZAM ISMAIL

    Thesis Submitted to the School of Graduate Studies, Universiti Putra Malaysia,

    in Fulfilment of Requirements for the Degree of Master of Science

    July 2008

  • ii

    Especially dedicated to……..

    Emak….in memory, may Allah bless her wherever she is,

    abah, family,

    friends and whoever has blown up my spirit..

    …thank you for the guidance, encouragement, and love given

    throughout my life…..

  • iii

    Abstract of thesis presented to the Senate of Universiti Putra Malaysia in fulfilment of

    the requirement for the degree of Master of Science.

    EXTRACTION OF -ORYZANOL AND TOCOPHEROLS

    FROM RICE (Oryza sativa) BRAN

    By

    ROSNIZAM ISMAIL

    July 2008

    Chairman : Associate Professor Azizah Abdul Hamid, PhD

    Faculty : Food Science and Technology

    The objective of this study was to extract -oryzanol and tocopherols from rice bran.

    Different extraction times and sequential extractions utilizing different solvents on -

    oryzanol and tocopherols levels from crude rice bran oil (CRBO) were studied. Rice

    bran was extracted using hexane with five different extraction times, while sequential

    extractions was carried out utilizing hexane, hexane/dichloromethane,

    dichloromethane and dichloromethane/methanol. Extraction of -oryzanol and

    tocopherols was further studied using precipitation and liquid-liquid separation from

    unsaponified fraction of CRBO. Precipitation was carried out by diluting the sample in

    hexane overnight at -20˚C. Liquid-liquid separations were carried out using hexane-

    methanol or hexane-acetonitrile. Solid and liquid portions formed from precipitation

    were further separated by liquid-liquid separations. The final stage of the extraction

    process was a combination of precipitation and single-stage chromatographic

  • iv

    separation. Results showed that percentage of extracted oil was not significantly

    different with the different extraction times used. However, 20 min extraction resulted

    in the highest -oryzanol level (p

  • v

    Abstrak tesis yang dikemukakan kepada Senat Universiti Putra Malaysia sebagai

    memenuhi keperluan untuk ijazah Master Sains.

    PENGEKSTRAKAN -ORYZANOL DAN TOKOFEROLS DARIPADA DEDAK BERAS (Oryza sativa)

    Oleh

    ROSNIZAM ISMAIL

    Julai 2008

    Pengerusi : Profesor Madya Azizah Abdul Hamid, PhD

    Fakulti : Sains dan Teknologi Makanan

    Kajian ini dijalankan dengan objektif untuk mengekstrak -orizanol dan tokoferol

    daripada dedak beras. Perbandingan dalam masa pengekstrakan dan pengekstrakan

    secara sekuel menggunakan pelarut yang berbeza telah dikaji ke atas jumlah -orizanol

    dan tokoferol daripada minyak dedak beras. Dedak beras yang telah distabilkan

    diekstrak dengan heksana dengan lima masa pengekstrakan yang berbeza. Manakala

    pengekstrakan sekuel dijalankan dengan menggunakan heksana,

    heksana/diklorometana, diklorometana dan diklorometana/metanol. Kajian pra-

    konsentrasi bagi -orizanol dan tokoferol selanjutnya telah dikaji dengan kaedah

    pemendakan dan kaedah pemisahan fasa cecair-cecair daripada bahagian tidak-

    tersaponifikasi (sebagai sampel) minyak dedak beras. Kaedah pemendakan telah

    dijalankan dengan mencampurkan sampel dalam heksana dan dibiarkan semalaman

    pada suhu -20˚C. Manakala kaedah pemisahan fasa cecair-cecair dijalankan dengan

    mencampurkan sampel dalam heksana-metanol atau heksana-asetonitril. Bahagian

  • vi

    pepejal dan cecair yang terbentuk daripada kaedah pemendakan telah selanjutnya

    dikaji dengan kaedah pemisahan fasa cecair-cecair. Bahagian terakhir kajian

    pengekstrakan bahan ini dijalankan dengan gabungan kaedah pemendakan dan kaedah

    pemisahan kromatografi turus. Keputusan telah menunjukkan peratusan minyak dedak

    beras yang terekstrak tidak berbeza secara signifikan dengan masa pengekstrakan yang

    berbeza. Walau bagaimanapun, pengekstrakan selama 20 minit telah memberi jumlah

    -orizanol yang tertinggi daripada masa pengekstrakan yang lain (p

  • vii

    10.99% dan tokoferol kepada 0.02%. Kajian ini mencadangkan satu kaedah alternatif

    dalam pengekstrakan -orizanol dan tokoferol daripada dedak beras.

  • viii

    ACKNOWLEDGEMENTS

    Alhamdulillah, praise to Allah s.w.t, The Almighty, for giving me strength, patience

    and ability to complete this project and thesis.

    Firstly, I’d like to express my appreciation and thank you so much to Associate

    Professor Dr. Azizah Abdul Hamid of the Department of Food Science, Faculty of

    Food Science and Technology, UPM, as the Chairman of my Supervisory Committee

    for her guidance, patience, advice and encouragement and most important, give me the

    chance to gain knowledge and experience through the challenging research. Precious

    experiences gained from being her graduate student and her commitment to help the

    success of my study will always be remembered in my heart.

    Beside, my deep sense of gratitude and respect goes to my co-supervisors, Associate

    Professor Badlishah Sham Baharin and Dr. Quek Siew Young (previously one of the

    supervisory committee, however, she was discontinued being a lecturer in UPM), for

    their sincere advice and support. I’d like to extend my appreciation to Associate

    Professor Dr. Nazamid Saari and Associate Professor Dr. Azizah Osman for their

    guidance, advice and encouraging interest in my study.

    My sincere thank also to all dedicated friend of my fellow graduate students and also

    to all helpful staff of the Faculty of Food Science and Technology. Sincere gratitude is

  • ix

    dedicated to Malaysian Government for the financial support provide through IRPA

    fund and to Graduate School of UPM for providing me with Biasiswa Pasca Siswazah.

    Finally, my deepest gratitude and appreciation goes to my beloved father, for his

    continuous support and to all my brothers and sister, thank you so much for their love

    and support who have been inspiring my life.

  • x

    I certify that an Examination Committee met on 1st of July 2008 to conduct the final

    examination of Rosnizam Ismail on his Master of Science Thesis entitled “Extraction

    of -oryzanol and tocopherols from rice (Oryza sativa) bran” in accordance with

    Universiti Pertanian Malaysia (Higher Degree) Act 1980 and Universiti Pertanian

    Malaysia (Higher Degree) Regulations 1981. The committee recommends that the

    candidate be awarded the relevant degree. Members of the Examination Committee

    are as follows:

    Azizah Osman, PhD

    Associate Professor

    Faculty of Food Science and Technology

    Universiti Putra Malaysia

    (Chairman)

    Yaakob Che Man, PhD

    Professor

    Faculty of Food Science and Technology

    Universiti Putra Malaysia

    (Internal Examiner)

    Aabdul Azis Ariffin, PhD

    Associate Professor

    Faculty of Food Science and Technology

    Universiti Putra Malaysia

    (Internal Examiner)

    Osman Hassan, PhD Professor

    Faculty of Science and Technology

    Universiti Kebangsaan Malaysia

    (External Examiner)

    _______________________________

    Hasanah Ghazali, PhD

    Professor and Deputy Dean

    School of Graduate Studies

    Universiti Putra Malaysia

    Date: 25 September 2008

  • xi

    This thesis was submitted to the Senate of Universiti Putra Malaysia and has been

    accepted as fulfillment of the requirements for the degree of Master of Science. The

    members of the Supervisory Committee were as follows:

    Azizah Abdul Hamid, PhD

    Associate Professor

    Faculty of Food Science and Technology

    Universiti Putra Malaysia

    (Chairman)

    Badlishah Sham Baharin, MSc

    Associate Professor

    Faculty of Food Science and Technology

    Universiti Putra Malaysia

    (Member)

    ______________________

    Aini Ideris, PhD

    Professor and Dean

    School of Graduate Studies

    Universiti Putra Malaysia

    Date: 16 Oktober 2008

  • xii

    DECLARATION

    I declare that the thesis is based on my original work except for quotations and

    citations, which have been duly acknowledged. I also declare that is not been

    previously and is not concurrently submitted for any degree at UPM or at any other

    institution.

    __________________

    Rosnizam Ismail

    Date:

  • xiii

    TABLE OF CONTENTS

    Page

    ABSTRACT iii

    ABSTRAK v

    ACKNOWLEDGEMENT viii

    APPROVAL x

    DECLARATION xii

    LIST OF TABLES xvi

    LIST OF FIGURES xviii

    LIST OF PLATES xix

    LIST OF ABBREVIATIONS xx

    CHAPTER

    1 INTRODUCTION 1

    2 LITERATURE REVIEW 5

    2.1 Overview of Rice 5

    2.2 Rice Bran 5

    2.2.1 Stabilization of Rice Bran 7

    2.2.2 Chemical Composition of Rice Bran 8

    2.2.3 Rice Bran Lipid 10

    2.3 -oryzanol 11

    2.3.1 Chemical Structure of -oryzanol 12

    2.3.2 Physiological Activity of -oryzanol 13

    2.4 Tocopherols 16

    2.4.1 Chemical Structure of Tocopherols 17

    2.4.2 Physiological Activity of Tocopherols 19

    2.5 -oryzanol and Tocopherols Extraction 22

    2.5.1 Sequential Chemical Extractions 23

    2.5.2 -oryzanol and Tocopherols Separation 25

    2.5.3 Liquid-liquid Separation and Precipitation Separation 27

    2.5.4 Adsorption Column Chromatography 29

    3 EXTRACTION OF CRUDE RICE BRAN OIL 31

    3.1 Introduction 31 3.2 Methodology 32

    3.2.1 Reagents and Solutions 32 3.2.2 Standard Solutions 33

    3.2.3 Rice Bran 33

  • xiv

    3.2.4 Effect of Different Extraction Times on

    CRBO Yield, -oryzanol and Tocopherols Levels 34

    3.2.5 Effect of Sequential Extractions on CRBO yield,

    -oryzanol and Tocopherols Levels 34

    3.2.6 Determination of -oryzanol and Tocopherols 35

    3.2.7 Determination of -oryzanol and Tocopherols

    High Performance Liquid Chromatography (HPLC) 38

    3.2.8 Statistical Analysis 40

    3.3 Results and Discussion 40

    3.3.1 Extraction of CRBO 40 3.3.2 Effect of Extraction Times and Sequential Extraction

    on -oryzanol 44

    3.3.3 Effect of Extraction Times and Sequential Extraction

    on Tocopherols 47

    3.4 Conclusion 53

    4 PRECONCENTRATION OF -ORYZANOL AND TOCOPHEROLS

    FROM UNSAPONIFIED FRACTION OF CRBO 54

    4.1 Introduction 54

    4.2 Methodology 55 4.2.1 Reagents and Solutions 55

    4.2.2 Extraction of CRBO 56

    4.2.3 Preparation of Unsaponified Fraction of CRBO 56

    4.2.4 Determination of -oryzanol and Tocopherols using HPLC 57

    4.2.5 Liquid-liquid Separation of Unsaponified Fraction of CRBO 57

    4.2.6 Precipitation of Unsaponified Fraction of CRBO 58

    4.2.7 Liquid-liquid Separation on Precipitation Fractions

    of Unsaponified Fraction of CRBO 58

    4.2.8 HPLC Determination of -oryzanol and Tocopherols 58

    4.2.9 Statistical Analysis 59

    4.3 Results and Discussion 60

    4.3.1 -oryzanol and Tocopherols Content of Unsaponified Fraction of CRBO 60

    4.3.2 Liquid-liquid Separation of Unsaponified Fraction of CRBO 61

    4.3.3 -oryzanol and Tocopherols obtained from Precipitation of Unsaponified Fraction of CRBO 66

    4.3.4 Liquid-liquid Separation on Precipitation Fractions of Unsaponified Fraction of CRBO 67

    4.4 Conclusion 73

    5 SEPARATION OF -ORYZANOL AND TOCOPHEROLS USING ADSORPTION COLUMN CHROMATOGRAPHY 74

    5.1 Introduction 74

  • xv

    5.2 Methodology 75 5.2.1 Reagents and Solutions 75 5.2.2 Unsaponified Fraction of CRBO 75

    5.2.3 Fractionation of -oryzanol and Tocopherol Using Silica Column Chromatography 76

    5.2.4 HPLC Determination of -oryzanol and Tocopherols 77

    5.2.5 Statistical Analysis 77

    5.3 Results and Discussion 79

    5.3.1 Adsorption Chromatographic Separation of -oryzanol 79

    5.3.2 -oryzanol Levels in Eluted Fraction of

    Chromatographic Separation 81

    5.3.3 Adsorption Chromatographic Separation of Tocopherols 85

    5.3.4 Tocopherols Levels in Eluted Fraction of

    Chromatographic Separation 87

    5.4 Conclusion 92

    6 SUMMARY AND RECOMMENDATIONS 93

    BIBLIOGRAPHY 96

    APPENDICES 109

    BIODATA OF STUDENT 120

    LIST OF PUBLICATIONS 121

  • xvi

    LIST OF TABLES

    Table Page

    2.1 Composition of paddy kernel 7

    2.2 Proximate chemical composition of rice bran (dry basis), percentage 9

    2.3 Lipids profile in crude rice bran oil 11

    2.4 Name and structural interrelationship of natural tocopherols 18

    3.1 Extracted CRBO levels with different extraction times and sequential extraction 41

    3.2 Effect of different extraction times and sequential extraction

    on -oryzanol levels from rice bran 45

    3.3 Effect of different extraction times on tocopherols levels

    from rice bran 48

    3.4 Effect of sequential extractions on tocopherols levels from rice bran 49

    4.1 -oryzanol and tocopherols levels in unsaponified fraction of CRBO 60

    4.2 -oryzanol and tocopherols levels of unsaponified fraction of CRBO obtained

    from liquid-liquid separation at 4˚C 63

    4.3 -oryzanol and tocopherols levels in unsaponified fraction of CRBO obtained

    from precipitation separation at -20˚C 67

    4.4 -oryzanol and tocopherols levels obtained from liquid-liquid

    separation (at 4˚C) on liquid fraction of unsaponified fraction of CRBO

    Precipitation 69

    4.5 -oryzanol and tocopherols levels obtained from liquid-liquid

    separation (at 4˚C) on solid fraction of unsaponified fraction of CRBO

    precipitation 72

    5.1 Recovered samples weight obtained from eluted fraction of

    chromatographic separation of -oryzanol 81

    5.2 -oryzanol levels obtained using silica column chromatography 82

  • xvii

    5.3 Recovered samples weight obtained from eluted fraction of

    chromatographic separation of tocopherols 87

    5.4 Tocopherols obtained using silica column chromatography 89

  • xviii

    LIST OF FIGURES

    Figure Page

    2.1 Diagram of Paddy Structure 6

    2.2 Molecular Structure of Individual -oryzanol According to Xu et al. (1999 14

    2.3 Diagram of Tocopherols Molecular Structure 18

    3.1 Flow Chart of Sequential Extractions of Rice Bran with

    Different Solvent Polarity 36

    3.2 Flow Chart of Saponification of CRBO for Determination

    of -oryzanol and Tocopherols 37

    3.3 Flow Chart of Sample Filtration Prior to HPLC Determination

    of -oryzanol and Tocopherols 38

    3.4 Chromatogram of -oryzanol Standard detected using

    C18 Novapak column 47

    3.5 Chromatogram of Tocopherols Standard detected using

    C18 Symmetry Column 51

    4.1 Experimental Layout of -oryzanol and Tocopherols Separation

    of Unsaponified Fraction of CRBO by Precipitation and

    Liquid-liquid Separation 59

    5.1 Experimental Layout of -oryzanol and Tocopherols Separation

    using Silica Column 78

    5.2 -oryzanol Absorbance obtained from Silica Column

    Chromatography Elution of Three Different Types of Samples 80

    5.3 Tocopherols Absorbance obtained from Silica Column

    Chromatography Elution of Three Different Types of Samples 86

    5.4 -oryzanol and Tocopherols Extraction from Rice bran 91

  • xix

    LIST OF PLATES

    Figure Page

    1.1 BERNAS factory that rice bran was taken at Kuala Selangor 109

    1.2 Unstabilized rice bran from rice milling was packed and to be sent to animal feed company 109

    1.3 Immediate rice bran stabilization process by using microwave

    in the factory 110

    1.4 Stabilized rice bran 110

    1.5 Crude rice bran oil and unsaponified fraction of crude rice bran oil 111

  • xx

    LIST OF ABBREVIATIONS

    C Degree Celsius

    GC/MS Gas chromatography/ mass spectroscopy

    HPLC High pressure liquid chromatography

    IU International Unit

    TE Tocopherol Equivalent

    ROS Reactive oxygen species

    CVD Cardiovascular disease

    LDL Low-density lipoprotein

    HDL High-density lipoprotein

    CRBO Crude rice bran oil

    NaOH Sodium hydroxide

    BHT Butylated hydroxytoluene

    mg Milligram

    g Gram

    kg Kilogram

    ppm Part per million

    ml Milliliter

    MHz Mega Hertz

    min minutes

    m Micrometer

    mm Millimeter

  • xxi

    nm Nanometer

    i.d. Internal diameter

    UV/Vis Ultraviolet/visible

    UV Ultraviolet

    SAS Statistical Analysis System

    MeOH Methanol

    MeCl2 Dichloromethane

    rpm Revolution per minute

    mol. wt Molecular weight

    CaCl2 Calcium chloride

    atm atmosphere

    P’ empirical solvent polarity

  • CHAPTER 1

    INTRODUCTION

    Rice (Oryza sativa) bran has gained much interest in recent years because it serves as

    an excellent source of beneficial -oryzanol, tocopherols and tocotrienols (Da Silva et

    al., 2006; Iqbal et al., 2005; Jennings and Akoh, 2000; Dunford and King, 2000). It

    has been viewed as a potential functional food and commercial source for use as food

    additive, pharmaceutical and in cosmetic product (Parrado et al., 2006; Lloyd et al.,

    2000). As an under-utilized by-product from paddy-milling, rice bran is potentially an

    inexpensive raw material. The obstacle hindering the use of rice bran for human

    consumption is its instability and rapid spoilage.

    Rice bran represents 10% of paddy (rough rice) weight fraction and reported to

    contain up to 17% protein, 23% lipid, 27% dietary fibre, vitamins (thiamine,

    riboflavin, niacin, tocopherols and tocotrienols), minerals (calcium, phosphorus and

    magnesium) and other bioactive compounds, in particular, -oryzanol (Parrado et al.,

    2006; Da Silva et al., 2006; Shin et al., 1997, Salunkhe et al., 1992; Saunders, 1990;

    Fedeli, 1983).

    Up to 28%, crude rice bran oil (CRBO) can be extracted from bran, making rice bran

    oil the richest oil from cereal (Da Silva et al., 2006). Several countries including Japan

    and India used the oil as speciality oil (Saunders, 1990; Prabhakar et al., 1986;

    Bhattacharyya et al., 1983). Furthermore, CRBO is one of the nature’s richest sources

  • 2

    of potent antioxidant including tocopherols, tocotrienols and -oryzanol, which are

    unique compared to other plants oil (Da Silva et al., 2006; Lloyd et al., 2000; Jennings

    et al., 2000; Das et al., 1998). These compounds in CRBO are believed to be

    responsible for hypocholesterolemic effect and reduction of aortic fatty streak

    (Pszczola, 2001; Kahlon et al., 1996; Rogers et al., 1993).

    -oryzanol has been shown to be a potent antioxidant and inhibits cholesterol

    oxidation in vitro better than that of tocopherols and tocotrienols. 24-methylene

    cycloartanyl ferulate exhibited the highest cholesterol antioxidation compared to other

    -oryzanol members in rice bran oil (Xu et al., 2001). It was reported that -oryzanol

    exhibited hypocholesterolemic action, decreased cholesterol absorption and plasma

    cholesterol level (Wilson et al, 2007; Vissers et al., 2000). In technological uses, the

    compound contributed to the rice bran oil stabilization at frying temperature and use as

    special cosmetic ingredient (Miller et al., 2003).

    Tocopherols is well known as an active free radical and reactive singlet oxygen

    scavenger that prevent peroxidation of lipid either in vivo or in vitro systems.

    Tocopherols has been repeatedly shown to have anticancer and anti-thrombosis

    properties; able to reduce cardiovascular disease (CVD) and offer protection against

    coronary heart disease by arresting free radical damages (Sylvester, 2002; Pszczola,

    2001; Cicero and Gaddi, 2001; Eintenmiller and Landen, 1999). Both -oryzanol and

    tocopherols are liposoluble compounds that are extracted in CRBO.

  • 3

    Various methods were used to separate or isolate both -oryzanol and tocopherols

    either from rice bran or other samples. Extraction methods used commonly involved

    solvent extraction followed by various concentration techniques such as adsorption

    column chromatography, preparative HPLC, chemical separation (such as

    esterification and transesterification and aminoalkylation), hydrogenation,

    crystallization, molecular distillation, supercritical extraction and others. Some

    methods involved sophisticated and expensive equipment and have certain drawbacks

    (Abidi, 2001; Sumner Jr. et al., 2001; Akihisa et al., 2000; Qureshi et al., 2000; Xu et

    al., 1999; Cheruckuri et al., 1999; Das et al., 1998; Hunt, 1997; Fizet, 1996; Baldwin

    et al., 1990; Takagi et al., 1984).

    Column chromatography was reported to be effective in separating desired

    compounds. Selective separation of the compounds of interest from rice bran may

    involve several complex and intensive unit operations. Beside, many procedures were

    time demanding procedures which enhance oxidation compounds and thermal

    degradation of the target compounds (Dunford et al., 2003; Guiochon and Lin, 2003;

    Diack et al., 1994; Dondi and Guiochon, 1992).