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Development of Nutraceuticals
targeting cancer
Catarina Duarte
Food & Health Unit
Nutraceuticals and controlled Delivery Lab
IBET/ ITQB-UNL
Oeiras, Portugal
Green Processes for developing health promoting products
Extraction /Fraccionation of Natural Compounds
Research interests:
Formulation โ€“ particle formation, encapsulation and
impregnation
Characterization and pre-clinical Bioactivity evaluation of bioproducts
Chemical, enzymatic and cell-based assays
Food&Health Unit
Nutraceuticals and Controlled Delivery Lab
POH was detected in
10%EtOH and 20%EtOH
extracts
Serra et al. (2010) J Supercri. Fluids, 55, 184-191
Sweet cherries
Development of POH-rich extracts
Application of High Pressure Technology for the development of natural extracts
rich in perillyl alcohol (POH)
Raw material:
Sweet cherry culls
(Saco variety)
POH
96h
Only two extracts (10%EtOH and 20%EtOH) inhibited cancer cell growth in a
time dependent manner and this effect is related with the presence of Perillyl
Alcohol
Cherry extracts induced cell cycle arrest in a different cell cycle checkpoint
than doxorrubicin suggesting that they can be used in combination with the
drug in chemotherapy
0
20
40
60
80
100
Control 4h 24h 48h 72h 96h
cell(%)
G1 S G2/M
Cherry extract-
10% EtOH
0
20
40
60
80
100
Control 4h 24h 48h 72h 96h
cell(%)
G1 S G2/M
Doxorubicina
0
20
40
60
80
100
120
Cellviability(%ofcontrol)
24h 48h 72h 96h
10%
EtOH
20%
EtOH
40%
EtOH
60%
EtOH
80%
EtOH
100%
EtOH
CO2
Antiproliferative effect on HT29 cells (human colorectal cancer cell line)
โ€ข Cell cycle analysis
Controlo
10% EtOH
20% EtOH
โ€ข Cell viability after 24, 48, 72 and 96h of proliferation
Serra et al. (2010) J Supercrit. Fluids, 55, 184-191
Serra et al. (2011) J Supercrit. Fluids,55 1007-1013
1st prize: โ€œInovation and Develo+ment of Products and Servicesโ€ category
Sweet cherries
Development of POH-rich extracts
Minutes
0 10 20 30 40 50 60 70 80 90 100 110 120 130
0
500
1000
1500
2000
2500
3000
3500
4000
4500
0
500
1000
1500
2000
2500
3000
3500
4000
4500
Detector 1-280nm
Laranja (2) TS
Ago2913075.dat
Detector 1-280nm
Laranja (3) TS
Ago2913076.dat
Detector 1-280nm
Laranja (4) TS
Ago2913077.dat
Detector 1-280nm
Laranja Dil 1:10
Jul2413094.dat
Sinensetin
Nobiletin
Tangeretin
Process: CO2+ EtOH (80:20 v/v); P=25MPa; T=323K; t=60min.
Tangeretina
Nobiletin
Sinensetin
Inรชs Silva (2013), Tese de mestrado
Citrus peels
Development of PMF-rich extracts
Application of Supercritical Fluid Technology for the development of natural extracts
rich in polymetoxylated flavones (PMF)
Sinensetin, tangeritin and nobiletin were
identified in citrus pell extracts.
Raw material:
Orange peels
(by-products of fruit juice
production)
Induction of apoptosis on HT29 cell spheroids
Control Citrus extract
(Red: viable cells; Green: apoptotic cells)
Cell viability
โ€ข 2D model
Orange extract inhibited the proliferation of
HT29 cells (antiproliferative effect was
dependent on spheroid size).
Orange extract induced apoptosis in HT29
spheroids(apoptotic cells are mainly located
on the surface of the spheroid).
โ€ข 3D model
Cell monolayer Cell spheroids with different sizes
Antiproliferative effect on HT29 cells (human colorectal cancer cell line)
Inรชs Silva (2013), Master thesis
Citrus peels
Development of PMF-rich extracts
Opuntia ficus-indica
Development of terpene-rich extracts
Raw material:
Opuntia ficus-indica
(by-products of fruit juice production)
Process: CO2+ EtOH+ H2O mixtures; P=20MPa; T=313K; t=180min.
Application of Pressurized Liquid Extracton for the development
of natural extracts rich in terpenes
fried lup #1 #2 #3 #4 #5 #6 #7 #8 #9 #10fried lup #1 #2 #3 #4 #5 #6 #7 #8 #9 #10
Terpene
detection by TLC
Opuntia extracts obtained with mixtures of CO2 and
EtOH presented high terpene content
Opuntia extract obtained with CO2:EtOH (60:40v/v) mixture (PLE2) presented the highest
antiproliferative effect. This effect is probably due to the presence of terpenes.
PLE-2 extracts increased drug sensitivity on HT29 dx cell population cells .
Antiproliferative effect on HT29 cells (human colorectal cancer cell line)
โ€ข Cell viability after 24 h of proliferation
0
20
40
60
80
100
1 2 3 4 5 6 7 8 9 10
Cellularviability
16 mg/mL 20 mg/mL 24 mg/mL
0
10
20
30
40
50
60
70
80
90
100
110
0 5 10 15 20
Cellviability(%ofcontrol)
Doxorubicin (ยตM)
Doxorubicin in HT29 dx
Doxorubicin in HT29
PLE-2 + Doxo in HT29 dx
โ€ข Chemosensitization effect in a drug resistant cell sub-
population (HT29 dx)
Joana Poejo(2014), Master thesis
Opuntia ficus-indica
Development of terpene-rich extracts
e-mail: cduarte@itqb.unl.pt;
http://www.itqb.unl.pt/labs/nutraceuticals-and-delivery
www.ibet.pt
Laboratรณrio de Nutracรชuticos e
Libertaรงรฃo Controlada
Oeiras, Portugal

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  • 2. Green Processes for developing health promoting products Extraction /Fraccionation of Natural Compounds Research interests: Formulation โ€“ particle formation, encapsulation and impregnation Characterization and pre-clinical Bioactivity evaluation of bioproducts Chemical, enzymatic and cell-based assays Food&Health Unit Nutraceuticals and Controlled Delivery Lab
  • 3. POH was detected in 10%EtOH and 20%EtOH extracts Serra et al. (2010) J Supercri. Fluids, 55, 184-191 Sweet cherries Development of POH-rich extracts Application of High Pressure Technology for the development of natural extracts rich in perillyl alcohol (POH) Raw material: Sweet cherry culls (Saco variety) POH
  • 4. 96h Only two extracts (10%EtOH and 20%EtOH) inhibited cancer cell growth in a time dependent manner and this effect is related with the presence of Perillyl Alcohol Cherry extracts induced cell cycle arrest in a different cell cycle checkpoint than doxorrubicin suggesting that they can be used in combination with the drug in chemotherapy 0 20 40 60 80 100 Control 4h 24h 48h 72h 96h cell(%) G1 S G2/M Cherry extract- 10% EtOH 0 20 40 60 80 100 Control 4h 24h 48h 72h 96h cell(%) G1 S G2/M Doxorubicina 0 20 40 60 80 100 120 Cellviability(%ofcontrol) 24h 48h 72h 96h 10% EtOH 20% EtOH 40% EtOH 60% EtOH 80% EtOH 100% EtOH CO2 Antiproliferative effect on HT29 cells (human colorectal cancer cell line) โ€ข Cell cycle analysis Controlo 10% EtOH 20% EtOH โ€ข Cell viability after 24, 48, 72 and 96h of proliferation Serra et al. (2010) J Supercrit. Fluids, 55, 184-191 Serra et al. (2011) J Supercrit. Fluids,55 1007-1013 1st prize: โ€œInovation and Develo+ment of Products and Servicesโ€ category Sweet cherries Development of POH-rich extracts
  • 5. Minutes 0 10 20 30 40 50 60 70 80 90 100 110 120 130 0 500 1000 1500 2000 2500 3000 3500 4000 4500 0 500 1000 1500 2000 2500 3000 3500 4000 4500 Detector 1-280nm Laranja (2) TS Ago2913075.dat Detector 1-280nm Laranja (3) TS Ago2913076.dat Detector 1-280nm Laranja (4) TS Ago2913077.dat Detector 1-280nm Laranja Dil 1:10 Jul2413094.dat Sinensetin Nobiletin Tangeretin Process: CO2+ EtOH (80:20 v/v); P=25MPa; T=323K; t=60min. Tangeretina Nobiletin Sinensetin Inรชs Silva (2013), Tese de mestrado Citrus peels Development of PMF-rich extracts Application of Supercritical Fluid Technology for the development of natural extracts rich in polymetoxylated flavones (PMF) Sinensetin, tangeritin and nobiletin were identified in citrus pell extracts. Raw material: Orange peels (by-products of fruit juice production)
  • 6. Induction of apoptosis on HT29 cell spheroids Control Citrus extract (Red: viable cells; Green: apoptotic cells) Cell viability โ€ข 2D model Orange extract inhibited the proliferation of HT29 cells (antiproliferative effect was dependent on spheroid size). Orange extract induced apoptosis in HT29 spheroids(apoptotic cells are mainly located on the surface of the spheroid). โ€ข 3D model Cell monolayer Cell spheroids with different sizes Antiproliferative effect on HT29 cells (human colorectal cancer cell line) Inรชs Silva (2013), Master thesis Citrus peels Development of PMF-rich extracts
  • 7. Opuntia ficus-indica Development of terpene-rich extracts Raw material: Opuntia ficus-indica (by-products of fruit juice production) Process: CO2+ EtOH+ H2O mixtures; P=20MPa; T=313K; t=180min. Application of Pressurized Liquid Extracton for the development of natural extracts rich in terpenes fried lup #1 #2 #3 #4 #5 #6 #7 #8 #9 #10fried lup #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 Terpene detection by TLC Opuntia extracts obtained with mixtures of CO2 and EtOH presented high terpene content
  • 8. Opuntia extract obtained with CO2:EtOH (60:40v/v) mixture (PLE2) presented the highest antiproliferative effect. This effect is probably due to the presence of terpenes. PLE-2 extracts increased drug sensitivity on HT29 dx cell population cells . Antiproliferative effect on HT29 cells (human colorectal cancer cell line) โ€ข Cell viability after 24 h of proliferation 0 20 40 60 80 100 1 2 3 4 5 6 7 8 9 10 Cellularviability 16 mg/mL 20 mg/mL 24 mg/mL 0 10 20 30 40 50 60 70 80 90 100 110 0 5 10 15 20 Cellviability(%ofcontrol) Doxorubicin (ยตM) Doxorubicin in HT29 dx Doxorubicin in HT29 PLE-2 + Doxo in HT29 dx โ€ข Chemosensitization effect in a drug resistant cell sub- population (HT29 dx) Joana Poejo(2014), Master thesis Opuntia ficus-indica Development of terpene-rich extracts