Fabrication of Self-Assembled (-)-Epigallocatechin gallate (EGCG) Ovalbumin-Dextran Conjugate Nanoparticles and Their Transport across Monolayers of Human.

Slides:



Advertisements
Similar presentations
Transport of PAMAM Dendrimers Across Biological Barriers Ghaith Al-Jayyoussi, Will Ford & Mark Gumbleton Welsh School of Pharmacy, Cardiff University,
Advertisements

Nano Technologies for Improved Oil & Gas Recovery.
Chp 4 Transport of Solutes and Water. Review 1- The intracellular and extracellular fluids are similar in osmotic concentration but very different in.
& 4 (A) (B) Fig. S1 Characterization of RLs E CM Figure S1. Characterization of RLs. (A) isolated RLs were subjected for hydrolysis.
Digestible compounds: protein amino acids
CELL COMPOUNDS Water Acids, Bases & Buffers Water Acids, Bases & Buffers.
Water, Solutions, and Membranes Roles of water in body functions Characteristics of water Solutions: composition, concentration, and pH Role of membranes.
Copyright © 2004 Lippincott Williams & Wilkins Chapter 2 Chemistry, Matter, and Life.
BRAIN DELIVERY OF PROTEINS BY THE INTRANASAL ROUTE OF ADMINISTRATION USING CATIONIC LIPOSOMES Presented by Mattia M. Migliore February 23, 2007 Graduate.
Improving solubility and cellular absorption of Paclitaxel with solid lipid nanoparticles and cyclodextrin Jong-Suep Baek, Jae-Woo So, Ji-Sook Hwang, Cheong-Weon.
What is energy? Energy: capacity to do work – Potential energy (Example: chemical bonds) – Kinetic energy (Energy of motion)
Determination of Hydrolyzable Tannins (Gallotannins and Ellagitannins) after Reaction with Potassium Iodate Zhang Hui J. Agric. Food Chem.2002,50,
Introduction What is a Biowaiver?
Chitosan/B-lactoglobulin core-shell nanoparticles as nutraceutical carriers Presenter: Jeong Youngjin.
A review: Using nanoparticles to enhance absorption and bioavailability of phenolic phytochemicals BILAL JAVED PhD BOTANY 09-ARID-1473 PMAS-ARID AGRICULTURE.
Formulation of an oral dosage form utilizing the properties of cubic liquid crystalline phases of glyceryl monooleate Ref.: European Journal of Pharmaceutics.
1/20 PRESENTED BY BRAHMABHATT BANSARI K. M. PHARM DEPARTMENT OF PHARMACEUTICS AND PHARMACEUTICAL TECHNOLGY L. M. COLLEGE OF PHARMACY.
AOCS 2014 MONIKA R. KULAK PROF. MILENA CORREDIG (SUPERVISOR) UNIVERSITY OF GUELPH, ON, CANADA Liposomal Nanoencapsulation of Bioactive Compounds and their.
Elements are the building blocks for all matter. Elements contain a single type of atom; elements cannot be further broken down by a chemical reaction.
PITAVASTATIN CONTAINING NANOEMULSIONS:
The first rechargeable battery was invented in 1859 Research during the 70s and 80s developed the rechargeable battery we use worldwide Cost of production.
Lecture 1     The Nature of ruminant Stomach   The stomach of ruminants has four compartments: The rumen The reticulum The omasum The abomasum   Collectively,
Proteins. Chemical composition of the proteins
13/11/
BIOCHEMISTRY REGENTS REVIEW
Design and development of ligand-appended polysaccharidic nanoparticles for the delivery of oxaliplatin in colorectal cancer  Anekant Jain, MPharm, Sanjay.
Aim: How are acids and bases different?
Weiping Jin1,2, Qingrong Huang2, Bin Li1
Chapter 18.2a The Digestive System.
RESULTS and DISCUSSION CONCLUSIONS and FUTURE APPROACH
Volume 59, Issue 5, Pages (May 2001)
Nucleate pool boiling heat transfer of TiO2–R141b nanofluids
Digestion.
Evaluation of a Highly Skin Permeable Low-Molecular-Weight Protamine Conjugated Epidermal Growth Factor for Novel Burn Wound Healing Therapy  Ji Hae Lee,
Performance improvement of vapor compression refrigeration cycle
Introduction What is a Biowaiver?
Centre of Polymer Systems
Polysaccharides Based Nanoparticles for Drug Delivery Application
Novel Polyglutamate-based Indocyanine green nanoparticles for photothermal cancer therapy Sam P. Tarassoli.
Food Effects on Gastrointestinal Transit Properties of Amphotericin B Solid Lipid Nanoparticles NASHIRU BILLA School of Pharmacy University of Nottingham,
Chitosan aqueous solution (0.1 mg/mL)
Preparation of magnetic β - glucan microspheres by microemulsion method for targeting drug delivery system Jun Hee Cho 1*, Sang Gil Ko1, Yangkyu Ahn1,
Understanding Solutions
Investigations of the mechanisms of absorption of lycopene from the gastro-intestinal tract of the rat. Faisal W., O'Driscoll C. M. and Griffin B. T.1.
Fe-Al binary Oxide Nano-Sorbent: Synthesis, Characterization and Phosphate Sorption Behavior Tofik Ahmed, Abi.M.Taddesse, Tesfahun Kebede, Girma Goro.
EFFECT OF STORAGE TEMPERATURE ON THE STABILITY OF TOTAL PARENTERAL NUTRITION ADMIXTURES PREPARED FOR INFANTS Acta Poloniae Pharmaceutica n Drug Research,
Unit 3: Biochemistry Part 1 Review
M M Additional file 2 - Silver staining of protein extract and tryptic digest run on SDS-PAGE. The figure shows.
Smart Hybrid Materials (SHMs)
Enhancement of Dietary Protein Digestion by Conjugated Bile Acids
Volume 138, Issue 3, Pages e2 (March 2010)
Digestibility of allergens extracted from natural rubber latex and vegetable foods  Takeshi Yagami, PhDa, Yuji Haishima, PhDa, Akitada Nakamura, PhDa,
Pharmacokinetics: Drug Absorption
Cross-matching.
Volume 123, Issue 5, Pages (November 2002)
Volume 59, Issue 5, Pages (May 2001)
Volume 128, Issue 5, Pages (May 2005)
Different applications of protein electrophorasis
Chemistry, Matter, and Life
Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract  Katawut Namdee, Mattaka Khongkow, Suwimon.
Pharmacokinetics: Drug Absorption
Molecular Therapy - Nucleic Acids
Domain Interactions in E
Understanding Solutions
Lab on a Chip Lab Chip, 2012, 12, 1591 COMMUNICATION
Amanda Solem, Nora Zingler, Anna Marie Pyle  Molecular Cell 
Molecular Therapy - Nucleic Acids
Smart Manipulation of Motor-Protein Movement
Ajay B. Antony, HSa, Robert S. Tepper, MDb, Kamal A. Mohammed, PhDa 
Development of Novel Formulations That Enhance Adenoviral-Mediated Gene Expression in the Lung in Vitro and in Vivo  Maria A. Croyle, Xuan Cheng, Arbans.
Presentation transcript:

Fabrication of Self-Assembled (-)-Epigallocatechin gallate (EGCG) Ovalbumin-Dextran Conjugate Nanoparticles and Their Transport across Monolayers of Human Intestinal Epithelial Caco-2 Cells ZHENG LI AND LIWEI GU Department of Food Science and Human Nutrition, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, Florida 32611 ABSTRACT NANOPARTICLE FABRICATION EGCG LOADING EFFICIENCY AND CAPACITY EGCG RELEASE FROM NANOPARTICLES Nanoparticles have the potential to increase bioavailability of nutraceutical compounds such as (-)-epigallocatechin gallate (EGCG). Ovalbumin was conjugated with dextran using the Maillard reaction. The resultant ovalbumin-dextran (O-D) conjugates were self-assembled with EGCG to form EGCG O-D conjugate nanoparticles at pH 5.2 after heating at 80 oC for 60 min. Ovalbumin in EGCG O-D conjugate nanoparticles were further cross-linked by glutaraldehyde for 24 hours at room temperature. EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles in aqueous suspension had particle sizes of 285 nm and 339 nm, and showed a spherical morphology. The loading efficiency of EGCG in these two nanoparticles was 23.4% and 30.0%, whereas the loading capacity was 19.6% and 20.9%, respectively. These nanoparticles showed positive zeta-potentials in a pH range from 2.5 to 4.0 but had negative charges at pH ≥ 5.0. EGCG O-D conjugate nanoparticles maintained a particle size of 183 nm-349 nm in simulated gastric fluid (SGF) and 188 nm-291 nm in simulated intestinal fluid (SIF) at 37oC for 2 hours, whereas cross-linked nanoparticles had a particle size of 294-527 nm in SGF and 206-300 nm in SIF, respectively. Limited release of EGCG was observed in both nanoparticle systems in simulated gastric and intestinal fluids without and with digestive enzymes. EGCG O-D conjugate nanoparticles significantly enhanced the apparent permeability coefficient (Papp) of EGCG on Caco-2 monolayers compared with EGCG solution, suggesting that these nanoparticles may improve the absorption of EGCG. Loading efficiency and loading capacity of EGCG in EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles. EGCG O-D conjugate nanoparticles Crosslinked EGCG Cumulative release of EGCG (%) 5 10 15 20 25 SGF without pepsin SGF with pepsin 30 40 50 SIF without pancreatin SIF with pancreatin Nanoparticles loading efficiency loading capacity (%) (w/w %) EGCG O-D conjugate nanoparticles 23.4 ± 2.9 19.6 ± 3.2 Cross-linked EGCG O-D conjugate nanoparticles 30.0 ± 4.9 20.9 ± 3.8 SDS-PAGE ANALYSIS PARTICLE CHARACTERISTICS IN DIFFERENT PH CONDITIONS pH condition 2.5 3.0 4.0 5.0 6.0 7.0 7.5 Particle size (nm) 200 400 600 800 1000 1200 EGCG O-D conjugate nanoparticles Crosslinked EGCG O-D conjugate nanoparticles 3 4 5 6 7 Zeta-potential (mV) -20 -10 10 20 30 Cumulative release of EGCG from EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles in (A) simulated gastric fluid (SGF, pH 4.0) without or pepsin for 0.5 hour and (B) simulated intestinal fluid (SIF, pH 6.0) without or pancreatin for 2 hours at 37oC. * indicates significant differences between simulated fluid without enzyme and fluid with enzyme. # indicates significant differences between EGCG O-D conjugate nanoparticles and cross-linked nanoparticles. EGCG ABSORPTION ON CACO-2 MONOLAYERS Time (min) 30 60 90 120 over initial value (%) TEER percentage 70 80 100 110 EGCG OVA-DEX conjugate nanoparticles EGCG Blank A Papp (10-6 cm/s) 0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 B * (A) protein stain and (B) carbohydrate stain. Lane M represents molecular weight marker. Lane 1, 2, 3, and 4 represent ovalbumin, dextran, ovalbumin/dextran physical mixture, and O-D conjugates, respectively. (A) Particle size and (B) zeta-potential of EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles in pH range from 2.5 to 7.5. PARTICLE CHARACTERISTICS PARTICLE SIZE IN SIMULATED FLUIDS Keywords: ovalbumin, ovalbumin-dextran conjugates, EGCG, nanoparticles Incubation time (Hour) 0.5 1 1.5 2 Particle size (nm) 200 400 600 800 1000 EGCG O-Dconjugate nanoparticles Crosslinked EGCG O-D conjugate nanoparticles 100 300 500 A B (A) Transepithelial electric resistance (TEER) and (B) apparent permeability coefficient (Papp) of EGCG in solution and EGCG O-D conjugate nanoparticles at 37oC. * indicate significant differences between nanoparticles and solutions at p ≤ 0.05. OBJECTIVE CONCLUSION In the present study, we applied the Maillard reaction to conjugate ovalbumin and dextran to form the O-D conjugates. Then, EGCG and O-D conjugates were self-assembled using a heating process to form EGCG O-D conjugate nanoparticles. Glutaraldehyde was used to cross-link ovalbumin in EGCG O-D conjugate nanoparticles. The aim of this study was to fabricate protein-polysaccharide nanoparticles with improved stability in the gastrointestinal tract and to enhance the absorption of loaded EGCG. Ovalbumin and dextran were conjugated using the Maillard reaction. EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles were formed using a heat-induced self-assembly. These particles showed a spherical morphology and had sizes of 285 nm and 339 nm in aqueous suspension. The loading efficiency of EGCG in these conjugate nanoparticles was 23.4% and 30.0%, whereas the loading capacity was 19.6% and 20.9%, respectively. EGCG O-D conjugate nanoparticles and cross-linked nanoparticles remained nano-sized in a pH range from 2.5 to 7.5, and the size remained stable in SGF and SIF. EGCG in EGCG O-D conjugate nanoparticles showed higher apparent permeability coefficient (Papp) on Caco-2 monolayers compared to EGCG solution. Particle size of EGCG O-D conjugate nanoparticles and cross-linked EGCG O-D conjugate nanoparticles in (A) simulated gastric fluid (SGF, pH 4.0) and (B) simulated intestinal fluid (SIF, pH 6.0) at 37oC for 0, 0.5, 1, 1.5, and 2 hour. Particle size and morphology of EGCG O-D conjugate nanoparticles (A1 and B1) and cross-linked EGCG O-D conjugate nanoparticles (A2 and B2).