multilayered nanoparticles for drug/gene delivery … nanoparticles for drug/gene delivery in...
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Multilayered Nanoparticles for Drug/Gene Delivery in Nanomedicine
OSC Drug Delivery Workshop
November 14, 2005
James F. Leary, Ph.D.SVM Professor of Nanomedicine
Professor of Basic Medical Sciences and Biomedical EngineeringMember: Purdue Cancer Center; Oncological Sciences Center;
Bindley Biosciences Center; Birck Nanotechnology CenterPurdue University, W. Lafayette, IN 47907
Email: [email protected]
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Our Goal is to Design Autonomous Nanomedical Systems
Definition: Self-guiding, adaptive, multicomponent systems on the nanoscale for diagnostic and therapeutic prevention or treatment of disease
Value: These “smart” nanomedical systems can deal with changing conditions, are error-correcting, and can provide proper dose of therapeutic response on a cell-by-cell basis
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Nanomedicine Conceptof Regenerative Medicine
“Fixing cells one cell at-a-time”• Conventional cancer therapies try to cut out the bad
cells (surgery), burn them out (radiation therapy), or poison the bad cells faster than the good cells (chemotherapy)! Conventional medicine removes diseased cells and does not attempt to fix them.
• Nanomedicine attempts to make smart decisions to either remove specific cells by induced apoptosis or repair them one cell-at-a-time (regenerative medicine). Single cell treatments will be based on molecular biosensor information that controls subsequent drug delivery to that single cell.
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What is Nanomedicine?Beyond the obvious application of nanotechnology to medicine, the
approach is fundamentally different than conventional medicine:Nanomedicine uses “nano-tools” (e.g. smart nanoparticles) that are roughly 1000 times smaller than a cell (knives to microsurgery to nanosurgery … )Nanomedicine is the treatment or repair (regenerative medicine, not just killing of diseased cells) of tissues and organs, WITHINindividually targeted cells, cell-by-cell (a nano “bottoms up”, rather than top-down approach)Nanomedicine typically combines use of molecular biosensors to provide for feedback control of treatment and repair. Most conventional medicine does not use feedback control. Drug use istargeted and adjusted appropriately for individual cell treatment at the proper dose for each cell (single cell medicine).
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YY
Y
Y
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Y
YY Y Y Cell targeting and entry
Intracellular targeting
Biomolecular sensing
Gene/drug delivery
Concept: Smart Boolean Targeted, Programmed Sequence of Events, Multilayered Nanomedicine Systems with
Biomolecular Sensors for Feedback Control of Gene/Drug Delivery within Single Cells
Y
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YY Y
Y Targeting molecules (e.g. an antibody, an DNA, RNA or peptide sequence, a ligand, a thioaptamer), in Boolean combinations for more precise nanoparticle delivery
Biomolecular sensors
Leary and Prow, US Patent pending 2004
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Biodegradable Biodegradable ““nanocapsulesnanocapsules””
Semiconductor Semiconductor nanocrystals or nanocrystals or
““Quantum DotsQuantum DotsTMTM””(Ref: Clark et al., 2004 submitted)
(Courtesy: Dr. Yuri Lvov)
Nanocrystals or Nanocapsules for Nanomedicine?
OR
Probable answer: Nanocrystals for ex-vivo optical diagnostics and some form of hybrid biodegradable nanocapsule with MRI contrast agent core for in-vivo simultaneous diagnostics and therapeutics (“theragnostics”).
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Example: Targeted Nanocrystal Delivery
14nm
HIV tat
Anti-CD95Naked
6xArg
14nm
Streptavidin coated nanocrystals;EM courtesy of Dr. Popov
Strept-avidin
Strept-avidin
Nanocrystals coated with nothing, anti-CD95, HIV tat fragment, or a 6xArg peptide were incubated with live cells for 1 hour and imaged with confocal microscopy:
Blue = Hoechst 33342, DNAGreen = NanocrystalsThese are composite images including Nomarski scattering
Copyright: Tarl Prow, Ph.D. Thesis (Leary lab) 2004
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Nanocapsule technology: LBL Assembly by Alternate Adsorption of Oppositely Charged Linear
Polyions and Nanoparticles or Proteins
The LBL-assembly regimes for more than 40 different compounds have been established.
LBL (layer-by-layer) self-assembly
Work with collaborator: Dr. Yuri Lvov
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A New and Better Approach to Nanocapsule Assembly?
Covalently Linked Biopolymers for Layer-by-Layer Assembly and Cleavable Layer-
by-Layer Disassembly
Desired result: Stable, reproducible, long-term biocompatible, multilayered
nanoparticles
A new collaboration at Purdue with Dr. Don Bergstrom…
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A New Approach to Nanocapsule Targeting to Cells
Use 50-60 nt dsDNA aptamer molecules for cell targeting. Aptamers are (1) much smaller than antibodies, (2) have lower immunogenicity in-vivo, and (3) allow biodistribution studies of nanoparticles (NP) to single NP level using PCR amplification of NP-attached aptamers labeled with reporter molecules
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Example: Design and Construction of Multilayered Nanoparticle Systems
Ref: Prow, TW, Kotov, N.A., Lvov, Y.M., Rijnbrand, R., Leary, J.F. “Nanoparticles, Molecular Biosensors, and Multispectral Confocal Microscopy”Journal of Molecular Histology, Vol. 35, No.6, pp. 555-564, 2004
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The Challenge: Optimal Drug Delivery to the Single Cell
A potential solution: Delivery a drug manufacturing (in-situ) factory, not a drug. Then manufacture exactly the optimal amount for that particular cell under feedback control of an upstream molecular biosensor.
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From the Greek “bios” = life and “mimesis” = imitation…
“Biomimicry is a new science that studies nature’s models and then imitates or takes inspiration from these designs and processes to solve human problems.”[from the preface of Biomimicry]
Biomimicry Biomimicry –– Can Nature Provide Can Nature Provide Some of the Answers?Some of the Answers?
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Concept of nanoparticle-based “nanofactories”(NF) manufacturing therapeutic genes inside living
cells for single cell treatments
cell membrane
Multilayered nanoparticle
The nanoparticle delivery system delivers the therapeutic gene template which uses the host cell machinery and local materials to manufacture therapeutic gene sequences that are expressed under biosensor-controlled delivery.
nucleus
cell
cytoplasm
Therapeutic gene
Biosensor control
YYYYYYYYYYYY
YYY
NF
NF
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Concept of nanoparticle-based “nanofactories”(NF) manufacturing therapeutic genes inside living
cells for single cell treatments
cell membrane
Multilayered nanoparticle
The nanoparticle delivery system delivers the therapeutic gene template which uses the host cell machinery and local materials to manufacture therapeutic gene sequences that are expressed under biosensor-controlled delivery.
nucleus
cell
cytoplasm
Therapeutic gene
Biosensor control
YYYYYYYYYYYY
YYY
NF
NF
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Data:Single-Cell HCV Antiviral Ribozyme(Rz)Therapy
A: DNA staining (blue) of nuclei; B: HCV biosensor staining green) C. HCV NSE protein staining (red) D: Composite image A-C
(1= Untreated cell) (2= Rz treated cell)
1 1
1
2 2
2
Result: Rz treated cell # 2 shows decrease in HCV NSE protein (red)
1 2
A B
D
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D.D.
A.A. B.B.
C.C.
Feasibility Study: Nanocapsule delivery of two reporter gene plasmids for possible binary transient gene therapy
Plasmid-transfected
Nanocapsule-transfected
Copyright: Tarl Prow, Ph.D. Thesis (Leary lab) 2004
Delivery of 2 different plasmids with lipid coated LBL. Huh-7 cells (Panels A. and B.) were transfected with a 1:1 mixture of pEGFP-C1 and pdsRed2-C1 or exposed to ~100nm layer-by-layer (LB) assembled nanocapsules containing a single layer of DNA (1:1 mixture of pEGFP-C1 and pdsRed2-C1) (Panels C. and D.). Although the transfection efficiency was low, there were cells expressing both EGFP (green) and dsRed (red) protein. All cells were counterstained with DAPI (blue).
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High-throughput Cell Separation for Delivery of Highly Enriched Cell Subpopulations for Gene Expression Microarray Analysis of Nanoparticle-Treated Cells
Fluorescence collection optics of LEAP instrument
Shooting at cells inside 384-well plates to eliminate undesired cells and capture desired cells for subsequent gene expression microarray analysis
LEAP™ (Laser-Enabled Analysis and Processing) has throughputs greater than 100,000 events/sec, high cell purity, yield and viability. It can process several cells or a billion cells with an expanded cell range including fragile cells. Another advantage is that it can analyze and purify biohazardous cells without generating aerosols .
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Voyage of the Nano-Surgeons
NASA-funded scientists are crafting microscopic vessels that can venture into the
human body and repair problems – one cell at a time.
January 15, 2002: It's like a scene from the movie "Fantastic Voyage." A tiny vessel -- far smaller than a human cell -- tumbles through a patient's bloodstream, hunting down diseased cells and penetrating their membranes to deliver precise doses of medicines.
Only this isn't Hollywood. This is real science.
Right: Tiny capsules much smaller than these blood cells may someday be injected into people's bloodstreams to treat conditions ranging from cancer to radiation damage. Copyright 1999, Daniel Higgins, University of Illinois at Chicago.
http://science.nasa.gov/headlines/y2002/15jan_nano.htm
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Nanomedicine - Continuous Therapy for Preventing Cancer in Astronauts
Engineered multilayered nanoparticles targeted to radiation-damaged cells can initiate repair of damaged DNA using DNA repair genes manufactured inside individual living cells under the control of molecular biosensor switches.
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Nanomedicine for Prevention of Radiation-Induced Cancer in Astronauts
Targeted nanoparticles
Seek out radiation-damaged cells
Cell entry and gene delivery
Expression of radiation-damage
biosensor
Expression of biosensor
Does the cell show signs of radiation-induced stress?
No Yes
Express therapeutic (DNA repair)
genes
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Nanoparticle Targeting Data
Conventional antibody labeling
Nanoparticle labeling
Note: Nuclei of cells are counter-stained blue with a DNA dye
Targeting strategies already developed can detect one rare cell in a million other cells (similar to the expected frequency of cancer cells in astronauts exposed to space radiation)
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Concept: Ionizing Radiation Activates Biosensor Mediated DNA Repair
Enzyme Expression
Irradiation
Normal Cell
Irradiated CellWith DNADamage
Cell WithRepaired DNA
Transcription of DNA Repair Enzymes Initiated by ARE Complex Binding
DNA repairX
No transcription of DNA repair enzymes in normal cells
Sequence to produce DNA repair
enzymeARE
biosensor Expression
Copyright: Tarl Prow, Ph.D. Thesis (Leary lab) 2004
ARE proteins
ARE proteins
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Data: ROS Activated Biosensor in Living Human Cells
Time (hrs): 0 24 60
Unstressed cells Stressed cellsFluorescence photographed
Treatment:
(No biosensors)ARE-GFP+(ARE biosensor
fluoresces green in the presence of ARE
stress proteins)
Methods: Cells were transfected with either ARE-GFP (stress biosensor) or TK-GFP (a control gene). 24 hours later the cells were stressed with a chemical to simulate space radiation stress. The cells were examined every 12 hours post treatment. Weak fluorescence was present at hour 48 and at hour 60 photographs were taken.
Source: Tarl Prow, Ph.D. Thesis(Leary lab) 2004
Stressed cells Control cellsControl cells
ARE-GFP+ARE biosensor background in unstressed cells
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Feasibility example: Production and testing of novel UV-damage specific DNA repair
enzymes with intracellular targeting sequences
1) Create genetically-modified DNA repair proteins that are specifically targeted to the cell’s nucleus or mitochondria to initiate repair at UV-induced DNA damage sites
a) Nuclear localization signals PKKRKRRL and PKKKRKRL at the C-terminus
b) Mitochondrial targeting sequence MALHSMRKARERWSFIRA and MGVFCLGPWGLGRKLRTFGKGPLQLLSRLCGDHLQ at the N-terminus
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T4 transfected DNA repair enzyme with no localization anchoring sequence, with transient expression
Wt-T4-PDG-GFP in CHO-XPG. Transient expression. 100x objective
Feasibility Results: Human cells transiently or stably transfected with missing DNA repair enzyme
T4 transfected DNA repair enzyme with mitochondrial localization anchoring sequence, with transient expression
MLS35-T4-PDG-GFP in CHO XPG. 100x objective
T4 transfected DNA repair enzyme with mitochondrial localization anchoring sequence, with stable expression
MLS18-T4-PDG-GFP in hXPA. 100x objective
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Feasibility Example: A Strategy for accelerating DNA repair in human cells• In humans, there is ONLY ONE mechanism to repair UV-induced damage to DNA
– Immune system suppressed 8-24 hrs.– DNA damage removal takes 24-48 hrs.
• However, simpler organisms have TWO and sometimes THREE repair systems• One of these repair systems is partially present in humans, BUT we are MISSING the
FIRST STEP
PCNAFEN-1POL β or δ/εLIG ILigIII/XRCC1
GLYCOSYLASE
AP LYASEAP ENDONUCLEASE
POLβLIGILigIII/XRCC1
OH^
XXUV Humans are
missing this repair enzyme which can be transfected into human cells
• Using nanoparticle/biosensor technology we can supply thismissing first step to enhance DNA repair in human cells
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T4 treatedNo T4 treatment
Un-irrad
20 J 0h
20 J 6h
Hxpa DNA repair-deficient human cells NLSI DNA repairable-human cellsNo T4 treatment T4 treated
Note: Comet streaks show attempts to repair DNA damage which should be completed in about 6 hours as opposed to normal 72 hours. NLSI cells successfully repair, control Hxpa cells do not.
Feasibility Results: DNA comet assays show evidence of accelerated DNA repair in transfected human cells
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Our MCF Team and Current CollaboratorsMolecular Cytometry Facility
(MCF)Director: James Leary
--------------------------------------------------UTMB
Jacob Smith* – mathematics and scientific programming Tarl Prow** – nanotechnology; confocal microscopy; molecular biosensors for HCVPeter Szaniszlo – HHV6/HIV; stem cells; microgenomics (UTMB)Nan Wang – cell culture, molecular biology assays (UTMB)Bill Rose–nanocapsule design (UTMB)------------------------------------------------
PurdueLab Dir: Lisa Reece – flow cytometry/ cell-bead sorting for proteomicsChristy Cooper- bioanalytical chemistry of nanocapsulesMeggie Grafton (Purdue) -BioMEMSEmily Haglund (Purdue)-nanocapsulesMary-Margaret Seale (Purdue) -nanocapsulesMichael Zordan (Purdue) - LEAP technology
Mathematics/StatisticsJames Hokanson*** (UTMB)Judah Rosenblatt (UTMB)Seza Orcun (Purdue)
Combinatorial chemistry/aptamersDavid Gorenstein (UTMB)Xianbin Yang (UTMB)Cagri Savran (Purdue)
BioinformaticsBruce Luxon (UTMB)Seza Orcun (Purdue)
Confocal ImagingMassoud Motamedi (UTMB)Gracie Vargas (UTMB)Paul Robinson (Purdue)
DNA RepairStephen Lloyd (Oregon Health Sciences Center)
ProteomicsAlex Kurosky (UTMB)Jo Davisson (Purdue)
Nanocrystal technologyNick Kotov (Univ. Michigan)Jo Davisson (Purdue)
Nanocapsule technologyYuri Lvov (Louisiana Tech U)Don Bergstrom (Purdue)Kinam Park (Purdue)
Microfluidics/engineeringRashid Bashir (Purdue)
LEAP technologyFred Koller (Cyntellect, Inc.San Diego, CA)
In-vivo retinal imaging Gerald Lutty group(Johns Hopkins Univ.)
* Texas A&M University
** Johns Hopkins University
*** recently deceased
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Leary, JF "Rare Event Detection and Sorting of Rare Cells" In: Emerging Tools for Cell Analysis: Advances in Optical Measurement Technology, Eds. G. Durack and J.P. Robinson, pp 49-72, 2000.Leary, JF, Reece, LM, Hokanson, JA, Rosenblatt, JI “Advanced “Real-time” Classification Methods for
Flow Cytometry Data Analysis and Cell Sorting” Proc. SPIE 4622: 204-210, 2002Prow, TW, Salazar, JH, Rose, WA, Smith, JN, Reece, LM, Fontenot, AA, Wang, N, Lloyd, RS, Leary, JF
"Nanomedicine – nanoparticles, molecular biosensors and targeted gene/drug delivery for combined single-cell diagnostics and therapeutics" Proc. SPIE 5318: 1-11, 2004.Szaniszlo, P, Wang, N, Sinha, M, Reece, LM, Van Hook, JW, Luxon, BA, Leary, JF "Getting the Right
Cells to the Array: Gene Expression Microarray Analysis of Cell Mixtures and Sorted Cells" Cytometry 59A: 191-202, 2004.Prow, TW, Kotov, NA, Lvov, YM, Rijnbrand, R, Leary, JF “Nanoparticles, Molecular Biosensors, and
Multispectral Confocal Microscopy” Journal of Molecular Histology, Vol. 35, No.6, pp. 555-564, 2004.Prow, TW, Rose, WA, Wang, N, Reece, LM, Lvov, Y, Leary, JF "Biosensor-Controlled Gene
Therapy/Drug Delivery with Nanoparticles for Nanomedicine" Proc. of SPIE 5692: 199 – 208, 2005.Leary, JF "Ultra High Speed Cell Sorting" Cytometry 67A:76–85, 2005Szaniszlo, P, Rose, WA, Wang, N, Reece, LM, Tsulaia, TV, Hanania, EG, Elferink, CJ, Leary, JF
“Scanning Cytometry with a LEAP: Laser-Enabled Analysis and Processing of Live Cells In Situ”Cytometry (In Press). Prow, T.W., Grebe, R., Merges, C., Smith, J.N., McLeod, D.S., Leary, J.F., Gerard A. Lutty, G.A. "Novel
therapeutic gene regulation by genetic biosensor tethered to magnetic nanoparticles for the detection and treatment of retinopathy of prematurity" Molecular Vision (in review) 2005Prow, T.W., Smith, J.N., Grebe, R., Salazar, J.H., Wang, N., Kotov, N., Lutty, G., Leary, J.F.
"Construction, Gene Delivery, and Expression of DNA Tethered Nanoparticles" Molecular Vision (in review) 2005Leary, J.F. and Prow, T.W. Multilayered Nanomedicine Delivery System and Method PCT/US05/06692
March 4, 2005.
A Few Relevant Recent References