Optoacoustic imaging identifies ovarian cancer using a microenvironment targeted theranostic wormhole mesoporous silica nanoparticle

At the intersection of the newly emerging fields of optoacoustic imaging and theranostic nanomedicine, promising clinical progress can be made in dismal prognosis of ovarian cancer. An acidic pH targeted wormhole mesoporous silica nanoparticle (V7-RUBY) was developed to serve as a novel tumor specif...

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Published inBiomaterials Vol. 182; pp. 114 - 126
Main Authors Samykutty, Abhilash, Grizzle, William E., Fouts, Benjamin L., McNally, Molly W., Chuong, Phillip, Thomas, Alexandra, Chiba, Akiko, Otali, Dennis, Woloszynska, Anna, Said, Neveen, Frederick, Peter J., Jasinski, Jacek, Liu, Jie, McNally, Lacey R.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.11.2018
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Abstract At the intersection of the newly emerging fields of optoacoustic imaging and theranostic nanomedicine, promising clinical progress can be made in dismal prognosis of ovarian cancer. An acidic pH targeted wormhole mesoporous silica nanoparticle (V7-RUBY) was developed to serve as a novel tumor specific theranostic nanoparticle detectable using multispectral optoacoustic tomographic (MSOT) imaging. We report the synthesis of a small, < 40 nm, biocompatible asymmetric wormhole pore mesoporous silica core particle that has both large loading capacity and favorable release kinetics combined with tumor-specific targeting and gatekeeping. V7-RUBY exploits the acidic tumor microenvironment for tumor-specific targeting and tumor-specific release. In vitro, treatment with V7-RUBY containing either paclitaxel or carboplatin resulted in increased cell death at pH 6.6 in comparison to drug alone (p < 0.0001). In orthotopic ovarian xenograft mouse models, V7-RUBY containing IR780 was specifically detected within the tumor 7X and 4X higher than the liver and >10X higher than in the kidney using both multispectral optoacoustic tomography (MSOT) imaging with secondary confirmation using near infrared fluorescence imaging (p < 0.0004). The V7-RUBY system carrying a cargo of either contrast agent or an anti-neoplastic drug has the potential to become a theranostic nanoparticle which can improve both diagnosis and treatment of ovarian cancer.
AbstractList At the intersection of the newly emerging fields of optoacoustic imaging and theranostic nanomedicine, promising clinical progress can be made in dismal prognosis of ovarian cancer. An acidic pH targeted wormhole mesoporous silica nanoparticle (V7-RUBY) was developed to serve as a novel tumor specific theranostic nanoparticle detectable using multispectral optoacoustic tomographic (MSOT) imaging. We report the synthesis of a small, < 40 nm, biocompatible asymmetric wormhole pore mesoporous silica core particle that has both large loading capacity and favorable release kinetics combined with tumor-specific targeting and gatekeeping. V7-RUBY exploits the acidic tumor microenvironment for tumor-specific targeting and tumor-specific release. In vitro, treatment with V7-RUBY containing either paclitaxel or carboplatin resulted in increased cell death at pH 6.6 in comparison to drug alone (p < 0.0001). In orthotopic ovarian xenograft mouse models, V7-RUBY containing IR780 was specifically detected within the tumor 7X and 4X higher than the liver and >10X higher than in the kidney using both multispectral optoacoustic tomography (MSOT) imaging with secondary confirmation using near infrared fluorescence imaging (p < 0.0004). The V7-RUBY system carrying a cargo of either contrast agent or an anti-neoplastic drug has the potential to become a theranostic nanoparticle which can improve both diagnosis and treatment of ovarian cancer.
Author McNally, Molly W.
Chuong, Phillip
Grizzle, William E.
Liu, Jie
McNally, Lacey R.
Chiba, Akiko
Otali, Dennis
Samykutty, Abhilash
Fouts, Benjamin L.
Thomas, Alexandra
Woloszynska, Anna
Said, Neveen
Frederick, Peter J.
Jasinski, Jacek
AuthorAffiliation Department of Pathology, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, United States of America
Department of Hematology and Oncology, Wake Forest School of Medicine, Winston-Salem, NC 27013, United States of America
β Department of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, NY 14263, United States of America
Department of Chemistry, Earlham College, Indianapolis, IN, 27013, United States of America
Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina 27013, United States of America
α Department of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY 14263, United States of America
Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America
Conn Center Materials Characterization, University of Louisville, Louisville, KY 40202, United States of America
Department of Forest Materials, North Carolina State University, Raleigh, NC 27695, United States
AuthorAffiliation_xml – name: Department of Pathology, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, United States of America
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– name: Department of Hematology and Oncology, Wake Forest School of Medicine, Winston-Salem, NC 27013, United States of America
– name: Conn Center Materials Characterization, University of Louisville, Louisville, KY 40202, United States of America
– name: π Department of Surgery, Wake Forest School of Medicine, Winston-Salem, NC 27013, United States of America
– name: α Department of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY 14263, United States of America
– name: Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America
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  organization: Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC 27013, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30118979$$D View this record in MEDLINE/PubMed
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Keywords Mesoporous silica nanoparticle
Asymmetric wormhole pore
Multispectral optoacoustic tomography
Extracellular pH
Ovarian cancer
Theranostic nanoparticle
Language English
License Copyright © 2018 Elsevier Ltd. All rights reserved.
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Notes Author Contributions
A.S., B.F., and P.C. synthesized nanoparticles and performed the physical characterization of the nanoparticles. J. J and J. L conducted additional physical characterization analysis of the particles. A.S, B.F, M.M., W.G., D.O., A.C., A. W-R, and N.S. performed in vitro studies. A.S. and L.M. developed the animal model and performed the imaging studies. L.M. and A.S. performed in vivo data analysis. A.C, A.T., and P.F. provided clinical expertise. L.M. supervised the project. All authors contributed to the discussion of the manuscript. A.S. and L.M. wrote the manuscript and edited by M.M., W.G. A.C., A.T., A. W-R., P.F., and L.M.
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Snippet At the intersection of the newly emerging fields of optoacoustic imaging and theranostic nanomedicine, promising clinical progress can be made in dismal...
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SubjectTerms Animals
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - pharmacokinetics
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Asymmetric wormhole pore
Carboplatin - administration & dosage
Carboplatin - pharmacokinetics
Carboplatin - pharmacology
Carboplatin - therapeutic use
Cell Line, Tumor
Extracellular pH
Female
Humans
Mesoporous silica nanoparticle
Mice
Mice, Nude
Multispectral optoacoustic tomography
Nanoparticles - chemistry
Ovarian cancer
Ovarian Neoplasms - diagnostic imaging
Ovarian Neoplasms - drug therapy
Ovarian Neoplasms - pathology
Paclitaxel - administration & dosage
Paclitaxel - pharmacokinetics
Paclitaxel - pharmacology
Paclitaxel - therapeutic use
Photoacoustic Techniques - methods
Porosity
Silicon Dioxide - chemistry
Theranostic Nanomedicine - methods
Theranostic nanoparticle
Tomography - methods
Tumor Microenvironment - drug effects
Title Optoacoustic imaging identifies ovarian cancer using a microenvironment targeted theranostic wormhole mesoporous silica nanoparticle
URI https://dx.doi.org/10.1016/j.biomaterials.2018.08.001
https://www.ncbi.nlm.nih.gov/pubmed/30118979
https://pubmed.ncbi.nlm.nih.gov/PMC6289590
Volume 182
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